Oleylamine-stabilized Cu0.9Ni0.1 nanoparticles as efficient catalyst for ammonia borane dehydrogenation

被引:23
作者
Li, Si-Jia [1 ,2 ]
Wang, Hong-Li [3 ]
Yan, Jun-Min [1 ,2 ]
Jiang, Qing [2 ]
机构
[1] Jilin Univ, State Key Lab Automot Simulat & Control, Changchun 130022, Jilin, Peoples R China
[2] Jilin Univ, Dept Mat Sci & Engn, Minist Educ, Key Lab Automobile Mat, Changchun 130022, Jilin, Peoples R China
[3] Changchun Univ Technol, Minist Educ, Key Lab Adv Struct Mat, Coll Mat Sci & Engn, Changchun 130012, Jilin, Peoples R China
基金
中国国家自然科学基金;
关键词
Ammonia borane dehydrogenation; Cupper-nickel nanocatalyst; Activity; Hydrogen; Heterogeneous catalysis; CHEMICAL HYDROGEN STORAGE; CORE-SHELL NANOPARTICLES; HIGHLY-ACTIVE CATALYST; SENSITIZED SOLAR-CELLS; FORMIC-ACID OXIDATION; HYDROLYTIC DEHYDROGENATION; BIMETALLIC NANOPARTICLES; MEDIATED SYNTHESIS; PD NANOPARTICLES; FACILE SYNTHESIS;
D O I
10.1016/j.ijhydene.2017.08.120
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Monodisperse CuNi nanoparticles are conveniently prepared by the reduction of cupric acetate and nickel(II) acetylacetonate in the presence of oleylamine and borane tributylamine under inert gas atmosphere. It is found that among the CuNi system, Cu0.9Ni0.1 shows the best performance for catalyzing the dehydrogenation of ammonia borane. In total, 2.5 equiv. of hydrogen per ammonia borane is generated even at room temperature with an initial turnover frequency value of 212.3 mol of H-2 (mol of Cu0.9Ni0.1)(-1).h(-1), which is comparable to the best Pd-based catalyst ever reported. The remarkable catalytic performance is attributed to the mild affiliation of oleylamine (OAm) to NPs, which not only stabilizes NPs to maintain good dispersion but also leaves sufficient surface active sites to facilitate the catalytic reaction. This low-cost and high catalytic performance catalyst makes it an exciting alternative towards the application of ammonia borane as a hydrogen storage material for fuel cell applications. (C) 2017 Hydrogen Energy Publications LLC. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:25251 / 25257
页数:7
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