钙钛矿(结构)
电阻随机存取存储器
量子点
光电子学
毫秒
材料科学
阅读(过程)
极性(国际关系)
物理
计算机科学
化学
电极
天文
量子力学
生物化学
政治学
法学
细胞
结晶学
作者
Meng-Cheng Yen,Chia-Jung Lee,Kang-Hsiang Liu,Yi Peng,Junfu Leng,Tzu-Hsuan Chang,Chun-Chieh Chang,Kaoru Tamada,Ya‐Ju Lee
标识
DOI:10.1038/s41467-021-24762-w
摘要
Abstract Field-induced ionic motions in all-inorganic CsPbBr 3 perovskite quantum dots (QDs) strongly dictate not only their electro-optical characteristics but also the ultimate optoelectronic device performance. Here, we show that the functionality of a single Ag/CsPbBr 3 /ITO device can be actively switched on a sub-millisecond scale from a resistive random-access memory (RRAM) to a light-emitting electrochemical cell (LEC), or vice versa, by simply modulating its bias polarity. We then realize for the first time a fast, all-perovskite light-emitting memory (LEM) operating at 5 kHz by pairing such two identical devices in series, in which one functions as an RRAM to electrically read the encoded data while the other simultaneously as an LEC for a parallel, non-contact optical reading. We further show that the digital status of the LEM can be perceived in real time from its emission color. Our work opens up a completely new horizon for more advanced all-inorganic perovskite optoelectronic technologies.
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