Alloyed palladium-nickel hollow nanospheres with interatomic charge polarization for improved hydrolytic dehydrogenation of ammonia borane

被引:36
作者
Du, Yuanxin [1 ]
Wang, Kun
Zhai, Qingxi
Chen, Akang
Xi, Zhiwei
Yan, Jian
Kang, Xi
Chen, Man
Yuan, Xiaoyou
Zhu, Manzhou [1 ]
机构
[1] Anhui Univ, Dept Chem, Hefei 230601, Anhui, Peoples R China
基金
中国国家自然科学基金;
关键词
Palladium-nickel hollow nanospheres; Hydrolytic dehydrogenation; Ammonia borane; Synergistic mechanism; First-principles calculation; CHEMICAL HYDROGEN STORAGE; METAL-ORGANIC FRAMEWORK; RUTHENIUM NANOPARTICLES; CATALYTIC HYDROLYSIS; REUSABLE CATALYST; OXYGEN REDUCTION; ROOM-TEMPERATURE; FACILE SYNTHESIS; GENERATION; EFFICIENT;
D O I
10.1016/j.ijhydene.2017.11.066
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
Hydrolysis reaction of ammonia borane (AB) has been considered as a safe and efficient hydrogen generation method, in which designing cost-effective and high-performance catalysts plays vital role. In this work, we have developed well dispersed palladium-nickel hollow nanospheres (PdNi HNSs) with tunable shell thiclmess"and compositions via a facile galvanic replacement approach. The as-prepared PdNi HNSs show composition-dependent catalysis in the hydrolytic dehydrogenation of AB. The Pd84Ni16/C exhibiting sphere-shaped hollow interiors with average 70 nm particle size and 10 nm thin wall, presents the highest catalytic activity with the turnover frequency of 76.0 (mol H-2 min(-1) (mol Pd)(-1)) and the activation energy of 33.5 kJ ma(-1). The superior catalytic effect of PdNi HNSs in enhancing hydrolysis efficiency of AB can be ascribed to two major factors: (1) high active surface areas of the unique hollow structure; (2) enhanced H adsorption attributed to the coupling between Pd and Ni induces polarization charges on Pd catalytic sites, which is indicated by the first-principles calculation and X-ray photoelectron spectroscopy studies. Furthermore, the catalysts exert good long-term recycling stability and catalytic activity for the hydrolytic dehydrogenation of AB. This work represents a strategy may hopefully be extended to synthesize other Pd-based hollow nanostructure with reduced Pd usage and increased catalytic active sites, and also sheds light on the exploration of utilizing interatomic interactions to regulate species adsorption/activation for highly efficient catalytic performance. (C) 2017 Hydrogen Energy Publications LLC. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:283 / 292
页数:10
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