Investigating the Superior Performance of Hard Carbon Anodes in Sodium‐Ion Compared With Lithium‐ and Potassium‐Ion Batteries

Author:

Guo Zhenyu1ORCID,Xu Zhen1ORCID,Xie Fei2ORCID,Jiang Jinglin1ORCID,Zheng Kaitian13ORCID,Alabidun Sarat1ORCID,Crespo‐Ribadeneyra Maria14ORCID,Hu Yong‐Sheng2ORCID,Au Heather1ORCID,Titirici Maria‐Magdalena15ORCID

Affiliation:

1. Department of Chemical Engineering Imperial College London London SW7 2AZ UK

2. Key Laboratory for Renewable Energy Beijing Key Laboratory for New Energy Materials and Devices Beijing National Laboratory for Condensed Matter Physics Institute of Physics Chinese Academy of Sciences Beijing 100190 China

3. Chemical Engineering Research Center State Key Laboratory of Chemical Engineering School of Chemical Engineering and Technology Tianjin University Tianjin 300072 China

4. School of Materials Science and Engineering Queen Mary University of London Mile End Road London E1 4NS UK

5. Advanced Institute for Materials Research (WPI‐AIMR) Tohoku University 2‐1‐1 Katahira, Aobaku, Sendai Miyagi 980–8577 Japan

Abstract

AbstractEmerging sodium‐ion batteries (NIBs) and potassium‐ion batteries (KIBs) show promise in complementing lithium‐ion battery (LIB) technology and diversifying the battery market. Hard carbon is a potential anode candidate for LIBs, NIBs, and KIBs due to its high capacity, sustainability, wide availability, and stable physicochemical properties. Herein, a series of hard carbons is synthesized by hydrothermal carbonization and subsequent pyrolysis at different temperatures to finely tune their structural properties. When tested as anodes, the hard carbons exhibit differing ion‐storage trends for Li, Na, and K, with NIBs achieving the highest reversible capacity. Extensive materials and electrochemical characterizations are carried out to study the correlation of structural features with electrochemical performance and to explain the specific mechanisms of alkali‐ion storage in hard carbons. In addition, the best‐performing hard carbon is tested against a sodium cathode Na3V2(PO4)3 in a Na‐ion pouch cell, displaying a high power density of 2172 W kg−1 at an energy density of 181.5 Wh kg−1 (based on the total weight of active materials in both anode and cathode). The Na‐ion pouch cell also shows stable ultralong‐term cycling (9000 h or 5142 cycles) and demonstrates the promising potential of such materials as sustainable, scalable anodes for beyond Li‐batteries.

Funder

China Scholarship Council

Engineering and Physical Sciences Research Council

Science and Technology Facilities Council

Publisher

Wiley

Subject

Mechanical Engineering,Mechanics of Materials,General Materials Science

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