Exploring highly porous Co2P nanowire arrays for electrochemical energy storage

被引:42
作者
Chen, Minghua [1 ]
Zhou, Weiwei [2 ]
Qi, Meili [1 ]
Yin, Jinghua [1 ]
Xia, Xinhui [3 ,4 ]
Chen, Qingguo [1 ]
机构
[1] Harbin Univ Sci & Technol, Sch Appl Sci, Key Lab Engn Dielect & Applicat, Minist Educ, Harbin 150080, Peoples R China
[2] Harbin Inst Technol Weihai, Sch Mat Sci & Engn, Weihai 264209, Peoples R China
[3] Zhejiang Univ, Key Lab Adv Mat & Applicat Batteries Zhejiang Pro, State Key Lab Silicon Mat, Hangzhou 310027, Zhejiang, Peoples R China
[4] Zhejiang Univ, Sch Mat Sci & Engn, Hangzhou 310027, Zhejiang, Peoples R China
基金
中国博士后科学基金;
关键词
Cobalt phosphides; Mesoporous arrays; Alkaline batteries; Energy storage; Phosphorization; LITHIUM-ION BATTERIES; ASYMMETRIC SUPERCAPACITORS; FACILE SYNTHESIS; HOLLOW SPHERES; METAL-OXIDES; PERFORMANCE; ANODE; CATHODE; NANOSTRUCTURES; NANOPARTICLES;
D O I
10.1016/j.jpowsour.2017.01.014
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
Controllable synthesis of mesoporous conductive metal phosphide nanowire arrays is critical for developing highly-active electrodes of alkaline batteries. Herein we develop a simple combined strategy for rational synthesis of mesoporous Co2P nanowire arrays by hydrothermal-phosphorization method. Free-standing mesoporous Co2P nanowires consisting of interconnected nanoparticles of 10-20 nm grow vertically to the substrate forming arrays. High electrical conductivity and large porosity are obtained in the arrays architecture. When characterized as the cathode of high-rate alkaline batteries, the designed Co2P nanowire arrays are proven with good electrochemical performance with a large capacity (133 mAh g(-1) at 1 A g(-1)), stable cycling life with a capacity retention of almost 100% after 5000 cycles at 10 A ri owing to the mesoporous nanowire structure with short ion/electron transport path. Our synthetic approach can be useful for construction of other porous metal phosphide arrays for energy storage and conversion. (C) 2017 Elsevier B.V. All rights reserved.
引用
收藏
页码:964 / 969
页数:6
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