Double-plasmonic-coupled heterojunction photocatalysts for highly-efficient full-spectrum-light-driven H2 evolution from ammonia borane

被引:7
|
作者
He, Yun [1 ]
Yang, Yang [1 ]
Bowen, Chris R. [2 ]
Shu, Zhan [1 ]
Zheng, Luxia [1 ]
Tu, Nengrong [1 ]
Lu, Taixu [1 ]
Li, Weijun [1 ]
Yang, Weiyou [1 ]
机构
[1] Ningbo Univ Technol, Inst Micro Nano Mat & Devices, Ningbo 315211, Peoples R China
[2] Univ Bath, Dept Mech Engn, Bath BA2 7AK, England
基金
中国国家自然科学基金;
关键词
Full-spectrum-light-driven; Localized surface plasmon resonance; Hot electrons; Photothermal; Heterojunction photocatalyst; OXYGEN-VACANCIES; HYDROGEN GENERATION; NANOWIRES; REDUCTION; G-C3N4; SOLAR;
D O I
10.1016/j.cej.2023.148299
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Methods to enhance the full-spectrum-light-driven water splitting for H-2 evolution remain one of the critically important issues to explore advanced photocatalysts. In this study, we present a novel double-plasmon-coupled semiconductor heterojunction photocatalyst with a large number of oxygen vacancies, produced via a simple two-step solvothermal process. These materials represent a new model system to study the kinetics process and catalytic activity of ammonia borane hydrolytic dehydrogenation in a full-spectrum-light-driven plasmonic semiconductor heterostructure. Upon irradiation with full-spectrum light, the resultant photocatalysts are capable of delivering H-2 generation rate up to 13,031 mu mol g(-1)h(-1), which is similar to 6 times greater than that of pristine MoO3-x counterpart. The excellent photocatalytic behavior is primarily attributed to the improved carrier separation, increased light absorption, and enhanced generation of "hot electrons", enabled by a synergistic photo- and thermo-catalytic effect. Consequently, the high performance of the novel photocatalyst derives from the design of a double-plasmonic-coupling effect and the photocatalyst containing Type-II heterojunctions.
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页数:12
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