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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.
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页数:11
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