Patent Grant
11417506
Embodiments disclosed herein relate to an apparatus including a thermal energy harvesting thermionic device integrated with at least one electronic component, and in one or more particularly exemplary embodiments a unitary apparatus including the thermal energy harvesting thermionic device and the at least one integrated electronic component. Also provided are related systems and methods, including systems incorporating the apparatus and methods of making and using the apparatus.
Existing electrochemical technologies, such as lithium-ion, lead-acid, and nickel-cadmium battery technology, have performance limitations and are burdened by limited operational durations due to limited energy storage. Further, existing electrochemical technologies include hazardous material subject to sometimes onerous handling, shipping, and disposal requirements. Furthermore, electrochemical technologies are also constrained by battery service and shelf-life limitations, particularly caused by electrochemical degradation under mechanical stress, and charge and discharge rates that limit operational lifetime.
The embodiments include systems, apparatus, and methods that involve a thermal energy harvesting thermionic device and at least one electronic component.
In an aspect, an apparatus is provided that includes an electronics layer comprising at least one electronic component, a thermal energy harvesting thermionic device to receive thermal energy and generate an electrical output for powering the at least one electronic component, and an intermediate layer positioned between the thermal energy harvesting thermionic device and the electronics layer. The thermionic device comprises a cathode, an anode spaced from the cathode, and a plurality of nanoparticles in at least one medium between the cathode and the anode to permit electron transfer between the cathode and the anode. The intermediate layer comprises a gradient thermal expansion material (TEM), and has a first surface with a first coefficient of thermal expansion (CTE) facing the thermal energy harvesting thermionic device, and a second surface with a second CTE facing the electronics layer. The first CTE is quantitatively closer than the second CTE to a CTE of a first surface of the thermal energy harvesting thermionic device facing the first surface of the intermediate layer. The second CTE is quantitatively closer than the first CTE to a CTE of a surface of the electronics layer facing the second surface of the first intermediate layer.
Another aspect provides a system comprising an apparatus and an electrically conductive path. The apparatus comprises an electronics layer comprising at least one electronic component, a thermal energy harvesting thermionic device configured to receive thermal energy and generate an electrical output for powering the at least one electronic component, and an intermediate layer. The thermal energy harvesting thermionic device comprises a cathode, an anode spaced from the cathode, and a plurality of nanoparticles in at least one medium between the cathode and the anode. The nanoparticles are configured to permit electron transfer between the cathode and the anode. The intermediate layer is positioned between the thermal energy harvesting thermionic device and the electronics layer. The intermediate layer comprises a gradient thermal expansion material (TEM). The intermediate layer has a first surface with a first coefficient of thermal expansion (CTE) facing the thermal energy harvesting thermionic device, and a second surface with a second CTE facing the electronics layer. The first CTE is quantitatively closer than the second CTE to a CTE of a first surface of the thermal energy harvesting thermionic device facing the first surface of the intermediate layer. The second CTE is quantitatively closer than the first CTE to a CTE of a surface of the electronics layer facing the second surface of the intermediate layer. The electrically conductive path is configured to electrically couple the thermal energy harvesting thermionic device and the at least one electronic component of the electronics layer.
In another aspect, a method is provided that includes providing an apparatus. In an embodiment of the method, an electronics layer comprising at least one electronic component is electrospray deposited. A thermal energy harvesting thermionic device is electrospray deposited. The thermal energy harvesting thermionic device comprises a cathode, an anode spaced from the cathode, and a plurality of nanoparticles in at least one medium contained between the cathode and the anode. The nanoparticles are configured to permit electron transfer between the cathode and the anode. An intermediate layer is electrospray deposited. The intermediate layer is positioned in the apparatus between the thermal energy harvesting thermionic device and the electronics layer. The intermediate layer comprises a gradient thermal expansion material (TEM). The intermediate layer has a first surface with a first coefficient of thermal expansion (CTE) facing the thermal energy harvesting thermionic device, and a second surface with a second CTE facing the electronics layer. The first CTE is quantitatively closer than the second CTE to a CTE of a first surface of the thermal energy harvesting thermionic device facing the first surface of the intermediate layer. The second CTE is quantitatively closer than the first CTE to a CTE of a surface of the electronics layer facing the second surface of the intermediate layer.
Other aspects disclosed herein include systems, devices, components, apparatus, methods, and processes. Features of these and other aspects will become apparent from the following detailed description of exemplary embodiments, taken in conjunction with the accompanying drawings.
The drawings referenced herein form a part of and are incorporated into the specification. Features shown in the drawings are meant as illustrative of only some embodiments, and not of all embodiments, unless otherwise explicitly indicated.
It will be readily understood that the components and features of the exemplary embodiments, as generally described herein and illustrated in the Figures, may be arranged and designed in a wide variety of different configurations. Thus, the following detailed description of the embodiments of the methods, devices, assemblies, apparatus, systems, compositions, etc. of the exemplary embodiments, as presented in the Figures, is not intended to limit the scope of the embodiments, as claimed, but is merely representative of selected embodiments.
The illustrated embodiments will be best understood by reference to the drawings, wherein like parts are designated by like numerals throughout. The following description is intended only by way of example, and illustrates certain selected embodiments of methods, devices, assemblies, apparatus, systems, etc. that are consistent with the embodiments as claimed herein.
Reference throughout this specification to “a select embodiment,” “one embodiment,” “an exemplary embodiment,” or “an embodiment” means that a particular feature, structure, or characteristic described in connection with the embodiment is included in at least one embodiment. Thus, appearances of the phrases “in a select embodiment,” “in one embodiment,” “in an exemplary embodiment,” or “in an embodiment” in various places throughout this specification are not necessarily referring to the same embodiment. The embodiments may be combined with one another in various combinations and modified to include features of one another.
Referring now more particularly to
System (102)
The system (102) may be in the form of a physical device, apparatus, machine, or equipment configured for use in a commercial or domestic domain. In exemplary embodiments, the system (102) may be embodied as or in a mobile telephone, cordless telephone, a consumer electronics device, a portable electronic device, a computer such as a laptop computer and a tablet computer, a personal digital assistant (PDA), a portable radio, a power tool, a watch, a calculator, a game system or controller, a camera, a video recorder, a portable television, a global positioning system (GPS), a data transfer device, a home-consumer appliance, a light source or system, a home product, a toy, headphones, a DVD or CD player, a MP3 player, a voice recorder, a sensor, a controller, a grooming instrument, an alarm system, a weapon such as a stun gun, a backup power source, military equipment, emergency equipment, utility equipment, vehicle control system, a telecommunication device, etc.
The system (102) is shown with an external (or system) housing (104). The system housing (104) can be made of any suitable material, including, for example, metal, plastic, composite, or aerogel material, or any combination thereof. The system housing (104) defines one or more compartments or cavities (106). Although
Many systems are conveniently cooled by natural convection and radiation or through the use of fluid movers, e.g., fans, especially fans internal to a system housing, such as the housing (104). In an embodiment, natural convection cooling is desirable, since natural convection cooling does not involve fans that may break down or consume harvested energy. Natural convection is based on fluid motion caused by density differences driven by a temperature difference. To promote natural convection cooling, the system housing (104) is depicted in
The compartment (106) contains several components, including an apparatus (110), an electrical conductive path (130), a heat-dissipation device (also referred to herein as a heat dissipation device (134)), a fluid-circulating device (136), a heat shield (150), an energy storage device (e.g., capacitor) (152), a controller (154), a temperature sensor (156), a switch (158), and a heat source (160). The system (102) may include fewer components than shown in
Each of the above-mentioned components will be described in greater detail below.
Apparatus (110)
The apparatus (110) includes a plurality of layers, including but not limited to, a substrate (122), a thermal energy harvesting thermionic device (114), a first intermediate layer (124), a second intermediate layer (126), and electronics layer (128) including at least one electronic component. As described herein, the first and second intermediate layers (124) and (126), respectively, are thermal expansion layers. It should be understood that the apparatus (110) may include additional or fewer layers than shown in
In an exemplary embodiment, the substrate (122), the first intermediate layer (124), second intermediate layer (126), the cathode (116), the anode (118) and the spacer (120) of the thermionic device (114), the and the electronics layer (128) are manufactured or made as a one-piece or unitary “printed” apparatus involving use of an electrospray apparatus, as discussed in further detail below, including with reference to
The apparatus (110) also includes an apparatus housing (112). In an embodiment, the apparatus housing (112) encloses the substrate (122), the first and second intermediate layers (124) and (126), respectively, the electronics layer (128), and the thermionic device (114). In an alternative embodiment, the apparatus housing (112) may enclose one or more but fewer than all of the substrate (122), the first and second intermediate layers (124) and (126), respectively, the electronics layer (128), and the thermionic device (114).
According to an exemplary embodiment, the apparatus housing (112) is made of an aerogel material. However, the housing (112) may be made of other materials, whether conductive, semi-conductive, or insulating. Representative materials include metals, alloys, plastics, glass, etc.
Thermal Energy Harvesting Thermionic Device (114)
The thermal energy harvesting thermionic device (114), shown in greater detail in
Exemplary embodiments of spacers are discussed below with reference to
As best shown in
The thermal energy harvesting thermionic device (114) operates on a thermionic power conversion principle to convert the thermal energy (162) supplied by the heat source (160) into electrical energy (electricity) by an emission of electrons from the cathode (116), which is also referred to herein as an emitter electrode. The production of electrons from the cathode (116) is controlled by barriers to the flow of electricity. The first barrier to be overcome involves establishing electron energy that is sufficiently large to exceed the work function of the cathode (116) to enable electron emission from a surface of the cathode (116), such as the second surface (116B) of the cathode (116). At lower temperatures, only a fraction of the electrons have sufficient energy to allow thermionic emission to proceed, thus limiting current flow. Intermediate and elevated temperatures provide higher energy than lower temperatures, with the intermediate temperatures giving rise to an increase in electron production at the second surface (116B) of the cathode (116) due to an increased or larger distribution of electrons with the required energy for emission. As kinetic energy of the electrons is dependent upon the temperature of the cathode (116), increasing the temperature of the cathode (116) (e.g., with a heat source such as (160)), results in an increase in electron emission, and hence electrical current.
The electrons emitted from the cathode (116) effectively cool the cathode (116) in a similar way that rain evaporating from roof carries away heat. The “hot” electrons emitted by the cathode (116) pass through the nano-fluid in the spacer (120) and heat the anode (118), which is also referred to herein as a collector electrode. This movement of electrons sets up a thermal gradient for a nanoscale heat engine.
Electrons flow from the cathode/emitter electrode (116), across the nano-fluid in the spacer (120), to the anode/collector electrode (118). As shown, the anode (118) is spaced from the cathode (116) by an inter-electrode gap containing the spacer (120). As mentioned above, a medium is contained in the spacer (120). The medium is in contact with facing surfaces (116B) and (118A) of the cathode (116) and the anode (118), respectively. According to an exemplary embodiment, the medium contains suspended nanoparticles to permit electron transfer between the cathode (116) and the anode (118). Thermal processes which involve the transport of the electrons across the nano-fluid in the electrode gap (without, or in an embodiment with minimal, resistively heating the nano-fluid) involve movement of nanoparticles within the medium in the spacer (120) to come close together or collide with each other and with the facing surfaces (116B) and (118A) of the electrodes (116) and (118), respectively. These collisions enable the hopping or transition of electrons in the direction of the electric field (i.e., current production). A reverse production of electrons from the anode (118) to the cathode (116) is suppressed by the electric field. In an embodiment, the electric field is supplied by the use of dissimilar electrode materials, e.g. metals, graphene, etc. The transmission of the electrons across the gap from the cathode (116) (emitter electrode) to the collector (118) (anode electrode) creates a flow of electrical energy, and when connected to a circuit, enables electrons to pass through an electrical load completing the circuit. Although not shown in the accompanying drawings, electrical current from the thermal energy harvesting thermionic device (114) to the load, e.g., the electronic component, via the electrical conductive path (130) may be smoothed via, for example, a trimming capacitor.
Recent improvements in thermionic power converters pertain to material selection based on work functions and corresponding work function values for the electrodes and using a fluid to fill the inter-electrode gap. Electron transfer density is limited by the materials of the electrodes and the materials of the fluid in the inter-electrode gap (i.e., the associated work functions). Representative and exemplary materials, features, conditions, etc. associated with thermal energy harvesting thermionic devices are described in further detail below, including in connection with
As noted, thermal energy causes electrons to flow from the cathode (116) to the anode (118). Accordingly, the heat source (160) is placed in closer proximity to the cathode (116) than the anode (118) of the thermal energy harvesting thermionic device (114) in an exemplary embodiment.
While in exemplary embodiments described above, the thermal energy harvesting thermionic device (114) harvests thermal energy from the heat source (160), in exemplary embodiments the thermionic device (114) also harvests ambient heat from air and uses the ambient heat to generate additional electricity. Additionally, excess electricity may be stored in a capacitor or other energy storage device (152) to meet varying demands for power for activating the heat source (160).
Substrate (122)
As best shown in
Electronics Layer (128)
As best shown in
Intermediate (Thermal Expansion) Layers (124) and (126)
The first intermediate layer (124), also referred to herein as a first thermal expansion layer, includes a first surface (124A) and an opposite second surface (124B). The first surface (124A) of the first intermediate layer (124) interfaces with a second surface (118B) of the anode (118). Surface (118B) is also referred to herein as a first surface of the thermal energy harvesting thermionic device (124). The second surface (124B) of the first intermediate layer (124) interfaces with the first surface (128A) of the electronics layer (128).
The first surface (124A) and the second surface (124B) of the first intermediate layer (124) have a first coefficient of thermal expansion (CTE) and a second CTE, respectively. In an embodiment, the first intermediate layer (124) is referred to as having a gradient CTE extending between the first and second surfaces (124A) and (124B), respectively. Measurement of the CTE of a surface shall be understood to mean the CTE of the material of which the surface is made. For example, the CTEs of the first surface (124A) and the second surface (124B) of the first intermediate layer (124) should be understood to mean the CTE of a first material of which the first surface (124A) is made and the CTE of a second material of which the second surface (124B) is made, respectively. Either linear coefficient of thermal expansion (LCTE) or volumetric coefficient of thermal expansion (VCTE) may be used for the various embodiments described herein. Further, the thermal expansion coefficient may be based on degrees Celsius, Kelvin, or Fahrenheit. Unless specified, the CTE is assumed to be the average linear coefficient of thermal expansion over the temperature range 20-300° C. and is expressed in terms of ppm/° C., and should be determined using a push-rod dilatometer in accordance with ASTM E228-11.
According to an exemplary embodiment, the first CTE of the first surface (124A) is quantitatively closer than the second CTE to a CTE of the first surface (118B) of the thermal energy harvesting thermionic device (114) positioned proximal to the first surface (124A) of the first intermediate layer (124). Additionally, the second CTE of the second surface (124B) is quantitatively closer than the first CTE to a CTE of the first surface (128A) of the electronics layer (128) positioned proximal to the second surface (124B) of the first intermediate layer (124). In an exemplary embodiment, the first CTE of the first surface (124A) of the first intermediate layer (124) is within plus or minus 10 percent of the CTE of the proximal first surface (118B) of the thermal energy harvesting thermionic device (114), and the second CTE of second surface (124B) of the first intermediate layer (124) is within plus or minus 10 percent of the CTE of the proximal first surface (128A) of the electronics layer (128). In another exemplary embodiment, the first CTE of the first surface (124A) of the first intermediate layer (124) is within plus or minus 2 percent of the CTE of the first surface (118B) of the thermal energy harvesting thermionic device (114), and the second CTE of the second surface (124B) of the first intermediate layer (124) is within plus or minus 2 percent of the CTE of the proximal first surface (128A) of the electronics layer (128).
Likewise, the second intermediate layer (126) includes a first surface (also referred to as a third surface) (126A) and an opposite second surface (also referred to as a fourth surface) (126B). The third surface (126A) of the second intermediate layer (126) interfaces with a second surface (122B) of the substrate (122). The fourth surface (126B) of the second intermediate layer (126) interfaces with the first surface (116A) of the cathode (116), also referred to herein as the second surface (116A) of the thermal energy harvesting thermionic device (114).
The third surface (126A) and the fourth surface (126B) of the second intermediate layer (126) have a third coefficient of thermal expansion (CTE) and a fourth CTE, respectively. In an embodiment, the second intermediate layer (126) is referred to as having a gradient CTE extending between the third and fourth surfaces (126A) and (126B), respectively. According to an exemplary embodiment, the third CTE of the third surface (126A) is quantitatively closer than the fourth CTE to a CTE of a surface (122B), referred to herein as the first surface (122B), of the substrate (122) positioned proximal to the third surface (126A) of the second intermediate layer (126). Additionally, the fourth CTE of the fourth surface (126B) is quantitatively closer than the third CTE to a CTE of the second surface (116A) of the thermionic device (114) positioned proximal to the fourth surface (126B). In an exemplary embodiment, the third CTE of the third surface (126A) of the second intermediate layer (126) is within plus or minus 10 percent of the CTE of the proximal second surface (122B) of the substrate (122), and the fourth CTE of the fourth surface (126B) of the second intermediate layer (126) is within plus or minus 10 percent of the CTE of the proximal second surface (116A) of the thermionic device (114). In another exemplary embodiment, the third CTE of the third surface (126A) of the second intermediate layer (126) is within plus or minus 2 percent of the CTE of the proximal second surface (122B) of the substrate (122), and the fourth CTE of the fourth surface (126B) of the second intermediate layer (126) is within plus or minus 2 percent of the CTE of the proximal second surface (116A) of the thermal energy harvesting thermionic device (114).
It should be noted that the terms “first,” second,” “third,” and “fourth” are assigned for explanatory and simplification purposes in connection with embodiments, and may differ throughout the specification and claims for different embodiments.
An exemplary embodiment in which the first and second intermediate layers have non-linear gradient coefficients of thermal expansion will now be described with reference to
In the exemplary embodiment of
Additionally, in the exemplary embodiment of
Another exemplary embodiment in which the first and second intermediate layers have linear gradient coefficients of thermal expansion will now be described with reference to
In the exemplary embodiment of
Similarly the exemplary embodiment of
Representative thermal expansion layers and methods of making the first and second intermediate layers, including with gradient coefficients of thermal expansion, are disclosed in U.S. patent application Ser. No. 16/416,849 filed May 20, 2019 entitled “Single-Nozzle Apparatus for Engineered Nano-Scale Electrospray Depositions,” U.S. patent application Ser. No. 16/416,858 filed May 20, 2019 entitled “Multi-Nozzle Apparatus for Engineered Nano-Scale Electrospray Depositions,” and in U.S. patent application Ser. No. 16/416,869 filed May 20, 2019 entitled “Method of Fabricating Nano-Structures with Engineered Nano-Scale Electrospray Depositions,” the detailed descriptions and drawings of which are incorporated herein by reference.
Certain embodiments disclosed in those applications relate to, among other things, an electrospray apparatus for implementing electrospraying techniques to fabricate structures (e.g., composites), including nano-structures (e.g., nano-composites) with tailored properties. In one aspect, the electrospray apparatus is provided with at least one reservoir to hold at least a first composition and a second composition, wherein the first and second compositions differ from one another. The first composition includes a first nano-structural material and a plurality of first grain growth inhibitor nano-particles including one or more first grain growth inhibitors. The first composition also includes a first tailoring solute and/or a plurality of first tailoring nano-particles. The second composition includes a second nano-structural material and a plurality of second grain growth inhibitor nano-particles including one or more second grain growth inhibitors. The second composition also includes a second tailoring solute and/or a plurality of second tailoring nano-particles. The electrospray apparatus also includes at least one nozzle operatively coupled to the reservoir(s) and a stage positioned proximate to the nozzle(s). The stage is adapted to hold the substrate (1222) and move relative to the nozzle(s). The electrospray apparatus further includes a surface profile determination device positioned proximate to the stage to obtain profile data of the substrate (1222). A control unit is operatively coupled to the device and the stage and regulates manufacture of a pinned nano-structure. The control unit forms a first deposition layer positioned proximal to the substrate, e.g., (1222) of
The nano-structural materials include, for example: Cu, FeCu, FeCo, MoSi, MoC, NbC, NiCr, TiC, NiAl, Mo2Si, NiCr/Cr3C2, Fe/TiC, Mo/TiC, WC/Co, or any of the forgoing alloys with one or more of Ti, TiC, Mn, W, B, Y, Cr, Mo, Ni, Zr, Ce, Fe, Al, Si, V, and mixtures of the foregoing metals. Grain-grown inhibitors include, for example: B, Si, Al, Cr, Ni, Mo, Hf, Ta, Fe, W, Zr, Ce, Ti, Mo, TiC, AlSi, TiSi, TiAl, and TiB2, and a combination thereof. In addition, materials such as rare earth metals, silicon-based carbides, titanium-based carbides, aluminum-based nitrides, titanium-based nitrides, BN, metal silicides, and metal aluminides may be used.
Electrically Conductive Path (130)
The electrical conductive path (130) includes one or more electrical conductors. The one or more electrical conductors can be, for example, one or more electricity-conveying members such as wires, traces, electrical ink, electrical lines, etc. Portions of the electrical conductive path (130) connected to or passing through parts or components, such as the heat dissipation device (134), and walls of the heat shield (150), are sometimes shown as broken or dashed lines passing through the parts or components for convenience sake.
The electrical conductive path (130) is established between the thermionic device (114) and electronic components of the electronics layer (128) to transfer electrical output from the thermionic device (114) to the electronics layer (128). The flow direction of electrons is represented by arrows (132) in
Heat Dissipation/Heat Dissipation Device (134)
In exemplary embodiments, the heat dissipating device (134) is positioned to reduce the temperature of the electrical conductive path (130). It should be understood that the use of the heat-dissipation device (134) and associated fluid-circulating device (136) and thermal reservoir (138) in the embodiment of
According to an exemplary embodiment, a design feature of an exemplary embodiment of the circuit is that the size, e.g., diameter, of the return wire or other electrical conductive path(s)/connector(s) (132) is small enough to transfer heat readily back to the cathode (116) without creating a large or excessive resistance. The temperature or average energy of electrons is reduced due to thermal exchange of heat leaving the anode (118) to the heat dissipation device (also referred to and embodied herein as a heat dissipating device) (134), such as a heat exchanger or a heat sink. The electron flow leaving the anode (118) and passing through the heat dissipation device (134) is thereby delivered to the electronics layer (128) via conductive path (132) with less thermal energy, thereby reducing likelihood that the electronics layer (128) will overheat. This reduced thermal energy is re-supplied to the cathode (116) via the conductive path (132) to maintain the thermionic device operating at a high efficiency. In an exemplary embodiment, the heat-dissipation device (134) is a microstructure array heat exchanger, and in an exemplary embodiment is the heat-dissipating device shown and described below in
The heat-dissipation device (134) may be embodied as, for example, a heat sink or a heat exchanger. In an exemplary embodiment, the heat-dissipation device (134) comprises a micro-structure array heat exchanger. Referring to
The heat-dissipation device (300) includes a plurality of rings, annular fins, or arcuate surfaces, hereinafter referred to as annular fins, and illustrated as first, second, and third annular fins (302), (304), and (306), respectively. Although three annular fins (302), (304), and (306) are shown in
In
The first, second, and third annular fins (302), (304), and (306), respectively, include corresponding openings, shown in
As shown in
In an exemplary mode of operation, heat conveyed by the electrical conductor (320) is removed in part by the fins (302), (304), and (306) and transmitted to the base (310), which together function as a heat sink.
Fluid-Circulating Device (136) and Thermal Reservoir (138)
The system (102) also includes a fluid-circulating device (136) operatively coupled to a thermal reservoir (138). The fluid-circulating device (136) may be, for example, one or more fans, impellers, blowers, or any device configured to facilitate fluid flow. Although the fluid-circulating device (136) is depicted in
Electrical Energy Storage Component (152)
The electrical energy storage device (152), also referred to herein as a storage device, is shown herein positioned internal to a housing (104) of the system (102), within the compartment (106). In an alternative embodiment, the electrical energy storage device (152) may be positioned external to the housing (104). In an exemplary embodiment, one or more capacitors are selected as the electrical energy storage device (152), although other devices capable of storing electrical energy, e.g., a charge, may be used, especially for meeting large electrical demand periods. Unless otherwise indicated, the term capacitor can include supercapacitor, micro-capacitor, micro-supercapacitor, and the like. Examples of electrical energy storage devices that may be used instead of or in combination with one or more capacitors include, without limitation, inductors, fuel cells, non-rechargeable batteries, rechargeable batteries, and other electrical energy storage elements.
Heat Source (160)
In an exemplary embodiment, heat is the by-product of resistance of a circuit component, including but not limited to resistors. In an exemplary embodiment, the heat source (160) comprises one or more resistors. Various types of resistors may be employed. In an exemplary embodiment, selection or employment of resistors is configurable. For example, resistors suitable for use as the heat source (160) may have a resistance in a range of, for example, about 0.01 ohms to about 10 k ohms (10,000 ohms) and/or a power dissipation rating of, for example, about 0.001 watts to about 1 or more megawatts. Other heating sources with low thermal resistance change may be used instead of or in addition to a resistor.
The heat source (160) is positioned proximal to the thermal energy harvesting thermionic device (114) so that the thermal energy generated by the heat source (160), when activated by the controller (154) closing the switch (158), thermally perturbs the thermal energy harvesting thermionic device (114).
Temperature Sensor (156)
The temperature sensor (156) may be embodied as one or more thermocouples. The temperature sensor (156) measures the temperature of the thermal energy harvesting thermionic device (114) or a component thereof, e.g., the cathode (116), the anode (118), the nano-fluid or spacer (120), or a temperature difference between two or more of the components.
Controller (154) and Switch (158)
The controller (154) monitors the temperature, as measured by the temperature sensor (156), for a temperature drop below a temperature threshold. In an embodiment, the temperature threshold is a temperature value. In another embodiment, the temperature threshold is a range of temperatures. The temperature threshold may be predetermined. For example, the temperature threshold may be any value between the freezing point and the boiling point of the nano-fluid (discussed below) of the thermal energy harvesting thermionic device (114). In another embodiment, the temperature threshold is a temperature difference (temperature gradient) between the cathode and anode.
In response to detection that the temperature (as monitored by the temperature sensor (156)) of the thermal energy harvesting thermionic device (114) has fallen below the temperature threshold, the controller (154) closes the switch (158). Electricity is supplied from the electrical energy storage device (152) to the heat source (160). As current (typically direct current (DC)) flows from the electrical energy storage device (152) to the heat source (160), the electrical energy is converted by the heat source (160) into heat (or thermal energy) (162).
In an exemplary embodiment, the controller (154) activates the heat source (160) to generate a temperature in a range of about −200° C. to about 2,000° C. In an exemplary embodiment, the temperature range is correlated with the composition of the nano-fluid. For example, at −200° C. the nano-fluid composition may include an alkali metal, and at the highest temperature range the nano-fluid composition may include molten salts. Similarly, in another embodiment, at room temperature, such as 25° C. to 200° C., the nano-fluid composition may include organics, such as toluene, alkanes, alkane thiols, and/or water, with each composition having respective operational temperatures or temperature ranges.
In an exemplary embodiment, the controller (154) closes the switch (158) for a period of about 4-10 seconds to about 100 seconds, which is sufficient time for the electrical energy storage device (152) to supply electricity to the heat source (160) to generate heat for harvesting by the thermal energy harvesting thermionic device (114). The amount of time selected for activating the heat source (160) may be based on various factors, including but not limited to the ambient temperature of the environment in which the system (102) is located, the temperature of the nano-fluid prior to activation, etc. The magnitude of the resulting current produced by the thermal energy harvesting thermionic device (114) will depend upon many factors, including the heat energy emitted by the heat source (160). In an exemplary embodiment, activating the heat source (160) for a limited duration, e.g. seconds, can increase the electrical output of the thermal energy harvesting thermionic device (114) for an extended duration, e.g. hours.
As explained above, the thermal energy (162) generated by the heat source (160), when activated by the controller (154) closing the switch (158), thermally perturbs the thermal energy harvesting thermionic device (114). The device (114) generates electricity for recharging of the electrical energy storage component (152). Eventually, the cycle will decrease to the point at which an outside electrical source, e.g., a battery or AC power source, should supply electricity to charge the electrical energy storage component (152).
The controller (154), which may be embodied as a control circuit, may include at least one processor (e.g., a microprocessor), at least one microcontroller, at least one programmable logic device (e.g., field programmable gate arrays, programmable array logic, programmable logic devices), at least one application specific integrated circuit, or the like, or combinations including one or more thereof. The controller (154) may include or operatively communicate with a memory or memory module. Memory or memory modules may be in the form of nonvolatile data stores, such as hard drives and/or nonvolatile memory. A non-exhaustive list of more specific examples of memory includes the following: a portable computer diskette, a hard disk, a dynamic or static random access memory (RAM), a read-only memory (ROM), an erasable programmable read-only memory (EPROM or Flash memory), a magnetic storage device, a portable compact disc read-only memory (CD-ROM), a digital versatile disk (DVD), a memory stick, and any suitable combination of the foregoing. The memory may store one or more software-based control applications that include instructions that the control circuit executes to perform the functions described herein.
Heat Shield (150)
As shown in
Electronics, particularly resistors, generate thermal energy in one or more of a number of ways, including through the use of resistors. In the apparatus (210) of the system (202) of
Thermal Energy Harvesting Thermionic Devices (114) and (214)
Embodiments of the thermal energy harvesting thermionic devices (114) and (214) are described in greater detail with reference to
Referring to
The thermal energy harvesting thermionic device (400) is sometimes referred to herein as a cell. In exemplary embodiments, the thermal energy harvesting thermionic device (400) is illustrated as a sheet or a plurality of adjacently positioned sheets or layers, e.g., that may be stacked or wound. A plurality of devices (400) may be organized as a plurality of cells, or a plurality of layers, with the cells or layers arranged in series or parallel, or a combination of both to generate electrical output at the desired voltage, current, and power.
The thermal energy harvesting thermionic device (400) includes an emitter electrode (also referred to herein as the cathode) (402) and a collector electrode (also referred to herein as the anode) (404) positioned to define an inter-electrode gap (or interstitial space) therebetween. In an embodiment, a spacer (406) of separation material, sometimes referred to herein as a standoff or spacer, maintains separation between the electrodes (402) and (404). While the spacer (406) is referred to herein in the singular, it should be understood that the spacer (406) may comprise a plurality of elements. The spacer (406) may be a dielectric or insulator, or comprise one or more materials that collectively exhibit electrically non-conductive properties. The spacer (406) is illustrated in direct contact with the electrodes (402) and (404). The electrodes (402) and (404) and the spacer (406) define a plurality of closed apertures (408), also referred to herein as cavities, in the inter-electrode gap. The apertures (408) extend in the Y direction between the electrodes (402) and (404) for a distance (410) in a range, for example, of about 1 nanometer (nm) to about 100 nm, or in a range, for example, of about 1 nm to about 20 nm. A fluid (412), also referred to as a nano-fluid (discussed further herein with reference to
In alternative embodiments, no spacer (406) is used and only the nano-fluid (412) is positioned between the electrodes (402) and (404). Accordingly, the thermal energy harvesting thermionic device (400) includes two opposing electrodes (402) and (404), optionally separated by the spacer (406) with a plurality of apertures (408) extending between the electrodes (402) and (404) and configured to receive the nano-fluid (412).
The emitter electrode (402) and the collector electrode (404) each may be fabricated from different materials, with the different materials having separate and different work function values. The work function of a material or a combination of materials is the minimum thermodynamic work, i.e., minimum energy, needed to remove an electron from a solid to a point in a vacuum immediately outside a solid surface of the material. The work function is a material-dependent characteristic. Work function values are typically expressed in units of electron volts (eV). Accordingly, the work function of a material determines the minimum energy required for electrons to escape the surface, with lower work functions generally facilitating electron emission.
The difference in work function values between the electrodes (402) and (404) due to the different electrode materials influences the voltage that can be achieved. Thus, to generate high power, the difference in work function values between the electrodes (402) and (404) is large in an exemplary embodiment. In an embodiment, the work function value of the collector electrode (404) is smaller than the work function value of the emitter electrode (402). The different work function values induces a contact potential difference between the electrodes (402) and (404) that has to be overcome, e.g., by the application of heat to the emitter electrode (402), to transmit electrons through the nano-fluid (412) within the apertures (408) from the emitter electrode (402) to the collector electrode (404). In an exemplary embodiment, the total of the work function value of the collector electrode (404) and the contact potential difference is less than or equal to the work function of the emitter electrode (402). Maximum flow occurs when the total of the work function value of the collector electrode (404) and the contact potential equals the work function value of the emitter electrode (402).
Both electrodes (402) and (404) emit electrons; however, once the contact potential difference is overcome, the emitter electrode (402) will emit significantly more electrons than the collector electrode (404), which is influenced by an electric field that suppresses electron production from the collector electrode (404). A net flow of electrons is transferred from the emitter electrode (402) to the collector electrode (404), and a net electron current (414) flows from the emitter electrode (402) to the collector electrode (404) through the apertures (408). This net electron current (414) causes the emitter electrode (402) to become positively charged and the collector electrode (404) to become negatively charged. Accordingly, the thermal energy harvesting thermionic device (400) generates an electron flow (414) that is transmitted from the emitter electrode (402) to the collector electrode (404).
The emitter electrode (402) may be manufactured with a first backing (416), which may comprise, for example, a polyester film, e.g., Mylar®, and a first layer (418) extending beneath the first backing (416). The first layer (418) may be comprised, for example, graphene, platinum (Pt), or other suitable materials. In an embodiment, the emitter electrode (402) has an emitter electrode thickness measurement (420) extending in the Y direction that is, for example, approximately 0.25 millimeters (mm), such measurement being non-limiting, or in a range of, for example, about 2 nm to about 0.25 mm, such measurements being non-limiting. The first backing (416) is shown in
In an exemplary embodiment, prior to assembly, the first layer (418) is sprayed onto the first backing (416) so as to embody the first layer (418) as a nanoparticle layer that is approximately 2 nm (i.e., the approximate diameter of a nanoparticle), where the 2 nm value should be considered non-limiting. In an embodiment, the thickness (424) of the first layer (418) may be in a range of, for example, about 1 nm to about 20 nm, or about 2 nm to about 20 nm. In another embodiment, the thickness (424) of the first layer (418) may be in a range of, for example, 0.01 mm to 0.125 mm. Generally, smaller thicknesses have higher energy densities and less wasted energy. The first backing (416) has a first outer surface (428). The first backing (416) and the first layer (or the nanoparticle layer) (418) define a first interface (430) therebetween. The first layer (or the nanoparticle layer) (418) defines a first surface (432) facing the inter-electrode gap. Alternative to spraying, the first layer (418) may be pre-formed and applied to the first backing layer (416), or vice versa, i.e., the first backing layer (416) applied to the first layer (418).
A first coating (434), such as cesium oxide (Cs2O), at least partially covers the first surface (432) to form an emitter surface (436) of the first electrode (402) that directly interfaces with a first spacer surface (438). Accordingly, the emitter electrode (402) of the embodiment illustrated in
In
In an embodiment, the second layer (448) is sprayed on to the second backing (446) to embody the second layer (448) as a second nanoparticle layer that is approximately 2 nm thick, where the 2 nm value should be considered non-limiting. The second layer measurement (454) of the second layer (448) may range from, for example, about 1 nm to about 20 nm, or about 2 nm to about 20 nm. In another embodiment, the second layer measurement (454) of the second layer (448) may be in a range of, for example, 0.01 mm to 0.125 mm. As discussed above in connection with the first layer (418), generally, smaller thicknesses have higher energy densities and less wasted energy. The second backing (446) has a second outer surface (458). The second backing (446) and the second layer/nanoparticle layer (448) define a second interface (460). The second layer (or the second nanoparticle layer) (448) defines a second surface (462) facing the inter-electrode gap. Alternatively to spraying, the second layer (448) may be pre-formed and applied to the second backing (446) or vice versa, i.e., the second backing (446) applied to the second layer (448).
A second coating (464), which may be comprised of cesium oxide (Cs2O), at least partially covers the second surface (462) to form a collector surface (466) of the collector electrode (404) that directly interfaces with a second surface (468) of the spacer (406). Accordingly, the collector electrode (404) of
In an exemplary embodiment, the first coating (434) and the second coating (464) are formed on the first and second surfaces (432) and (462), respectively. In an embodiment, an electrospray or a nano-fabrication technique is employed to form or apply the first and second coatings (434) and (464), respectively. The first and second coatings (434) and (464) can be applied in one or more predetermined patterns that may be the same as or different from one another.
In one or more exemplary embodiments, a percentage of surface area coverage of each of the first surface (432) and second surface (462) with the respective coating layers (434) and (464) (e.g., Cs2O) is within a range of at least 50%, and up to 70%, and in at least one embodiment is about 60%. The Cs2O coatings (434) and (464) reduce the work function values of the electrodes (402) and (404) from the work function values of, for example, platinum (Pt), which is an embodiment is 5.65 electron volts (eV), and aluminum (Al), which in an embodiment is 4.28 eV. The emitter electrode (402) with the coating layer (434) of Cs2O has a work function value ranging from about 0.5 to about 2.0 eV, and in an embodiment is approximately 1.5 eV, and the collector electrode (404) with the coating layer (464) of Cs2O has a work function value of about 0.5 to about 2.0 eV, and in an embodiment is approximately 1.5 eV.
Various modifications may be made to the thermal energy harvesting thermionic device (400) discussed herein. For example, either or both of the first backing (416) and the second backing (446) may be eliminated, particularly where the first layer (418) and/or the second layer (448) have relatively large thicknesses.
In an embodiment, the electrodes (402) and (404) are comprised of graphene, and are referred to herein as graphene electrodes (402) and (404). The graphene electrodes (402) and (404) can exhibit work function values below 1.0 eV when coated with cesium oxide, gold, tungsten, and other elements and compounds. Sulfur may be incorporated into the coatings (434) and (464) to improve the bonding of the coatings (434) and (464) to the graphene electrodes (402) and (404), respectively, particularly where the first and second layers (418) and (448) of the electrodes (402) and (404) comprise graphene and the sulfur creates covalent bonding between the electrodes (402) and (404) and their respective coatings (434) and (464). The respective work function values of the electrodes (402) and (404) can be made to differ, even when both are comprised of graphene, for example by incorporating different coatings (434) and (464) into the electrodes (402) and (404). Suitable graphene electrodes are available through ACS (Advanced Chemical Suppliers) Materials, and include Trivial Transfer Graphene™ (TTG 10055).
In an embodiment, the surface area coverage on the emitter electrode (402) or the collector electrode (404) with Cs2O is spatially resolved, e.g., applied in a pattern or non-uniform across the length of the corresponding surface, and provides a reduction in a corresponding work function to a minimum value. In an exemplary embodiment, the work function value, from a maximum of about 2.0 eV is reduced approximately 60-80% corresponding to the surface coverage of the Cs2O, e.g. cesium oxide. The lower work function values of the electrodes (402) and (404) improve operation of the thermal energy harvesting thermionic device (400) as described herein.
Platinum (Pt) coated on copper foil and aluminum (Al) materials optionally are selected for the first and second electrodes (402) and (404), respectively, due to at least some of their metallic properties, e.g., strength and resistance to corrosion, and the measured change in work function values when the thermionic emissive material of Cs2O or other materials disclosed herein is layered thereon. Alternative materials may be used, such as graphene, noble metals including, and without limitation, rhenium (Re), osmium (Os), ruthenium (Ru), iridium (Ir), rhodium (Rh), and palladium (Pd), or any combination of these metals. In addition, and without limitation, non-noble metals such as gold (Au), tungsten (W), tantalum (Ta), and molybdenum (Mo), and combinations thereof, may also be used. For example, and without limitation, tungsten (W) nanoparticles may be used rather than platinum (Pt) nanoparticles to form the first surface (432), and gold (Au) nanoparticles may be used rather than aluminum (Al) nanoparticles to form the second surface (462). Accordingly, the selection of the materials used to form the nanoparticle surfaces (432) and (462) can be principally based on the work functions of the electrodes (402) and (404), and more specifically, the difference in the work functions once the electrodes (402) and (404) are fully fabricated.
The selection of the first and second coatings (434) and (464), e.g., thermionic electron emissive material, on the first surface (432) and second surface (462), respectively, may be partially based on the desired work function value of the electrodes (402) and (404), respectively, and chemical compatibility between the deposited materials, and the deposited thermionic electron emissive materials of the first and second coatings (434) and (464), respectively. Deposition materials include, but are not limited to, thorium, aluminum, cerium, and scandium, as well as oxides of alkali or alkaline earth metals, such as cesium, barium, calcium, and strontium, as well as combinations thereof and combinations with other materials. In at least one embodiment, the thickness of the layer of patterned thermionic electron emissive material of the first and second coatings (434) and (464) is approximately 2 nm, where the 2 nm value should be considered non-limiting. Accordingly, the electrodes (402) and (404) have highly desirable work functions.
The spacer (500) includes a plurality of interconnected edges or walls (502). The edges (502) have a thickness or edge measurement (504) in the range of, for example, about 2.0 nm to about 0.25 mm. In the illustrated embodiment, the interconnected edges (502) collectively define a plurality of hexagonal apertures, also referred to herein as cavities (506), in a honeycomb array (508). The cavities (506) extend in a direction parallel to the Y-axis. The spacer (500) may be configured as a uniform or relatively uniform layer, e.g., contiguous and with or without limited apertures. The apertures or cavities, either uniformly or non-uniformly provided across the width and/or length of the spacer material, may be in a range of, for example, greater than 0 mm (e.g., 2 nm) to about 0.25 mm in the Y-axis direction, similar to an embodiment of the spacer (406) of
Referring to
Referring to
The spacers (500) and (570), shown in
As shown in
With respect to the first electrode (562), the first lateral side edge (530) extends in the lateral direction Z beyond the first lateral support side edge (514) of the spacer (500), (570) by a third distance (536), and the second lateral support side edge (516) of the spacer (500), (570) extends in the lateral direction Z beyond the second lateral side edge (532) by a fourth distance (528).
With respect to the second electrode (564), the first lateral support side edge (514) of the spacer (500), (570) extends in the lateral direction Z beyond the third lateral side edge (540) by a fifth distance (526), and the fourth lateral side edge (542) extends in the lateral direction Z beyond the second lateral support side edge (516) of the spacer (500), (570) by a sixth distance (548).
In embodiments, the third distance (536), the fourth distance (528), the fifth distance (526), and the sixth distance (548) may be the same or different from one another and within a range of, for example, approximately 1.1 nm to approximately 10 microns. The spacer (500), (570) may have a lateral measurement (518) with respect to the Z-axis greater than lateral measurements (534) and (544) of the electrodes (562) and (564), respectively. The spacer design and measurements shown and described herein reduce a potential for electrodes, such as the electrodes (402) and (404), to contact one another when the spacer (500), (570) is incorporated into the device (400) of
Each of the lateral support side edges (514) and (516) may receive at least one layer of an electrically insulating sealant that electrically isolates the portions (550) and (552) of the electrodes (562) and (564), respectively, that extend beyond the lateral support side edges (514) and (516), respectively. Further, as described above, each of the electrodes (562) and (564) may be offset from the spacer (500), (570) to reduce the potential for the electrodes (562) and (564) contacting each other and creating a short circuit.
In exemplary embodiments, the at least one spacer (500) and/or (570), which in exemplary embodiments are dielectric spacers, as shown and described in
Referring to
At least one layer of a dielectric coating (610), such as a monolayer of alkanethiol material, is deposited on the Au nanoparticle clusters (604) and the Ag nanoparticle clusters (606) to form a dielectric barrier thereon. In an exemplary embodiment, the deposit of the dielectric coating (610) is performed via electrospray. The alkanethiol material of the dielectric coating (610) includes, but is not limited to, dodecanethiol and/or decanethiol. Additionally or alternatively, the dielectric coating (610) may be a halogenoalkane or alkyl halide, in which one or more of the hydrogen atoms of the alkane are replaced by halogen atom(s), i.e., fluorine, chlorine, bromine, or iodine. The deposit of the dielectric coating (610), such as alkanethiol, reduces coalescence of the nanoparticle clusters (604) and (606). In at least one embodiment, the nanoparticle clusters (604) and (606) have a diameter in the range of about 1 nm to about 3 nm. In an exemplary embodiment, the nanoparticle clusters (604) and (606) have a diameter of about 2 nm. In an exemplary embodiment, the Au nanoparticle clusters (604) and the Ag nanoparticle clusters (606) are tailored to be electrically conductive with charge storage features (i.e., capacitive features), minimize heat transfer through associate spacer apertures, such as the spacer apertures (506) of
The Au nanoparticle clusters (604) according to exemplary embodiments are dodecanethiol functionalized gold nanoparticles. In exemplary embodiments, the AU nanoparticle clusters (604) have an average particle size of about 1 nm to about 3 nm, at about 2% (weight/volume (grams/ml)). According to exemplary embodiments, the Ag nanoparticle clusters (606) are dodecanethiol functionalized silver nanoparticles. In certain embodiments, the Ag nanoparticle clusters (606) have an average particle size of about 1 nm to about 3 nm, at about 0.25% (weight/volume percent). In an embodiment, the average particle size of both the Au and Ag nanoparticle clusters (604) and (606) is at or about 2 nm. The Au and Ag cores of the nanoparticle clusters (604) and (606) are selected for their abilities to store and transfer electrons. In an embodiment, a 50%-50% mixture of Au and Ag nanoparticle clusters (604) and (606) are used. However, a mixture in the range of 1-99% Au-to-Ag could be used as well. Electron transfers are more likely to occur between nanoparticle clusters (604) and (606) with different work functions. In an exemplary embodiment, a mixture of nearly equal (molar) numbers of two different nanoparticle clusters (604) and (606), e.g., Au and Ag, provides good electron transfer. Accordingly, nanoparticle clusters are selected based on particle size, particle material (with the associated work function values), mixture ratio, and electron affinity.
Conductivity of the nano-fluid (602) can be increased by increasing concentration of the nanoparticle clusters (604) and (606). The nanoparticle clusters (604) and (606) may have a concentration within the nano-fluid (602) of, for example, about 0.1 mole/liter to about 2 moles/liter. In at least one embodiment, the Au and Ag nanoparticle clusters (604) and (606) each have a concentration of at least 1 mole/liter. In at least one embodiment, a plurality of Au and Ag nanoparticle clusters (604) and (606) are mixed together in a dielectric medium (608) to form a nano-fluid (602), the nano-fluid (602) residing in, for example, the apertures (408) of
The stability and reactivity of colloidal particles, such as Au and Ag nanoparticle clusters (604) and (606), are determined largely by a ligand shell formed by the alkanethiol coating (610) adsorbed or covalently bound to the surface of the nanoparticle clusters (604) and (606). The nanoparticle clusters (604) and (606) tend to aggregate and precipitate, which can be prevented by the presence of a ligand shell of the non-aggregating polymer alkanethiol coating (610) enabling these nanoparticle clusters (604) and (606) to remain suspended. Adsorbed or covalently attached ligands can act as stabilizers against agglomeration and can be used to impart chemical functionality to the nanoparticle clusters (604) and (606). Over time, the surfactant nature of the ligand coatings is overcome and the lower energy state of agglomerated nanoparticle clusters is formed. Over time, agglomeration may occur due to the lower energy condition of nanoparticle cluster accumulation and occasional addition of a surfactant may be used. Examples of surfactants include, without limitation, Tween® 20 and Tween® 21.
In the case of the nano-fluid (602) of
Thermally-induced Brownian motion causes the nanoparticle clusters (604) and (606) to move within the dielectric medium (608), and during this movement the nanoparticle clusters (604) and (606) occasionally collide with each other and with the electrodes (402) and (404). As the nanoparticle clusters (604) and (606) move and collide within the dielectric medium (608), the nanoparticle clusters (604) and (606) chemically and physically transfers charge. The nanoparticle clusters (604) and (606) transfer charge chemically when electrons (612) hop between electrodes, e.g., from and to the electrodes (402) and (404) of
The nanoparticle clusters (604) and (606) transfer charge physically (i.e., undergo transient charging) due to the ionization of the nanoparticle clusters (604) and (606) upon receipt of an electron, and the electric field generated by the differently charged electrodes (402) and (404). The nanoparticle clusters (604) and (606) become ionized in collisions when they gain or lose an electron (612). Positive and negative charged nanoparticle clusters (604) and (606) in the nano-fluid (602) migrate to the negatively charged collector electrode (404) and the positively charged emitter electrode (402), respectively, providing an electrical current flow. This ion current flow is in the opposite direction from the electron current flow, but less in magnitude than the electron flow.
Some ion recombination in the nano-fluid (602) may occur, which diminishes both the electron and ion current flow. Electrode separation may be selected at an optimum width (or thickness in the Y direction in
In an exemplary embodiment, when the emitter electrode (402) and the collector electrode (404) are initially brought into close proximity, the electrons of the collector electrode (404) have a higher Fermi level than the electrons of the emitter electrode (402) due to the lower work function of the collector electrode (404). The difference in Fermi levels drives a net electron current that transfers electrons from the collector electrode (404) to the emitter electrode (402) until the Fermi levels are equal, i.e., the electrochemical potentials are balanced and thermodynamic equilibrium is achieved. The transfer of electrons between the emitter electrode (402) and the collector electrode (404) results in a difference in charge between the emitter electrode (402) and the collector electrode (404). This charge difference sets up the voltage of the contact potential difference and an electric field between the emitter electrode (402) and the collector electrode (404), where the polarity of the contact potential difference is determined by the material having the greatest work function. With the Fermi levels equalized, no net current will flow between the emitter electrode (402) and the collector electrode (404). Accordingly, electrically coupling the emitter electrode (402) and the collector electrode (404) with no external load results in attaining the contact potential difference between the electrodes (402) and (404) and no net current flow between the electrodes (402) and (404) due to attainment of thermodynamic equilibrium between the two electrodes (402) and (404).
The thermal energy harvesting thermionic device (400) can generate electric power (e.g., at room temperature) with or without additional heat input. Heat added to the emitter electrode (402) will raise the temperature of the emitter electrode (402) and the Fermi level of the emitter electrode (402) electrons. With the Fermi level of the emitter electrode (402) higher than the Fermi level of the collector electrode (404), a net electron current will flow from the emitter electrode (402) to the collector electrode (404) through the nano-fluid (412), (602). If the device (400) is placed into an external circuit, such that the external circuit is connected to the electrodes (402) and (404), the same amount of electron current will flow through the external circuit from the collector electrode (404) to the emitter electrode (402). Heat energy added to the emitter electrode (402) is carried by the electrons (612) to the collector electrode (402). The bulk of the added energy is transferred to the external circuit for conversion to useful work, some of the added energy is transferred through collisions of the nanoparticle clusters (604) and (606) with the collector electrode (404), and some of the added energy is lost to ambient as waste energy. As the energy input to the emitter electrode (402) increases, the temperature of the emitter electrode (402) increases, and the electron transmission from the emitter electrode (402) increases, thereby generating more electron current. As the emitter electrode (402) releases electrons onto the nanoparticle clusters (604) and (606), energy is stored in the thermal energy harvesting thermionic device (400). Accordingly, the thermal energy harvesting thermionic device (400) generates, stores, and transfers charge and moves heat energy associated with a temperature difference, where added thermal energy causes the production of electrons to increase from the emitter electrode (402) into the nano-fluid (412), (602).
The nano-fluid (602) can be substituted into the device (400) of
As the electrons (612) hop from nanoparticle cluster (604) and (606) to nanoparticle cluster (604) and (606), single electron charging effects that include the additional work required to hop an electron (612) onto a nanoparticle cluster (604) and (606) if an electron (612) is already present on the nanoparticle cluster (604) and (606), determine if hopping additional electrons (612) onto that particular nanoparticle cluster (604) and (606) is possible. Specifically, the nanoparticle clusters (604) and (606) include a voltage feedback mechanism that prevents the hopping of more than a predetermined number of electrons to the nanoparticle cluster (604) and (606). This prevents more than the allowed number of electrons (612) from residing on the nanoparticle cluster (604) and (606) simultaneously. In an embodiment, only one electron (612) is permitted on any nanoparticle cluster (604) and (606) at any one time. Therefore, during conduction of current through the nano-fluid (602), a single electron (612) hops onto the nanoparticle cluster (604) and (606). The electron (612) does not remain on the nanoparticle cluster (604) and (606) indefinitely, but hops off to either the next nanoparticle cluster (604) and (606) or the collector electrode (404) through collisions resulting from the Brownian motion of the nanoparticle clusters (604) and (606). However, the electron (612) does remain on the nanoparticle cluster (604) and (606) long enough to provide the voltage feedback required to prevent additional electrons (612) from hopping simultaneously onto the nanoparticle clusters (604) and (606). The hopping of electrons (612) across the nanoparticle clusters (604) and (606) avoids resistive heating associated with current flow in a media. Notably, the thermal energy harvesting thermionic device (400) containing the nano-fluid (602) does not require pre-charging by an external power source in order to introduce electrostatic forces. This is due to the device (400) being self-charged with triboelectric charges generated upon contact between the nanoparticle clusters (604) and (606) due to Brownian motion. Accordingly, the electron hopping across the nano-fluid (602) is limited to one electron (612) at a time residing on a nanoparticle cluster (604) and (606).
As the electron current starts to flow through the nano-fluid (602), a substantial energy flux away from the emitter electrode (402) is made possible by the net energy exchange between emitted and replacement electrons (612). The replacement electrons from an electrical conductor connected to the emitter electrode (402) do not arrive with a value of energy equivalent to an average value of the Fermi energy associated with the material of emitter electrode (402), but with an energy that is lower than the average value of the Fermi energy. Therefore, rather than the replacement energy of the replacement electrons being equal to the chemical potential of the emitter electrode (402), the electron replacement process takes place in the available energy states below the Fermi energy in the emitter electrode (402). The process through which electrons are emitted above the Fermi level and are replaced with electrons below the Fermi energy is sometimes referred to as an inverse Nottingham effect. Accordingly, a low work function value of, for example, about 0.5 eV for the emitter electrode (402) allows for the replacement of the emitted electrons with electrons with a lower energy level to induce a cooling effect on the emitter electrode (402).
As described this far, the principal electron transfer mechanism for operation of the device (400) is thermionic energy conversion or harvesting. In some embodiments, thermoelectric energy conversion is conducted in parallel with the thermionic energy conversion. For example and referring to
A plurality of thermal energy harvesting thermionic devices (400) is distinguished by at least one embodiment having the thermoelectric energy conversion features described herein. The nano-fluid (412), (602) is selected for operation of the thermal energy harvesting thermionic devices (400) within one or more temperature ranges. In an embodiment, the temperature range of the associated thermal energy harvesting thermionic device (400) is controlled to modulate a power output of the device (400). In general, as the temperature of the emitter electrode (402) increases, the rate of thermionic emission therefrom increases. The operational temperature ranges for the nano-fluid (602) are based on the desired output of the thermal energy harvesting thermionic device (400), the temperature ranges that optimize thermionic conversion, the temperature ranges that optimize thermoelectric conversion, and fluid characteristics. Therefore, different embodiments of the nano-fluid (602) are designed for different energy outputs of the device (400).
For example, in an embodiment, the temperature of the nano-fluid (412), (602) is maintained at less than 250° C. to avoid deleterious changes in energy conversion due to the viscosity changes of the dielectric medium (608) above 250° C. In an embodiment, the temperature range of the nano-fluid (602) for substantially thermionic emission is only approximately room temperature (i.e., about 20° C. to about 25° C.) up to about 70-80° C., and the temperature range of the nano-fluid (602) for thermionic and thermo-electric conversion is above 70-80° C., with the principal limitations being the temperature limitations of the materials. In an exemplary embodiment, the nano-fluid (602) for operation including thermoelectric conversion includes a temperature range that optimizes the thermoelectric conversion through optimizing the power density within the thermal energy harvesting thermionic device (400), thereby optimizing the power output of the device (400). In at least one embodiment, a mechanism for regulating the temperature of the nano-fluid (602) includes diverting some of the energy output, e.g., heat, of the device (400) into the nano-fluid (602). Accordingly, the apertures (408) of specific embodiments of the thermal energy harvesting thermionic device (400) may be filled with the nano-fluid (602) to employ thermoelectric energy conversion with thermionic energy conversion above a particular temperature range, or thermionic energy conversion by itself below that temperature range.
As described herein, in at least one embodiment, the dielectric medium (608) has thermal conductivity values less than about 1.0 watt per meter-Kelvin (W/m·K). In at least one embodiment, the thermal conductivity of the dielectric medium (608) is about 0.013 watt per meter-Kelvin (W/m·K), as compared to the thermal conductivity of water at about 20 degrees Celsius (° C.) of about 0.6 W/m·K. Accordingly, the nano-fluid (602) minimizes heat transfer, such as through the apertures (408) of
As shown in
Examples of a first factor include, but are not limited to, enhanced phonon and electron transfer between the plurality of nanoparticle clusters (604) and (606) within the nano-fluid (602), enhanced phonon and electron transfer between the plurality of nanoparticle clusters (604) and (606) and the first electrode (402), and enhanced phonon and electron transfer between the plurality of nanoparticle clusters (604) and (606) and the second electrode (404).
A second factor is an enhanced influence of Brownian motion of the nanoparticle clusters (604) and (606) in a confining environment between the electrodes (402) and (404) to, e.g., less than about 10 nm inter-electrode distance (410). As the distance (410) between the electrodes (402) and (404) decreases below about 10 nm, fluid continuum characteristics of the nano-fluid (412), (602) with the suspended nanoparticle clusters (604) and (606) is altered. For example, as the ratio of particle size to volume of the apertures (408) increases, random and convection-like effects of Brownian motion in a dilute solution dominate. Therefore, collisions of the nanoparticle clusters (604) and (606) with the surfaces of other nanoparticle clusters (604) and (606) and the electrodes (402) and (404) increase thermal and electrical conductivity values due to the enhanced phonon and electron transfer.
A third factor is the at least partial formation of matrices of the nanoparticle clusters (604) and (606) within the nano-fluid (602). Under certain conditions, the nanoparticle clusters (604) and (606) will form matrices within the nano-fluid (602) as a function of close proximity to each other with some of the nanoparticle clusters (608) remaining independent from the matrices. In an embodiment, the formation of the matrices is based on the factors of time and/or concentration of the nanoparticle clusters (604) and (606) in the nano-fluid (602).
A fourth factor is the predetermined nanoparticle clusters (604) and (606) density, which in an embodiment is about one mole per liter. Accordingly, apertures (408) containing the nano-fluid (602) with a distance (410) of about 1 nm to less than about 10 nm causes an increase in the thermal and electrical conductivity values of the nano-fluid (602) therein.
In addition, the nanoparticle clusters (604) and (606) have a small characteristic length, e.g., about 2 nm, and the clusters (604) and (606) are often considered to have only one dimension. This characteristic length restricts electrons in a process called quantum confinement, which increases electrical conductivity. The collision of particles with different quantum confinement facilitates transfer of charge to the electrodes (402) and (404). The thermal energy harvesting thermionic device (400) has an enhanced electrical conductivity value greater than about 1 Siemens per meter (S/m) as compared to the electrical conductivity of drinking water of about 0.005 S/m to about 0.05 S/m. Also, the embodiments of the device (400) with the enhanced thermal conductivity have a thermal conductivity value greater than about 1 W/m·K as compared to the thermal conductivity of water at 20 degrees Celsius (° C.) of about 0.6 W/m·K.
Thermionic emission of electrons (612) from the emitter electrode (402) and the transfer of the electrons (612) across the nano-fluid (602) from one nanoparticle cluster (604) and (606) to another nanoparticle cluster (604) and (606) through hopping are both quantum mechanical effects.
Release of electrons from the emitter electrode (402) through thermionic emission as described herein is an energy selective mechanism. A thermionic barrier in the apertures (408) between the emitter electrode (402) and the collector electrode (404) is induced through the interaction of the nanoparticles (604) and (606) inside the apertures (408) with the electrodes (402) and (404). The thermionic barrier is at least partially induced through the number and material composition of the plurality of nanoparticle clusters (604) and (606). The thermionic barrier induced through the nano-fluid (602) provides an energy selective barrier on the order of magnitude of about 1 eV. Accordingly, the nano-fluid (602) provides an energy selective barrier to electron emission and transmission.
To overcome the thermionic barrier and allow electrons (612) to be emitted from the emitter electrode (402) above the energy level needed to overcome the barrier, materials for the emitter electrode (402) and the collector electrode (404) are selected for their work function values and Fermi level values. The Fermi levels of the two electrodes (402) and (404) and the nanoparticle clusters (604) and (606) will try to align by tunneling electrons (612) from the electrodes (402) and (404) to the nanoparticle clusters (604) and (606). The difference in potential between the two electrodes (402) and (404) (described elsewhere herein) overcomes the thermionic barrier, and the thermionic emission of electrons (612) from the emitter electrode (402) occurs with sufficient energy to overcome the thermionic block. Notably, and in general, for cooling purposes, removing higher energy electrons from the emitter electrode (402) causes the emission of electrons (612) to carry away more heat energy from the emitter electrode (402) than is realized with lower energy electrons. Accordingly, the energy selective barrier is overcome through the thermionic emission of electrons at a higher energy level than would be otherwise occurring without the thermionic barrier.
Once the electrons (612) have been emitted from the emitter electrode (402) through thermionic emission, the thermionic barrier continues to present an obstacle to further transmission of the electrons (612) through the nano-fluid (602). Smaller inter-electrode gaps on the order of about 1 nm to about 10 nm, as compared to those gaps in excess of 100 nm, facilitate electron hopping, i.e., field emission, of short distances across the apertures (408). Energy requirements for electron hopping are much lower than the energy requirements for thermionic emission; therefore, the electron hopping has a significant effect on the energy generation characteristics of the device (400). The design of the nano-fluid (602) enables energy selective tunneling, e.g., electron hopping, that is a result of the barrier (which has wider gap for low energy electrons) which results in electrons above the Fermi level being a principal hopping component. In an exemplary embodiment, direction of the electron hopping is determined through the selection of the different materials for the electrodes (402) and (404) and their associated work function and Fermi level values. The electron hopping across the nano-fluid (602) transfers heat energy with electrons (612) across the apertures (408) while maintaining a predetermined temperature gradient such that the temperature of the nano-fluid (602) is relatively unchanged during the electron transfer. Accordingly, the emitted electrons transport heat energy from the emitter electrode (402) across the apertures (408) to the collector electrode (404) without increasing the temperature of the nano-fluid (602).
In an embodiment, the thermal energy harvesting thermionic device (400) is configurable with respect to the physical dimensions therein. In an exemplary embodiment, the device (400) has a length measurement, in a direction along the X-axis in
The first (top) harvester unit (701A) includes an emitter electrode (cathode) (702A) having a coating (734A), a collector electrode (anode) (704A) having a coating (764A), and a chamber (or aperture) interposed between the electrodes (702A) and (704A) filled with nano-fluid (708A) and surrounded on opposite sides by insulating spacers (706A,1) and (706A,2). The second (middle) harvester unit (701B) includes an emitter electrode (cathode) (702B) having a coating (734B), a collector electrode (anode) (704B) having a coating (764B), and a chamber (or aperture) between the electrodes (702B) and (704B) filled with nano-fluid (708B) and surrounded on opposite sides by insulating spacers (706B,1) and (706B,2). The third (bottom) harvester unit (701C) includes an emitter electrode (cathode) (702C) having a coating (734C), a collector electrode (anode) (704C) having a coating (764C), and a chamber (or aperture) between the electrodes (702C) and (704C) filled with nano-fluid (708C) and surrounded on opposite sides by insulating spacers (706C,1) and (706C,2).
A first insulating layer (770A) is positioned above the first harvester unit (701A). A second insulating layer (770B) is interposed between the first harvester unit (701A) and the second harvester unit (701B). A third insulating layer (770C) is interposed between the second harvester unit (701B) and the third harvester unit (701C). A conductive plate (772) is positioned below the third harvester unit (701C) as a thermal conductor for transmitting heat from a heat source to the thermal energy harvesting thermionic device (700). In another embodiment, reference numeral (772) may be the heat generating source.
The emitter electrodes (cathodes) (702A), (702B), and (702C) may be made of any of the materials described herein. In an exemplary embodiment, the emitter electrodes (702A), (702B), and (702C) are made of a copper foil coated with platinum (Pt). The emitter electrode coatings (734A), (734B), and (734C) may be comprised of cesium oxide. The emitter electrode coatings (734A), (734B), and (734C) may cover, for example, about 60 to 80 percent of the surface area of their respective emitter electrodes. The collector electrodes (anodes) (704A), (704B), and (704C) likewise may be made of any of the materials described herein. In an exemplary embodiment, the collector electrodes (704A), (704B), and (704C) are made of tungsten foil. The collector electrode coatings (764A), (764B), and (764C) may be comprised of cesium oxide. The collector electrode coatings (764A), (764B), and (764C) may cover, for example, about 60 to about 80 percent of the surface area of their respective collector electrodes.
The nano-fluids (708A), (708B), and (708C) may be, for example, any of the materials described above in connection with
The insulating spacers (706A,1), (706A,2), (706B,1), (706B,2), (706C,1), and (706C,2) and the insulating layers (770A), (770B), and (770C) may be comprised of, for example, an alkanethiol. The spacers may have a multi-layer (e.g., five-layer) structure, with each layer at least one micron in thickness.
For the purposes of illustration, the thermal energy harvesting thermionic device (700) has been shown with three thermionic units (701A), (701B), and (701C) stacked on one another. It should be understood that the device (700) may include fewer (two) or more thermionic units than shown. Although
The thermal energy harvesting thermionic device (700) may be substitute into the apparatus (110) or (210) for the thermionic device (114) or (214), respectively.
Embodiment for Manufacturing the Apparatus (110) and (210)
Referring to
Exemplary electrospray and nano-fabrication technique(s) and associated equipment, including three-dimensional printing and four-dimensional printing (in which the fourth dimension is varying the nanoscale composition during printing to tailor properties) for forming the substrate (122), the thermionic device (114) (including the cathode (116), the anode (118), and the spacer (120) with nano-fluid), the first intermediate layer (124) and the second intermediate layer (126), and the electronics layer (128) with one or more electronic components, as well as other components (e.g., housing (112)), layers and coatings discussed herein, including those of the device (400) and the apparatus (110) and (210), are set forth in U.S. Application Publication No. 2015/0251213 published Sep. 10, 2015 entitled “Electrospray Pinning of NanoGrained Depositions,” U.S. patent application Ser. No. 16/416,849 filed May 20, 2019 entitled “Single-Nozzle Apparatus for Engineered Nano-Scale Electrospray Depositions,” U.S. patent application Ser. No. 16/416,858 filed May 20, 2019 entitled “Multi-Nozzle Apparatus for Engineered Nano-Scale Electrospray Depositions,” and in U.S. patent application Ser. No. 16/416,869 filed May 20, 2019 entitled “Method of Fabricating Nano-Structures with Engineered Nano-Scale Electrospray Depositions,” the detailed descriptions and drawings of which are incorporated herein by reference. The apparatus and methods of those applications may be practiced alone or in combination with one another for making the various layers and components of the apparatus, e.g., (110) and (210), disclosed herein. Generally, those applications include disclosures of embodiments regarding, among other things, a composition including a nano-structural material, grain growth inhibitor nanoparticles, and/or at least one of a tailoring solute or tailoring nanoparticles. Any one of more of those compositional components (e.g., grain growth inhibitors) may be excluded from the embodiments described herein.
A simplified diagram of an electrospray apparatus or system is generally designated by reference numeral (900) in
Embodiment for Operating the Systems (102) and (202)
Referring to
In an exemplary embodiment, system (202) uses environmental heat or heat from an outside heat source for generating electricity from the thermal energy harvesting thermionic device (214) and powering the electronics of the electronics layer (228).
Another embodiment for generating electric power with a thermal energy harvesting thermionic device to operate one or more electronic components of the electronics layer (228) of the apparatus (210) will now be described. The apparatus (210) is positioned so that the cathode (216) is proximal to the electronics layer (228). An electrical path is established from the thermionic device (214) of the apparatus (210) to the electronics layer (228) of the apparatus (210). A heat-dissipating device (e.g., device (234) of
Nano-Electronic Component Embodiments
As described above, the electronics layers (128) and (228) each include at least one electronic component. In certain exemplary embodiments described below with reference to
A quantum island (also referred to in embodiments as a quantum dot) (1310) is shown in the center of the circuit diagram (1300). Positioned between the source electrode (1302) and the quantum island (1310) is a first junction (1312), and positioned between the drain electrode (1304) and the quantum island (1310) is a second junction (1314). The gate electrode (1306) is capacitively coupled to the quantum island (1310), as represented in
Conductive traces (or lines) (1420), (1422), and (1424) are electrically connected to the source electrode (1402), the drain electrode (1404), and the gate electrode (1406), respectively. Although not shown, if a backgate electrode was present, as in
In
In an exemplary embodiment, the gate electrode (1406) is positioned approximately ninety degrees from the source electrode (1402) and the drain electrode (1404). In an exemplary embodiment, the gate electrode (1406) is co-planar with the source electrode (1402) and the drain electrode (1404).
Operation of SETs is based on the Coulomb blockade effect. Electrons pass between the source electrode (1302), (1402) and the drain electrode (1304), (1404) one-by-one onto and off of the quantum island (1310), (1410). Electrons lack sufficient energy to transfer between the either the source electrode (1302), (1402) or the drain electrode (1304), (1404) and the quantum island (1310), (1410) when the gate voltage and the bias voltage (between the source and the drain electrodes) are zero. When the energy of the system reaches the Coulomb energy, e.g., by increasing the bias voltage, an electron transfers between the source electrode (1302), (1402) and the quantum island (1310), (1410), then the quantum island (1310), (1410) and the drain electrode (1304), (1404). The Coulomb blockage is lifted by the increased voltage to allow electron travel through the island (1310), (1410). The Coulomb energy, EC, is given by Equation (1) below:
EC=e2/2C Equation (1)
wherein e is the charge on an electron, and C is the total capacitance of the source and drain junctions and the gate electrode, which the quantum island (1310), (1410) is capacitively coupled to.
The Coulomb gap voltage, e/C, is the voltage necessary to lift the blockade and transfer an electron across the spaces (1426) and (1428) to and from the quantum island (1310), (1410). When the bias voltage between the source electrode (1302), (1402) and the drain electrode (1304), (1404) is greater than the Coulomb gap voltage, electrons actively travel across the spaces (1426) and (1428) one-by-one resulting in a current through the transistor independent of the gate bias. In operation according to an embodiment, the bias voltage between the source and drain electrode is maintained below the Coulomb gap voltage, and the Coulomb blockage effect, and hence the electron transfer across the spaces (1426) and (1428), is controlled by altering the gate voltage.
In order to see the quantization of the electron flow (known as the Coulomb staircase), the thermal energy is less than the Coulomb gap voltage. For a SET to operate at room temperature, kT<<e2/2C, which translates into the capacitance C<<e2/2kT˜3.09×10−18 F. The capacitance (CNP) of a sphere is C=q/V where q is total charge and V=q/47πεor, where εo is the permittivity of free space, and r is the radius of the nanoparticle. Substituting for the voltage, V, and solving for the capacitance, results in C=4πεor that is less than 3×10−18F. Accounting for the uniform monolayer (of dielectric constant ε) on a spherical nanoparticle, the capacitance can be expressed as CNP=ANPεoε (r+d)/rd where ANP is the surface area if a sphere (4πr2), and d is the thickness of conductive coating (0.5 nm). Substituting for the surface area of the sphere results in the equation CNP=4πεεor(r+d)/d. The coated nanoparticles have a capacitance of less than 0.6×10−18F which enables operating temperatures substantially above room temperature. Thus, in an embodiment a 1 nm SET (wherein the 1 nm is the characteristic dimension of the smallest working features, e.g., the island) avoids thermally-induced random tunneling events and operates at elevated temperatures.
The first SET (1501A) includes a first source electrode (1502A), a first drain electrode (1504A), and a first quantum island (1510A) positioned between and spaced from the first source electrode (1502A) and the first drain electrode (1504A). The first SET (1501A) further includes a first gate electrode (1506A) positioned perpendicular or relatively perpendicular from the first source and drain electrodes (1502A) and (1504A). The first SET (1501A) includes one or more first nanoscale connections (1534A) between the first source electrode (1502A) and the first quantum island (1510A) and between the first quantum island (1510A) and the first drain electrode (1504A).
Similarly, the second SET (1501B) includes a second source electrode (1502B), a second drain electrode (1504B), and a second quantum island (1510B) positioned between and spaced from the second source electrode (1502B) and the second drain electrode (1504B). The second SET (1501B) further includes a second gate electrode (1506B) positioned perpendicular or relatively perpendicular from the second source and drain electrodes (1502B) and (1504B), respectively. The second SET (1501B) includes second nanoscale connections (1534B) between the second source electrode (1502B) and the second quantum island (1510B) and between the second quantum island (1510B) and the second drain electrode (1504B).
The one or more nanoscale connectors (1534A) establish a first connection or junction between the first source electrode (1502A) and the first quantum island (1510A) embodied as a single nanometer-scale conductive particle and a second connection or junction between the first drain electrode (1504A) and the second quantum island (1510A) embodied as a single nanometer-scale conductive particle. In an embodiment, one or more of the nanoscale connectors (1534A) extend lengthwise continuously between the first source electrode (1502A) and the first drain electrode (1504A), coming within 1 nanometer of, and in a particularly exemplary embodiment coming into contact with, the first quantum island (1510A). In another exemplary embodiment, one or more first nanoscale connectors extend from the first source electrode (1502A) to the quantum island (1510A), and one or more different second nanoscale connectors extend from the first drain electrode (1504A) to the first quantum island (1510A).
Likewise, one or more nanoscale connectors (1534B) establish a third connection or junction between the second source electrode (1502B) and the second quantum island (1510B) embodied as a single nanometer-scale conductive particle and a fourth connection or junction between the second drain electrode (1504B) and the second quantum island (1510B) embodied as a single nanometer-scale conductive particle. In an embodiment, one or more of the nanoscale connectors (1534B) extend lengthwise continuously between the second source electrode (1502B) and the second drain electrode (1504B), coming within 1 nanometer of, and in a particularly exemplary embodiment coming into contact with, the second quantum island (1510B). In another exemplary embodiment, one or more third nanoscale connectors extend from the second source electrode (1502B) to the second quantum island (1510B), and one or more different fourth nanoscale connectors extend from the second drain electrode (1504B) to the second quantum island (1510$).
Although nanoscale connectors (e.g., (1534A, 1534B)) are not illustrated in the embodiments of
The chip (1500) includes an encapsulate (1536), shown in phantom in
Representative materials for the chip (1500) and its various components are discussed below. The same materials may be used for the embodiments illustrated in
In an exemplary embodiment, the substrate (or wafer) (1532) is made of an inert, dielectric material, especially but not limited to glossy polymers. Representative, non-limiting materials that may be used for the substrate include, for example, epoxies, ceramic nano-particle-filled resins (e.g., Grandio™), silica nanoparticle-reinforced epoxies (e.g., Futura Bond™) polydimethylsiloxane (PDMS), polymethylmethacrylate (PMMA), polymethacrylate (PMA), polyvinylalcohol (PVA), polyvinylchloride (PVC), polyacrylic acid (PAA), Mercon™, phenyl-C61-butyric acid methyl ester (PCBM), pentacene, carbazoles, phthalocyanine, and aerogels, such as silica, aluminum, chromia, graphene oxide, and tin oxide aerogels. In an exemplary embodiment, the substrate (1532) is not made of (i.e., is free of) a semiconductor material, such as silicon, gallium, arsine, carbides, etc.
In an exemplary embodiment, the surface of the substrate (1532) is hydrophobic. For example, inherently hydrophobic materials such as PDMS may be selected as the substrate (1532) to provide the hydrophobic surface. In another embodiment, the surface of a non-hydrophobic (hydrophilic) substrate (1532) may be treated, such as with plasma, to render the surface hydrophobic.
The source electrodes (1502A), (1502B), the drain electrodes (1504A), (1504B), the gate electrodes (1506A), (1506B), the backgate electrode (not shown in
In an exemplary embodiment, the quantum islands (1510A), (1510B) are comprised of a conductive material, such as a metal, including, for example, gold, silver, and/or copper, or a conductive non-metal, such as graphene or an alkanethiol. In another exemplary embodiment, the quantum islands (1510A), (1510B) each comprise a substantially non-conductive core with a conductive coating. The core shape may be that of a sphere, for example. An exemplary core material is polystyrene latex (PSL). Suitable conductive coatings include, for example, gold, silver, copper, and/or graphene.
In an exemplary embodiment, any one or more of the electrodes (1502A), (1502B), (1504A), (1504B), (1506A), and (1506B) (as well as backgate electrode if present (see (1308) in
In an exemplary embodiment the nanoscale connectors (1534A) and (1534B) each comprise one or more conductive carbon nanotubes (CNT), and in an exemplary embodiment the connectors (1534A) and (1534B) are conductive Single Wall Carbon Nanotubes (SWCNTs). Commercial suppliers of SWCNTs include U.S. Research Nanomaterials, although the SWCNTs that may be used in connection with the embodiments described herein are not limited to SWCNTs supplied by that commercial supplier.
Representative encapsulates (1536) include aerogels, such as silica, alumina, chromia, graphene oxide, and tin oxide aerogels.
Representative dimensions for the chip (1500) and its various components are discussed below. The same dimensions may be used for the embodiments illustrated in
The size of the substrate (or wafer) (1532) is not particularly limited. According to an exemplary embodiment, the substrate (1532) has a thickness (in the z-direction in
The electrodes (1502A), (1502B), (1504A), (1504B), (1506A), and (1506B) (as well as backgate electrodes if present (see (1308) in
In an exemplary embodiment, the quantum islands (1510A), (1510B) are each a single nanometer-scale conductive particle (or nanoparticle). According to an exemplary embodiment, the single nanometer-scale conductive particle has an effective size of not greater than 10 nanometers, such as in a range of about 1 nanometer to about 10 nanometers, or in a range of about 1 nanometer to about 5 nanometers. In another embodiment, the single nanometer-scale conductive particle is less than 1 nanometer. The effective size is the largest dimension of the nanoparticle. In the event that the single nanometer-scale conductive particle is a sphere, for example, the effective size will be the diameter of the spherical particle.
In exemplary embodiments, the nanoscale connectors (e.g., SWCNTs) have lengths in a range of 10 to 100 nanometers. In an additional exemplary embodiment, the nanoscale connectors (e.g., SWCNTs) have a diameter of about 1 nanometer.
In an exemplary embodiment, the encapsulate (1536) has a thickness in a range of 10 nanometers (nm) to 100 nanometers.
The electrospray apparatus (1600) has capillary needle (1602) with a central passage (1604) through which liquid material is received from a syringe pump (1605) via a conduit (1608) that communicates with the top of the capillary needle (1602). In an embodiment, induction heating coils (1624) wrap around the capillary needle (1602), serving to heat the liquid material (1604). Fewer or more induction heating coils (1624) than shown may be used, or the induction heating coils may be eliminated. A Faraday cage (1626) around the capillary needle (1602) and the induction heating coils (1624) shield the environment from electromagnetic radiation generated by the induction heating coils (1624). A vented heat shield (1628) positioned outside the Faraday cage (1626) performs a similar shielding function with respect to heat generated by the induction heating coils (1624).
An electrospray nozzle or print head (referred to hereinafter as a print head in the interest of brevity) (1610) is coupled to the bottom of the capillary needle (1602) to receive the liquid material (not shown) from the capillary needle (1602) with a capillary tube (1611). While the capillary needle (1602) and the capillary tube (1611) are shown as separate but communicating structures, alternatively, the capillary tube (1611) may form part of the capillary needle (1602). The capillary tube (1611) is configured for transporting the liquid material out of the capillary needle (1602) to the print head (1610).
In an exemplary embodiment, the print head (1610) comprises an ultrafine conductive hollow needle to concentrate electric fields around its outlet orifice. The orifice opening can be selected from several hundred nanometers to a few microns, such as 100 nm to 10,000 nm, depending upon the material to be deposited.
An extractor electrode (1622) is coupled to the print head (1610). As shown in
Additionally, the extractor electrode (1622) also generates a magnetic field in an exemplary embodiment. The generated magnetic field can serve to limit dispersion of the stream of droplets. When discharged from the print head (1610), the electrosprayed droplets are charged. The charge tends to disperse the droplets from one another. More specifically, the charge imparts a force on the particles that is orthogonal to both the magnetic field lines and the motion of the charged particles. If the magnetic field is strong relative to the velocity of the charged particle, however, the charge particles will tend to orbit magnetic field lines while moving along the lines. Thus, the dispersive tendencies of the stream of charged droplets are countered by the magnetic field.
The extractor electrode (1622) is shaped to provide both the electric field and magnetic field with characteristics useful for extracting liquid material from the electrospray nozzle (1610), driving the stream of droplets (1656) toward to the moving stage (1636), and focusing the stream of droplets (1656) on a deposition area (1652) (see
As previously mentioned, the deposition area (1652) of the moving stage (1636) serves as the target for the stream of droplets (1656). In an embodiment, the moving stage (1636) is configured for moving relative to the print head (1610) in three orthogonal dimensions. In an embodiment, the moving stage (1636) is a piezo-flexure guided stage providing bidirectional repeatability on a nanometer scale. The moving stage (1636) is typically electrically grounded so that the moving stage (1636) forms a planar endpoint for the electrical field. In an exemplary embodiment, the moving stage (1636) comprises a utility base plate (1634), a cooling chuck (1632) and an object holder (1630) having the previously mentioned deposition area (1652) on an upward facing surface of the object holder (1630). The object holder (1630) is configured for providing a surface for the fabrication of an object (1678) that results from the electrospray process, and more particularly the EMAF technique. The cooling chuck (1632) is positioned underneath the object holder (1630) and coupled thereto. The cooling chuck (1632) is configured for cooling the object holder (1630), typically with one or more thermoelectric cooling chips that use, for example, DC current to pump heat from the object holder (1630) to the utility base plate (1634). The utility base plate (1634) is exposed to ambient air and may be cooled with natural convection or forced air flow. The utility base plate (1634) has wiring (1644) for powering the cooling chuck (1632) and for any sensors that may be embedded in the object holder (1630). The utility base plate (1634) has an enclosure gas inlet (1620) to inject gases into the enclosure cavity (1618). Example gases include inert gases such as nitrogen, argon, and the like.
The exemplary electrospray apparatus (1600) has an enclosure (1614) coupled to the print head (1610) and the capillary needle (1602). In the exemplary embodiment, the enclosure (1614) is made of quartz, but other suitable materials may be used. The enclosure (1614) is shaped such that when placed in contact with the moving stage (1636), the enclosure (1614) and moving stage (1636) collectively define an enclosure cavity (1618) that serves as a controlled environment for the electrospray process. The enclosure (1614) has an enclosure floating frame (1616) that is slidingly coupled to the outer edges of the central part of the enclosure (1614). The enclosure floating frame (1616) maintains contact with the moving stage (1636) as the moving stage (1636) moves vertically over short distances and horizontally with respect to the enclosure (1614) and floating frame (1616). Maintaining contact between the enclosure floating frame (1616) and the moving stage (1636) keeps the enclosure cavity (1618) fully enclosed during electrospray object fabrication. An enclosure gasket (1648) on the bottom of the enclosure floating frame (1616) improves the seal of the enclosure cavity (1618) and allows the moving stage (1636) to move laterally without breaking the seal. In the exemplary embodiment, the enclosure gasket (1648) is made of felt, but in other embodiments may be made of other suitable materials, including but not limited to those typically used for gaskets.
In exemplary embodiments, an Electrical Mobility Aerosol Focusing (EMAF) technique is employed for electrospraying. According to this EMAF technique, charged nanoparticles in aerosolized droplets discharged from the print head (1610) are guided by a precise position by a concentrated electromagnetic field generated by the extractor electrode (1622).
In an embodiment for carrying out the EMAF technique, a stream of droplets (1656) emerges from a Taylor cone (1650) that forms on the tip of the print head (1610) when the electric field draws the liquid material in the aerosol from the print head (1610). Dispersion of the stream of droplets (1656) is limited by the magnetic field. A region on the fabricated object (1678) where the stream of droplets (1656) impacts is referred to as the deposition area (1652). In an embodiment, the fabricated object (1678) comprises successive deposition layers. In another embodiment, the fabricated object (1678) comprises a single deposition layer. In yet another embodiment, the fabricated object (1678) comprises single-layer structures and multi-layer structures. In another embodiment, a pre-formed substrate or wafer (such as (332)) is positioned on the object holder (1630) prior to electrospraying. In still another embodiment, the substrate or wafer (such as (332)) is fabricated on the object holder (1630), and constitutes the deposition area (1652) for deposition of electrodes, traces, quantum islands, and any other features of the SETs and related circuits.
The moving stage (1636) moves laterally while the stream of droplets (1656) impacts on the fabricated object (1678) (or object holder (1630)), forming the current deposition layer over all or part of the deposition area (1652), be it previous deposition layers or the object holder (1630). The distance between the print head (1610) and the deposition area (1652) is referred to as the stand-off distance (1654) or distance-to-deposition. In exemplary embodiments, the stand-off distance is in a range of 0.5 mm to 5 mm. If no other actions are taken, that is, if the moving stage 436) is not moved downwardly, e.g., vertically, the stand-off distance (1654) will change as the stream of droplets (1656) impacts on the fabricated object (1678) and adds layer(s) of deposited material. On the next pass, creating the next deposition layer, the stand-off distance (1654) would be reduced, if no other action is taken. In an exemplary embodiment, the stand-off distance (1654) is maintained at or near a target stand-off distance. The maintenance of a constant stand-off distance can be achieved by adjusting the moving stage (1636) vertically as necessary.
In an exemplary embodiment, the syringe pump (1605) controls the flow rate of the liquid materials to affect the distribution of the spray so as to obtain a monodispersed droplet production. In an exemplary embodiment, the monodispersed droplets each contain a statistical average of a single nanoparticle per monodispersed droplet. The number of nanoparticles per droplet can be controlled by selection of an appropriate concentration of nanoparticles for a given droplet size.
In an exemplary embodiment, the flow rate is controlled in combination with the moving stage (1636) to produce print velocities in a range of, for example, 0.0001 mm (0.1 micron) to 100 mm per second. In an exemplary embodiment, the volumetric flow rate is, by way of example and not limitation, about 0.1 picoliters (0.1×10−12 liters) per second. An example of a suitable moving stage is an XYZ piezo stage (LP300) from MadCityLabs, although this example is not intended to be limiting as there are other acceptable commercial moving stages.
Electrospray, also known as electrostatic atomization, typically involves the atomization of a liquid through the Coulombic interaction of charges and the applied electric field. Electrostatic atomization offers several advantages over alternative atomization techniques. Electrospray droplet streams are mainly due to the net charge on the surface of the droplets and the Coulombic repulsion of the droplets. This net charge causes the droplets to disperse, preventing their coalescence.
The trajectory of a charged droplet can be guided by the electrostatic field. According to an embodiment, the electrical power supplied to the extractor electrode (1622) for generating the electrostatic field is a 10 microamp square wave signal at a frequency of 22 kHz driven at 10 kilovolts peak-to-peak. In addition, the electrical mobility aerosol focusing is characterized in embodiments by previously deposited structures or layers acting as an intense electric field concentrator to attract subsequent droplets in-flight to the nanostructure. Another advantage of this type of atomization is the ability to control the size distribution of the spray and under specific electrodynamic operating conditions, obtain a monodispersed spray.
The electrical mobility of the in-flight droplets depends on, at least, the particle size and the electrical charge. The smaller the particle and/or the higher the electrical charge, the higher the electrical mobility. The electrical mobility, Zp, is in general dependent on the particle diameter dp, as shown by Equation (2):
Zp=neC(dp)/3πηdp Equation (2)
wherein dp is the aerosol particle diameter, n is the number of electrical charges on the particle, e is the elementary charge, C is the Cunningham slip correction factor, which is a function of the aerosol diameter, and η is the gas viscosity.
Without wishing to be bound by theory, electrospray can be described as being characterized by the formation of the liquid meniscus at a capillary tip (Smith, 1986) which results from a number of forces acting on the interface, including surface tension, gravitational, electrostatics, inertial, and viscous forces. Sir Geoffrey Taylor was the first to calculate analytically a conical shape for the meniscus through the balance of surface tension and electrical normal stress forces which we now know is called the “Taylor cone” in electrospray and appears in the cone-jet mode (Taylor, 1964). Monodispersed ink droplets are ejected from the cone due to the accumulation of charge.
In the cone-jet mode, liquid leaves the capillary in the form of an axisymmetric cone with a thin jet emitted from its apex. The small jet of liquid issuing out of the print head is electrostatically charged when subjected to an intense electric field at the tip of the print head (Birmingham, et al., 2001). The charged droplets are propelled away from the print head by the Coulomb force and are dispersed out as a result of charge on the droplets. In conventional practice, the droplets are approximately 10 microns in diameter. In exemplary embodiments described herein, the droplets in connection deposition of all layers and structures are nanodroplets having diameters of, for example, 20 nanometers to 100 nanometers.
In exemplary embodiments, the droplets are comprised of a suspension (e.g., colloidal suspension) or ink containing the nanoparticles. During flight and/or after impact, the droplets containing the nanoparticles rapidly evaporate in microseconds, leaving only the nanoparticle.
Referring back to
In order to achieve higher production rates, such as by practicing parallel device fabrication or serial device fabrication, multiple print heads (1610) can be used. According to an embodiment, the electrospray apparatus (1600) has more than one capillary needle (1602) and more than one print head (1610), e.g., with each print head (1610) associated with a respective capillary needle (1602). In another embodiment, the electrospray apparatus (1600) has a capillary needle (1602) associated with a plurality of capillary tubes (1611) and a plurality of print heads (1610), e.g., with each of the print heads (1610) associated with a respective capillary tube (1611). According to the above-described and other multiple print head embodiments, each print head (1610) may be associated with a respective extractor electrode (1622). An example of a multi-head electrospray apparatus is illustrated in FIG. 8 of U.S. Application Publication No. 2015/0251213.
The utility of a multi-nozzle electrospray apparatus is apparent from the following example. According to an embodiment, electrospraying a droplet with a diameter of 100 nm at 10 kHz (10,000 per second) ejections, the printing flow rate from a single electrospray capillary is 5 to 100 femtoliters (5×10−15 L) per second. To achieve drop overlap to ensure good conductivity of metal nanoparticle traces, a print speed of 100 microns per second would result in a printing time of 10 seconds for a 10 micron-size square. Extrapolating to a standard Very Large Scale Integrated (VLSI) chip with an area of 1 cm2 at a dense patterning at 10 nm resolution, 100 nozzles would take about a day to complete the VLSI chip, which represents an excellent production rate compared to current industrial processes.
The exemplary electrospray apparatus (1700) of
The main control unit (1784) uses the profile data to control the electrospray apparatus (1700) during deposition of the next deposition layer. For deposition of the next deposition layer, the main control unit (1784) has the moving stage (1736) move vertically as necessary to maintain the stand-off distance (1754) at the target stand-off distance, based on the profile data of the proceeding deposition layer. It should be understood, however, that the structures fabricated with the exemplary electrospray apparatus (1700) may be comprised of a single deposition layer.
The main control unit (1784) also uses the profile data to compensate for errors in the previous deposition layers. If the profile data of the proceeding deposition layer indicates that some region of the fabricated object (1778) is too thick, the main control unit (1784) can correct on the next deposition layer by slowing the flow rate of liquid material from the print head (1710) when over that region. Likewise, if the profile data of the proceeding deposition layer indicates that some region of the fabricated object (1778) is too thin, the main control unit (1784) can correct on the next deposition layer by increasing the flow rate of liquid material through the print head (1710) when over that region.
The main control unit (1784) is connected by main control unit communication links (1796) to one or more sub-control units. The apparatus (1700) is illustrated including a first sub-control unit (1786) for controlling the moving stage (1736), a second sub-control unit (1788) for controlling the extractor electrode (1722), and a third sub-control unit (1790) for controlling a heater (such as heater (1658) of
Although not shown, the apparatus (1600) or (1700) can include a microscope to study droplet ejection, precise placement, and other aspects of the deposition process. An example of a suitable microscope is a Scanning Electron Microscope (SEM).
An exemplary method for fabricating a Single Electron Transistor (SET), such as but not limited to the SETs illustrated in
Ambient conditions (e.g., temperature, humidity, and gas composition (e.g., air)) may be practiced in carrying out the various steps described herein.
Fabrication of the Substrate (1802)
Referring now to the flowchart (1800) of
As mentioned above, in an exemplary embodiment the substrate (1432), (1532) is made of a material that is inert and/or dielectric, including polymers, especially but not limited to glossy polymers. Representative, non-limiting materials that may be used for the substrate (1432), (1532) include, for example, epoxies, ceramic nano-particle-filled resins (e.g., Grandio™), silica nanoparticle-reinforced epoxies (e.g., Futura Bond™), polydimethylsiloxane (PDMS), polymethylmethacrylate (PMMA), polymethacrylate (PMA), polyvinylalcohol (PVA), polyvinylchloride (PVC), polyacrylic acid (PAA), Mercon™, phenyl-C61-butyric acid methyl ester (PCBM), pentacene, carbazoles, phthalocyanine, and aerogels, such as silica, aluminum, chromia, graphene oxide, and tin oxide aerogels. In an exemplary embodiment, the substrate (1432), (1532) is not made of, and is free of, a semiconductor material, such as silicon, gallium, arsine, carbides, etc. The substrate (1432), (532) is deposited using monodispersed droplets in an exemplary embodiment.
In accordance with an embodiment, the substrate-forming material can be introduced into the electrospray apparatus (1600) or (1700) in a precursor form, including but not limited to monomeric, oligomeric, or pre-polymer form and be subject to polymerization initiated by, for example, the electrospray charge. In accordance with other embodiments, the substrate material may be introduced into the electrospray apparatus (1600) or (1700) as a solution, emulsion, or suspension, and in an embodiment as nanoparticles suspended in a solvent or liquid medium. In an exemplary embodiment, one or more surfactants may also be included to prevent agglomeration of the nanoparticles. Representative surfactants include, but are not limited to, TRITON®-100X, TWEEN®-20, and TWEEN®-80.
In an exemplary embodiment, the substrate-forming material is deposited as nano-scale droplets (or nanodroplets) having diameters in a range of, for example, 20 nanometers to 100 nanometers. During flight and/or upon impact on the object holder (1630), (1730), the carrier liquid evaporates, leaving the deposited nanoparticles to cure and build on one another.
In an exemplary embodiment, the surface of the resulting substrate is hydrophobic. Certain of the above exemplary materials, such as PDMS, are inherently hydrophobic materials. Others may be rendered hydrophobic by, for example, subjecting the surfaces to ionized gas (plasma) treatment.
The electrospray apparatus (1600) or (1700) allows for precise control over substrate thickness and topography. In an embodiment, the substrate is deposited by electrospray additive manufacturing to a thickness of 1 nanometer to 10 microns, although that range is not necessarily limiting. Control over the electrospray process can, in an exemplary embodiment, produce a substrate with a substantially planar surface. In an exemplary embodiment, the substantially planar surface is sufficiently planar to meet strict semiconductor fabrication requirements. In an embodiment, surface variations, as measured by a profilometer, of the area on which the SET is to be deposited are not greater than 5 nanometers, and in an exemplary embodiment not greater than 1 nanometer.
Electrospray Deposition of Electrodes (1804)
The electrodes (e.g., source (1402), (1502A), (1502B), drain (1404), (1504A), (1504B), gate (1406), (1506A), (1506B), and/or backgate) are fabricated directly on the substrate (e.g., (1432), (1532)) via electrospray deposition, more particularly an Electrical Nobility Aerosol Focusing (EMAF) technique. In an exemplary embodiment, the electrospray apparatus (1600) or (1700) is used to practice the EMAF technique.
Representative metals for forming the electrodes include, but are not limited to, gold, silver, and/or copper, although this list is not exhaustive. A representative non-metal for forming the electrodes includes, but is not limited to, graphene, although this list is likewise not limiting. The various electrodes (e.g., source, drain, gate, backgate) can be made of the same material or different materials in any combination.
The electrode-forming droplets discharged from the electrospray apparatus may be comprised of a solution, emulsion, or suspension, and in an embodiment as nanoparticles suspended, dissolved, or otherwise contained in a liquid carrier. In an exemplary embodiment, one or more colloidal inks are used for deposition of the electrodes. In an embodiment, the liquid carrier comprises an organic liquid such as an alcohol, aliphatic hydrocarbon, ester, ketone, others, and combinations including one or more of the same. During flight and/or upon impact on the target surface, the carrier liquid evaporates, leaving the deposited nanoparticle.
In an exemplary embodiment, the electrode-forming droplets comprise aerosols of monodispersed nanodroplets 20 nanometers to 100 nanometers in diameter. In an exemplary embodiment, the nanodroplets are deposited to overlap with one another in an exemplary embodiment to ensure good conductivity. By way of example only, a volumetric flowrate of about 0.1 picoliters per second may be practiced.
Electrospray Deposition of Conductive Traces (1806)
The conductive traces (e.g., conductive lines (1420), (1422), and (1424) in
Electrification of Electrodes (1808)
The electrodes are grounded to a checked ground on an electrical outlet. The software goes circuit by circuit to check similar to the electronic memory is quality-assured today. All the electrodes are grounded which creates the island target for the fast electrical mobility of the aerosol.
The charges on the nanoparticles and the electrodes average out to deposit the nanoparticles equidistance from electrodes. The electrification of the electrodes is used to precisely place the nanoparticle within the nanocircuit island location. The voltage applied guides the charged nanoparticle to its grounded location.
Electrospray Deposition of Quantum Island (1810)
The quantum islands (e.g., (1310), (1410), (1510A), and (1510B) are deposited using the EMAF technique to electrospray nanodroplets. In an embodiment, the nanodroplets include a conductive particle in a liquid carrier. The conductive particle that forms the quantum island is, according the exemplary embodiments, a metal such as, for example, gold, silver, and/or copper, or a conductive non-metal, such as graphene. The conductive coating may, in turn include a coating comprising, for example, an alkane thiol. In another exemplary embodiment, the conductive particle comprises a substantially non-conductive core with a conductive coating. The core shape may be that of a sphere, for example. An exemplary core material is polystyrene latex (PSL). Suitable conductive coatings include, for example, gold, silver, copper, graphene and/or alkane thiols. In exemplary embodiments the carrier is a colloidal ink discussed above with reference to the electrodes. During flight and/or upon impact on the target surface, the carrier liquid evaporates, leaving the deposited nanoparticle.
Deposition of Nanoscale Connections (1812)
The semiconductor connections or junctions between the electrodes and the quantum island are formed by nanoscale connectors. In an exemplary embodiment, those connectors are carbon nanotubes, and in a particular embodiment conductive single wall carbon nanotubes (SWCNTs). As described above with reference to
The nanoscale connectors can be deposited, for example, using the electrospray apparatus (1600) or (1700). In an exemplary embodiment, the connectors (e.g., SWCNTs) are deposited as droplets in which the SWCNTs (or other connectors) are suspended in a carrier liquid. An example of a suitable carrier liquid for forming the droplets and entraining the SWCNTs is water. During flight and/or upon impact on the target surface, the carrier liquid (e.g., water) evaporates, leaving the deposited connector(s).
The suspension density affects the number of SWCNTs deposited. For example, a suspension having a SWCNTs suspension density of 10 μg/ml an average of one SWCNT per microliter of suspension. At such suspension densities, however, SWCNTs can agglomerate into bundles, reducing the uniformity of the suspension. To mitigate this problem, the SWCNT suspensions may be subject to horn sonication and subsequently filtered to remove larger bundles remaining after sonication.
Dielectrophoresis (1814)
When the conductive traces (e.g., (1420), (1422), and (1424) in
The nanoscale connectors act as a bridge spanning the gaps between the electrodes and the single nanometer-scale conductive particle that serves as a quantum island. In an embodiment, after subject to DEP, one or more nanoscale connections establish a first junction between a source electrode and single nanometer-scale conductive particle and a second junction between the drain electrode and the single nanometer-scale conductive particle. In an embodiment, one or more of the SWCNTs extend lengthwise continuously between the source electrode and the drain electrode, coming within 1 nanometer of, and in a particularly exemplary embodiment coming into contact with, the nanometer-scale conductive particle. In another exemplary embodiment, one or more first SWCNTs extend from the source electrode to the single nano-scale conductive particle, and one or more second SWCNTs extend from first drain electrode to the single nano-scale conductive particle.
Initially, the CNTs expand into the gap and bring the two electrodes closer together. Once the bridging began, the primary effect of further CNT deposition is to fill in gaps in the network.
In-situ monitoring of the CNT DEP may be employed by measuring the current, voltage, and phase angle during deposition. The process is monitored by measuring the root-mean-square current amplitude (e.g., 6 mA to 30 mA) and relative phase angle (with the voltage from 0 to 30 degrees) during deposition. In an embodiment, DEP is terminated when the current reaches (e.g., plateaus at) a maximum. The measured data allow for a correlation between the CNT network densities thus establishing the feasibility of a closed-loop system suitable for industrial applications.
In a set of non-limiting experiments, initially the out-of-phase component, which is linearly related to the capacitance in a simple circuit model, rose quickly, and reached a transition point, at approximately one minute, where it changed. This change occurred as the SWCNTs began to bridge the electrode gap. Initially, the SWCNTs were expanding into the gap and bringing the two electrodes closer together. Once the bridging to the coated nanoparticle began, the primary effect of further SWCNT deposition was terminated. The SWCNT were able to rapidly connect to the coated nanoparticle because of the limited distance needed for alignment.
Once formed, the CNT/SWCNT or other connector network quality may be assessed using, for example, scanning electron microscopy (SEM) image analysis.
In an exemplary embodiment, the method comprises deposition of individual CNTs between arrays of electrodes and the assembly of large-area CNT networks. This exemplary DEP technique uses many electrospray-patterned electrodes to assemble CNT networks on a wafer in a manner appropriate for massively parallel device fabrication. The CNTs are deposited only where desired, resulting in negligible wasting of CNTs. In an exemplary embodiment, the technique can be used in a closed-loop system, enabling large-scale industrial application.
Encapsulation (1816)
Encapsulation (1816) of the nanoelectronics is performed principally to protect the SET from interfering effects such as background charge, excessive heat, and/or other hazardous conditions.
As mentioned above, the encapsulation material may be comprised of an aerogel, such as silica, alumina, chromia, graphene oxide, and tin oxide aerogels. The apparatus (1600) or (1700) can be adapted to apply a sol-gel for formation of aerogels. The aerogel may be formed, for example, by printing or spraying a sol-gel onto a surface and allowing the sol-gel to dry at a suitable temperature and pressure, such as atmospheric temperature and atmospheric pressure. According to an embodiment, the sol-gel is sprayed from a print head having a 0.4 mm internal diameter orifice at flow rate in a range of 2 to 5 ml/min, with an applied electrical power of about 20 kilovolts peak-to-peak and a frequency of 22 kHz to generate the monodispersed droplets that are electrically propelled towards the wafer. According to an embodiment, the wafer is moved in the X-Y plane at about 50 mm/second.
According to an embodiment, to prepare the sol-gel, tetraethyl-ortho-silicate (TEOS) is diluted in alcohol (e.g., anhydrous ethanol or isopropanol) to about 10-20% TEOS. A catalyst (e.g., an acid such as dilute HCl, 1M) is added dropwise to the TEOS/alcohol solution while stirring, then allowed to sit (e.g., 24-48 hours) to permit polymerization of the silicate and generation of a sol-gel. The sol-gel is diluted with alcohol and stored at a relatively low temperature (e.g., refrigeration) to slow further polymerization. Before use, the sol-gel may be diluted as for electrospray application to a desired coating thickness.
Electrospraying sol-gel creates a thin film aerogel condensation event. Electrospraying may be conducted in a heated (or elevated temperature) environment to cure the sol-gel and form the aerogel. Suitable elevated temperatures include, for example, 35° C. to 40° C. Cure temperature affects pore size. Generally, pore size increases with increased cure temperature, and decreases with decreased cure temperature. Gel time can be reduced by reducing the amount of alcohol and/or by adding additional catalyst (e.g., an acid such as HCl), although excess catalyst can result in shorter polymeric chains.
One or more energy harvesting devices having nano-scale characteristics can be employed as power sources for circuits including the SETs described herein. The energy harvesting devices described herein provide, for example, a stable voltage of about 1.1 V.
The thermal energy harvesting thermionic devices of exemplary embodiments described herein facilitate generating electrical energy via a long-lived, battery-like device for any size-scale electrical application. Thermal energy harvesting thermionic devices of exemplary embodiments have a conversion efficiency superior to presently available single and double conventional batteries. In addition, the devices of exemplary embodiments described herein may be incorporated into an apparatus for charging a secondary battery and/or powering an electrical load, such as a power-consumption device. The thermal energy harvesting thermionic devices of exemplary embodiments described herein are light weight, compact, and have a relatively long operating life with an electrical power output at a useful value. Furthermore, in addition to the tailored work functions, the nanoparticle clusters of exemplary embodiments described herein are multiphase nano-composites that include thermoelectric materials. The combination of thermoelectric and thermionic functions within a single device further enhances the power generation capabilities of the thermal energy harvesting thermionic devices.
The conversion of heat into usable electricity enables energy harvesting capable of offsetting, or even replacing, the reliance of electronics on conventional power supplies, such as electrochemical batteries, especially when long-term operation of a large number of electronic devices in dispersed locations is required. Energy harvesting distinguishes itself from batteries and hardwire power owing to inherent advantages, such as outstanding longevity measured in years, little maintenance, and minimal disposal and contamination issues. The thermal energy harvesting thermionic devices of exemplary embodiments described herein demonstrate a novel electric generator with low cost for efficiently harvesting thermal energy. The devices of exemplary embodiments described herein initiate electron flow due to the differences in the Fermi levels of the electrodes without the need for an initial temperature differential or thermal gradient, although in exemplary embodiments heat sources are used to generate the temperature differentials over the course of use.
The thermal energy harvesting thermionic devices of exemplary embodiments described herein are scalable across a large number of power generation requirements. The devices may be designed for applications requiring electric power in the milliwatts (mW), watts (W), kilowatts (kW), and megawatts (MW) ranges.
The production of renewable, sustainable, green energy resources is the critical innovation for sustainable development of human civilization. Embodiments disclosed herein include one or more thermal energy harvesting thermionic devices to power electricity-consuming electronics. Further embodiments disclosed herein include one or more thermal energy harvesting thermionic devices to complement the power of a battery or other electricity-generating system (e.g., an electrical outlet of an AC source) to power electricity-consuming devices. In exemplary embodiments, the thermionic device is a nanoscale energy harvester, and in further exemplary devices is the sole power supply. In an exemplary embodiment, the thermionic device can cause the at least one electronic component of the electronics layer to be substantially autogenous or self-powered.
Aspects of the present embodiments are described herein with reference to one or more of flowchart illustrations and/or block diagrams of methods and apparatus (systems) according to the embodiments. It should be understood that the sequence of steps in those flowcharts may be changed. Further, additional steps may be included and/or illustrated steps omitted.
While particular embodiments have been shown and described, it will be understood to those skilled in the art that, based upon the teachings herein, changes and modifications may be made without departing from its broader aspects. Therefore, the appended claims are to encompass within their scope all such changes and modifications as are within the true spirit and scope of the embodiments. Furthermore, it is to be understood that the embodiments are solely defined by the appended claims. It will be understood by those with skill in the art that if a specific number of an introduced claim element is intended, such intent will be explicitly recited in the claim, and in the absence of such recitation no such limitation is present. For non-limiting example, as an aid to understanding, the following appended claims contain usage of the introductory phrases “at least one” and “one or more” to introduce claim elements. However, the use of such phrases should not be construed to imply that the introduction of a claim element by the indefinite articles “a” or “an” limits any particular claim containing such introduced claim element to the embodiments containing only one such element, even when the same claim includes the introductory phrases “one or more” or “at least one” and indefinite articles such as “a” or “an”; the same holds true for the use in the claims of definite articles. As used herein, the term “and/or” means either or both (or any combination or all of the terms or expressed referred to).
The corresponding structures, materials, acts, and equivalents of all means or step plus function elements in the claims below are intended to include any structure, material, or act for performing the function in combination with other claimed elements as specifically claimed. The description of the present embodiments has been presented for purposes of illustration and description, but is not intended to be exhaustive or limited to the embodiments in the form disclosed. Many modifications and variations will be apparent to those of ordinary skill in the art without departing from the scope and spirit of the embodiments. The embodiments were chosen and described in order to best explain the principles of the embodiments and the practical application, and to enable others of ordinary skill in the art to understand the embodiments for various embodiments with various modifications and combinations with one another as are suited to the particular use contemplated. Accordingly, the scope of protection of the embodiment(s) is limited only by the following claims and their equivalents.
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