电化学
材料科学
镍
钴
超级电容器
配体(生物化学)
金属
耐久性
电极
无机化学
氢氧化物
电化学能量转换
化学工程
金属氢氧化物
电解质
冶金
复合材料
化学
物理化学
生物化学
受体
工程类
作者
Dongxuan Guo,Yan Zhang,Wei-Feng Sun,Dawei Chu,Bonan Li,Lichao Tan,Huiyuan Ma,Haijun Pang,Xinming Wang,Lulu Zhang
标识
DOI:10.1021/acsami.9b11894
摘要
The use of high electrochemical active binary nickel–cobalt sulfides/phosphides/selenides (Ni–Co–X, X = S, P, Se) as electrochemical energy storage materials still has a space for improvement because they become electrochemically unstable during long-term use. Herein, a facile and cost-effective dual-ligand synergistic modulation tactic is described to substantially improve the durability of Ni–Co–X (X = S, P, Se) at the atomic level by partially substituting S, P, and Se ligands into the nickel–cobalt hydroxide precursor, respectively. Remarkably, the dual-ligand electrodes on Ni-foam achieve superior durability and high electrochemical activity when used as positive electrodes in supercapacitors. Impressively, the density functional theory calculations demonstrate that the OH ligand in NiCo2(MOH)x (M = S, P, Se) could attract electrons from metal–S/metal–P/metal–Se bonds to the metal–O bond, enhancing the binding energy of metal–S/metal–P/metal–Se bonds and improving the long-term durability of Ni–Co–X (X = S, P, Se) in alkaline electrolytes. Moreover, OH and S/P/Se ligands could effectively alter the electron structure and result in favorable electrochemical activity. Overall, this tactic could offer an exciting avenue to achieve long-term durability and electrochemical activity of supercapacitor electrodes simultaneously.
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