Tailoring transient-amorphous states: towards fast and power-efficient phase-change memory and neuromorphic computing.
Tailoring transient-amorphous states: towards fast and power-efficient phase-change memory and neuromorphic computing.
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DOI:
10.1002/adma.201402696
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发表时间:
2014-11-26
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影响因子:
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通讯作者:
Elliott SR
中科院分区:
文献类型:
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作者:
Lee TH;Loke D;Huang KJ;Wang WJ;Elliott SR
DOI: 10.1002/adma. 201402696 crucial, especially for neuromorphic-computing applications of PCM technology, such as electronic synapses,[4, 5] or bio-inspired arithmetic-computing devices,[6] in which many electric pulses are used in a complicated way to induce phase transitions. However, few systematic researches regarding the physics underlying this interaction have been reported yet. We report here new methodologies to overcome these limitations by tailoring transient amorphous (TA) states of PC materials. Applying multiple electrical-excitation pulses in a well-programmed manner not only enables the development of a fast, low-power and efficient (parallel-writing) form of PCM, but also provides an opportunity even for achieving biologylike neuromorphic functionalities, which can benefit from a dynamic control of TA-states. We first demonstrate the temporal evolution of TA-states upon the application of a stimulus pulse. Three different stimulus pulses, each having a different amplitude (V St) or length (d St), were employed, while allowing an unbiased time period (d TS) between the low-voltage/high-voltage (LO-HI) stimulus and ACT pulses. Each stimulus pulse represents a different region in the voltage-width (VW) diagram in Figure 1a, and causes a different influence on the TA states, as shown in Figure 1 b. In any case, the TA-phases generated from the stimulus pulse always show shorter minimum ACT lengths (the minimum ACT pulse length for full crystallization) than that for the melt-quenched amorphous (a-) state (60 ns; see Figure S2), which means that exposure to the stimulus pulse always gives rise to faster crystallisation (Figure 1c). In addition, the stronger (and wider) is the stimulus pulse, the shorter the minimum ACT length becomes. A more interesting observation is that, when there exists an unbiased period between two LO-HI pulses, all the TA-states show a spontaneous transition (or relaxation) to other TA-states, each of which presents, progressively, a longer minimum ACT length, up to a characteristic time (∼ 1 µs).The TA-states can be represented by their cluster-size distribution that form the basis of kinetic theory of nucleation, and the shortening of the ACT time upon a stimulus pulse may be described by their evolution. On the microscopic scale, the TA-states may be described by their degree of medium-range order in the disordered-network structure that fluctuates locally and temporally upon excitations. Numerical computations [14–16] based on the kinetic theory of nucleation have shown that, in response to a temperature change, the cluster population of the melt-quenched amorphous phase nam evolves gradually to the steady-state distribution nss at an elevated temperature in a finite amount of time.[17] This time dependence is a consequence of the thermally-activated process during the growth of