纳米
钙钛矿(结构)
材料科学
微晶
二极管
发光二极管
光电子学
纳米晶
光伏
卤化物
纳米技术
化学工程
光伏系统
化学
无机化学
复合材料
工程类
冶金
生物
生态学
作者
Zhengguo Xiao,Ross A. Kerner,Lianfeng Zhao,Nhu L. Tran,Kyung Min Lee,Tae‐Wook Koh,Gregory D. Scholes,Barry P. Rand
出处
期刊:Nature Photonics
[Nature Portfolio]
日期:2017-01-16
卷期号:11 (2): 108-115
被引量:1260
标识
DOI:10.1038/nphoton.2016.269
摘要
Organic–inorganic hybrid perovskite materials are emerging as highly attractive semiconductors for use in optoelectronics. In addition to their use in photovoltaics, perovskites are promising for realizing light-emitting diodes (LEDs) due to their high colour purity, low non-radiative recombination rates and tunable bandgap. Here, we report highly efficient perovskite LEDs enabled through the formation of self-assembled, nanometre-sized crystallites. Large-group ammonium halides added to the perovskite precursor solution act as a surfactant that dramatically constrains the growth of 3D perovskite grains during film forming, producing crystallites with dimensions as small as 10 nm and film roughness of less than 1 nm. Coating these nanometre-sized perovskite grains with longer-chain organic cations yields highly efficient emitters, resulting in LEDs that operate with external quantum efficiencies of 10.4% for the methylammonium lead iodide system and 9.3% for the methylammonium lead bromide system, with significantly improved shelf and operational stability. Perovskite nanocrystal LEDs featuring long-chain ammonium cations offer improved stability and efficiency.
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