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Construction of S-scheme 0D/2D heterostructures for enhanced visible-light-driven CO2 reduction
被引:100
|作者:
Gong, Shuaiqi
[1
]
Teng, Xue
[1
]
Niu, Yanli
[1
]
Liu, Xuan
[1
]
Xu, Mingze
[1
]
Xu, Chen
[1
]
Ji, Lvlv
[2
]
Chen, Zuofeng
[1
]
机构:
[1] Tongji Univ, Shanghai Key Lab Chem Assessment & Sustainabil, Sch Chem Sci & Engn, 1239 Siping Rd, Shanghai 200092, Peoples R China
[2] Zhejiang Sci Tech Univ, Key Lab Adv Text Mat & Mfg Technol, Hangzhou 310018, Peoples R China
基金:
中国国家自然科学基金;
关键词:
S-scheme;
0D/2D heterojunction;
InVO4 quantum dots;
CO2;
reduction;
Photocatalysis;
QUANTUM DOTS;
PHOTOCATALYTIC REDUCTION;
ATOMICALLY-THIN;
CARBON NITRIDE;
EFFICIENT;
CONVERSION;
HETEROJUNCTION;
FABRICATION;
SHEETS;
CHARGE;
D O I:
10.1016/j.apcatb.2021.120521
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:
Zero-dimensional quantum dots (QDs) and two-dimensional nanosheets represent two kinds of distinctive materials with unique properties. Here, we describe the fabrication of step-scheme (i.e. S-scheme) 0D/2D hetero-structure with InVO4 QDs and g-C3N4 (CN) ultrathin nanosheets for photocatalytic CO2 reduction. The formation of S-scheme heterostructure facilitates the separation of electron-hole pairs and reduces the recombination of charge carriers. Moreover, the light-absorption edge of InVO4/CN is extended to 605 nm because of the strong visible light absorption of InVO4 QDs. The 0D/2D hybrid enables highly selective photocatalytic reduction of CO2 to CO (93.3 %) at a decent rate of 69.8 mu mol g(-1) h(-1) under visible light irradiation. Density functional theory (DFT) results suggest that the formation of InVO4/CN heterostructure can enhance CO2 adsorption/activation, stabilize COOH* intermediates and allow rapid CO desorption as the major product. This study opens up a new possibility for construction of novel S-scheme heterostructure for photocatalytic applications.
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页数:11
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