Lattice Strain and Charge Localization Dual Regulation of Phosphorus‐Doped CoSe2/MXene Catalysts Enable Kinetics‐Enhanced and Dendrite‐Free Lithium‐Sulfur Batteries

Author:

Wang Jing1,Xu Yucong1,Zhuang Yanhui1,Li Yuhang1,Chang Hao‐Hsiang2,Min Huihua3,Shen Xiaodong1,Chen Han‐Yi2,Yang Hao1ORCID,Wang Jin1ORCID

Affiliation:

1. College of Materials Science and Engineering Nanjing Tech University Nanjing 211816 P. R. China

2. Department of Materials Science and Engineering National Tsing Hua University 101, Sec. 2, Kuang‐Fu Road Hsinchu 300044 Taiwan

3. Electron Microscope Lab Nanjing Forestry University Nanjing Jiangsu 210037 P. R. China

Abstract

AbstractPhase engineering is considered an effective strategy to regulate the electrocatalytic activity of catalysts for Li–S batteries (LSBs). However, the underlying origin of phase‐dependent catalytic ability remains to be determined, which significantly impedes the design principles of high‐performance catalytic materials for LSBs. Herein, heteroatom‐doped engineering can trigger phase transformation from mixed‐phased cubic and orthorhombic cobalt diselenide into pure orthorhombic structure with a tensile strain and enhanced charge localization. The upshift of the d‐band center and enhanced Bader charge at Se sites synergistically strengthen the interaction with Li and S sites in polysulfide species, thus endowing the transformed P‐MoSe2/MXene with high catalytic activity and uniform lithium deposition for LSBs. Consequently, the P‐CoSe2/MXene Li–S batteries demonstrate a high‐rate capability of 603 mAh g−1 at 4C, and an excellent cyclability of 652 mAh g−1 at 1C over 500 cycles with a degradation rate of 0.076% per cycle. The work provides an in‐depth insight into the fundamental design principles of effective catalysts for LSBs.

Funder

National Natural Science Foundation of China

Priority Academic Program Development of Jiangsu Higher Education Institutions

Publisher

Wiley

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