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Amorphous NiP supported on rGO for superior hydrogen generation from hydrolysis of ammonia borane
被引:92
|作者:
Du, Xiaoqiong
[1
]
Yang, Chenlu
[1
]
Zeng, Xiang
[1
]
Wu, Tong
[1
]
Zhou, Yinghui
[3
]
Cai, Ping
[1
]
Cheng, Gongzhen
[1
]
Luo, Wei
[1
,2
]
机构:
[1] Wuhan Univ, Coll Chem & Mol Sci, Wuhan 430072, Hubei, Peoples R China
[2] Nankai Univ, Minist Educ, Key Lab Adv Energy Mat Chem, Tianjin 300071, Peoples R China
[3] Kingfa SCI & Tech CO LTD, Guangzhou 510663, Guangdong, Peoples R China
基金:
中国国家自然科学基金;
关键词:
Transition metal phosphides;
NiP/rGO;
Hydrogen storage;
Ammonia borane;
EVOLUTION REACTION;
EFFICIENT ELECTROCATALYST;
CATALYTIC HYDROLYSIS;
NICKEL NANOPARTICLES;
METHYLAMINE BORANE;
ROOM-TEMPERATURE;
GRAPHENE OXIDE;
AMINE BORANE;
DEHYDROGENATION;
STORAGE;
D O I:
10.1016/j.ijhydene.2017.04.052
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:
Transition metal phosphide based amorphous NiP/rGO hybrids have been successfully synthesized through a facile one-pot co-reduction method. The prepared NiP/rGO hybrids are characterized by powder X-ray diffraction (XRD), inductively coupled plasma-atomic emission spectroscopy (ICP-AES), X-ray photoelectron spectroscopy (XPS), transmission electron microscope (TEM) and energy dispersive X-ray detector (EDX) techniques. Compared with Ni/rGO, the resulted Ni91P9/rGO hybrid exhibits superior catalytic activity toward hydrogen generation from hydrolysis of ammonia borane (NH3BH3), with turnover frequency (TOP) value of 13.3 min(-1). The activation energy (Ea) of Ni91P9/rGO for this reaction is calculated to be 34.7 kJ mol(-1), which is much lower than those of the other reported catalysts. This superior catalytic performance may be due to the good dispersibility of Ni-91/D-9 nanoparticles and the synergistic electronic interactions between nickel and phosphorus. (C) 2017 Hydrogen Energy Publications LLC. Published by Elsevier Ltd. All rights reserved.
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页码:14181 / 14187
页数:7
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