P-doped CNTs encapsulated nickel hybrids with flower-like structure as efficient catalysts for hydrogen evolution reaction

被引:44
作者
Jing, Shengyu [1 ,3 ]
Wang, Dourong [1 ,2 ]
Yin, Shibin [2 ]
Lu, Jiajia [2 ]
Shen, Pei Kang [2 ]
Tsiakaras, Panagiotis [3 ,4 ,5 ]
机构
[1] China Univ Min & Technol, Sch Informat & Control Engn, Xuzhou 221116, Jiangsu, Peoples R China
[2] Guangxi Univ, State Key Lab Proc Nonferrous Met & Featured Mat, Guangxi Key Lab Electrochem Energy Mat, Collaborat Innovat Ctr Sustainable Energy Mat, Nanning 530004, Peoples R China
[3] Univ Thessaly, Sch Engn, Dept Mech Engn, Lab Alternat Energy Convers Syst, Volos 38834, Greece
[4] Ural Fed Univ, Lab Mat & Devices Electrochem Power Ind, 19 Mira St, Ekaterinburg 620002, Russia
[5] RAS, Inst High Temp Electrochem, Lab Electrochem Devices Based Solid Oxide Proton, Ekaterinburg 620990, Russia
关键词
Water splitting; Hydrogen evolution; Catalyst; P-doped carbon nanotubes; Nickel foam; CARBON NANOTUBES; BIFUNCTIONAL ELECTROCATALYST; OXYGEN REDUCTION; NI FOAM; COBALT; NITROGEN; NANOPARTICLES; NITRIDE; MOFS; PHOSPHORUS;
D O I
10.1016/j.electacta.2018.12.055
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
Electrochemical water splitting attracted an increasing attention as a promising approach to produce high-purity hydrogen. Both the design and synthesis of low-cost and high-performance catalysts for hydrogen evolution reaction (HER) remain challenging. Herein, an in-situ growth of carbon nanotubes encapsulated Ni particles on nickel foam is described. This catalyst is synthesized via a one-step chemical vapor deposition (CVD) at different temperatures followed by P-doping treatment (P-doped Ni@CNTs/NF). The corresponding physicochemical and electrochemical results illustrate that the P-doped Ni@CNTs/NF prepared at 600 degrees C with flower-like structure exhibits excellent activity and stability for HER in acidic electrolytes. In 0.5 MH2SO4 aqueous solution, the sample shows a small overpotential value of -135.2 mV to achieve a current density of -10 mA cm(-2), which also displays acceptable long-term stability for lasting 20 h. This work provides a facile approach to prepare a cost-effective catalyst with high efficiency and might promote further study of the transition metal catalysts for hydrogen evolution in acid environments. (C) 2018 Elsevier Ltd. All rights reserved.
引用
收藏
页码:142 / 149
页数:8
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