材料科学
钴
电化学
化学工程
磷化物
杰纳斯
沸石咪唑盐骨架
电导率
催化作用
纳米技术
无机化学
化学
金属
金属有机骨架
电极
吸附
物理化学
有机化学
冶金
工程类
作者
Zichao Yan,Yaru Liang,Weibo Hua,Xia‐Guang Zhang,Wei‐Hong Lai,Zhe Hu,Wanlin Wang,Jian Peng,Sylvio Indris,Yunxiao Wang,Shulei Chou,Huan Liu,Shi Xue Dou
出处
期刊:ACS Nano
[American Chemical Society]
日期:2020-07-16
卷期号:14 (8): 10284-10293
被引量:95
标识
DOI:10.1021/acsnano.0c03737
摘要
Electrode materials with high conductivity, strong chemisorption, and catalysis toward polysulfides are recognized as key factors for metal-sulfur batteries. Nevertheless, the construction of such functional material is a challenge for room-temperature sodium-sulfur (RT-Na/S) batteries. Herein, a multiregion Janus-featured CoP-Co structure obtained via sequential carbonization-oxidation-phosphidation of heteroseed zeolitic imidazolate frameworks is introduced. The structural virtues include a heterostructure existing in a CoP-Co structure and a conductive network of N-doped porous carbon nanotube hollow cages (NCNHCs), endowing it with superior conductivity in both the short- and long-range and strong polarity toward polysulfides. Thus, the S@CoP-Co/NCNHC cathode exhibits superior electrochemical performance (448 mAh g-1 remained for 700 times cycling under 1 A g-1) and an optimized redox mechanism in polysulfides conversion. Density functional theory calculations present that the CoP-Co structure optimizes bond structure and bandwidth, whereas the pure CoP is lower than the corresponding Fermi level, which could essentially benefit the adsorptive capability and charge transfer from the CoP-Co surface to Na2Sx and therefore improve its affinity to polysulfides.
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