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Bright Lead-Free Inorganic CsSnBr3 Perovskite Light-Emitting Diodes

Authors
Heo, Jung -MinCho, HimchanLee, Seong-ChulPark, Min -HoKim, Joo SungKim, HobeomPark, JinwooKim, Young-HoonYun, Hyung JoongYoon, EojinKim, Dong-HyeokAhn, SoyeongKwon, Sung-JooPark, Chan-YulLee, 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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Park, Min-Ho
College of Engineering (Department of Materials Science and Engineering)
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