Hierarchical Se-Ti <sub>3</sub> C <sub>2</sub> @CNTs Catalytic Network for High-Stability Li–S Batteries: Synergistic Polysulfide Anchoring and Conversion
The practical application of lithium-sulfur (Li-S) batteries is plagued by the polysulfide shuttle effect and sluggish redox kinetics. Herein, a high-temperature selenization strategy is proposed to construct a selenium-rich interface via reactions between surface functional groups and selenium sources, yielding a selenium-doped Ti<sub>3</sub>C<sub>2</sub> quantum dots composite with carbon nanotubes (Se-Ti<sub>3</sub>C<sub>2</sub> QDs@CNTs) as the cathode material. Microstructural characterizations confirm that Se doping modulates the QDs' electronic structure to form polar active sites, reinforcing polysulfide anchoring. Kinetic analysis reveals that uniformly dispersed Se-Ti<sub>3</sub>C<sub>2</sub> QDs on the 3D carbon network form catalytic centers, which synergistically suppress the shuttle effect and accelerate the redox kinetics. Benefiting from the conductive CNT framework and rapid charge transfer of QDs, the composite achieves efficient sulfur utilization and stable cycling, providing an innovative route for high-performance Li-S battery design.
Authors
- Na Huang (ORCID: https://orcid.org/0009-0007-2870-8042)
- Qinhua. Gu
- Ying Liu (ORCID: https://orcid.org/0000-0002-6628-6377)
- Yiqi Cao (ORCID: https://orcid.org/0000-0001-5238-0840)
- Wenjuan Han (ORCID: https://orcid.org/0009-0001-9306-4956)
- Yujie Qi
- Zhaofeng Zhai
- Li Wang
- Ming Lu
- Chuyan Zhang
- Xiao Tao
- Bingsen Zhang
Institutions
- Jilin Normal University (CN)
- Jilin University (CN)
- Chinese Academy of Sciences (CN)
- Institute of Metal Research (CN)
- Chery Automobile (China) (CN)
- Jilin Medical University (CN)
- Changchun Institute of Technology (CN)
- Ministry of Education (BD)
Publication Details
- Journal
- Nano Letters
- Published
- 2026-03-12
- DOI
- https://doi.org/10.1021/acs.nanolett.5c05926
- Primary Topic
- Advanced Battery Materials and Technologies
- Type
- article
- Field-Weighted Citation Impact
- 0.00