In-situ construction of Bi-MOF-derived S-scheme BiOBr/CdIn2S4 heterojunction with rich oxygen vacancy for selective photocatalytic CO2 reduction using water

被引:4
|
作者
Shen, Mengting [1 ]
Li, Yang [1 ]
Luo, Tianhang [1 ]
Wang, Zhen [1 ]
Zhou, Man [1 ]
Wang, Yanan [1 ]
Xu, Song [1 ]
Li, Zhongyu [1 ,2 ,3 ]
机构
[1] Changzhou Univ, Sch Petrochem Engn, Jiangsu Key Lab Adv Catalyt Mat & Technol, Changzhou 213164, Peoples R China
[2] Changzhou Univ, Adv Catalysis & Green Mfg Collaborat Innovat Ctr, Changzhou 213164, Peoples R China
[3] Changzhou Univ, Sch Environm Sci & Engn, Changzhou 213164, Peoples R China
基金
中国国家自然科学基金;
关键词
Metal-organic frameworks; Photocatalytic performance; S-scheme heterojunction; MOF-BiOBr/CdIn(2)S(4 )heterojunction; Photocatalytic CO2 reduction; BIOBR;
D O I
10.1016/j.seppur.2024.129713
中图分类号
TQ [化学工业];
学科分类号
0817 ;
摘要
In this study, a highly selective MOF-BiOBr/CdIn2S4 (MOF-BiOBr/CIS) heterostructure with CdIn(2)S(4 )nanosheets grown in situ on the tubular structure derived from Bi-MOF-based BiOBr was successfully constructed using a hydrothermal method. Under simulated solar light without sacrificial or photosensitizing agents, the 20-MOFBiOBr/CIS composite exhibited excellent photocatalytic CO2 performance, achieving production rates of 30.18 mu mol g(- 1) h(- 1) for CO and 1.50 mu mol g(- 1) h(- 1) for CH4. Compared to pure MOF-BiOBr and CdIn2S4, the CO production rates were increased by approximately 9 and 116 times, respectively. It was revealed that the 20MOF-BiOBr/CIS composite with rich oxygen vacancy exhibited close interfacial contact and efficient charge transfer. The formation of MOF BiOBr/CdIn2S4 heterojunction thereby provided efficient CO2 photocatalytic reduction. The CO selectivity of 20-MOF-BiOBr/CIS reached 83.4 %, and the MOF-BiOBr/CIS heterojunction exhibited good stability over multiple cycles. Furthermore, a mechanism for enhanced photocatalytic CO2 reduction by the MOF-BiOBr/CIS heterojunction was also proposed.
引用
收藏
页数:11
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