In Situ Formation of AgCo Stabilized on Graphitic Carbon Nitride and Concomitant Hydrolysis of Ammonia Borane to Hydrogen

被引:27
作者
Wang, Qi [1 ]
Xu, Caili [1 ]
Ming, Mei [1 ]
Yang, Yingchun [2 ]
Xu, Bin [3 ]
Wang, Yi [1 ]
Zhang, Yun [1 ]
Wu, Jie [1 ]
Fan, Guangyin [1 ]
机构
[1] Sichuan Normal Univ, Coll Chem & Mat Sci, Chengdu 610068, Sichuan, Peoples R China
[2] Chengdu Univ Informat Technol, Coll Resources & Environm, Chengdu 610225, Sichuan, Peoples R China
[3] Sichuan Univ Sci & Engn, Sch Chem & Environm Engn, Zigong 643000, Peoples R China
来源
NANOMATERIALS | 2018年 / 8卷 / 05期
基金
中国国家自然科学基金;
关键词
graphitic carbon nitride; bimetallic catalyst; ammonia borane; hydrogen generation; CORE-SHELL NANOPARTICLES; RUTHENIUM NANOPARTICLES; HIGHLY EFFICIENT; SODIUM-BOROHYDRIDE; ALLOY NANOPARTICLES; CATALYTIC-ACTIVITY; OXYGEN REDUCTION; FACILE SYNTHESIS; FUEL-CELLS; GENERATION;
D O I
10.3390/nano8050280
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The development of highly-efficient heterogeneous supported catalysts for catalytic hydrolysis of ammonia borane to yield hydrogen is of significant importance considering the versatile usages of hydrogen. Herein, we reported the in situ synthesis of AgCo bimetallic nanoparticles supported on g-C3N4 and concomitant hydrolysis of ammonia borane for hydrogen evolution at room temperature. The as-synthesized Ag0.1Co0.9/g-C3N4 catalysts displayed the highest turnover frequency (TOF) value of 249.02 mol H-2 center dot(mol(Ag)center dot min)(-1) for hydrogen evolution from the hydrolysis of ammonia borane, which was higher than many other reported values. Furthermore, the Ag0.1Co0.9/g-C3N4 catalyst could be recycled during five consecutive runs. The study proves that Ag0.1Co0.9/g-C3N4 is a potential catalytic material toward the hydrolysis of ammonia borane for hydrogen production.
引用
收藏
页数:10
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