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Facile synthesis of nitrogen-doped carbon nanotubes encapsulating nickel cobalt alloys 3D networks for oxygen evolution reaction in an alkaline solution
被引:105
|作者:
Yu, Jie
[1
]
Zhong, Yijun
[1
]
Zhou, Wei
[1
]
Shao, Zongping
[1
,2
,3
]
机构:
[1] Nanjing Tech Univ, Coll Chem Engn, Jiangsu Natl Synerget Innovat Ctr Adv Mat SICAM, State Key Lab Mat Oriented Chem Engn, 5 Xin Mofan Rd, Nanjing 210009, Jiangsu, Peoples R China
[2] Nanjing Tech Univ, Coll Energy, State Key Lab Mat Oriented Chem Engn, Jiangsu Natl Synerget Innovat Ctr Adv Mat SICAM, 5 Xin Mofan Rd, Nanjing 210009, Jiangsu, Peoples R China
[3] Curtin Univ, Dept Chem Engn, Perth, WA 6845, Australia
关键词:
Water splitting;
Non-precious transition metals;
Metal alloy nanoparticles;
Synergistic effects;
Oxygen evolution reaction;
BIFUNCTIONAL ELECTROCATALYST;
REDUCTION REACTION;
GRAPHENE;
HYDROGEN;
WATER;
NANOPARTICLES;
CATALYST;
OXIDES;
STABILITY;
CATHODE;
D O I:
10.1016/j.jpowsour.2016.11.023
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:
Efficient oxygen evolution reaction (OER) catalysts are required to facilitate the large-scale exploitation of renewable energy resources and applications in electrochemical energy conversion technologies. Here, we show that metal alloy-based hybrids can provide higher electrocatalytic activity than their individual metal-based hybrids. In particular, NiCo alloys encapsulated within nitrogen-doped carbon nanotubes (NiCo@NCNTs) showed higher OER activities in an alkaline solution than the individual metal hybrids (Ni@NCNTs and Co@NCNTs), highlighting a synergy between the Ni and Co components. NiCo@NCNTs pyrolyzed at 800 degrees C displayed an overpotential of similar to 41 mV at a current density of 10 mA cm(-2) and were more stable than IrO2 during 1000-cycle accelerated durability testing at a scan rate of 100 mV s(-1). (C) 2016 Elsevier B.V. All rights reserved.
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页码:26 / 33
页数:8
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