Mechanical Activation of Graphite for Na‐Ion Battery Anodes: Unexpected Reversible Reaction on Solid Electrolyte Interphase via X‐Ray Analysis

Author:

Lee Su Chan12,Kim Young Hwan1ORCID,Park Jae‐Ho1,Susanto Dieky1,Kim Ji‐Young3,Han Jonghyun1ORCID,Jun Seong Chan2,Chung Kyung Yoon14ORCID

Affiliation:

1. Energy Storage Research Center Korea Institute of Science and Technology (KIST) Hwarang‐ro 14‐gil 5, Seongbuk‐gu Seoul 02792 South Korea

2. Nano‐Electro Mechanical Device Laboratory School of Mechanical Engineering Yonsei University 50 Yonsei‐ro, Seodaemun‐gu Seoul 03722 South Korea

3. Advanced Analysis Center Korea Institute of Science and Technology (KIST) Hwarang‐ro 14‐gil 5, Seongbuk‐gu Seoul 02792 South Korea

4. Division of Energy & Environmental Technology, KIST School Korea University of Science and Technology Seoul 02792 South Korea

Abstract

AbstractAlthough sodium‐ion batteries (SIBs) offer promising low‐cost alternatives to lithium‐ion batteries (LIBs), several challenges need to be overcome for their widespread adoption. A primary concern is the optimization of carbon anodes. Graphite, vital to the commercial viability of LIBs, has a limited capacity for sodium ions. Numerous alternatives to graphite are explored, particularly focusing on disordered carbons, including hard carbon. However, compared with graphite, most of these materials underperform in LIBs. Furthermore, the reaction mechanism between carbon and sodium ions remains ambiguous owing to the structural diversity of disordered carbon. A straightforward mechanical approach is introduced to enhance the sodium ion storage capacity of graphite, supported by comprehensive analytical techniques. Mechanically activated graphite delivers a notable reversible capacity of 290.5 mAh·g−1 at a current density of 10 mA·g−1. Moreover, it maintains a capacity of 157.7 mAh·g−1 even at a current density of 1 A·g−1, benefiting from the defect‐rich structure achieved by mechanical activation. Soft X‐ray analysis revealed that this defect‐rich carbon employs a sodium‐ion storage mechanism distinct from that of hard carbon. This leads to an unexpected reversible reaction on the solid electrolyte surface. These insights pave the way for innovative design approaches for carbon electrodes in SIB anodes.

Funder

National Research Foundation of Korea

Ministry of Science and ICT, South Korea

Korea Institute of Science and Technology

Publisher

Wiley

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