钙钛矿(结构)
材料科学
发光二极管
卤化物
发光
碘化物
二极管
纳米晶
八面体
薄膜
光电子学
结晶学
无机化学
晶体结构
纳米技术
化学
作者
Nan Li,Sofia Apergi,Christopher C. S. Chan,Yongheng Jia,Fangyan Xie,Qiong Liang,Gang Li,Kam Sing Wong,Geert Brocks,Shuxia Tao,Ni Zhao
标识
DOI:10.1002/adma.202202042
摘要
Abstract 3D mixed‐halide perovskite‐based red emitters combine excellent charge‐transport characteristics with simple solution processing and good film formation; however, light‐emitting diodes (LEDs) based on these emitters cannot yet outperform their nanocrystal counterparts. Here the use of diammonium halides in regulating the formation of mixed bromide–iodide perovskite films is explored. It is found that the diammonium cations preferentially bond to Pb–Br, rather than Pb–I, octahedra, promoting the formation of quasi‐2D phases. It is proposed that the perovskite formation is initially dominated by the crystallization of the thermodynamically more favorable 3D phase, but, as the solution gets depleted from the regular A cations, thin shells of amorphous quasi‐2D perovskites form. This leads to crystalline perovskite grains with efficiently passivated surfaces and reduced lattice strain. As a result, the diammonium‐treated perovskite LEDs demonstrate a record luminance (10745 cd m −2 ) and half‐lifetime among 3D perovskite‐based red LEDs.
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