| Literature DB >> 32150404 |
Dongxin Ma1, Petar Todorović1, Shadi Meshkat2, Makhsud I Saidaminov1, Ya-Kun Wang1, Bin Chen1, Peicheng Li3, Benjamin Scheffel1, Rafael Quintero-Bermudez1, James Z Fan1, Yitong Dong1, Bin Sun1, Chao Xu4, Chun Zhou1, Yi Hou1, Xiyan Li1, Yuetong Kang5, Oleksandr Voznyy2, Zheng-Hong Lu3, Dayan Ban4, Edward H Sargent1.
Abstract
Metal halide perovskites show promise for light-emitting diodes (LEDs) owing to their facile manufacture and excellent optoelectronic performance, including high color purity and spectral stability, especially in the green region. However, for blue perovskite LEDs, the emission spectrum line width is broadened to over 25 nm by the coexistence of multiple reduced-dimensional perovskite domains, and the spectral stability is poor, with an undesirable shift (over 7 nm) toward longer wavelengths under operating conditions, degradation that occurs due to phase separation when mixed halides are employed. Here we demonstrate chloride insertion-immobilization, a strategy that enables blue perovskite LEDs, the first to exhibit narrowband (line width of 18 nm) and spectrally stable (no wavelength shift) performance. We prepare bromide-based perovskites and then employ organic chlorides for dynamic treatment, inserting and in situ immobilizing chlorides to blue-shift and stabilize the emission. We achieve sky-blue LEDs with a record luminance over 5100 cd/m2 at 489 nm, and an operating half-life of 51 min at 1500 cd/m2. By device structure optimization, we further realize an improved EQE of 5.2% at 479 nm and an operating half-life of 90 min at 100 cd/m2.Entities:
Year: 2020 PMID: 32150404 DOI: 10.1021/jacs.9b12323
Source DB: PubMed Journal: J Am Chem Soc ISSN: 0002-7863 Impact factor: 15.419