A Hierarchical CdS Quantum Dot/Polymeric Carbon Nitride Nanosheet Heterostructure with Close Contact Interfaces for Enhanced Photocatalytic CO2 Reduction

被引:6
作者
Guo, Yongkang [1 ]
Wu, Jiaming [1 ]
Zhang, Ran [1 ]
Ocran, Gideon Abaidoo [1 ]
An, Yonglin [1 ]
Li, Keyan [1 ]
An, Sufeng [2 ]
Guo, Xinwen [1 ]
机构
[1] Dalian Univ Technol, PSU DUT Joint Ctr Energy Res, Sch Chem Engn, State Key Lab Fine Chem, Dalian 116024, Peoples R China
[2] SINOPEC Dalian Res Inst Petr & Petrochem Co Ltd, Dalian 116045, Peoples R China
基金
中国博士后科学基金; 中国国家自然科学基金;
关键词
PCN nanosheets; CdS quantumdots; heterojunction; hierarchical structure; photocatalytic CO2 reduction; HYDROGEN EVOLUTION; G-C3N4; CONSTRUCTION; COMPOSITES; TUBES; DOTS;
D O I
10.1021/acssuschemeng.3c07345
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Polymeric carbon nitride (PCN)-based materials have gained increasing attention as visible-light-responsive photocatalysts for solar energy conversion, but their limited light absorption ability and low photocatalytic performance are far from satisfactory. Herein, we reported a hierarchical CdS quantum dot/polymeric carbon nitride nanosheet heterojunction for notably enhanced CO2 conversion under visible light. Through a solvothermal process, the CdS quantum dots were uniformly distributed and tightly anchored over the surface of hierarchical PCN nanosheets, which are conducive for the formation of a close contact interface and the efficient transfer of the charge carriers across the interface. Furthermore, the optimal heterostructure owns a larger specific surface area, an enhanced light-harvesting capacity, a shortened charge transfer distance, and adequately exposed reaction sites. In consequence, the CO generation rate of the heterojunction reached 2810 mu mol g(-1) h(-1), which is nearly two times of that of the pure CdS photocatalysts and four times of that of the PCN nanosheets. This work provides an opportunity to get insight into the heterostructure between PCN and narrow-bandgap metal sulfide, which demonstrates a type I band alignment.
引用
收藏
页码:6132 / 6144
页数:13
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