Electron Trapping Prolongs the Lifetime of Charge-Separated States in 2D Perovskite Nanoplatelet-Hole Acceptor Complexes

被引:9
|
作者
He, Sheng [1 ]
Jin, Tao [1 ]
Ni, Anji [1 ]
Lian, Tianquan [1 ]
机构
[1] Emory Univ, Dept Chem, Atlanta, GA 30322 USA
基金
美国国家科学基金会;
关键词
CESIUM-LEAD-HALIDE; EXCITON DISSOCIATION; ANION-EXCHANGE; QUANTUM DOTS; NANOCRYSTALS; SURFACE; EFFICIENCY; SINGLE; PHOTOLUMINESCENCE; PASSIVATION;
D O I
10.1021/acs.jpclett.2c03815
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Two-dimensional (2D) lead halide perovskite nanoplatelets (NPLs) are promising materials for blue light emission because of the strong quantum confinement in the 2D morphology. However, the identity of carrier traps and the trap influence on charge transfer in these NPLs remain unclear. Herein, transient absorption studies revealed two types of electron traps in 3 monolayer lead bromide perovskite NPLs with trapping lifetime of 9.0 +/- 0.6 and 516 +/- 59 ps, respectively, while no hole traps were observed. Systematic charge transfer experiments show that electron traps have negligible influence on ultrafast electron transfer or hole transfer but extend the half-lifetime of the charge-separated state from 2.1 +/- 0.1 to 68 +/- 3 ns after hole transfer, which is explained by the reduced electron- hole overlap. This work contributes to the understanding of the fundamental carrier dynamics in 2D perovskite NPLs and offers guidelines for boosting their performance in optoelectronics and photocatalysis.
引用
收藏
页码:2241 / 2250
页数:10
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