Edge stabilization in reduced-dimensional perovskites

Li Na Quan(University of Toronto), Dongxin Ma(University of Toronto), Yong‐Biao Zhao(University of Toronto), Oleksandr Voznyy(University of Toronto), Haifeng Yuan(University of Toronto), Eva Bladt(University of Antwerp), Jun Pan(Zhejiang University of Technology), F. Pelayo Garcı́a de Arquer(University of Toronto), Randy P. Sabatini(University of Toronto), Zachary Piontkowski(University of Rochester), Abdul‐Hamid Emwas(King Abdullah University of Science and Technology), Petar Todorović́(University of Toronto), Rafael Quintero‐Bermudez(University of Toronto), Grant Walters(University of Toronto), James Z. Fan(University of Toronto), Mengxia Liu(University of Toronto), Hairen Tan(University of Toronto), Makhsud I. Saidaminov(University of Toronto), Liang Gao(University of Toronto), Yiying Li(University of Toronto), Dalaver H. Anjum(King Abdullah University of Science and Technology), Nini Wei(King Abdullah University of Science and Technology), Jiang Tang(Wuhan National Laboratory for Optoelectronics), David W. McCamant(University of Rochester), Maarten B. J. Roeffaers(KU Leuven), Sara Bals(University of Antwerp), Johan Hofkens(Max Planck Institute for Polymer Research), Osman M. Bakr(King Abdullah University of Science and Technology), Zheng‐Hong Lu(University of Toronto), Edward H. Sargent(University of Toronto)
Nature Communications
January 10, 2020
Cited by 226Open Access
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Abstract

Abstract Reduced-dimensional perovskites are attractive light-emitting materials due to their efficient luminescence, color purity, tunable bandgap, and structural diversity. A major limitation in perovskite light-emitting diodes is their limited operational stability. Here we demonstrate that rapid photodegradation arises from edge-initiated photooxidation, wherein oxidative attack is powered by photogenerated and electrically-injected carriers that diffuse to the nanoplatelet edges and produce superoxide. We report an edge-stabilization strategy wherein phosphine oxides passivate unsaturated lead sites during perovskite crystallization. With this approach, we synthesize reduced-dimensional perovskites that exhibit 97 ± 3% photoluminescence quantum yields and stabilities that exceed 300 h upon continuous illumination in an air ambient. We achieve green-emitting devices with a peak external quantum efficiency (EQE) of 14% at 1000 cd m −2 ; their maximum luminance is 4.5 × 10 4 cd m −2 (corresponding to an EQE of 5%); and, at 4000 cd m −2 , they achieve an operational half-lifetime of 3.5 h.


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