CuxCo1-xO Nanoparticles on Graphene Oxide as A Synergistic Catalyst for High-Efficiency Hydrolysis of Ammonia-Borane

被引:209
作者
Feng, Kun [1 ]
Zhong, Jun [1 ]
Zhao, Binhua [1 ]
Zhang, Hui [1 ]
Xu, Lai [1 ]
Sun, Xuhui [1 ]
Lee, Shuit-Tong [1 ]
机构
[1] Soochow Univ, Jiangsu Key Lab Carbon Based Funct Mat & Devices, Inst Funct Nano & Soft Mat Lab FUNSOM, Suzhou 215123, Peoples R China
基金
中国国家自然科学基金;
关键词
graphene oxide; heterogeneous catalysis; hydrogen storage; hydrolysis mechanism; nanoparticles; X-RAY-ABSORPTION; HYDROGEN GENERATION; NICKEL NANOPARTICLES; METAL NANOPARTICLES; DEHYDROGENATION; CARBON; NANOSTRUCTURES; SPECTROSCOPY; PERFORMANCE; MICROSCOPY;
D O I
10.1002/anie.201604021
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Ammonia-borane (AB) is an excellent material for chemical storage of hydrogen. However, the practical utilization of AB for production of hydrogen is hindered by the need of expensive noble metal-based catalysts. Here, we report CuxCo1-xO nanoparticles (NPs) facilely deposited on graphene oxide (GO) as a low-cost and high-performance catalyst for the hydrolysis of AB. This hybrid catalyst exhibits an initial total turnover frequency (TOF) value of 70.0 (H-2) mol/(Cat-metal) mol.min, which is the highest TOF ever reported for noble metal-free catalysts, and a good stability keeping 94 % activity after 5 cycles. Synchrotron radiation-based X-ray absorption spectroscopy (XAS) investigations suggested that the high catalytic performance could be attributed to the interfacial interaction between CuxCo1-xO NPs and GO. Moreover, the catalytic hydrolysis mechanism was studied by in situ XAS experiments for the first time, which reveal a significant water adsorption on the catalyst and clearly confirm the interaction between AB and the catalyst during hydrolysis.
引用
收藏
页码:11950 / 11954
页数:5
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