Adsorption‐Enhanced Bismuth Oxide Efficiently Convert CO <sub>2</sub> to Formate Over a Wide Potential Window
Electrochemical conversion of carbon dioxide (CO<sub>2</sub>) into high-value-added chemicals using clean energy is a processing method to reduce carbon emissions and store energy. The unsatisfactory adsorption and activation of CO<sub>2</sub> suppress electrochemical reduction over a narrow potential window. Herein, we synthesized CO<sub>2</sub> adsorption-enhanced bismuth oxide nanosheets (syn-Bi<sub>2</sub>O<sub>3</sub>) using a one-pot low-temperature water bath method. The syn-Bi<sub>2</sub>O<sub>3</sub> exhibited marked Faradic efficiency (FE<sub>formate</sub>) over 94% in a wide potential window from -0.43 to -1.31 V versus RHE in the flow cell, and demonstrated an appreciable FE<sub>formate</sub> of 94.5% at a partial current density of 661.9 mA cm<sup>-2</sup>. The in situ spectroscopy and theoretical calculation unraveled the distinct formate production performance of the syn-Bi<sub>2</sub>O<sub>3</sub> catalyst, which was contributed by its adsorption of CO<sub>2</sub> and promoting the subsequent formation of intermediates. Furthermore, coupled with the simulated solar cell with the 4 layer 3-cell stacks, the solar to formate and overall solar-to-fuel reach 19.34% and 20.23% with over 0.21 A, respectively. This work provides insights into the practical application of electrochemical CO<sub>2</sub> reduction for formate production driven by solar energy.
Authors
- Guiwei He (ORCID: https://orcid.org/0009-0005-2023-559X)
- Shengjie Bai (ORCID: https://orcid.org/0000-0002-2023-6841)
- Chen Liao (ORCID: https://orcid.org/0009-0009-0687-8758)
- Tengfei Ma (ORCID: https://orcid.org/0009-0008-6748-4851)
- Ya Liu (ORCID: https://orcid.org/0009-0005-5866-3178)
- Y. Ren
- Liejin Guo
- Dan Lei
- Feng Wang
Institutions
- Xi'an Jiaotong University (CN)
Publication Details
- Journal
- Small
- Published
- 2026-01-08
- DOI
- https://doi.org/10.1002/smll.202512691
- Primary Topic
- CO2 Reduction Techniques and Catalysts
- Type
- article
- Field-Weighted Citation Impact
- 0.00