共轭体系
材料科学
电化学
聚合物
纳米技术
金属
配位聚合物
配体(生物化学)
组合化学
电极
化学工程
化学
冶金
物理化学
工程类
复合材料
生物化学
受体
作者
Jian Xie,Xue‐Feng Cheng,Xun Cao,Jinghui He,Wei Guo,Dong‐Sheng Li,Zhichuan J. Xu,Yizhong Huang,Jianmei Lu,Qichun Zhang
出处
期刊:Small
[Wiley]
日期:2019-10-25
卷期号:15 (49): e1903188-e1903188
被引量:69
标识
DOI:10.1002/smll.201903188
摘要
Abstract Conjugated coordination polymers have become an emerging category of redox‐active materials. Although recent studies heavily focus on the tailoring of metal centers in the complexes to achieve stable electrochemical performance, the effect on different substitutions of the bridging bonds has rarely been studied. An innovative tailoring strategy is presented toward the enhancement of the capacity storage and the stability of metal–organic conjugated coordination polymers. Two nanostructured d‐π conjugated compounds, Ni[C 6 H 2 (NH) 4 ] n (Ni‐NH) and Ni[C 6 H 2 (NH) 2 S 2 ] n (Ni‐S), are evaluated and demonstrated to exhibit hybrid electrochemical processes. In particular, Ni‐S delivers a high reversible capacity of 1164 mAh g −1 , an ultralong stability up to 1500 cycles, and a fully recharge ability in 67 s. This tailoring strategy provides a guideline to design future effective conjugated coordination‐polymer‐based electrodes.
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