Catalytic Hydrolysis of Ammonia Borane via Cobalt Palladium Nanoparticles

被引:261
作者
Sun, Daohua [1 ,2 ]
Mazumder, Vismadeb [1 ]
Metin, Onder [1 ,3 ]
Sun, Shouheng [1 ]
机构
[1] Brown Univ, Dept Chem, Providence, RI 02912 USA
[2] Xiamen Univ, Dept Chem & Biochem Engn, Coll Chem & Chem Engn, Xiamen 361005, Peoples R China
[3] Ataturk Univ, Dept Chem, Fac Sci, TR-25240 Erzurum, Turkey
基金
中国国家自然科学基金;
关键词
ammonia borane hydrolysis; bimetallic nanoparticles; cobalt-palladium alloy catalyst; heterogeneous catalysis; hydrogen storage; MONODISPERSE NICKEL NANOPARTICLES; HYDROGEN GENERATION SYSTEM; DEHYDROGENATION; NANOCLUSTERS; STORAGE; DISSOCIATION;
D O I
10.1021/nn2016666
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Monodisperse 8 nm CoPd nanoparticles (NPs) with controlled compositions were synthesized by the reduction of cobalt acetylacetonate and palladium bromide in the presence of oleylamine and trioctylphosphine. These NPs were active catalysts for hydrogen generation from the hydrolysis of ammonia borane (AB), and their activities were composition dependent. Among the 8 nm CoPd catalysts tested for the hydrolysis of AB, the Co35Pd65 NPs exhibited the highest catalytic activity and durability. Their hydrolysis completion time and activation energy were 5.5 min and 27.5 kJ mol(-1), respectively, which were comparable to the best Pt-based catalyst reported. The catalytic performance of the CoPd/C could be further enhanced by a preannealing treatment at 300 degrees C under air for 15 h with the hydrolysis completion time reduced to 3.5 min. This high catalytic performance of Co35Pd65 NP catalyst makes it an exciting alternative in pursuit of practical implementation of AB as a hydrogen storage material for fuel cell applications.
引用
收藏
页码:6458 / 6464
页数:7
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