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Bright Lead-Free Inorganic CsSnBr3Perovskite Light-Emitting Diodes

Cited 23 time in Web of Science Cited 27 time in Scopus
Authors

Heo, Jung-Min; Cho, Himchan; Lee, Seong-Chul; Park, Min-Ho; Kim, Joo Sung; Kim, Hobeom; Park, Jinwoo; Kim, Young-Hoon; Yun, Hyung Joong; Yoon, Eojin; Kim, Dong-Hyeok; Ahn, Soyeong; Kwon, Sung-Joo; Park, Chan-Yul; Lee, Tae-Woo

Issue Date
2022-08
Publisher
American Chemical Society
Citation
ACS Energy Letters, Vol.7 No.8, pp.2807-2815
Abstract
© 2022 American Chemical Society.Tin-based perovskites have emerged as lead-free alternatives, but their application in perovskite light-emitting diodes (PeLEDs) has been limited due to the low chemical stability and inhomogeneity of the inorganic CsSnBr3 films using solution processing. Here, we demonstrate bright (∼160 cd m-2) CsSnBr3 PeLEDs made by introducing co-additives consisting of SnF2 and a grain-growth inhibitor (1,3,5-tris(N-phenylbenzimidazol-2-yl)benzene). The use of co-additives increased the number of nucleation sites during the crystallization process of CsSnBr3, and consequently yielded uniform CsSnBr3 films with decreased grain size and improved defect passivation. The crystallization-controlled CsSnBr3 PeLEDs had a maximum luminance of ∼160 cd m-2, i.e., ∼7500 times brighter than than that of the control devices (without additive, 0.02 cd m-2), and a long device lifetime of ∼30 h at 58 cd m-2. Our work suggests that control of the crystallization of CsSnBr3 during film formation is an important requirement to increase the luminescence efficiency and stability of tin-based PeLEDs.
ISSN
2380-8195
URI
https://hdl.handle.net/10371/189430
DOI
https://doi.org/10.1021/acsenergylett.2c01010
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