可靠的卤化物包光体晶闸管中挥发性和非挥发性响应的解耦

Naresh-Kumar Pendyala, Cedric Gonzales, Antonio Guerrero
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引用次数: 0

摘要

卤化物包晶对于制造用于神经形态应用的高能效忆阻器极具吸引力。然而,与其他技术相比,可重复性、稳定性和对开关行为的理解仍然落后。在本文中,通过开发高度可重现的器件,我们对包晶体忆阻器有了深层次的了解。该方法基于一种高度稳定的过氧化物配方(MAPbBr3),并使用预氧化银(AgI)作为缓冲层。在这里,我们展示了可靠的过氧化物忆阻器,其器件产量接近 100%,挥发性响应的稳定性达到 104 个周期,非挥发性响应的线性增效/抑制条件充分。通过使用这些器件,我们了解了易失性和非易失性双响应的性质。研究表明,施加短 SET 电压(VSET)脉冲会导致过氧化物材料内部的离子位移,并在触点附近形成离子双层。离子的位移会增加器件的串联电阻,并导致离子在 V < VSET 时扩散回包晶的波动响应。另一种情况是,长 VSET 脉冲导致电流逐渐增加,出现化学感应和非挥发性响应。观察到的非挥发性机制与 Ag+ 导电丝的形成有关。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Decoupling Volatile and Nonvolatile Response in Reliable Halide Perovskite Memristors

Decoupling Volatile and Nonvolatile Response in Reliable Halide Perovskite Memristors
Halide perovskite is very attractive for the fabrication of energy-efficient memristors for neuromorphic applications. However, reproducibility, stability, and understanding the switching behavior still lag in comparison to other technologies. Herein, a deep-level understanding of perovskite memristors is obtained by the development of highly reproducible devices. The approach is based on a highly stable perovskite formulation (MAPbBr3) and the use of preoxidized silver (AgI) as a buffer layer. Here, reliable perovskite memristors with device yields approaching 100%, stabilities of >104 cycles for volatile response, and adequate conditions for linear potentiation/depression for nonvolatile response are demonstrated. Using these devices, the nature of the dual volatile and nonvolatile response is understood. It is shown that applying short SET voltage (VSET) pulses leads to ion displacement inside the perovskite material with the formation of an ionic double layer close to the contacts. The displacement of the ions contributes to the series resistance of the device and to a volatile response with ions diffusing back to the perovskite at V < VSET. Alternatively, long VSET pulses lead to a gradual increase in current, the appearance of a chemical inductor, and a nonvolatile response. The observed nonvolatile regime is related to the formation of Ag+ conductive filaments.
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CiteScore
17.30
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