Increased Active Sites by in Situ Growth of CoP Quantum Dots on CdS/rGO To Achieve Efficient Photocatalytic H2 Production

被引:41
作者
An, Hua [1 ]
Yan, Xiaoqing [1 ]
Li, He [1 ]
Yang, Bolun [1 ]
Wei, Jinjia [1 ]
Yang, Guidong [1 ]
机构
[1] Xi An Jiao Tong Univ, Sch Chem Engn & Technol, XJTU Oxford Int Joint Lab Catalysis, Xian 710049, Shaanxi, Peoples R China
基金
中国国家自然科学基金;
关键词
active sites; charge transfer; internal electric field; photocatalytic H-2 generation; quantum dots; REDUCED GRAPHENE OXIDE; GRAPHITIC CARBON NITRIDE; HYDROGEN-PRODUCTION; CHARGE SEPARATION; CDS; NANOPARTICLES; COCATALYST; HYBRID; WATER; PERFORMANCE;
D O I
10.1021/acsaem.9b00439
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
Constructing numerous surface active sites to realize quick charge transfer and efficient adsorption of water molecule is of significant importance for extremely improving the photocatalytic H-2 production activity of catalyst. In this work, new ternary CoP/CdS/rGO photocatalysts were prepared using hydrothermal assisted by thermal phosphorization method. In situ growth of CoP quantum dots (QDs) is employed as the surface active sites on the CdS/rGO surface to accelerate photogenerated electrons transport and strengthen surface photo-reaction of the samples. According to the experimental and DFT calculation results, an internal electric field is built at the interface of CdS/graphene and CoP/graphene, respectively. Under solar light irradiation, the photogenerated electrons would directionally transfer from CdS to CoP QDs via the "charge transfer channel" of graphene, resulting in the efficient separation of electron-hole pairs. As a result, the ternary composites achieve unexpectedly high-efficient photocatalytic hydrogen generation activities (1.104 mmol.h(-1)), which exceed 6.8 times that of CdS. This research verifies that the introduction of more active sites is the key factor for the improvement of photocatalytic H-2 generation and provides a valuable strategy for the synthesis of high performance graphene-based photocatalyst.
引用
收藏
页码:4195 / 4204
页数:19
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