Differential negative resistance memory

Information

  • Patent Grant
  • 7745808
  • Patent Number
    7,745,808
  • Date Filed
    Friday, December 28, 2007
    16 years ago
  • Date Issued
    Tuesday, June 29, 2010
    14 years ago
Abstract
The invention relates to a DNR (differential negative resistance) exhibiting device that can be programmed to store information as readable current amplitudes and to methods of making such a device. The stored data is semi-volatile. Generally, information written to a device in accordance with the invention can maintain its memory for a matter of minutes, hours, or days before a refresh is necessary. The power requirements of the device are far reduced compared to DRAM. The memory function of the device is highly stable, repeatable, and predictable. The device can be produced in a variety of ways.
Description
FIELD OF THE INVENTION

This invention relates to devices exhibiting differential negative resistance and to methods of forming and using such devices.


BACKGROUND

Devices that exhibit differential negative resistance (DNR), also often referred to as negative differential resistance or negative differential conductance, do not function in agreement with Ohm's law. Instead, an increase in absolute voltage produces a decrease in absolute current, at least over a portion of an applied voltage range.


A DNR device that it commonly used in integrated circuits, particularly logic circuitry, is the tunnel diode (or Esaki diode). The DNR effect is displayed in tunnel diodes as a current dip in the forward I-V characteristics. For a certain range of forward voltages the current through the diode actually falls, instead of increasing, making it useful in certain switching applications, for instance.


It has recently been discovered that a chalcogenide glass structure may be configured with an excess of metal ions, e.g., Ag ions, to exhibit DNR behavior. U.S. patent application Ser. No. 10/193,529 by the inventor describes such a DNR exhibiting device suitable for use as a tunnel diode. This related application is incorporated by reference herein in its entirety. The DNR behavior of the device is characterized by a very good peak-to-valley current ratio evident in its forward I-V curve. It would be advantageous if such DNR behavior could be utilized for a memory function.


SUMMARY

The invention relates to a DNR (differential negative resistance) structure, which can be programmed to store information as an absolute DNR current maximum, thereby forming a memory element. The memory element is semi-volatile and therefore, can store data for longer periods than standard DRAM memory elements, which must be frequently refreshed. Generally, information written to a DNR memory element will retain its programmed state for minutes, hours, or days before a refresh is necessary.


The DNR structure can be produced in a variety of ways. One method of processing the structure is by blanket deposition and patterning of electrode layers, chalcogenide glass layers, and metal-chalcogenide layers. Another fabrication method is a processing-in-via method using similar layers.


Additional processing steps are performed to add silver or copper to the device to induce the DNR effect, thus enabling DNR structure to thereafter function as a DNR memory element. One way the DNR effect can be induced in the structure is by adding silver layers to the resistance variable region thereof. Annealing can be incorporated into this method as well. Another way of inducing the DNR effect is by performing an annealing step. A third way of inducing the DNR effect is by applying a negative voltage pulse to the structure at its top electrode. After the initial inducement of DNR effect, the structure can function as a memory element by exhibiting the DNR behavior in a predictable, repeatable, and stable fashion.


The DNR memory element functions by storing data as separate, maintainable maximum current states, which are programmed when voltages are applied to the memory element. As an example, a first current amplitude state may be provided when a first programming voltage potential is applied to the DNR structure. Thereafter, when a read voltage is applied, a first read current is obtained. A second read current state may be produced when a second programming voltage potential is applied to the DNR structure. Thereafter, upon application of the read voltage, a second, different read current amplitude may be read. The programmed current amplitude states are read during a read operation and are also maintained in the memory element for a relatively long time without refreshing after the programming voltages are removed (as compared to conventional DRAM). The programmed current amplitude states can be read by a sense amplifier in electrical communication with the DNR memory element. The observable DNR memory of the structure is highly stable, repeatable, and predictable, making for an excellent memory device.


In an alternative embodiment, analog memory states are possible with the DNR memory. Multiple voltage pulses can increase or decrease the amplitude of the readable current amplitude states. In this way the ultimate current read at the DNR device can be finely tuned throughout an analog range.


These and other advantages and features of the present invention will be more apparent from the following detailed description and drawings which illustrate various embodiments of the invention.





BRIEF DESCRIPTION OF THE DRAWINGS


FIG. 1 shows a DNR memory device in accordance with the invention.



FIG. 1
a is a graph illustrating typical DNR memory behavior exhibited by devices in accordance with the invention.



FIGS. 2 through 9 show a partial cross-section of a wafer during processing in accordance with an embodiment of the invention, with FIG. 9 showing a substantially complete device in accordance with that embodiment.



FIGS. 10 through 17 show a partial cross-section of a wafer during processing in accordance with another embodiment of the invention, with FIG. 17 showing a substantially complete device in accordance with that embodiment.



FIG. 18 shows a device in accordance with another embodiment of the invention.



FIGS. 19 through 21 depict portions of memory arrays in accordance with the invention.



FIG. 22 is a depiction of a system incorporating devices in accordance with the invention.





DETAILED DESCRIPTION

In the following detailed description, reference is made to the accompanying drawings, which are a part of the specification, and in which is shown by way of illustration various embodiments whereby the invention may be practiced. These embodiments are described in sufficient detail to enable those skilled in the art to make and use the invention. It is to be understood that other embodiments may be utilized, and that structural, logical, and electrical changes, as well as changes in the materials used, may be made without departing from the spirit and scope of the present invention. Additionally, certain processing steps are described and a particular order of processing steps is disclosed; however, the sequence of steps is not limited to that set forth herein and may be changed as is known in the art, with the exception of steps or acts necessarily occurring in a certain order.


The terms “wafer” and “substrate” are to be understood as interchangeable and as including any foundation suitable for supporting a DNR memory element of the invention. Preferably, the substrate is silicon, silicon-on-insulator (SOI) or silicon-on-sapphire (SOS), doped and undoped semiconductors, epitaxial layers of silicon supported by a base semiconductor foundation, and other semiconductor structures. Furthermore, when reference is made to a “wafer” or “semiconductor substrate” in the following description, previous process steps may have been utilized to form regions, junctions or material layers in or on the base semiconductor structure or foundation. In addition, the semiconductor substrate need not be silicon-based, but could be based on silicon-germanium, germanium, gallium arsenide, or other known semiconductor materials. Further, the substrate need not be semiconductor-based at all, but can be any material suitable for supporting an integrated circuit, for instance, polymer, glass, metals, insulated metals, ceramics, and other materials.


Now referring to the figures, where like reference numbers designate like elements, substantially complete DNR memory devices 8, 100, 100′, and 100″ incorporating DNR memory elements in accordance with various embodiments of the invention are respectively shown in FIGS. 1, 9, 17, and 18. These shown structures 8, 100, 100′, and 100″, while not limiting, are illustrative of the invention. A basic structure of the device of a first exemplary embodiment of the invention is shown in FIG. 1. It is an exemplary DNR-exhibiting memory element 8 that can be programmed to store information as stable current states at read voltage(s) in response to applied programming voltages. A first programming voltage can increase the current at a read voltage. A second programming voltage can decrease the current at a read voltage. The stored data (readable absolute current amplitude) is semi-volatile, meaning that it retains a stored data state for relatively long periods of time, e.g., minutes, hours, or even days. The stored data is not necessarily completely non-volatile and may require some refreshing.



FIG. 1 shows the DNR memory device 8 supported by a substrate 1. Over the substrate is an optional insulating layer 2, which can be Si3N4, for example. An electrode (serving typically as the anode) is provided over the substrate 1 as layer 3. Over layer 3 a resistance variable region is formed of a chalcogenide-based glass layer 4 and an optional metal layer 5. The chalcogenide-based glass layer 4 is preferably GexSe1-x, where x is about 18-40, with 20, 25, and 40 being preferred. The chalcogenide-based glass layer 4 should also incorporate a metal, preferably silver or copper, with silver typically being preferred over copper. The metal can be incorporated into the chalcogenide-based glass layer 4 by doping or co-evaporation, for example. The chalcogenide-based glass layer 4 can be doped with metal by photo- or thermal diffusion. The metal layer 5 can comprise silver or copper, depending on with which metal the chalcogenide-based glass layer 4 is to be doped. It is the resistance variable region that stores data as multiple readable current amplitudes programmed in response to applied voltages. The voltages are applied by a second electrode, which can be layer 6. This electrode can be silver or copper, if desired. As stated above, layer 5 is optional and if not utilized, layer 6 should include the metal with which the chalcogenide-based glass layer 4 is to be doped; silver or copper as appropriate. The device 8 may be electrically isolated by an insulating layer 7.


The FIG. 1 device 8 may be constructed by successive blanket depositions of the various layers of the device 8 over a substrate, which are subsequently etched to form individual devices in a manner similar to that described with respect to the embodiment shown in FIGS. 2-9. Alternatively, a via can be formed in an insulating layer and device 8 can be formed by deposition of the various layers within the via in a manner similar to that described below with respect to the embodiments shown in FIGS. 10-17.


Throughout the detailed description reference is made to applied voltages used to achieve the current amplitude memory states. These described current amplitudes and voltages can be positive or negative and the devices described herein can function in equivalent ways based on either positive or negative applied voltages. The exemplary voltages are applied at the upper electrode of the DNR devices.


The memory element of the invention stores data based on its ability to change to and maintain discrete observable (when a read voltage is applied) current amplitude states by utilizing DNR behavior over a predictable range of applied DC voltage potentials. The memory element typically is connected to electrodes (see layers 3 and 6 in FIG. 1) on either side of a resistance variable region, which typically includes a chalcogenide-based glass. The top electrode is generally the cathode and provides a negative potential to the memory element.


Typical DNR behavior of the memory element of the device is illustrated generally by the graph of FIG. 1a. The graph of FIG. 1a shows an I-V (current-voltage) curve for an embodiment of the invention upon application of voltage potentials up to about 1.0 V. The memory is read by applying a voltage in region A of the graph, preferably a voltage corresponding to the peak absolute current produced in this region by a non-programmed device, which is shown in the graph to be about 0.26 V. By applying voltages in regions B-E, which are programming regions, the peak absolute current at the read voltage can be shifted to increase or decrease. After programming with a voltage in the regions B-E, the shifted current is maintained in a semi-volatile memory. Two extreme current-shifting voltages, one increasing and one decreasing the peak absolute readable current, can be used to write a first and a second memory state for semi-volatile digital memory, each of which can be read at about 0.26 V.



FIG. 1
a shows the five exemplary applied voltage ranges A, B, C, D, and E, which can influence the ultimate readable current in the DNR memory. Voltages within region A should be considered read voltages. No matter how the device is written by voltages in regions B-E, it is always read at the same read voltage, e.g., 0.26 V in FIG. 1a, which is related to the peak absolute current amplitude of the device in region A. DNR behavioral response is best exhibited in the regions B-E. An applied voltage within region B, defining a range of about 0.36 V to about 0.55 V, will result in a relatively small increase in readable current in the programmed device when read at the read voltage, e.g., 0.26 V. An applied voltage within region C, defining a range of about 0.55 V to about 0.74 V, will result in a relatively small decrease in programmed readable current. An applied voltage within region D, defining a range of about 0.74 V to about 1.0 V, results in a relatively larger increase in programmed readable current at the read voltage. An applied voltage in region E, which extends beyond 1.0 V, results in a relatively larger decrease in programmed readable current. Thus, by using programming voltages in the range of D and E, one can cause significant shifts, upward for region D and downward for region E, in the current read at the read voltage, e.g., 0.26 V.


The memory element can be written-to very quickly, thereby meeting or exceeding the programming timing requirements of standard memory circuitry used in the art. Programming to either the first or second readable current states can be performed in about 8 ns or less, easily fast enough for present memory applications.


Although the memory states of the DNR memory are generally discussed herein as digital memory, it is also possible to use the device as an analog memory as well. To program the device as analog memory, a plurality of write voltages selected from regions B-E can be used to change the current read by the read voltage to a plurality of respective different values. Voltages from each region shift the readable current to a designated degree and current shifts from multiple voltages can be compounded so that multiple current levels can be written to and read from the DNR element by the read voltage. The analog memory is, like the digital memory, semi-volatile.


Returning again to discussion of digital memory, where two different current states are used for storage, the semi-volatile data retention for the memory element in the higher and lower current amplitude states can be stable for minutes, hours, and even days without refreshing. A regular refresh may be needed for long-term memory storage. The refresh can be provided by the application of a stabilizing voltage potential of about the same magnitude as that required to program the memory element to its set current state. Thus, for example, to refresh data written by an applied voltage in region B, the same voltage in region B can be applied. Likewise, to refresh data written by a voltage in region C, the same voltage in region C can be applied. The refresh voltage application does not disturb the written state of the memory element, but stabilizes the memory element to maintain the stored data.


The data stored in the DNR-exhibiting memory element can be read by a sensing device in electrical communication with the memory element upon application of a designated read voltage, which is typically a voltage in region A of the graph in FIG. 1a. As noted, for the exemplary device depicted in FIG. 1a, the exemplary read voltage is at about 0.26 V. The designated read voltage corresponds to a peak absolute current amplitude exhibited by a non-programmed device corresponding to a voltage in region A. The sensing device (e.g., sense amplifier 304 shown in FIGS. 19, 20, and 21) in communication with the memory element (e.g., structure 8 or 100) can be set up to read relative high or low current amplitude through the memory element, which relates to the first memory state and second memory state. Suitable sensing devices for sensing the multiple current levels of the analog DNR memory can also be provided.


As an example of use of the DNR device as a memory element, a “1” can be represented by an increased current level obtained by programming the device using a voltage in region B (for small current increase) or in region D (for larger current increase). The programmed “1” value would be read by application of a voltage of about 0.26 V, which produces the increased read current relative to the observable current of a non-programmed device at the read voltage. For instance, if the non-programmed current corresponding to the designated read voltage is x μA, the programmed “1” would be read as (x+y) μA, where y is the current amplitude increase resulting from programming. The “0” state may be represented by the non-programmed current level of x μA, or alternatively can be represented by a lowered current obtained by programming the device with a voltage in the range of C or E. In this instance, the “0” value would be read by application of about 0.26 V, which would produce a read current of about (x−z) μA, where z is the decrease in current amplitude resulting from programming. Note that the above described correlation between writing voltages and data written, i.e., a “1” or a “0,” is arbitrary and can just as easily be reversed.


It is also possible to reset (as opposed to refresh) the memory device (e.g., device 8 or 100) to a completely non-programmed state. By applying about a 2.0 V or greater potential to the device, it can be reset to have no stored information so that it can be freshly written-to by application of a programming voltage, which sets the memory element to a particular memory state.


The programming of the DNR memory has been discussed above as utilizing DC voltages, however, it is also possible to use AC voltage programming. The voltage potential requirements to obtain the maximum current increase or decrease to the programmed memory states varies depending on AC pulse width. For pulses greater than 500 ns, the voltage potential amplitude requirements are similar for voltage requirements when using DC voltage programming.



FIGS. 2 through 9 illustrate another exemplary embodiment of a DNR memory device 100 in accordance with the invention at various stages of processing. FIG. 2 shows a section of a substrate 10 for supporting a plurality of memory devices 100 in accordance with the invention. Although only a single device 100 cross-section is shown at various stages of processing for the sake of clarity of description, it is intended that a plurality of such devices 100 be fabricated simultaneously in an array of M×N memory cells. It is further intended that such arrays of memory cells can be stacked, one above another, to increase the density and total memory capacity of the integrated circuit.


The substrate 10 in FIG. 2 can be any suitable material for supporting an integrated circuit, for example, monocrystalline silicon, or a polymer material. Over the substrate 10 is a layer of insulating material 12. This layer 12 is optional and can be silicon dioxide, silicon nitride, borophosphosilicate glass (BPSG) or other insulative materials; it can be deposited as is known in the art. Over the substrate 10 or optional insulating layer 12 is formed a conductive layer 14, which will later serve as the bottom electrode (e.g., anode) of the device 100. This conductive layer 14 can be any material suitable for an integrated circuit interconnect since it can also serve as a column line or row line and a common bottom electrode for multiple memory devices 100 of the array. The conductive layer 14 can be, e.g., doped polysilicon, or a metal such as silver, tungsten, titanium, nickel, platinum, tantalum, other metals, alloys or combinations of these and other metals, or metal nitrides. This conductive layer 14 can be blanket deposited as is known in the art.



FIG. 3 shows a stage of processing subsequent to that shown in FIG. 2. Over the conductive layer 14 is formed a chalcogenide-based glass layer 18. This layer 18 is preferably a germanium selenide glass composition of formula GexSe100−x, where x is preferably in the range of about 18 to about 43, and more preferably is about 20, 25, or 40. This glass layer 18 can be about 100 Å to about 300 Å in thickness, preferably about 150 Å. The glass layer 18 can be formed by any suitable method. Preferred methods of deposition are evaporation, co-sputtering the components, sputtering from a proportional source, or chemical vapor deposition (CVD). The glass layer 18 can serve as a glass backbone for the device. The glass layer 18 also incorporates a metal, such as silver, for example. Silver can be incorporated in to the glass layer 18 by co-sputtering or doping (e.g., photo- or thermal diffusion), for example.


Optionally, a thin layer of metal 19, such as silver, can be deposited over the glass layer 18 prior to the forming of a metal-chalcogenide layer 20 thereover. By adding this thin metal layer 19 it can be ensured that the glass layer 18 incorporates enough metal to enable the DNR functioning of the ultimate device.



FIG. 4 shows a stage of processing subsequent to that shown in FIG. 3. Over the glass layer 18 (or thin metal layer 19 if used) is formed a metal-chalcogenide layer 20. If optionally used, is it preferred that the thin metal layer 19 be the same metal as that of the metal-chalcogenide layer 20. The metal of the metal-chalcogenide layer 20 is preferably silver (as is the thin metal layer 19). As an alternative, the metal of the metal-chalcogenide layer 20 can be copper. The other component of the metal-chalcogenide layer 20 is a chalcogenide material, preferably selenium. Combined, the two preferred components form silver selenide (Ag2Se) as layer 20. Additional silver can be incorporated into the Ag2Se (Ag2+xSe) layer as elemental silver, silver ions, or silver compounds or alloys. This preferred combination of components should contain enough silver to donate silver to an adjacent chalcogenide glass layer (e.g., layer 18) during the operation of the memory device 100. The metal-chalcogenide layer 20 can be formed by evaporative deposition, sputtering, co-sputtering, or other known methods. The metal-chalcogenide layer 20 can be about 200 Å to about 1,000 Å thick. It is preferably thicker than the underlying glass layer 18 in a ratio of thickness of about 1:1 to about 5:1 compared to the glass layer 18. More preferably, the ratio is between 2:1 and 3.1:1.



FIG. 5 shows a stage of processing subsequent to that shown in FIG. 4. A second chalcogenide-based glass layer 22 is formed over the metal-chalcogenide layer 20. The forming of the second glass layer 22 completes a resistance variable region with layers 18 and 20. The second glass layer 22 can be made of the same materials (e.g., GexSe100−x) as the first glass layer 18. Additionally, the second glass layer 22 can also have the same stoichiometry as the first glass layer 18. The second glass layer 22 preferably is about 50 Å to about 500 Å thick, and more preferably about 150 Å thick. Again, like the first glass layer 18, the second glass layer 22 can be deposited by evaporation, sputtering, co-sputtering, CVD, or other known techniques.



FIG. 6 shows the formation of an optional metal layer 24 over the second glass layer 22. If the thin metal layer 19 optionally formed over layer 18 is not used, then this optional metal layer 24 should be incorporated into the device. Preferably, this optional metal layer 24 is the same metal as that of the metal-chalcogenide layer 20, e.g., preferably silver or copper. Silver is preferred over copper for most applications. Typically, the metal layer 24 is thin, e.g., 500 Å or less, with less than 200 Å being preferred.



FIG. 7 shows a stage of processing subsequent to that shown by FIG. 6 (or FIG. 5 if the optional metal layer 24 is not desired). A second conductive layer 26 is formed over the metal layer 24 (or second glass layer 22 if layer 24 is omitted). The second conductive layer 26 is a top electrode (e.g., cathode) of the device 100 and can be made of the same materials as the lower electrode conductive layer 14. Alternatively, and particularly if the optional metal layer 24 or the optional metal layer 19 over layer 18 are not utilized, the second conductive layer 26 should be silver; the first conductive layer 14 can then be another metal, such as platinum, tantalum, tungsten, titanium, aluminum, or copper.


As shown by FIG. 8, after forming the various layers 14, 18, 19, 20, 22, 24, 26 of the device 100, the wafer is patterned with a photoresist mask 27 and etched using insulating layer 12 as an etch stop layer to leave stacks. Alternatively, the lower electrode conductive layer 14 can be the etch-stop. The stacks will define the substantially complete memory devices 100. After removing the photoresist 27, an insulating layer 16 is deposited over the stacks to electrically isolate them from one another and other devices. The insulating layer 16 can be any of those known in the art, such as oxide, silicon oxide, silicon nitride, or other dielectric materials, but is preferably parylene. Using parylene for layer 16 allows its deposition to be low temperature. If layer 16 is parylene, it is deposited by vapor phase deposition. Once electrically isolated, the DNR memory device 100 is substantially complete. Electrical connections can be made between the DNR memory device and other devices of the integrated circuit.


Another embodiment of the invention utilizing an alternative processing method is illustrated by FIGS. 10-17. The alternative embodiment utilizes processing-in-via methodology. As shown in FIG. 10, the processing can begin with the same material layers as the preceding embodiment. A substrate 10′ is provided. Over the substrate can be the optional insulating layer 12′. Over the substrate 10′ or optional insulating layer 12′ (if utilized) is a conductive layer 14′, which will serve as a bottom electrode (e.g., anode) for the memory device 100′. A thick dielectric layer 15 is provided over the conductive layer 12′. The dielectric layer 15 should be of a material appropriate for the formation of a via therein. Each of these layers can comprise the same materials and be formed like the respective layers discussed above in the former embodiment, with the exception of the dielectric layer 15, which must be appropriate for etching a via.


As shown in FIG. 11, the dielectric layer 15 is patterned and etched by standard known methods (e.g., photolithography and etching) to form a via 17 down to and exposing a portion of the conductive layer 14′. Now referring to FIG. 12, a chalcogenide-based glass layer 18′ is formed over the conductive layer 14′ and within the via 17. Typically, the glass layer 18′ is conformally deposited. The glass layer 18′ can be optionally etched-back to leave the glass layer 18′ remaining only within a lower portion of the via 17. Again, this glass layer 18′ is preferably germanium selenide (GexSe100−x) of the same stoichiometry and thickness as described above in relation to the respective layer 18 of the above-discussed embodiment. Additionally, the glass layer 18′ will also incorporate a metal as does respective layer 18.


As shown in FIG. 13, a metal-chalcogenide layer 20′ is formed over the glass layer 18′ and within the via 17. This metal-chalcogenide layer 20′, too, is typically conformally deposited, but may be etched-back to leave the material only within a lower portion of the via 17. As with the first embodiment, an optional thin layer of metal 19′, such as silver, can be (conformally) deposited over the glass layer 18′ prior to the forming of the metal-chalcogenide layer 20′. Also, the metal of the metal-chalcogenide layer 20′ is preferably silver (as is the thin metal layer 19′ if used). As an alternative, the metal of the metal-chalcogenide layer 20′ can be copper. The other component of the metal-chalcogenide layer 20′ is a chalcogenide material, again, preferably selenium for an Ag2Se composition. However, the chalcogenide component can be another chalcogenide material as well. The metal-chalcogenide layer 20′ should be deposited like, and have a similar thickness to, the respective layer 20 described in the previous embodiment.


Now referring to FIG. 14, a second chalcogenide-based glass layer 22′ is formed over the metal-chalcogenide layer 20′ and within the via 17. The second glass layer 22′ is formed of the same materials, in the same preferred thickness range, and by the same methods as discussed for the same layer 22 in the first embodiment. Again, like the other layers 18′, 20′ within the via 17, the second glass layer 22′ is conformally deposited, but can likewise be etched-back if desired. Upon forming the second glass layer 22′ (with layers 18′ and 20′) the resistance variable region of the device 100′ is substantially complete.



FIG. 15 shows an optional thin metal layer 24′ formed over the second glass layer 22′ and within the via 17. As with the previously described embodiment, the optional metal layer 24′ is preferably the same metal as that of the metal-chalcogenide layer 20′, e.g., preferably silver or copper. Again, the optional metal layer 24′ is about 300 Å or less, with less than 50 Å being preferred. As with the other layers 18′, 20′, 22′, the optional metal layer 24′ may be conformally deposited and then etched back if desired.


Now referring to FIG. 16, a second conductive layer 26′ is formed over the second glass layer 22′ (or optional metal layer 24′ if present). The second conductive layer 26′ is a top electrode (e.g., cathode) of the memory device 100′. The second conductive layer 26′ can be formed similarly to the respective layer 26 of the previous embodiment and of like materials. Typically, layer 26′ is conformally deposited. After forming the second conductive layer 26′, the wafer can be patterned and etched so that the layers 18′, 19′, 20′, 22′, 24′, and 26′ are removed down to the level of the dielectric layer 15 beside the via 17, as shown in FIG. 17. As shown in FIG. 17, an insulating layer 28 is formed over the wafer, covering the first dielectric layer 15 and the second conductive layer 26′. Insulating layer 28 can be parylene, similarly to layer 16 in the previous embodiment. This layer 28 can be planarized by RIE or CMP methods, if desired.


At this point in processing the device 100′ is substantially structurally complete. Remaining processing can include forming electrical connections to peripheral devices, such as sense amplifiers or logic circuitry. Also, additional arrays having memory cells like the just-described device 100′ can be formed over the dielectric layer 28.


Another embodiment of the invention is shown in FIG. 18. This device 100″ can be formed by a process similar to either embodiment described above (i.e., blanket deposition of layers or in-via processing). If the blanket deposition processing of the first embodiment is utilized, insulating layer 16′ is utilized. If the in-via processing of the second embodiment is utilized, dielectric layer 15′ and insulating layer 28′ are utilized. In this third embodiment, additional chalcogenide-based glass layers 118 and 218 are formed alternating with additional metal-chalcogenide layers 120, 220 to form a portion of the resistance variable region of the device 100″. These additional alternating layers 118, 120, 218, 220 can be formed with the same processing steps discussed for respective layers 18 and 20 in the previous embodiments and can have the same material composition and physical dimensions. Further, this embodiment is not limited to only the number of additional alternating layers of glass layers 118, 218 and metal-chalcogenide layers 120, 220 shown, but additional such alternating layers can be added as well if desired or found to be appropriate.


Regardless of which processing embodiment described above or which ultimate structure for the device 100, 100′, or 100″ is fabricated, during processing, either before or after the device is substantially complete, a variety of steps can be utilized to induce the DNR memory effect in the structure to activate the memory element of the devices 100, 100′, and 100″ so that they will thereafter function by exhibiting DNR memory behavior as illustrated in FIG. 1a. Any of the following DNR inducement methods can be used whether the device is used as a digital memory or analog memory. The following methods of inducting the DNR effect result in making the device silver-rich (or copper-rich if that is the metal of choice). A silver-rich device incorporates greater than about 30% silver into the bottom chalcogenide-based glass layer 4, 18, 18′, and 18″. Preferably, about 30% to about 53% silver is incorporated into a silver-rich device in this way.


A first method of inducing DNR behavior is accomplished by ensuring saturation (e.g., at least 30% doping of the resistance variable region) of the device with silver by depositing an optional silver layer, e.g., layer 5 or 19, over the first chalcogenide-based glass layer, e.g., layer 4 or 18, during processing. The optional silver layer (e.g., 5 or 19) can absorbed into the chalcogenide-based layer upon subsequent processing (e.g., forming layer 20) or by photodissolution or thermal diffusion prior to subsequent processing. If the optional silver layer is excluded and instead the top electrode (e.g., layer 6 or 26) comprises metal to be diffused into the resistance variable region, the device stack can be annealed at 100° C. for about 1 hour. Another means of making the DNR structure silver-rich when the metal-chalcogenide layer 20 is Ag2Se is to make that layer thicker, e.g., up to about 250 Å to about 400 Å thick. Either of these methods can also incorporate a brief annealing process, e.g., heating the structure to about 200° C. for about 5 minutes, preferably in an inert ambient, upon forming the metal-chalcogenide layer 20 or after completion of the device.


In an alternative embodiment, the DNR effect can be induced by annealing the structure after the device is substantially structurally complete, as shown by device 8, 100, 100′, and 100″ in FIGS. 1, 9, 17, and 18, respectively. This achieves movement of silver from at least one of the overlying layers, e.g., 5, 19, 20, 22, 24, or 26, into the bottom chalcogenide-based glass layer, e.g., 4 or 18. The annealing parameters depend somewhat on the stoichiometry of the layers, e.g., layers 18, 20, and 22, but in general fall within a defined range. If the device incorporates glass layers (e.g., 18 and 22) having Ge40Se60 stoichiometry the DNR behavior can be induced by annealing the structure at about 50° C. for about 60 minutes. If the device is not especially silver-rich, it can be annealed at about 150° C. for about 30 minutes. If the device includes glass layers (e.g., 18 and 22) with Ge25Se75 stoichiometry it can be annealed at about 100° C. for about 60 minutes to induce the DNR behavior; this is particularly effective if the top conductive layer, e.g., layer 26, comprises silver or if the optional metal layer, e.g., layer 24, is utilized and is silver. In general, if annealing is the method of inducing the DNR behavior in the device, anneal parameters in the range of about 50° C. to about 150° C. and about 1 minute to about 60 minutes are preferred.


A third alternative for inducing DNR behavior in the memory device is by application of an AC voltage potential to the device at the top electrode (e.g., layer 6 or 26). This also causes migration of silver into the bottom chalcogenide-based glass layer. The negative voltage amplitude of the AC pulse will depend on the thickness of the bottom chalcogenide-based glass layer 4, 18, 18′ and 18″ and on the pulse width. For instance, for a shorter pulse width a higher amplitude is necessary to convert the cell into a DNR memory. Voltage pulses in the range of about −500 mV to about −2 V for about 5 ns to about 500 ns can be used. Preferably a voltage of about −1 V for about 10 ns is used to induce the DNR behavior. The DNR-inducing voltage pulse can be performed once a completed device (see FIGS. 1, 9, 17, and 18) is connected to a voltage source. The pulse alters the electrical nature of the device and inducing subsequent DNR behavior therein. After the initial inducement of DNR behavior in a completed device (by any of the just described methods), the device will permanently function with the DNR memory effect upon application of the first and second memory states potentials at the top electrode, as shown in FIG. 1a.


Now referring to FIG. 19, the memory device 100 (shown for exemplary purposes) can be incorporated into an array 310 as shown. For the sake of clarity only a portion of the array 310 is shown; however, the array can consist of M×N memory cells having memory devices 100, as desired. The memory device 100 can be addressed at the intersection of a column line 300 and a row line 302. The row line 302 can link each device 100 in electrical connection therewith to a sensing device 304 for reading the information stored in the device as a designated current amplitude. The sensing device 304 can be a sense amplifier tuned to current amplitudes of the selected read voltage of FIG. ° 1a.


An alternative embodiment is shown in the partial array 310 of FIG. 20. Access transistors 306 can be utilized at each memory device 100. The access transistors 306 can be fabricated and structured as is known in the art and can be positioned anywhere convenient to the memory devices 100. Otherwise the array 310 of FIG. 20 is structured and functions like that shown by FIG. 19.


Another embodiment is shown in FIG. 21 where, instead of access transistors 306, isolation diodes 308 are utilized to access the memory devices 100. The diodes 308 can be fabricated and structured as is known in the art and can be positioned anywhere convenient to the memory devices 100, even incorporated into the device 100 itself as layers thereof. Otherwise, the array 310 of FIG. 21 is structured and functions like that shown by FIG. 19. The array 310 shown by FIGS. 19-21 can be utilized whether the memory devices are digital or analog.



FIG. 22 shows a typical processor-based system 400, which includes a memory circuit 448, for example, a programmable RAM, employing devices 8, 100, 100′, or 100″, in accordance with the invention. A processor system, such as computer system, generally comprises a central processing unit (CPU) 444, such as a microprocessor, a digital signal processor, or other programmable digital logic devices. Such devices communicate with an input/output (I/O) device 446 over a bus 452. The memory 448 communicates with the system over the bus 452, typically by a memory controller.


In the case of a computer system, the processor may include peripheral devices, such as a disk drive 454 and a CDROM drive 456, which also communicate with the CPU 444 over the bus 452. Memory 448 is preferably constructed as an integrated circuit, which includes one or more memory devices. If desired, the memory 448 may be combined with the processor, for example CPU 444, in a single integrated circuit.


The processes and devices described above are merely illustrative of but a few of the preferred methods and typical devices that could be used and produced in accordance with the invention. The above description and drawings illustrate embodiments, which achieve the objects, features, and advantages of the present invention. However, it is not intended that the present invention be strictly limited to the above-described and illustrated embodiments. Any modifications, though presently unforeseeable, of the present invention that come within the spirit and scope of the following claims should be considered part of the present invention.

Claims
  • 1. A differential negative resistance memory device, comprising: a substrate;a first conductive layer over said substrate;a first germanium selenide layer over said first conductive layer;a silver selenide layer over said first germanium selenide layer;a second germanium selenide layer over said silver selenide layer, wherein said first and second germanium selenide layers have a chemical formula GexSe100-x, x being in the range of about 18-43;a silver layer over said second germanium selenide layer; anda second conductive layer over said silver layer;wherein at least said first germanium selenide layer is configured to exhibit a differential negative resistance memory such that it is programmable to a higher current flow read state and a lower current flow read state in response to applied first and second programming voltages, respectively.
  • 2. The differential negative resistance memory device of claim 1, wherein differential negative resistance memory is semi-volatile.
  • 3. The differential negative resistance memory device of claim 1, wherein a current flow read state programmed to said memory device is maintained for at least a minute without refreshing.
  • 4. The differential negative resistance memory device of claim 1, wherein said higher current flow read state is increased relative to a non-programmed current amplitude at a read voltage.
  • 5. The differential negative resistance memory device of claim 1, wherein said lower current flow read state is decreased relative to a non-programmed current amplitude at a read voltage.
  • 6. A processor system, comprising; a processor;a differential negative resistance memory device, said memory device comprising;a first electrode and a second electrode; anda resistance variable region separating said first and second electrodes and in electrical communication therewith, said resistance variable region being configured so as to exhibit differential negative resistance memory behavior as storing at least one memory state as a read current in response to an applied voltage.
  • 7. The processor system of claim 6, wherein said memory device can be programmed to a first read current state upon application of a first voltage potential and to a second read current state upon application of a second voltage potential.
  • 8. The processor system of claim 6, wherein said at least one memory state is semi-volatile.
  • 9. The processor system of claim 6, wherein said at least one memory state written to said memory device is retained for at least a minute without refreshing.
  • 10. The processor system of claim 7, wherein said first read current state is increased relative to a non-programmed read current at a read voltage.
  • 11. The processor system of claim 7, wherein said second read current state is decreased relative to a non-programmed read current at a read voltage.
Parent Case Info

This application is a divisional of U.S. patent application Ser. No. 11/001,306, filed Dec. 2, 2004, now U.S. Pat. No. 7,329,558, which is a divisional application of U.S. Pat. No. 7,050,327, application Ser. No. 10/410,567, filed Apr. 10, 2003, the entirety of each of which is incorporated by reference.

US Referenced Citations (185)
Number Name Date Kind
3271591 Ovshinsky Sep 1966 A
3622319 Sharp Nov 1971 A
3743847 Boland Jul 1973 A
3961314 Klose et al. Jun 1976 A
3966317 Wacks et al. Jun 1976 A
3983542 Ovshinsky Sep 1976 A
3988720 Ovshinsky Oct 1976 A
4177474 Ovshinsky Dec 1979 A
4181913 Thornburg Jan 1980 A
4267261 Hallman et al. May 1981 A
4269935 Masters et al. May 1981 A
4312938 Drexler et al. Jan 1982 A
4316946 Masters et al. Feb 1982 A
4320191 Yoshikawa et al. Mar 1982 A
4405710 Balasubramanyam et al. Sep 1983 A
4419421 Wichelhaus et al. Dec 1983 A
4499557 Holmberg et al. Feb 1985 A
4597162 Johnson et al. Jul 1986 A
4608296 Keem et al. Aug 1986 A
4637895 Ovshinsky et al. Jan 1987 A
4646266 Ovshinsky et al. Feb 1987 A
4664939 Ovshinsky May 1987 A
4668968 Ovshinsky et al. May 1987 A
4670763 Ovshinsky et al. Jun 1987 A
4671618 Wu et al. Jun 1987 A
4673957 Ovshinsky et al. Jun 1987 A
4678679 Ovshinsky Jul 1987 A
4696758 Ovshinsky et al. Sep 1987 A
4698234 Ovshinsky et al. Oct 1987 A
4710899 Young et al. Dec 1987 A
4728406 Banerjee et al. Mar 1988 A
4737379 Hudgens et al. Apr 1988 A
4766471 Ovshinsky et al. Aug 1988 A
4769338 Ovshinsky et al. Sep 1988 A
4775425 Guha et al. Oct 1988 A
4788594 Ovshinsky et al. Nov 1988 A
4795657 Formigoni et al. Jan 1989 A
4800526 Lewis Jan 1989 A
4809044 Pryor et al. Feb 1989 A
4816878 Kano et al. Mar 1989 A
4818717 Johnson et al. Apr 1989 A
4843443 Ovshinsky et al. Jun 1989 A
4845533 Pryor et al. Jul 1989 A
4847674 Sliwa et al. Jul 1989 A
4853785 Ovshinsky et al. Aug 1989 A
4891330 Guha et al. Jan 1990 A
5128099 Strand et al. Jul 1992 A
5159661 Ovshinsky et al. Oct 1992 A
5166758 Ovshinsky et al. Nov 1992 A
5177567 Klersy et al. Jan 1993 A
5219788 Abernathey et al. Jun 1993 A
5238862 Blalock et al. Aug 1993 A
5272359 Nagasubramanian et al. Dec 1993 A
5296716 Ovshinsky et al. Mar 1994 A
5314772 Kozicki May 1994 A
5315131 Kishimoto et al. May 1994 A
5335219 Ovshinsky et al. Aug 1994 A
5341328 Ovshinsky et al. Aug 1994 A
5350484 Gardner et al. Sep 1994 A
5359205 Ovshinsky Oct 1994 A
5360981 Owen et al. Nov 1994 A
5406509 Ovshinsky et al. Apr 1995 A
5414271 Ovshinsky et al. May 1995 A
5500532 Kozicki et al. Mar 1996 A
5512328 Yoshimura et al. Apr 1996 A
5512773 Wolf et al. Apr 1996 A
5534711 Ovshinsky et al. Jul 1996 A
5534712 Ovshinsky et al. Jul 1996 A
5536947 Klersy et al. Jul 1996 A
5543737 Ovshinsky Aug 1996 A
5591501 Ovshinsky et al. Jan 1997 A
5596522 Ovshinsky et al. Jan 1997 A
5608231 Ugajin et al. Mar 1997 A
5687112 Ovshinsky Nov 1997 A
5694054 Ovshinsky et al. Dec 1997 A
5714768 Ovshinsky et al. Feb 1998 A
5726083 Takaishi Mar 1998 A
5751012 Wolstenholme et al. May 1998 A
5761115 Kozicki et al. Jun 1998 A
5789277 Zahorik et al. Aug 1998 A
5815008 Williamson, III et al. Sep 1998 A
5825046 Czubatyj et al. Oct 1998 A
5841150 Gonzalez et al. Nov 1998 A
5846889 Harbison et al. Dec 1998 A
5896312 Kozicki et al. Apr 1999 A
5912839 Ovshinsky et al. Jun 1999 A
5914893 Kozicki et al. Jun 1999 A
5920788 Reinberg Jul 1999 A
5933365 Klersy et al. Aug 1999 A
5998066 Block et al. Dec 1999 A
6011757 Ovshinsky Jan 2000 A
6072716 Jacobson et al. Jun 2000 A
6077729 Harshfield Jun 2000 A
6084796 Kozicki et al. Jul 2000 A
6087674 Ovshinsky et al. Jul 2000 A
6117720 Harshfield Sep 2000 A
6141241 Ovshinsky et al. Oct 2000 A
6143604 Chiang et al. Nov 2000 A
6177338 Liaw et al. Jan 2001 B1
6236059 Wolstenholme et al. May 2001 B1
RE37259 Ovshinsky Jul 2001 E
6297170 Gabriel et al. Oct 2001 B1
6300684 Gonzalez et al. Oct 2001 B1
6316784 Zahorik et al. Nov 2001 B1
6329606 Freyman et al. Dec 2001 B1
6339544 Chiang et al. Jan 2002 B1
6348365 Moore et al. Feb 2002 B1
6350679 McDaniel et al. Feb 2002 B1
6376284 Gonzalez et al. Apr 2002 B1
6388324 Kozicki et al. May 2002 B2
6391688 Gonzalez et al. May 2002 B1
6404665 Lowrey et al. Jun 2002 B1
6414376 Thakur et al. Jul 2002 B1
6418049 Kozicki et al. Jul 2002 B1
6423628 Li et al. Jul 2002 B1
6429064 Wicker Aug 2002 B1
6437383 Xu Aug 2002 B1
6462984 Xu et al. Oct 2002 B1
6469364 Kozicki Oct 2002 B1
6473332 Ignatiev et al. Oct 2002 B1
6480438 Park Nov 2002 B1
6487106 Kozicki Nov 2002 B1
6487113 Park et al. Nov 2002 B1
6501111 Lowrey Dec 2002 B1
6507061 Hudgens et al. Jan 2003 B1
6511862 Hudgens et al. Jan 2003 B2
6511867 Lowrey et al. Jan 2003 B2
6512241 Lai Jan 2003 B1
6514805 Xu et al. Feb 2003 B2
6531373 Gill et al. Mar 2003 B2
6534781 Dennison Mar 2003 B2
6545287 Chiang Apr 2003 B2
6545907 Lowrey et al. Apr 2003 B1
6555860 Lowrey et al. Apr 2003 B2
6563164 Lowrey et al. May 2003 B2
6566700 Xu May 2003 B2
6567293 Lowrey et al. May 2003 B1
6569705 Chiang et al. May 2003 B2
6570784 Lowrey May 2003 B2
6576921 Lowrey Jun 2003 B2
6586761 Lowrey Jul 2003 B2
6589714 Maimon et al. Jul 2003 B2
6590807 Lowrey Jul 2003 B2
6593176 Dennison Jul 2003 B2
6597009 Wicker Jul 2003 B2
6605527 Dennison et al. Aug 2003 B2
6613604 Maimon et al. Sep 2003 B2
6621095 Chiang et al. Sep 2003 B2
6625054 Lowrey et al. Sep 2003 B2
6642102 Xu Nov 2003 B2
6646297 Dennison Nov 2003 B2
6649928 Dennison Nov 2003 B2
6667900 Lowrey et al. Dec 2003 B2
6671710 Ovshinsky et al. Dec 2003 B2
6673648 Lowrey Jan 2004 B2
6673700 Dennison et al. Jan 2004 B2
6674115 Hudgens et al. Jan 2004 B2
6687153 Lowrey Feb 2004 B2
6687427 Ramalingam et al. Feb 2004 B2
6690026 Peterson Feb 2004 B2
6696355 Dennison Feb 2004 B2
6707712 Lowery Mar 2004 B2
6714954 Ovshinsky et al. Mar 2004 B2
20020000666 Kozicki et al. Jan 2002 A1
20020072188 Gilton Jun 2002 A1
20020106849 Moore Aug 2002 A1
20020123169 Moore et al. Sep 2002 A1
20020123170 Moore et al. Sep 2002 A1
20020123248 Moore et al. Sep 2002 A1
20020127886 Moore et al. Sep 2002 A1
20020163828 Krieger et al. Nov 2002 A1
20020168820 Kozicki Nov 2002 A1
20020190350 Kozicki Dec 2002 A1
20030001229 Moore et al. Jan 2003 A1
20030027416 Moore Feb 2003 A1
20030035314 Kozicki Feb 2003 A1
20030035315 Kozicki Feb 2003 A1
20030048744 Ovshinsky et al. Mar 2003 A1
20030156463 Casper et al. Aug 2003 A1
20030156468 Campbell et al. Aug 2003 A1
20030212724 Ovshinsky et al. Nov 2003 A1
20030212725 Ovshinsky et al. Nov 2003 A1
20040035401 Ramachandran et al. Feb 2004 A1
20040042259 Campbell et al. Mar 2004 A1
20040045565 Mua et al. Mar 2004 A1
Foreign Referenced Citations (5)
Number Date Country
56126916 Oct 1981 JP
WO 9748032 Dec 1997 WO
WO 9928914 Jun 1999 WO
WO 0048196 Aug 2000 WO
WO 0221542 Mar 2002 WO
Related Publications (1)
Number Date Country
20080128674 A1 Jun 2008 US
Divisions (2)
Number Date Country
Parent 11001306 Dec 2004 US
Child 12003573 US
Parent 10410567 Apr 2003 US
Child 11001306 US