Engineering Spin State in Spinel Co3O4 nanosheets by V‐Doping for Bidirectional Catalysis of Polysulfides in Lithium–Sulfur Batteries

Author:

Zhou Wei1,Chen Minzhe1,Zhao Dengke1,Zhu Chuheng1,Wang Nan2,Lei Wen3ORCID,Guo Yan4,Li Ligui15

Affiliation:

1. New Energy Research Institute School of Environment and Energy Higher Education Mega Center South China University of Technology Guangzhou 510006 China

2. Siyuan laboratory Guangzhou Key Laboratory of Vacuum Coating Technologies and New Energy Materials Department of Physics Jinan University Guangzhou Guangdong 510632 China

3. The State Key Laboratory of Refractories and Metallurgy Wuhan University of Science and Technology Wuhan 430081 China

4. Guangdong‐Hong Kong‐Macau Joint Laboratory for Photonic‐Thermal‐Electrical Energy Materials and Devices Institute of Applied Physics and Materials Engineering University of Macau Taipa Macau SAR 999078 China

5. Guangdong Provincial Key Laboratory of Advance Energy Storage Materials South China University of Technology Guangzhou 510640 China

Abstract

AbstractThe slow bidirectional conversion and fast shuttling of lithium polysulfides (LiPSs) remain the main obstacles that inhibit the practical application of lithium sulfur batteries (LSBs). Here, by engineering the in‐spin state of spinel oxides, V doping‐induced hexagonal nanosheets (V‐Co3O4 NS) with intermediate spin state (IS, t2g5 eg1) can form stable bond order toward LiS* based on the ligand field theory and molecular orbital theory, thus effectively accelerating the sulfur conversion kinetics. Owing to these merits, the V‐Co3O4 NS modified separator base battery achieves a high areal capacity of 15.37 mAh cm−2 with sulfur loading of 15.4 mg cm−2, and it displays a low‐capacity attenuation of 0.015% each cycle at 3.0 C for 1900 cycles.

Funder

National Natural Science Foundation of China

National Defense Science and Technology Innovation Fund of the Chinese Academy of Sciences

Guangdong Provincial Key Laboratory of Advanced Energy Storage Materials

Publisher

Wiley

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