Sb, N co-doped bagasse-derived carbon activated by antimony acetate toward efficient oxygen reduction catalysis
Biomass-derived carbon electrocatalysts are promising low-cost alternatives to platinum-based catalysts for the oxygen reduction reaction (ORR) and can greatly promote the practical application of metal-air batteries. However, rational fabrication of high-performance biomass carbon catalysts with well-defined active structures remains challenging. Herein, an antimony and nitrogen co-doped bagasse-derived carbon catalyst (Sb-N-C-1100) was fabricated via a facile antimony acetate-assisted activation strategy. The synergistic effects of high-temperature pyrolysis, antimony species evaporation, and chemical activation construct a hierarchical porous nanostructure with large specific surface area, moderate graphitization degree, and abundant SbN x species. Electrochemical tests demonstrate that the optimized Sb-N-C-1100 catalyst delivers excellent ORR catalytic activity with a favorable four-electron reaction pathway, outstanding cycling stability, and superior methanol poisoning resistance. This work provides a feasible route for the rational design and microstructure regulation of high-efficiency biomass-based ORR electrocatalysts for advanced energy conversion and storage devices.
Authors
- Yikang Ji (ORCID: https://orcid.org/0009-0002-0950-9383)
- Errui Wang (ORCID: https://orcid.org/0009-0001-3089-1989)
- Jing Tang (ORCID: https://orcid.org/0000-0003-4815-5522)
- Jiahao Guo (ORCID: https://orcid.org/0000-0002-6829-0927)
- Yuan Ren (ORCID: https://orcid.org/0000-0002-3991-5342)
- Shengbiao Zheng (ORCID: https://orcid.org/0000-0002-1192-8221)
- Haijun Yao
- Jie Chen
Institutions
- Anhui University (CN)
- Anhui University of Science and Technology (CN)
- Anhui Science and Technology University (CN)
Publication Details
- Journal
- Journal of Power Sources
- Published
- 2026-09-16
- DOI
- https://doi.org/10.1016/j.jpowsour.2026.241527
- Primary Topic
- Electrocatalysts for Energy Conversion
- Type
- article
- Field-Weighted Citation Impact
- 0.00