钙钛矿(结构)
材料科学
可塑性
记忆电阻器
突触可塑性
峰值时间相关塑性
变质塑性
神经形态工程学
光电子学
纳米晶
长时程增强
纳米技术
化学
计算机科学
电子工程
人工神经网络
生物化学
机器学习
工程类
复合材料
受体
结晶学
作者
Sixian Liu,Jiuhui Guan,Lei Yin,Lue Zhou,Junli Huang,Yuncheng Mu,Shuyao Han,Xiaodong Pi,Gang Liu,Pingqi Gao,Shu Zhou
标识
DOI:10.1021/acs.jpclett.2c02900
摘要
Exploring new materials and structures to construct synaptic devices represents a promising route to fundamentally approach novel forms of computing. Nanocrystals (NCs) of halide perovskites possess unique charge transport characteristics, i.e., ionic–electronic coupling, holding considerable promise for energy-efficient and reconfigurable artificial synapses. Herein, we report solution-processed thin-film memristors from all-inorganic CsPbBr3 perovskite NCs, functioning as an electrically programmable analog memory with good stability. The devices are demonstrated to successfully emulate a number of essential synaptic functions with low power consumption, including reversible potentiation and depression, short-term plasticity (STP), paired-pulse facilitation (PPF), and long-term plasticity (LTP), such as spike-number-dependent plasticity (SNDP), spike-rate-dependent plasticity (SRDP), spike-timing-dependent plasticity (STDP), and spike-voltage-dependent plasticity (SVDP). It is proposed that a coupled capacitive and inductive phenomenon originating from charge trapping and ion migration in CsPbBr3 NC films, controlled by the amplitude and timing of the programming pulses, defines the degree of synaptic plasticity. A transition emerges from the fast trap-related capacitive regime to a slow ionic inductive regime, which enables continuous change of the film resistance and the magnitude of the electronic current, analogous to the synaptic weight modulation in biological synapses.
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