Harnessing electrochemical CO<sub>2</sub> reduction and assisted water electrolysis <i>via</i> constrained thermodynamic modeling
Electrochemical CO<sub>2</sub> reduction reaction (CO<sub>2</sub>RR) and assisted water electrolysis (AWE) using organic compounds offer promising pathways for sustainable energy conversion. However, the thermodynamic feasibility and efficiency of these processes are strongly influenced by CO<sub>2</sub> phase transitions (both gaseous and aqueous) and operating conditions, such as temperature and pH. This study systematically examines the thermodynamic behavior of CO<sub>2</sub>RR and AWE by calculating Gibbs free energy (Δ<i>G</i>), enthalpy (Δ<i>H</i>), and theoretical potentials (<i>E</i><sub>TN</sub> and <i>E</i><sub>RE</sub>) over a broad temperature range (0-1000 °C) and varying pH conditions. Pourbaix diagrams for key CO<sub>2</sub>-derived products, including CO, hydrocarbons, organic acids, and alcohols, are constructed to assess their stability across different electrochemical environments. The analysis reveals that in aqueous-phase CO<sub>2</sub> systems, equilibrium potentials shift due to the effects of CO<sub>2</sub> speciation. In alkaline conditions, dissolved CO<sub>2</sub> undergoes sequential conversion into HCO<sub>3</sub><sup>-</sup> and CO<sub>3</sub><sup>2-</sup>, resulting in increased overpotentials in CO<sub>2</sub>RR. Conversely, gaseous CO<sub>2</sub> maintains a stable equilibrium potential, mitigating pH-induced fluctuations that could hinder reaction selectivity and efficiency. In AWE, the phase transition during reaction conditions lowers oxidation potentials, resulting in enhanced energy efficiency. The calculated <i>V</i><sub>TN</sub> and <i>V</i><sub>RE</sub> values demonstrate that organic oxidation reactions in AWE require substantially lower energy inputs than conventional oxygen evolution reactions, providing a thermodynamic advantage for energy-efficient hydrogen production. This study establishes a comprehensive thermodynamic framework for CO<sub>2</sub> electrochemical conversion, integrating Pourbaix diagrams and temperature-dependent electrochemical modeling to optimize reaction conditions and energy efficiency. These insights contribute to the rational design of electrocatalytic systems and the development of scalable CO<sub>2</sub> conversion technologies for industrial applications.
Authors
- Uk Sim (ORCID: https://orcid.org/0000-0001-7767-495X)
- Subramani Surendran (ORCID: https://orcid.org/0000-0003-0750-3199)
- Hyojung Lim (ORCID: https://orcid.org/0009-0007-5287-2993)
- Joon Bo Shim
- Jinuk Choi (ORCID: https://orcid.org/0000-0002-2070-8466)
- Seonghyeon Park
- Gyoung Hwa Jeong
Institutions
- Luoyang Normal University (CN)
Publication Details
- Journal
- Physical Chemistry Chemical Physics
- Published
- 2025-01-01
- DOI
- https://doi.org/10.1039/d5cp01408e
- Citations
- 9
- Primary Topic
- CO2 Reduction Techniques and Catalysts
- Type
- article
- Field-Weighted Citation Impact
- 3.27
Funders
- National Research Foundation of Korea
- Korea Institute of Energy Technology Evaluation and Planning