Embodiments described herein relate generally to a memory element.
There is a resistance change memory as a memory device. The resistance change memory is less influenced by shrinking and is capable of achieving a large capacity, and is therefore drawing attention as a next-generation nonvolatile memory. The resistance change memory is composed of resistance change elements (cells), and utilizes the characteristic that the resistance of a resistance change film is changed by applying a voltage to the film via upper and lower electrodes to pass a current through the film. Examples of the resistance change film include a large number of oxide films such as transition metal oxide films. In the case where, for example, a transition metal oxide film is used as the resistance change film, the initial state is high resistive, and the forming operation for making the film low resistive in the beginning may be performed. However, the forming operation may take a long time.
In general, according one embodiment, a memory element includes: a first electrode layer; a second electrode layer including a metal element; and a memory layer provided between the first electrode layer and the second electrode layer, the memory layer including an oxide layer, and a platinum group metal being dispersed in at least part of the oxide layer, an absolute value of a standard Gibbs free energy of formation of an oxide of an element included in the oxide layer being larger than an absolute value of a standard Gibbs free energy of formation when the metal element changes to an oxide.
Hereinbelow, embodiments are described with reference to the drawings. In the following description, identical components are marked with the same reference numerals, and a description of components once described is omitted as appropriate.
As shown in
The memory element 1 shown in
The absolute value of the standard Gibbs free energy of formation of the oxide contained in the oxide layer is larger than the absolute value of the standard Gibbs free energy of formation when the metal element contained in the electrode layer 20 changes to an oxide. The standard Gibbs free energy of formation of the oxide contained in the oxide layer is expressed as ΔGa (kJ/mol, 298.15 K), for example. The standard Gibbs free energy of formation when the metal element contained in the electrode layer 20 changes to an oxide is expressed as ΔGb. In this case, the absolute value of ΔGa is larger than the absolute value of ΔGb.
The memory element 1 further includes a selector 40.
An electric potential of a negative polarity (a first polarity) can be applied to the electrode layer 10 via the bit line 80, and an electric potential of a positive polarity (a second polarity) can be applied to the electrode layer 20 via the word line 90. Furthermore, an electric potential of a positive polarity can be applied to the electrode layer 10 via the bit line 80, and an electric potential of a negative polarity can be applied to the electrode layer 20 via the word line 90. That is, the memory cell array 100 includes a bipolar memory element 1.
The platinum group metal is at least one selected from the group consisting of platinum (Pt), palladium (Pd), iridium (Ir), rhodium (Rh), osmium (Os), and ruthenium (Ru). The oxide layer in which a platinum group metal is introduced is formed by, for example, PVD (physical vapor deposition), CVD (chemical vapor deposition), ALD (atomic layer deposition), or the like.
The electrode layer 10 contains, for example, at least one selected from the group consisting of tungsten (W), aluminum (Al), titanium nitride (TiN), and the like. The electrode layer 20 contains, for example, at least one selected from the group consisting of platinum (Pt), ruthenium (Ru), cobalt (Co), tungsten (W), titanium (Ti), titanium nitride (TiN), and the like.
The oxide layer included in the memory layer 30 contains at least one selected from the group consisting of hafnium oxide (HfOx), zirconium oxide (ZrOx), tantalum oxide (TaOx), niobium oxide (NbOx), titanium oxide (TiOx), and the like. The coefficients of the elements of the composition formulae of these oxides are deviated from the stoichiometric coefficients. The selector 40 is, for example, a field effect transistor, a tunnel diode, or the like,
Operations of the memory element 1 are described.
It is possible to switch to a low resistance state by the set operation from the initial state, or switch to a high resistance state by the reset operation.
By an electric field being applied to the memory layer 30, the oxygen in the memory layer 30 is ionized. The oxygen ions are minus ions, and therefore the oxygen ions move through the memory layer 30 in an oxygen deficient state and are diffused to the side of the electrode layer 20, which is an anode. The oxygen ions can fill the oxygen defect in an oxygen deficient state near the electrode layer 20. The electrons possessed by the oxygen ions flow to the electrode layer 20.
Thereby, a high resistance region 30h with a high resistance is produced near the interface between the electrode layer 20 and the memory layer 30, Here, since the absolute value of ΔG (free energy of formation of oxide of constituent element in the memory layer 30) is larger than the absolute value of ΔG (free energy of formation of oxide of the electrode layer 20), the oxygen ions in the memory layer 30 fill the oxygen deficient portion of the resistance change layer near the interface with the electrode layer 20, and form the high resistance region 30h. The oxide in the high resistance region 30h is in a state of the stoichiometric composition or a state near the stoichiometric composition. That is, assuming that the state of the memory layer 30 shown in
The oxygen ions are diffused to the side of the electrode layer 10, which is an anode. Consequently, the oxygen concentration of the high resistance region 30h is decreased. The electrons possessed by the oxygen ions flow to the electrode layer 10. That is, the high resistance region 30h disappears, and the memory layer 30 returns to the low resistance state. Changing the state of the memory layer 30 from the high resistance state to the low resistance state is defined as the set operation. The state of the memory element in the low resistance state is taken as, for example, information “1”.
Thus, in the memory element 1, the polarity of the voltage applied to the memory layer 30 is changed to produce or eliminate the high resistance region 30h formed near the electrode layer 20; thereby, information can be written or erased.
In the memory element 1 according to the first embodiment, a platinum group element is introduced in the oxide layer. The platinum group element is substituted with part of the metal element of the oxide layer. The platinum group element has the property of being less likely to form an oxide, and therefore a reaction is less likely to occur between an oxygen ion and the platinum group element. Thus, oxygen ions and the metal in the oxide layer near the anode react with good efficiency, and the high resistance region 30h is stably produced near the anode.
The platinum group element has a catalytic action. Therefore, the ionization of the oxygen in the oxide layer is promoted. That is, the oxygen is ionized by the application of an electric field and the catalytic action of the platinum group element. Consequently, in the memory element 1 of the embodiment, the memory layer 30 can be reset or set by a relatively low voltage as compared to a memory layer in which no platinum group element is introduced. Thereby, the power consumption of the memory element is reduced.
When the resetting and setting of the memory layer 30 are possible at a low voltage, the electrical load on the memory layer 30 is reduced. Therefore, the durability of the memory element is improved.
The memory element 1 is not what is called a filament-type memory element, In the memory element 1, the oxygen concentration in the oxide layer in contact with the entire region of the electrode layer 20 changes. Thus, in the memory element 1, the forming operation essential to the filament-type memory element is not needed.
For example, in the case where a resistance change layer formed of a transition metal oxide film is used, an operation called the forming operation takes a long time. The forming operation turns a high resistance filament to a low resistance state. A large current may flow at the time of forming or setting, and the resistance change film may be broken. In addition, due to the forming, the resistance at the time of setting will become too low and a large reset current will flow; thus, a drive circuit element and a protection circuit element may be broken. In addition, the forming may cause phenomena in which the voltage and the current value in setting and resetting vary, the difference between the set voltage and the reset voltage is reduced, and the voltage threshold of the lead cannot be established.
When resistance changes occur due to the oxidation of part of the filament formed in the forming and the re-breaking of the oxide layer formed, there is a trade-off between increasing the number of times of data retention and increasing the data retention time, and thereby reliability may not be ensured. In the first embodiment, since the forming operation is not needed, these faults are less likely to occur.
In the first embodiment, the production and elimination of the high resistance region 30h occur stably. Therefore, the resistance difference between the low resistance state that is the ON state and the high resistance state that is the OFF state (Roff/Ron ratio) is large, and the possibility of false reading is reduced. Furthermore, since the resistance difference (Roff/Ron ratio) is high, separation into resistance states becomes possible. Therefore, a multiple-valued operation is enabled, Thereby, the integration degree of the memory device is further increased.
In the first embodiment, the memory layer 30 is not made a multiple-layer structure, and a platinum group metal is introduced into the memory layer 30. Therefore, the manufacturing process is simplified, and an increase in manufacturing costs is not caused.
The concentration distribution of the platinum group metal in the memory layer 30 is shown on the right side of the drawings of memory elements of
In memory elements 2A and 2B according to the second embodiment, in the memory layer 30, the concentration of the platinum group metal in the oxide layer is higher on the electrode layer 20 side than on the electrode layer 10 side.
For example, in the memory element 2A shown in
In the memory element 2A, the concentration of the platinum group metal near the interface between the electrode layer 20 and the memory layer 30 is high. Therefore, the oxygen deficiency of the oxide layer near the interface between the electrode layer 20 and the memory layer 30 can be compensated for by oxygen ions more easily. That is, the high resistance region 30h is more stably produced and eliminated near the interface between the electrode layer 20 and the memory layer 30. Thereby, the durability of the memory element is further improved.
The structure in which the concentration of the platinum group metal in the oxide layer is higher on the electrode layer 20 side than on the electrode layer 10 side is not limited to the structure shown in the memory element 2A. For example, like the memory element 2B shown in
The concentration distribution of the platinum group metal in the memory layer 30 is shown on the right side of the drawings of memory elements of
The structure of the memory layer 30 is not limited to the structure of the second embodiment described above, and also a structure in which the structure of the second embodiment is turned upside down is possible. In this case, the material of the electrode layer 10 and the material of the electrode layer 20 may be exchanged.
For example, in memory elements 3A and 3B according to the third embodiment, in the memory layer 30, the concentration of the platinum group metal in the oxide layer is lower on the electrode layer 20 side than on the electrode layer 10 side.
For example, in the memory element 3A shown in
In the memory element 3A, the concentration of the platinum group metal near the interface between the electrode layer 10 and the memory layer 30 is high. Therefore, the oxygen deficiency of the oxide layer near the interface between the electrode layer 10 and the memory layer 30 can be compensated for by oxygen ions more easily. That is, the high resistance region 30h is more stably produced and eliminated near the interface between the electrode layer 10 and the memory layer 30. Thereby, the durability of the memory element is further improved.
The structure in which the concentration of the platinum group metal in the oxide layer is lower on the electrode layer 20 side than on the electrode layer 10 side is not limited to the structure shown in the memory element 3A. For example, like the memory element 3B shown in
The embodiments have been described above with reference to examples. However, the embodiments are not limited to these examples. More specifically, these examples can be appropriately modified in design by those skilled in the art. Such modifications are also encompassed within the scope of the embodiments as long as they include the features of the embodiments. The components included in the above examples and the layout, material, condition, shape, size and the like thereof are not limited to those illustrated, but can be appropriately modified.
The term “on” in “a portion A is provided on a portion B” refers to the case where the portion A is provided on the portion B such that the portion A is in contact with the portion B and the case where the portion A is provided above the portion B such that the portion A is not in contact with the portion B.
Furthermore, the components included in the above embodiments can be combined as long as technically feasible. Such combinations are also encompassed within the scope of the embodiments as long as they include the features of the embodiments, In addition, those skilled in the art could conceive various modifications and variations within the spirit of the embodiments. It is understood that such modifications and variations are also encompassed within the scope of the embodiments.
While certain embodiments have been described, these embodiments have been presented by way of example only, and are not intended to limit the scope of the inventions. Indeed, the novel embodiments described herein may be embodied in a variety of other forms; furthermore, various omissions, substitutions and changes in the form of the embodiments described herein may be made without departing from the spirit of the inventions. The accompanying claims and their equivalents are intended to cover such forms or modifications as would fall within the scope and spirit of the invention.
This application is based upon and claims the benefit of priority from U.S. Provisional Patent Application 61/804404, filed on Mar. 22, 2013; the entire contents of which are incorporated herein by reference.
Number | Date | Country | |
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61804404 | Mar 2013 | US |