材料科学
卤化物
光电子学
电极
铅(地质)
钙钛矿(结构)
电阻随机存取存储器
纳米尺度
纳米技术
电阻式触摸屏
计算机科学
无机化学
化学
结晶学
物理化学
地质学
地貌学
计算机视觉
作者
Shuping Ge,Xinwei Guan,Yutao Wang,Chun‐Ho Lin,Yimin Cui,Yunxia Huang,Xinran Zhang,Ruoxuan Zhang,Xiaosong Yang,Tom Wu
标识
DOI:10.1002/adfm.202002110
摘要
Abstract 3D organic–inorganic and all‐inorganic lead halide perovskites have been intensively pursued for resistive switching memories in recent years. Unfortunately, instability and lead toxicity are two foremost challenges for their large‐scale commercial applications. Dimensional reduction and composition engineering are effective means to overcome these challenges. Herein, low‐dimensional inorganic lead‐free Cs 3 Bi 2 I 9 and CsBi 3 I 10 perovskite‐like films are exploited for resistive switching memory applications. Both devices demonstrate stable switching with ultrahigh on/off ratios (≈10 6 ), ultralow operation voltages (as low as 0.12 V), and self‐compliance characteristics. 0D Cs 3 Bi 2 I 9 ‐based device shows better retention time and larger reset voltage than the 2D CsBi 3 I 10 ‐based device. Multilevel resistive switching behavior is also observed by modulating the current compliance, contributing to the device tunability. The resistive switching mechanism is hinged on the formation and rupture of conductive filaments of halide vacancies in the perovskite films, which is correlated with the formation of AgI x layers at the electrode/perovskite interface. This study enriches the library of switching materials with all‐inorganic lead‐free halide perovskites and offers new insights on tuning the operation of solution‐processed memory devices.
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