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All-inorganic perovskite quantum dot light-emitting memories

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 switc...

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Detalles Bibliográficos
Autores principales: Yen, Meng-Cheng, Lee, Chia-Jung, Liu, Kang-Hsiang, Peng, Yi, Leng, Junfu, Chang, Tzu-Hsuan, Chang, Chun-Chieh, Tamada, Kaoru, Lee, Ya-Ju
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8298456/
https://www.ncbi.nlm.nih.gov/pubmed/34294699
http://dx.doi.org/10.1038/s41467-021-24762-w
Descripción
Sumario: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.