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Hydrolytic dehydrogenation of ammonia borane and methylamine borane catalyzed by graphene supported Ru@Ni core-shell nanoparticles
被引:115
作者:
Cao, Nan
[1
]
Su, Jun
[2
]
Luo, Wei
[1
]
Cheng, Gongzhen
[1
]
机构:
[1] Wuhan Univ, Coll Chem & Mol Sci, Wuhan 430072, Hubei, Peoples R China
[2] Huazhong Univ Sci & Technol, Wuhan Natl Lab Optoelect, Wuhan 430074, Hubei, Peoples R China
基金:
中国国家自然科学基金;
关键词:
Core-shell nanoparticles;
Ammonia borane;
Methylamine borane;
Graphene;
Hydrogen storage;
HYDROGEN GENERATION;
STABILIZED RUTHENIUM(0);
NANOCLUSTERS CATALYST;
ROOM-TEMPERATURE;
STORAGE;
ELECTROCATALYSTS;
REGENERATION;
HYDRAZINE;
OXIDATION;
LITHIUM;
D O I:
10.1016/j.ijhydene.2013.10.059
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:
Ru@Ni core-shell nanoparticles (NPs) supported on graphene have been synthesized by one-step in situ co-reduction of aqueous solution of ruthenium (III) chloride, nickel (II) chloride, and graphene oxide (GO) with ammonia borane (AB) as the reducing agent under ambient condition. The as-synthesized NPs exhibit much higher catalytic activity for hydrolytic dehydrogenation of AB than the monometallic, bimetallic alloy (RuNi/graphene), and graphene-free core-shell (Ru@Ni) counterparts. Additionally, the Ru@Ni/graphene NPs facilitate the hydrolysis of AB, with the turnover frequency (TOP) value of 340 mol H-2 min(-1) (mol Ru)(-1), which is among the highest value reported on Ru-based NPs so far, and even higher than the reversed Ni@Ru NPs. Furthermore, the as-prepared NPs exert satisfied durable stability and magnetically recyclability for the hydrolytic dehydrogenation of AB and methylamine borane (MeAB). Moreover, this simple synthetic method can be extended to other Ru-based bimetallic core-shell systems for more applications. Copyright (C) 2013, Hydrogen Energy Publications, LLC. Published by Elsevier Ltd. All rights reserved.
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页码:426 / 435
页数:10
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