Zou Rujia, Yuen Muk Fung, Yu Li, Hu Junqing, Lee Chun-Sing, Zhang Wenjun
State Key Laboratory for Modification of Chemical Fibers and Polymer Materials, College of Materials Science and Engineering, Donghua University, Shanghai 201620, China.
Center of Super-Diamond and Advanced Films (COSDAF), Department of Physics and Materials Science, City University of Hong Kong, Hong Kong.
Sci Rep. 2016 Feb 1;6:20264. doi: 10.1038/srep20264.
We developed a new electrode comprising thin carbon layer coated hierarchical NiCo2S4 core-shell nanowire arrays (NiCo2S4@C CSNAs) on graphene/Ni foam (Ni@G) substrates. The electrode showed outstanding electrochemical characteristics including a high specific capacitance of 253 mAh g(-1) at 3 A g(-1), high rate capability of 163 mAh g(-1) at 50 A g(-1) (~64.4% of that at 3 A g(-1)), and long-term cycling stability with a capacity retention of 93.9% after 5000 cycles. Comparative studies on the degradation of hierarchical NiCo2S4 CSNA electrodes with and without carbon coatings revealed that the morphology pulverization, structural separation at core/shell interface, and irretrievably chemical composition change of NiCo2S4 CSNAs electrode are major factors that deteriorate the electrochemical performance of the electrodes without carbon coating. The favorable roles of carbon coatings on hierarchical NiCo2S4 CSNAs were further clarified: (1) serving as a physical buffering layer that suppresses the structural breakdown; (2) retarding the chemical composition conversion of the NiCo2S4 CSNAs; and (3) providing extra path for charge transition in addition to the NiCo2S4 core nanowires. Understanding of the degradation mechanisms and the significance of the surface carbon coatings would provide useful guidelines for the design of new electrode materials for high-performance electrochemical devices.
我们开发了一种新型电极,该电极由在石墨烯/泡沫镍(Ni@G)基底上涂覆有薄碳层的分级NiCo2S4核壳纳米线阵列(NiCo2S4@C CSNAs)组成。该电极表现出优异的电化学特性,包括在3 A g(-1)时具有253 mAh g(-1)的高比电容,在50 A g(-1)时具有163 mAh g(-1)的高倍率性能(约为3 A g(-1)时的64.4%),以及长期循环稳定性,在5000次循环后容量保持率为93.9%。对有碳涂层和无碳涂层的分级NiCo2S4 CSNA电极降解的对比研究表明,NiCo2S4 CSNAs电极的形态粉碎、核/壳界面处的结构分离以及不可挽回的化学成分变化是导致无碳涂层电极电化学性能恶化的主要因素。进一步阐明了碳涂层对分级NiCo2S4 CSNAs的有利作用:(1)作为物理缓冲层抑制结构破坏;(2)延缓NiCo2S4 CSNAs的化学成分转变;(3)除了NiCo2S4核纳米线外,还为电荷转移提供额外路径。对降解机制和表面碳涂层重要性的理解将为高性能电化学器件新型电极材料的设计提供有用的指导。