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The present invention relates to electrical circuits for signal processing, such as for system control, characterization or modeling. More particularly, the invention relates to electrical components that have fractional order (FO) impedances, their methods of manufacture, and their use in signal processing.
Generally, electrical components can be used to perform analog, real time calculus operations for scientific or engineering applications. More specifically, electrical components with FO impedances can be used to perform FO calculus operations, which are particularly important in many applications.
Impedance is defined as the ratio of the voltage across a device to the current through the device. In alternating current (ac) systems, it is defined as the ratio of the amplitudes of the voltage and current along with the phase lead or lag between the two.
Standard electrical components include resistors, capacitors, and inductors. Each component has some characteristics that are time-related and some that are important overall. A resistor is a simple component that creates an electrical voltage across its terminals that is proportional to the electrical current that passes through it. If the applied voltage changes, the current responds substantially immediately, without significant delay or lag in time. Overall, the resistor's terminal voltage can induce a voltage loss in a circuit. Additionally, a resistor dissipates energy equal to its instantaneous voltage times its current.
A capacitor also has time-related and overall characteristics. In relation to time, when a voltage is newly applied, a capacitor initially does not respond with a new terminal voltage but retains the original. It then slowly responds, conforming the terminal voltage to the applied voltage over a response period. In an alternating current (AC) system, a capacitor's current leads its voltage by one-quarter cycle, a phase shift of +90 degrees. Overall, the ideal capacitor alternates between storing energy from a circuit during one period and discharging it back into the circuit during the next. Ideally, it dissipates no energy.
An inductor, is similar to a capacitor, except that it responds over time to a change in applied current, rather than a change in applied voltage. Like a capacitor, it ideally stores and then releases energy rather than dissipating it. In an alternating current (AC) system, an inductor's current lags its voltage by one-quarter cycle, a phase shift of −90 degrees. Standard electrical components perform within their respective categories, such as resistors, capacitors or inductors, and have no significant mixing of characteristics. They are considered to have integer-order impedances.
However, electrical components need not be limited to the separate characteristics of ideal resistors, capacitors or inductors. It would be useful if components had characteristics that were somewhere between the characteristics of standard components. A component may have characteristics, such as a fractional order electrical impedance, that are between the characteristics of a resistor and a capacitor. For example, the characteristics could be a combination of some of the immediate, current-based response and voltage loss of a resistor with some of the time-delayed response to changes in voltage seen in capacitors.
In general, the impedance of an electrical component can be expressed as a Laplace transfer function that is proportional to s−α, where α is a number that describes the characteristics of the component. The phase shift between a device's current and its voltage is incorporated in the exponent. The phase shift, in degrees, is given by φ=−α*90. Specifically, the impedance of a standard resistor, R, can be expressed as R*s−α, with α equal to zero. The impedance of an ideal capacitor is proportional to s−1. The impedance of an ideal inductor is proportional to s1. Such impedances are of integer-order.
Ideal resistors, capacitors or inductors have α's exactly equal to 0, 1, or −1, respectively. However, actual electrical components do not have exactly integer α values. Very high quality capacitors, such as those made from polypropylene or polystyrene, have α values of 0.999 to 0.9999 or better. (See, e.g., Westerlund, et al, “Capacitor Theory,” in IEEE Trans. on Dielectrics and Electrical Insulation, 1 (1994) 5.). Even poor resistors, capacitors and inductors have α's within 5% of their ideal integer values.
Fractional order impedance can be approximated from a network of standard (integer-order impedance) components. For example, Newton approximations of impedances with α's of −½, ½, ⅓ and ¼ can be implemented using networks of resistors, capacitors and inductors, as reported by Carlson et al. in IEEE Tran. on Circuits and Systems 7 (1964) 210. Similarly, the combination of a battery, circuit terminals that connect to the battery, and corrosion between the battery terminals and the circuit terminals, can have an impedance with an α near ½ at very long time scales. Combinations like this are referred to as Warburg impedances.
In contrast to standard components with substantially integer-order impedances or combinations of components that form noninteger-order impedances, it would be useful to have a single electrical component with a non-integer value of α, giving a fractional order impedance and a phase shift that is not restricted to the values of −90, 0 or +90 degrees. For example, a component could have characteristics between those of a resistor and a capacitor, such as an exemplary α of −0.7. This would give the electrical designer more options in selecting the phase and energy storage/dissipation relationships for a particular need. Such fractional order components could be used to implement electrical circuits and methods that are not conventionally available.
Conventional calculus methods have been used to solve important problems for scientists, engineers, and consumers. An example is the PID controller circuit that is commonly used for automated control, such as for control of electrical motors or electrical heaters. Conventional calculus uses differentiation and integration to discrete, integer orders. For example, first or second derivatives, or first or second integrals, are used. Integer order differentiation may be expressed as having a Laplace transfer function proportional to sn, with n being an integer. Likewise, integer order integration may be expressed by a Laplace transfer function proportional to s−n.
In contrast, fractional order calculus is a generalization of conventional calculus that allows differentiation and integration to fractional order (FO). FO methods can be particularly important in solving nonlinear problems, such as performing automatic control, pattern recognition, system characterization, signal processing, and modeling of biological or chemical processes, vibration, viscoelasticity, damping, chaos, fractals, diffusion, wave propagation, percolation and irreversability. Similar to traditional calculus operations, FO differentiation and integration can be expressed with Laplace transfer functions sr and s−r, respectively. However, with FO calculus, r is any real number, such as a fraction 1/n.
Various methods have been used to perform fractional order calculus operations. Complicated electrical networks that approximate FO impedances (discussed above) have been used to approximate FO calculus operations, as reported by Carlson et al. in IEEE Tran. on Circuits and Systems 7 (1964) 210. Additionally, fractional order calculus operations have been simulated by digitally approximating the problems and calculating approximate solutions. Digital approximations are necessarily limited in bandwidth, highly consumptive of computer resources, and can suffer from numerical instabilities due to finite precision arithmetic. These limitations can make digital techniques impractical or incapable of solving many problems, such as controlling fast processes or “stiff” processes, which involve strong opposing forces.
Fractional order calculus methods can be particularly important in solving scientific or engineering problems. However, digital approximations to implementation of FO transfer functions have important limitations that may render digital techniques impractical or incapable of solving many problems. Analog approximations require extensive networks of components to approximate the needed FO impedances. Thus, there is a need for a single electrical component with fractional order impedance, which can be used to simply implement FO calculus operations or for other uses.
In one embodiment, the present invention provides an electrical component that has a fractional order impedance.
In another embodiment, the present invention provides a material that has a fractional order impedance.
In another embodiment, the present invention provides a partially oxidized platinum complex of Formula (III):
[A]x[Pt(L)bZy] (III)
wherein
A is an aromatic cation;
L is a ligand selected from the group consisting of oxalate, cyano;
Z is an anion;
x is 1, 2 or a non-integer between 1 and 2;
b is an integer 1-4; and
y is 0 or a non-integer between 0 and 2
and all hydrates thereof.
In another embodiment, the invention provides a composite material comprising the combination of at least one host and at least one partially oxidized platinum complex of formula IV:
[A]x[Pt(L)bZy] (IV)
wherein
A is a cation;
L is a ligand selected from the group consisting of oxalate, cyano;
Z is an anion;
x is 1, 2 or a non-integer between 1 and 2;
b is an integer 1-4; and y is 0 or a non-integer between 0 and 2,
and all hydrates thereof, and wherein the host is selected from the group consisting of a polymer, a copolymer, and combinations thereof.
In a preferred embodiment, the invention provides composite material comprising the combination of a host and a partially oxidized platinum complex of formula III, wherein the host is selected from the group consisting of a polymer, a copolymer, and combinations thereof.
In another embodiment, the invention provides composite material comprising the combination of a host and a partially oxidized platinum complex of formula III, wherein the host includes sol-gel material.
In another embodiment, the present invention provides a method for making an electrical component that has a fractional order impedance.
In another embodiment, the present invention provides an electrical circuit that implements a fractional order calculus operation.
In another embodiment, the present invention provides an automatic control circuit that uses an electrical component that has a fractional order impedance.
The foregoing general description and the following detailed description are merely exemplary and explanatory and are not restrictive of the invention as claimed.
The accompanying drawings, which are incorporated in and constitute a part of this specification, illustrate exemplary embodiments of the invention and, together with the description, serve to explain the principles of the invention. In the drawings:
FIGS. 10 to 14 are schematic diagrams showing additional exemplary electrical circuits using fractor order impedance components.
Reference will now be made in detail to the present exemplary embodiments of the invention illustrated in the accompanying drawings. Whenever possible, the same reference numbers will be used throughout the drawings to refer to the same or like parts. Also, where the different embodiments have similar structures, the same reference numbers are usually used.
The present invention is particularly useful for use in analog circuits for performing FO calculus operations for scientific and engineering applications, such as automatic control, system characterization or system modeling. The present invention includes an electrical component with a fractional impedance, its methods of manufacture and it use.
The nanowires 204 are electrically conductive, either with only insignificant electrical resistance or with desired electrical resistances. For example, the nanowires 204 may be made of metal-metal polymer chains or of any other material convenient to creating nanowires of desired conductivity or resistance. The polymer chains may be one-dimensional and may be formed of a partially oxidized metal complex, such as a partially oxidized platinum complex. The partial oxidization may be done through any convenient method, such as photo-oxidation. The complex 203 may include some nanowires that touch each other, but, over the complex 203, the nanowires 204 may be prepared so as to reduce bundling of individual wires. Bundling may be reduced by using large cations that force individual wires apart and allow individual atomic wires to be isolated. Furthermore, cations having any structure that allows for formation of the nanowire complex may be used. For example, the cations may potentially be chiral in structure.
The nanowires 204 are encapsulated in a host material 205. The host material 205 may have a specific conductivity, including being non-conductive. For example, the host material 205 may be a polymer, a co-polymer, or any mixture thereof. It may also have any material density or form, such as a solid, liquid, gel, or sol-gel, that is convenient for retaining the complex 203's wire-to-wire spacing and orientation, so as to retain a desired fractional order impedance. Alternatively, as discussed below, some nanowires 204 may be only partially encapsulated by the host material 205 so as to provide electrical contact with the complex 203.
Some parts of the complex 203 may be electrically connected to component terminals 202. For example, some nanowires 204 may extend into a volume of electrically conductive material 206 so as to allow for conveniently forming electrical connection between a part of the complex 203 and a component terminal 202. A second component terminal 202 may be similarly connected to a volume of conductive material 206 and a part of the complex 203.
The nanowires 204 may be randomly oriented, as shown schematically in
Electrical signals may be conducted through an FO electrical component 200 like that in
For example,
In an embodiment of the present invention, in order to avoid bundling of individual metal-metal polymer chains (i.e., nanowires) and to control their structure, partially oxidized platinum complexes were prepared with the small cations replaced by large cationic ligands. These ligands are characterized by a localized charge surrounded by an extensive, relatively non-polar organic framework.
In the example of bisoxalatoplatinate complexes, the large ligands fit within the approximately 2.85 Å gap between sequential bisoxalatoplatinate centers, while also forcing neighboring platinum-platinum chains apart through steric hindrance.
In one embodiment, the present invention provides a partially oxidized platinum complex of Formula (III):
[A]x[Pt(L)bZy] (III)
wherein
A is an aromatic cation;
L is a ligand selected from the group consisting of oxalate, cyano;
Z is an anion;
x is 1, 2 or a non-integer between 1 and 2;
b is an integer 1-4; and
y is 0 or a non-integer between 0 and 2
and all hydrates thereof. Z may include, but is not limited to choride, bromide, fluoride, iodide, or FHF.
In an exemplary embodiment, partially oxidized platinum complexes of Formula III form crystals with a length:width ratio of about 20:1 to about 100:1. However, those skilled in the art would recognize that the nanowires may have other length:width ratios that are convenient to having a desired fractional order impedance of the complex 203. The nanowires may have a distribution of lengths. Additionally, the nanowires may be, but are not limited to being, sized, oriented and positioned so as to form a substantially fractal structure.
In a preferred embodiment, an aromatic cation A may be, but is not limited to, a pyridine, a pyrimidine, a pyridazine, a quinoline, an isoquinoline, a quinazoline, a quinoxaline, or mixtures thereof and may be optionally substituted with 1-4 substituents. Substituents include hydrogen, alkyl, alkoxy, amino, alkyl(N-alkylamino), alkyl-(N,N-dialkylamino), hydroxy, arylalkyl and heteroarylalkyl. In a preferred embodiment, aryl ammonium salts, such as N-methyl isoquinoline, are prepared and utilized to satisfy both of the above discussed prerequisites. These aryl ammonium salts also have the advantages of being readily synthesized and easily modified.
In a more preferred embodiment, L is oxalate, b is 2 and y is 0. In another more preferred embodiment, L is cyano, b is 4 and y is 0. In a most preferred embodiment, Ar is N-methylisoquinoline, L is oxalate, b is 2 and y is 0.
Although partially oxidized platinum complexes have the potential for use in materials applications, their handling and orientation presents certain unique problems. The tendency of some of these complexes to lose waters of hydration can lead to a significant decrease in their conductive properties. Encapsulation of these “nanowires” within a host such as, for example, a polymer matrix was found to reduce the loss of water problem and facilitate sample manipulation and orientation.
The presence of a host that encapsulates the partially oxidized platinum complexes also allows for the incorporation of additional complexes within the host. Examples of such additional complexes could include optically active complexes or charge-transfer complexes. Optically active complexes could include non-linear optical (NLO) complexes.
In an embodiment, the invention provides a composite material comprising the combination of at least one host and at least one partially oxidized platinum complex of formula IV:
[A]x[Pt(L)bZy] (IV)
wherein
A is a cation;
L is a ligand selected from the group consisting of oxalate, cyano;
Z is an anion;
x is 1, 2 or a non-integer between 1 and 2;
b is an integer 1-4; and y is 0 or a non-integer between 0 and 2,
and all hydrates thereof, and wherein the host is selected from the group consisting of a polymer and a copolymer.
In a preferred embodiment, partially oxidized platinum complexes of Formula IV form crystals with a length:width ratio of about 20:1 to about 100:1.
In a preferred embodiment, the invention provides composite material comprising the combination of a host and a partially oxidized platinum complex of Formula III, wherein the host is selected from the group consisting of a polymer and a copolymer. In a more preferred embodiment, the polymer forms a film with a thickness of about 25 to about 250 microns. In a most preferred embodiment, the polymer is selected from the group consisting of polyvinylalcohol (PVA), polymethyl methacrylate (PMMA) and mixtures thereof. In a more preferred embodiment, the partially oxidized platinum complexes include K1.6[Pt(Ox)2].2H2O, Co0.8[Pt(Ox)2].2H2O or a mixture thereof.
Polyaniline sulfonic (referred to as PAni) acid was found to be an effective polymer for modifying the electrical properties of the bulk material. Addition of polyaniline sulfonic acid (purchased as a 5% wt/wt solution from Sigma Aldrich) was used to reduce the overall impedance of the PVA polymer, hence a PVA/PAni copolymer.
Humidity has been found to allow ions in the material to become more mobile and move the organic polymer matrix (e.g., PVA/Pani). Thus, the impedance of the material decreases as the relative humidity increases. Humidity has been controlled using saturated salt solutions in a sealed chamber to produce specific humidities. However, more specific control may be obtained using a controlled system of moist and dry air to generate desired humidities.
The nanowire prepared below in Examples 1 and 2 was characterized by scanning electron microscopy (SEM), see
For the preparation of a nanowire encapsulated by PVA as shown in Examples 3 and 4, the PVA (Mw of about 89,000 to about 98,000) and (NH4)2Ce(IV)(NO3)6 (99.99%+) were purchased from Aldrich Chemicals and used as supplied. Bisoxalato platinate salts K2[Pt(Ox)2].2H2O and Co[Pt(Ox)2].6H2O were prepared by the method of Krogmann et al. in Chem. Ber. 99 (1966) 3402 and by the method of Schultz et al. in Inorg. Chem. 17 (1978) 1313, respectively. These salts were then oxidized in an aqueous solution of (NH4)2Ce(IV)(NO3)6 to give K1.6[Pt(Ox)2].2H2O and Co0.8[Pt(Ox)2].6H2O, respectively. The copper-colored, microcrystalline products were washed with chilled water and dried in a dessicator.
In Example 4, [NH2Bu2]2[Pt(Ox)2].H2O was prepared via reaction of Ag2[Pt(Ox)2].2H2O with [NH2Bu2]Cl in H2O. The insoluble AgCl was coagulated via gentle warming and filtered off under vacuum. Removal of the solvent gave the yellow solid in good yield. The partially oxidized platinum complex [NH2Bu2]x[Pt(Ox)2] was prepared by chemical oxidation of [NH2Bu2]2[Pt(Ox)2] with a solution of 0.1M (NH4)2Ce(NO3)6. PVA (400 mg) was dissolved in H2O (10 mL) with heating and stirring, once the cloudy solution had turned clear, it was cooled and the PAni was added via pipette to give the PVA/PAni copolymer solution. The polyaniline sulfonic acid was purchased from Sigma-Aldrich as a 5% wt. solution in water). The PVA/Pani copolymer was poured onto the [NH2BU2]x[Pt(Ox)2] material and allowed to dry at room temperature to give a dark, pliable film in which the dispersed [NH2Bu2]x[Pt(Ox)2] material could be seen. Polymer film thicknesses in all Examples 3 and 4 were determined with a micrometer gauge.
C10H10N]2[Pt(Ox)2].H2O was prepared via reaction of Ag2[Pt(Ox)2].2H2O with [C10H10N] in H2O. The insoluble AgI was coagulated via gentle warming and filtered off under vacuum. Removal of the solvent gave the yellow product in good yield and the composition was confirmed via microanalysis. A saturated solution of [C10H10N]2[Pt(Ox)2] (4 mL) was filtered through a 1 μm filter and placed in an electrolytic chamber fitted with gold wire electrodes. A 1.25V voltage was applied and after a 24 hour period, long, dark fibers were observed to have formed. The fibers, which did not undergo decomposition, were dried in air for several days to provide a nanowire. SEM analysis revealed a network of fibers of up to about 1 cm in length and approximately 20 μm or less in diameter, giving an aspect ratio of about 5,000:1 or greater.
[C10H10N]2[Pt(Ox)2] was prepared using any of the reported and well established synthetic procedures. [C10H10N]2[Pt(Ox)2] (102.2 mg, 0.155 mmol) was dissolved in 1M CF3SO3H (10 mL) with stirring under argon. A solution of 0.1M (NH4)2Ce(NO3)6 (0.3 mL, 0.03 mmol) was added dropwise and a gray, fibrous material was observed to form. This nanowire product was thoroughly washed with ice-cold water and stored at 5° C. SEM analysis was similar to that reported in the previous example.
PVA (200 mg) was dissolved in water (10 mL) by heating at 75° C. until a clear solution was obtained. The partially oxidized platinum complexes K1.6[Pt(Ox)2].2H2O and Co0.8[Pt(Ox)2].6H2O were separately dissolve quantities sufficient for the desired composite concentration and were added at room temperature to the PVA solution. This mixture was then poured into a Petri dish and stirred occasionally to ensure homogeneous dispersion of the complexes in the medium. After approximately 3 days, thin composite films were obtained.
[NH2Bu2]2[Pt(Ox)2] (100 mg) was dissolved in 1M CF3SO3H (15 mL) partially oxidized with 0.1M (NH4)Ce(IV)(NO3)6 to give a mass of fine, coppery, needle-shaped material. The material was poured into a Petri dish and allowed to dry out at room temperature for several days. Approximately 87 mg of nanowire product was collected. PVA (200 mg) was dissolved in water (10 mL) and heated and stirred at approximately 65° C. until all the material dissolved. After cooling, polyaniline sulfonic acid (873 mg) was added to make the polyaniline sulfonic acid concentration approximately 17.9% by weight. The nanowire product [NH2Bu2]x[Pt(Ox)2] was then added and the resulting slurry was allowed to evaporate at room temperature for several days to give a pliable black film in which the needles of [NH2Bu2]x[Pt(Ox)2] were visible.
The properties of conductivity and the real and imaginary components of capacitance were measured for each of the prepared partially oxidized platinum complexes and for each of the composites (i.e., complexes encapsulated in a host material). It was discovered that their overall physical properties of the composites varied depending upon the orientation of the complexes. In addition, for the complexes in general, electrical properties varied depending on the identity of the cation or cations present and/or the optional anion depicted as Z in Formulae III and IV, which includes Formulae I and II.
A linear, passive, two-lead electronic device with generalized Warburg impedance can be described in the fractional order impedance, a “fractance,” of the form:
where the magnitude of the impedance is ZC ohms at reference frequency fC, α is a non-integer exponent, and √{square root over (−1)}. Impedance spectroscopy of a representative fractional order impedance device, i.e., fractor, is shown in
The fractional form of Equation 1 holds over the frequency band of interest, at least three decades of frequency. This distinguishes the fractor from approximations of fractance created from networks of discrete conventional integer order elements. At some upper frequency, the impedance is often dominated by parasitic by-pass capacitance due to the electrode layers. The fractance devices will have electrical limitations of voltage, current, and operating temperature, just as with other passive electronic elements.
The form of Equation 1 admits to description of all conventional ideal passive electronic components, e.g., inductors (α=−1), resistors (α=0), and capacitors (α=1). The claims made herein specifically exclude the conventional inductor and resistor (α=−1 and 0) and the class of “lossy” bipolar capacitors with dissipation factors (referred to as “tan δ”) up to 0.3. Also excluded are the unipolar electrolytic capacitors with dissipation factors up to 0.5 as conventionally used as filters.
Fractance can also be written in terms of angular frequency, ω=2πf, notation with τ=1/(2πfC) as
and Laplace form, with s=jω, as
In the latter form, it becomes evident that fractance is described by the fractional order integral of order α.
As such, parallel and series arrangements of circuits having fractional order impedance is possible where the algebraic rules for combining impedances into equivalent circuits apply. For example, an example of a low pass filter is shown in
Further, electrical elements with FO impedances in conjunction with operational amplifiers can be used to implement FO calculus operations. For example,
The voltage at circuit input terminal 110 is Vin, and the voltage at circuit output terminal 120 is Vout. Therefore, circuit 100 has a transfer function according to equation (4)
where α is a fraction between zero and one. Circuit 100 is merely exemplary, and those skilled in the art will recognize that fractional order calculus operations may be implemented using other electrical circuits and using other values of impedance order α.
Of course, FO automatic controllers are not limited to the exemplary circuits of FIGS. 7 to 9 but may be made of various circuitries. Automatic controller 400 may be applied to controlling various processes, such as electrical motor speed, electrical heater operation, and electrical power voltage or current supplies.
Moreover, placing the fractor in the input position as shown in
With the fractor, it is therefore possible to create fractional order operators of orders obtained by exponent arithmetic. Given one fractor of order a and another of order β, an operator of order γ=β−α can be created as shown in
Cascading amplifier circuits of the form of
A proportional plus fractional order integral (PIλ) controller, described by Equation 10, can be formed using the diagram of
Summing the outputs of
In addition, phase compensation over broad bands is possible. As shown in
When the circuit of
Positive polarity configurations are also useful.
It should be apparent that the foregoing circuits are exemplary and numerous other circuits can be achieved in accordance with the present invention.
It has been further found that similar results can be obtained with properly designed platinum-free systems. A fractional impedance device, i.e., a fractor, can be constructed from roughened metal (or other conducting material) surfaces held face to face by a spacer. The surfaces may be roughened by sand blasting, bead blasting, chemical etching, lithographic techniques, or other techniques. The space between the plates is filled with electrically conducting polymer doped with acid and containing ionic materials so as to provide multiple pathways and charge carriers for the conduction of electricity. These composite materials possess, on a localized scale, a variety of impedance and capacitance values due to the fractal surface of the roughened metal plates, and a variety of activation barriers for the charge carriers.
One specific example, but not the only example, of such a system is two square copper plates, roughened by sand or bead blasting, held about 1.0 mm apart containing a solution made from 28 mL water, 28 mL 95% ethanol, 14 mL TEOS, 2 drops of nitric acid, drops of 5% polyaniline sulfate, and 2.805 grams of lithium nitrate. The experimental results from such a configuration are shown in
Those skilled in the art will appreciate that various modifications can be made in the present invention without departing from the spirit or scope of the invention. Thus, it is intended that the present invention cover the modifications and variations of this invention provided they come within the scope of the appended claims and their equivalents.
This application claims the benefit of U.S. Provisional application 60/660,325, filed on Mar. 11, 2005.
Number | Date | Country | |
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60660325 | Mar 2005 | US |