Accelerated Li+ Desolvation for Diffusion Booster Enabling Low‐Temperature Sulfur Redox Kinetics via Electrocatalytic Carbon‐Grazfted‐CoP Porous Nanosheets

Author:

Zhang Xin1,Li Xiangyang2,Zhang Yongzheng1ORCID,Li Xiang1,Guan Qinghua3,Wang Jian34ORCID,Zhuang Zechao5,Zhuang Quan2,Cheng Xiaomin1,Liu Haitao6,Zhang Jing7,Shen Chunyin1,Lin Hongzhen3,Wang Yanli1,Zhan Liang1ORCID,Ling Licheng1

Affiliation:

1. State Key Laboratory of Green Chemical Engineering and Industrial Catalysis Key Laboratory of Specially Functional Polymeric Materials and Related Technology (Ministry of Education) State Key Laboratory of Chemical Engineering East China University of Science and Technology Shanghai 200237 P. R. China

2. Inner Mongolia Key Laboratory of Carbon Nanomaterials Nano Innovation Institute (NII) Inner Mongolia Minzu University Tongliao Inner Mongolia 028000 P. R. China

3. i‐Lab & CAS Key Laboratory of Nanophotonic Materials and Device Suzhou Institute of Nano‐Tech and Nano‐Bionics, Chinese Academy of Sciences Suzhou Jiangsu 215123 P. R. China

4. Helmholtz Institute Ulm (HIU) / Karlsruhe Institute of Technology D89081 Ulm Germany

5. Department of Chemistry Tsinghua University Beijing 100084 P. R. China

6. Laboratory of Computational Physics Institute of Applied Physics and Computational Mathematics Beijing 100088 P. R. China

7. School of Materials Science and Engineering Xi'an University of Technology Xi'an Shanxi 710048 P. R. China

Abstract

AbstractLithium–sulfur (Li–S) batteries are famous for their high energy density and low cost, but prevented by sluggish redox kinetics of sulfur species due to depressive Li ion diffusion kinetics, especially under low‐temperature environment. Herein, a combined strategy of electrocatalysis and pore sieving effect is put forward to dissociate the Li+ solvation structure to stimulate the free Li+ diffusion, further improving sulfur redox reaction kinetics. As a protocol, an electrocatalytic porous diffusion‐boosted nitrogen‐doped carbon‐grafted‐CoP nanosheet is designed via forming the NCoP active structure to release more free Li+ to react with sulfur species, as fully investigated by electrochemical tests, theoretical simulations and in situ/ex situ characterizations. As a result, the cells with diffusion booster achieve desirable lifespan of 800 cycles at 2 C and excellent rate capability (775 mAh g−1 at 3 C). Impressively, in a condition of high mass loading or low‐temperature environment, the cell with 5.7 mg cm−2 stabilizes an areal capacity of 3.2 mAh cm−2 and the charming capacity of 647 mAh g−1 is obtained under 0 °C after 80 cycles, demonstrating a promising route of providing more free Li ions toward practical high‐energy Li–S batteries.

Funder

National Natural Science Foundation of China

Fundamental Research Funds for the Central Universities

Natural Science Foundation of Inner Mongolia

Publisher

Wiley

Subject

Electrochemistry,Condensed Matter Physics,Biomaterials,Electronic, Optical and Magnetic Materials

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