Cs2 CuBr4 perovskite quantum dots confined in mesoporous CuO framework as a p-n type S-scheme heterojunction for efficient CO2 photoconversion
文献类型： 外文期刊
作者： Zhang, Zhijie 1 ; Li, Xun 1 ; Tang, Huiling 1 ; Wu, Junhao 3 ; Yao, Chunxia 2 ; Li, Kui 3 ;
作者机构： 1.Shanghai Inst Technol, Sch Mat Sci & Engn, Shanghai 201418, Peoples R China
2.Shanghai Acad Agr Sci, Inst Agrofood Stand & Testing Technol, Shanghai 201403, Peoples R China
3.Hainan Univ, Sch Chem & Chem Engn, Haikou 570228, Peoples R China
关键词： Photocatalytic CO 2 conversion; Mesoporous CuO; Cs 2 CuBr 4; Perovskite quantum dots; S -scheme heterojunction
期刊名称：CHINESE CHEMICAL LETTERS （ 影响因子：9.4； 五年影响因子：7.3 ）
ISSN： 1001-8417
年卷期： 2024 年 35 卷 11 期
页码：
收录情况： SCI
摘要： Heterojunction engineering is recognized as a promising strategy to modulate the photocatalytic properties of semiconductors. Herein, lead-free Cs2CuBr4 2 CuBr 4 perovskite quantum dots (PQDs) were confined in a mesoporous CuO framework and a p-n type S-scheme heterojunction of Cs2CuBr4/CuO 2 CuBr 4 /CuO (CCB/CuO) photocatalyst was fabricated. Experimental characterizations confirmed the effective confinement of the Cs2CuBr4 2 CuBr 4 PQDs in the mesoporous CuO framework, which enabled intimate contact in the interface of CCB/CuO heterojunction, thus facilitating the interfacial charge migration and separation between p-type CuO and n-type Cs2CuBr4. 2 CuBr 4 . Owing to the outstanding charge transport property and CO2 2 adsorption capacity, the developed CCB/CuO heterojunction exhibited remarkably enhanced photocatalytic CO2 2 conversion efficiency with an electron consumption rate ( R electron ) of 281.1 }mol g -1 h -1 , which was approximately 2.8 times higher than that of pristine Cs2CuBr4. 2 CuBr 4 . These findings provide some insights into the rational engineering design of lead-free perovskite-based heterostructures for efficient photocatalytic CO2 2 conversion. (c) 2024 Published by Elsevier B.V. on behalf of Chinese Chemical Society and Institute of Materia Medica, Chinese Academy of Medical Sciences.
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