Tuning Microstructures of Hard Carbon Anode by Rapid Pre-foaming Strategy for Superhigh-Rate Sodium-ion Storage Performance in Low-plateau Region
Fabricating suitable microstructures containing closed pore volume , closed pore size, interlayer spacing as well as C=O content in the glucose-based hard carbon (Glu-HC) can greatly enhance its electrochemical performance in sodium-ion batteries (SIBs) at low-voltage below 0.1 V. Unfortunately, the blistering nature of D-glucose makes it difficult to regulate precisely these microstructures for achieving an excellent Na + storage performance, especially at high rates. Herein, D-glucose was rational pretreated by modulating KMnO 4 addition and hot acid-washing time to promote its condensation and aromatization, and avoid a foaming phenomenon. During carbonization , a deep chemical cross-liking reaction can be generated in the pretreated D-glucose to obtain HC concurrently featuring with these favorable microstructures. The optimal HC anode (HC-1100) shows high initial coulombic efficiency (89.62%), large total capacity of 421.6 and 215.3 mAh g −1 at 0.1 and 20 A g −1 , respectively. Besides, it delivers high plateau capacities of 303.31 and 193.1 mAh g −1 at 0.1 and 5 A g −1 along with 87% capacity retention for 2000 cycles, far surpassing than these reported HC anodes. Additionally, the HC-1100//Na 3 V 2 (PO 4 ) 3 full cell exhibits high energy density of 194 Wh kg −1 . Furthermore, Na + storage behaviors and theoretical calculations demonstrates that the HC material owning high C=O content, suitable closed pore size (0.9 nm) and interlayer spacing (0.5 nm) possesses a superior ultrahigh-rate performance. This work provides a significative guidance for rational constructing high-performance HC anode. Glucose-based hard carbon with rich C=O group, high closed pore volume, suitable closed pore size and large interlayer spacing was precisely prepared by combining rapid pre-foaming and high-temperature carbonization strategy. As sodium-ion battery anode, it showed superhigh plateau capacities of 303.31 and 193.1 mAh g −1 at 0.1 and 5 A g −1 , far exceeding than that of commercial HC anode.
Authors
- Bo Sun (ORCID: https://orcid.org/0000-0003-4349-690X)
- Fangzhi Zheng
- Ping Xiao (ORCID: https://orcid.org/0000-0002-6063-3681)
- Zechen Li (ORCID: https://orcid.org/0009-0001-2399-1666)
- Ping Li (ORCID: https://orcid.org/0009-0001-7203-0271)
- Ziang Wang (ORCID: https://orcid.org/0009-0005-1728-5473)
- Ping Xu (ORCID: https://orcid.org/0000-0002-1516-4986)
- Qiang Ye (ORCID: https://orcid.org/0000-0001-9384-1180)
- Tao Li (ORCID: https://orcid.org/0000-0001-9634-0314)
- Sijia Liao
- Yankun Sun (ORCID: https://orcid.org/0009-0009-5886-1325)
- Chong Xu (ORCID: https://orcid.org/0009-0000-1784-9180)
- Ting Pan
- Shuang Liu (ORCID: https://orcid.org/0000-0001-6022-2738)
- Dong Sun
Institutions
- China University of Petroleum, Beijing (CN)
- Henan Province Quality and Technical Supervision Bureau (CN)
Publication Details
- Journal
- Energy storage materials
- Published
- 2025-04-26
- DOI
- https://doi.org/10.1016/j.ensm.2025.104283
- Citations
- 17
- Primary Topic
- Advancements in Battery Materials
- Type
- article
- Field-Weighted Citation Impact
- 12.42
Funders
- National Natural Science Foundation of China
- Science Foundation of China University of Petroleum, Beijing