作者
Li Na Quan,David Ma,Yongbiao Zhao,Oleksandr Voznyy,Haifeng Yuan,Eva Bladt,Jun Pan,F. Pelayo García de Arquer,Randy P. Sabatini,Zachary Piontkowski,Abdul-Hamid Emwas,P. Todorovic,Rafael Quintero-Bermudez,Grant Walters,James Fan,Mengxia Liu,Hairen Tan,Makhsud I. Saidaminov,Liang Gao,Yiying Li,Dalaver H. Anjum,Nini Wei,Jiang Tang,David W. McCamant,Maarten B. J. Roeffaers,Sara Bals,Johan Hofkens,Osman M. Bakr,Zheng-Hong Lu,Edward H. Sargent
摘要
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.