Interfacial engineering of 0D/2D CoMn2O4 nanoparticles/CdS nanosheets p-n heterostructures for boosted photocatalytic H2 production and U (VI) reduction

被引:6
作者
Bao, Yining [1 ]
Zeng, Qingru [2 ]
Ning, Shunyan [2 ]
Zhao, Wei [1 ]
Wang, Longfei [1 ]
Wang, Xinpeng [1 ]
Wei, Yuezhou [2 ]
Zeng, Deqian [2 ]
机构
[1] Guangxi Univ, Sch Resources Environm & Mat, Nanning 530004, Peoples R China
[2] Univ South China, Sch Nucl Sci & Technol, Hengyang 421001, Peoples R China
基金
中国国家自然科学基金;
关键词
CdS nanosheets; CoMn; 2; O; 4; nanoparticles; p-n heterojunction; Photocatalytic H 2 production; Uranium(VI) photoreduction; CHARGE-TRANSFER; CDS NANOWIRES; HETEROJUNCTION; SHELL; COMPOSITE; OXYGEN; PERFORMANCE; SPHERES;
D O I
10.1016/j.ijhydene.2024.04.285
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
Developing effective heterojunction photocatalysts that efficiently separate charge carriers and improve lightharvesting capabilities is crucial in addressing energy and environmental issues. Herein, a unique nanocomposite photocatalyst is constructed by attaching CoMn2O4 nanoparticles onto 2D CdS nanosheets for H2 production and U(VI) reduction. The optimized 2% CoMn2O4/CdS nanocomposite showcases the highest photocatalytic H2 production efficiency, 5.8 times higher than CdS nanosheets. Additionally, the U(VI) reduction rate constant of 2% CoMn2O4/CdS is 0.0192 min-1, approximately 1.9 folds over the pristine CdS (0.0101 min-1). The exceptional photocatalytic performance toward photocatalytic H2 evolution and U(VI) reduction reactions directly result from the electronic integration between CoMn2O4/CdS p-n heterojunction, facilitated by the efficient photoexcited charge separation. Feasible photocatalytic mechanisms are proposed through experimental analyses and theoretical calculations. This study provides a straightforward method for designing effective CdSbased heterostructured photocatalysts, contributing to the advancement of solar-to-H2 conversion and environmental abetment.
引用
收藏
页码:586 / 595
页数:10
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