Tailoring oxygen vacancies on bismuth using one-dimensional BiSI for efficient CO2 electrolysis to formate

Authors
Jeon, JihoBang, Hyeon-SeokKo, Young-JinHuh, EugeneKang, JinsuZhang, XiaojieKa, SeohyeonKim, YeongjinLee, Woong HeeKim, KyeongsuYu, Hak KiOh, Hyung-SukChoi, Jae-Young
Issue Date
2025-11
Publisher
Elsevier BV
Citation
Chemical Engineering Journal, v.523
Abstract
The electrochemical reduction of CO2 to formate represents a promising strategy for carbon mitigation and energy storage. However, achieving selectivity and productivity at industrially relevant current densities remains a critical challenge. Herein, we report a defect-engineered bismuth electrocatalyst with abundant surface oxygen vacancies (OV-Bi), synthesized via electrochemical reduction of exfoliated one-dimensional BiSI—a van der Waals materials. The facile removal of sulfur and iodine during reduction promotes the formation of oxygen vacancies, which lower the energy barrier for *OCHO intermediate formation, thereby steering the reaction pathway toward formate. The resulting OV-Bi electrode exhibits a record-high partial current density for formate production of 465.7 mA cm−2 on a 5 cm2 electrode, while maintaining Faradaic efficiency above 90 % and stable operation for over 24 h at 100 mA cm−2. Electron spin resonance spectroscopy confirmed a substantial increase in oxygen vacancy concentration, and in situ/Operando X-ray absorption spectroscopy revealed dynamic electronic structure evolution under CO2RR conditions. These findings demonstrate that oxygen vacancy engineering significantly enhances catalytic CO2 adsorption and reduction, offering a viable strategy for designing next-generation high-performance electrocatalysts for scalable CO2-to-formate electrolysis.
Keywords
REDUCTION; METALS; OXIDE; ACID; One-dimensional (1D) materials; Oxygen vacancy; Electrocatalysts; CO2 reduction reaction (CO2RR); Formate; BiSI
ISSN
1385-8947
URI
https://pubs.kist.re.kr/handle/201004/153605
DOI
10.1016/j.cej.2025.168350
Appears in Collections:
KIST Article > 2025
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