Bright Lead-Free Inorganic CsSnBr3 Perovskite Light-Emitting Diodes
- 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
- Aug-2022
- Publisher
- AMER CHEMICAL SOC
- Citation
- ACS ENERGY LETTERS, v.7, no.8, pp.2807 - 2815
- Journal Title
- ACS ENERGY LETTERS
- Volume
- 7
- Number
- 8
- Start Page
- 2807
- End Page
- 2815
- URI
- http://scholarworks.bwise.kr/ssu/handle/2018.sw.ssu/42963
- DOI
- 10.1021/acsenergylett.2c01010
- ISSN
- 2380-8195
- Abstract
- 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 (similar to 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 similar to 160 cd m(-2), i.e., similar to 7500 times brighter than than that of the control devices (without additive, 0.02 cd m(-2)), and a long device lifetime of similar to 30 hat 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.
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