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.
引用
收藏
页码:26 / 33
页数:8
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