Is Soft Carbon a More Suitable Match for SiOx in Li‐Ion Battery Anodes?

Author:

Sun Qing12ORCID,Zeng Guifang345,Li Jing12,Wang Shang5,Botifoll Marc6,Wang Hao7,Li Deping1,Ji Fengjun1,Cheng Jun1,Shao Huaiyu8,Tian Yanhong5,Arbiol Jordi6,Cabot Andreu39ORCID,Ci Lijie12ORCID

Affiliation:

1. State Key Laboratory of Advanced Welding and Joining School of Materials Science and Engineering Harbin Institute of Technology (Shenzhen) Shenzhen 518055 China

2. Key Laboratory for Liquid‐Solid Structural Evolution & Processing of Materials (Ministry of Education) School of Materials Science and Engineering Shandong University Jinan 250061 China

3. Catalonia Institute for Energy Research – IREC Sant Adrià de Besòs Barcelona 08930 Spain

4. Department of Electronic and Biomedical Engineering Universitat de Barcelona Barcelona 08028 Spain

5. State Key Laboratory of Advanced Welding and Joining Harbin Institute of Technology Harbin 150001 China

6. Catalan Institute of Nanoscience and Nanotechnology (ICN2) CSIC and BIST Campus UAB Bellaterra Barcelona 08193 Spain

7. Land Transport Authority of Singapore Singapore 179102 Singapore

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

9. ICREA Pg. Lluis Companys Barcelona 08010 Spain

Abstract

AbstractSilicon oxide (SiOx), inheriting the high‐capacity characteristic of silicon‐based materials but possessing superior cycling stability, is a promising anode material for next‐generation Li‐ion batteries. SiOx is typically applied in combination with graphite (Gr), but the limited cycling durability of the SiOx/Gr composites curtails large‐scale applications. In this work, this limited durability is demonstrated in part related to the presence of a bidirectional diffusion at the SiOx/Gr interface, which is driven by their intrinsic working potential differences and the concentration gradients. When Li on the Li‐rich surface of SiOx is captured by Gr, the SiOx surface shrinks, hindering further lithiation. The use of soft carbon (SC) instead of Gr can prevent such instability is further demonstrated. The higher working potential of SC avoids bidirectional diffusion and surface compression thus allowing further lithiation. In this scenario, the evolution of the Li concentration gradient in SiOx conforms to its spontaneous lithiation process, benefiting the electrochemical performance. These results highlight the focus on the working potential of carbon as a strategy for rational optimization of SiOx/C composites toward improved battery performance.

Funder

National Natural Science Foundation of China

Publisher

Wiley

Subject

Biomaterials,Biotechnology,General Materials Science,General Chemistry

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