4.7 Article

Efficient hydrogen production from ammonia borane hydrolysis catalyzed by TiO2-supported RuCo catalysts

期刊

INTERNATIONAL JOURNAL OF HYDROGEN ENERGY
卷 46, 期 5, 页码 3964-3973

出版社

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.ijhydene.2020.10.234

关键词

Ruthenium; Cobalt; Ammonia borane; Hydrogen generation; Catalyzed hydrolysis

向作者/读者索取更多资源

The hydrolysis of ammonia borane is a reliable method for hydrogen production, and TiO2-supported RuCo catalysts synthesized in this study exhibit excellent catalytic performance, especially in alkaline solutions. The Ru1Co9/TiO2 catalyst with a Ru/Co molar ratio of 1:9 shows low activation energy and high turnover frequency for the hydrolysis of ammonia borane. Anatase TiO2-supported catalysts demonstrate better catalytic activity compared to rutile TiO2-supported catalysts or mixtures of anatase and rutile TiO2-supported catalysts.
Hydrolysis of ammonia borane provides a reliable pathway for hydrogen production, while suitable catalysts are indispensable to make the hydrolysis reaction reach a considerable rate. In the present work, a series of TiO2-supported RuCo catalysts have been fabricated by coprecipitation and subsequent reduction of Ru3+ and Co2+ on the surface of TiO2 nanoparticles. Transmission electron microscopy and elemental mapping have verified the good distribution of metal species in the catalysts. The fabricated catalysts have shown excellent performance for catalyzing ammonia borane hydrolysis, especially in alkaline solutions with 0.5 M NaOH. For Ru1Co9/TiO2 in which Ru/Co molar ratio is 1:9, the active energy of catalyzed ammonia borane hydrolysis is 33.25 kJ/mol, and a turnover frequency based on Ru as high as 1408 mol(H2)/(mol(Ru).min) is obtained at 25 degrees C. Moreover, when different types of TiO2 substrates are used, anatase TiO2-supported catalysts show better catalytic activity than their counterparts with rutile TiO2 as substrate or mixture of anatase and rutile TiO2 as substrate. (C) 2020 Hydrogen Energy Publications LLC. Published by Elsevier Ltd. All rights reserved.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.7
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据