钙钛矿(结构)
材料科学
荧光
结晶
光电子学
二极管
发光二极管
化学工程
光学
化学
结晶学
物理
工程类
作者
Wei Yang,Xinxin Ban,Xiaoli He,Xinmei Huang,Xiaoyu Wang,Yong Zhang,Chun‐Hong Gao
标识
DOI:10.1021/acs.jpcc.3c07799
摘要
Efficient and stable green emission of perovskite light-emitting diodes (PeLEDs) is an essential element for their potential applications in full-color displays and solid-state lighting, aspiring to become a new generation of light-emitting devices. Rational manipulation of the entire electroluminescence process is expected to prepare high-performance devices. Hence, to generate effective green PeLEDs that simultaneously reduce energy loss during electron–photon conversion and increase light outcoupling, a simple device architecture is suggested. Consequently, in our research, we utilized thermally activated delayed fluorescent materials DTC-mBPSB and BTBC-DPS to modify the hole transport layer. Employing efficient interfacial engineering to modulate the growth of perovskite crystals resulted in dense perovskite films and effectively reduced the density of defective states by providing lone electron pairs to neutralize unsaturated Pb2+ via oxygen atoms in the passivation group of the S═O bond. Furthermore, this approach increases the carrier transport abilities and thus facilitates the occurrence of more radiative recombination. Hence, this approach contributes to the realization of EQE of 11.04% (DTC-mBPSB) and 13.97% (BTBC-DPS), respectively, for green PeLEDs emitted at 512 nm and enhances the operational stability, establishing a foundation for subsequent studies.
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