多硫化物
电催化剂
材料科学
纳米技术
拉曼光谱
电导率
化学
法拉第效率
密度泛函理论
电化学
共价键
碳纳米管
电解质
催化作用
化学工程
有机化学
电极
计算化学
物理化学
工程类
物理
光学
作者
Jie Xu,Weiqiang Tang,Chao Yang,Ingo Manke,Nan Chen,Feili Lai,Ting Xu,Shuhao An,Бо Лю,Zhiliang Zhang,Yongjie Cao,Nan Wang,Shuangliang Zhao,Dongfang Niu,Renjie Chen
出处
期刊:ACS energy letters
[American Chemical Society]
日期:2021-08-12
卷期号:6 (9): 3053-3062
被引量:109
标识
DOI:10.1021/acsenergylett.1c00943
摘要
The catalysis of covalent organic frameworks (COFs) in Li–S chemistry is largely blocked by a weak chemical interaction and low conductivity. Herein, a new kind of diketopyrrolopyrrole (DPP)-based COF is in situ fabricated onto the carbon nanotube (CNT) surface (denoted as COF@CNT) to uncover the electrocatalysis behavior by its strong chemical interaction and highly conductive property. We declare that the electrocatalytic activity of DPP-COF can be maximized by introducing an appropriate content of CNT (66 wt %); the analyses including density functional theory calculations, X-ray photoelectron spectroscopy, Fourier transform infrared, and Raman show that the DPP moiety can mediate the conversion of polysulfides contributed by a C═O/C–O bonding conversion. Hence, the modified battery shows a 0.042% decay rate over 1000 cycles and achieves a desirable capacity of 8.7 mAh cm–2 with 10 mg cm–2 sulfur loading and lean electrolyte (E/S = 5). This work will inspire the rational design of COF@support hybrids for various electrocatalysis applications.
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