Unveiling the bifunctional modulation evoked by bromine doping of CoP towards efficient hydrolytic hydrogen generation

被引:13
|
作者
Yuan, Chongyang [1 ]
Xu, Tian [1 ]
Guo, Miao [1 ]
Sun, Yahui [1 ]
Zhang, Tengfei [2 ]
Yu, Xuebin [1 ]
机构
[1] Fudan Univ, Dept Mat Sci, Shanghai 200433, Peoples R China
[2] Nanjing Univ Aeronaut & Astronaut, Coll Mat Sci & Technol, Ctr Hydrogenergy, Nanjing 210016, Jiangsu, Peoples R China
关键词
Hydrogen generation; Catalysis; Morphology modulation; Anion doping; Electronic structure; AMMONIA BORANE; DEHYDROGENATION; CATALYST; NANOPARTICLES; CHALLENGES; EVOLUTION; STORAGE; CARBON; COBALT;
D O I
10.1016/j.apcatb.2023.123562
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 efficient and economical catalysts for hydrolytic hydrogen production from chemical hydrogen storage materials such as ammonia borane and NaBH4 is highly desirable but challenging. Herein, Br doped CoP nanoparticles in a carbon-based polyhedron with controllable morphology were developed as such an efficient hydrogen generation catalyst, and the bifunctional modulation of Br doping was explored. Firstly, regulating the doping content of Br results in the formation of more and larger nanopores in the CoP polyhedron, exposing more accessible active sites. Secondly, Co vacancies are introduced via Br doping, which significantly optimizes the electronic structure of Co atom, thus boosting AB and water dissociation, i.e., the rate-determining step (RDS). Therefore, the Br1-CoP@C catalyst with optimal composition exhibited a superb turnover frequency (TOF) of 67.3 min-1, implying an astonishing over 3-fold improvement compared with CoP@C. These findings showcase a novel and promising approach to build high-efficiency nanocatalysts for hydrogen production and beyond.
引用
收藏
页数:9
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