摘要
Field-induced ionic motions in all-inorganic CsPbBr3 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/CsPbBr3/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.
| 原文 | 英語 |
|---|---|
| 文章編號 | 4460 |
| 期刊 | Nature Communications |
| 卷 | 12 |
| 發行號 | 1 |
| DOIs | |
| 出版狀態 | 已發佈 - 2021 12月 1 |
ASJC Scopus subject areas
- 一般化學
- 一般生物化學,遺傳學和分子生物學
- 多學科
- 一般物理與天文學
指紋
深入研究「All-inorganic perovskite quantum dot light-emitting memories」主題。共同形成了獨特的指紋。引用此
- APA
- Standard
- Harvard
- Vancouver
- Author
- BIBTEX
- RIS