作者
Ya‐Kun Wang,Fanglong Yuan,Yitong Dong,Jiaoyang Li,Andrew Johnston,Bin Chen,Makhsud I. Saidaminov,Chun Zhou,Xiaopeng Zheng,Yi Hou,Koen Bertens,Hinako Ebe,Dongxin Ma,Zhengtao Deng,Shuai Yuan,Rui Chen,Laxmi Kishore Sagar,Jiakai Liu,James Z. Fan,Peicheng Li,Xiyan Li,Yuan Gao,Man‐Keung Fung,Zheng‐Hong Lu,Osman M. Bakr,Liang‐Sheng Liao,Edward H. Sargent
摘要
Abstract The all‐inorganic nature of CsPbI 3 perovskites allows to enhance stability in perovskite devices. Research efforts have led to improved stability of the black phase in CsPbI 3 films; however, these strategies—including strain and doping—are based on organic‐ligand‐capped perovskites, which prevent perovskites from forming the close‐packed quantum dot (QD) solids necessary to achieve high charge and thermal transport. We developed an inorganic ligand exchange that leads to CsPbI 3 QD films with superior phase stability and increased thermal transport. The atomic‐ligand‐exchanged QD films, once mechanically coupled, exhibit improved phase stability, and we link this to distributing strain across the film. Operando measurements of the temperature of the LEDs indicate that KI‐exchanged QD films exhibit increased thermal transport compared to controls that rely on organic ligands. The LEDs exhibit a maximum EQE of 23 % with an electroluminescence emission centered at 640 nm (FWHM: ≈31 nm). These red LEDs provide an operating half‐lifetime of 10 h (luminance of 200 cd m −2 ) and an operating stability that is 6× higher than that of control devices.