异质结
光催化
材料科学
钙钛矿(结构)
还原(数学)
铅(地质)
化学工程
光电子学
电荷(物理)
纳米技术
化学
催化作用
工程类
物理
地质学
几何学
地貌学
量子力学
生物化学
数学
作者
Zhipeng Zhang,Bingzhe Wang,Hai‐Bing Zhao,Jin‐Feng Liao,Zichun Zhou,Tanghao Liu,Bingchen He,Qi Wei,Shi Chen,Hong‐Yan Chen,Dai‐Bin Kuang,Ying Li,Guichuan Xing
标识
DOI:10.1016/j.apcatb.2022.121358
摘要
Lead-free double perovskites with superior stability have been considered as promising non-toxic substitutes to their lead-contained counterparts in photocatalysis. However, the severe charge recombination greatly restricts their potential as high-performance photocatalysts. Herein, for the first time, we present a self-assembled heterostructure of lead-free double perovskite Cs 2 AgBiBr 6 nanocrystals (NCs) on the surface of MXene nanosheets via mutual electrostatic attraction. The presence of MXene nanosheets effectively promotes the formation of free charge carriers in Cs 2 AgBiBr 6 NCs via reducing the exciton binding energy. Additionally, the ultrafast photogenerated electron transfer from Cs 2 AgBiBr 6 to MXene with a timescale of 1.1 ps largely prolongs the charge carrier lifetime by two times. As a result of the efficient charge separation and electron extraction, the Cs 2 AgBiBr 6 /MXene heterostructures achieve a high photoelectron consumption yield of 50.6 µmol g −1 h −1 for photocatalytic CO 2 reduction, which surpasses most previously reported lead-free perovskite-based catalysts. • A novel self-assembled double perovskite/MXene heterostructure was prepared through a facile solution method. • The presence of MXene nanosheets effectively prolongs the charge carrier lifetime by two times. • The Cs 2 AgBiBr 6 /MXene heterostructures achieve a high electron consumption yield for photocatalytic CO 2 reduction.
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