Co-CoOx supported onto TiO2 coated with carbon as a catalyst for efficient and stable hydrogen generation from ammonia borane

被引:0
|
作者
Guang Yang [1 ]
Shuyan Guan [1 ]
Sehrish Mehdi [2 ,3 ]
Yanping Fan [1 ]
Baozhong Liu [1 ]
Baojun Li [1 ,3 ]
机构
[1] College of Chemistry and Chemical Engineering, Henan Polytechnic University
[2] Department of Chemistry, The Women University, Kutchery Campus
[3] College of Chemistry, Zhengzhou University
基金
中国国家自然科学基金;
关键词
D O I
暂无
中图分类号
TQ116.2 [氢气]; TQ426 [催化剂(触媒)];
学科分类号
080502 ; 0817 ; 081705 ;
摘要
Ammonia borane(AB) can be catalytically hydrolyzed to provide hydrogen at room temperature due to its high potentaial for hydrogen storage. Non-precious metal heterogeneous catalysts have broad application in the field of energy catalysis. In this article, catalysts precursor is obtained from Co-Ti-resorcinol-formaldehyde resin by sol–gel method. Co/TiO2@N-C(CTC) catalyst is prepared by calcining the precursor under high temperature conditions in nitrogen atmosphere. Co-CoOx/TiO2@N-C(COTC) is generated by the controllable oxidation reaction of CTC. The catalyst can effectively promote the release of hydrogen during the hydrolytic dehydrogenation of AB. High hydrogen generation at a specific rate of 5905 m L min-1gCo-1is achieved at room temperature. The catalyst retains its 85% initial catalytic activity even for its fifth time use in AB hydrolysis. The synergistic effect among Co, Co3O4and TiO2promotes the rate limiting step with dissociation and activation of water molecules by reducing its activation energy. The applied method in this study promotes the development of non-precious metals in catalysis for utilization in clean energy sources.
引用
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页码:236 / 243
页数:8
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