Electrochemical Reduction of Carbon Dioxide by in-situ Generated Hydrogen at Porous Cu-Fe Foam-Like Catalysts: Efficiency Towards Formic Acid Formation | ||
| Egyptian Journal of Chemistry | ||
| Articles in Press, Accepted Manuscript, Available Online from 02 November 2025 | ||
| Document Type: Original Article | ||
| DOI: 10.21608/ejchem.2025.401455.12010 | ||
| Authors | ||
| Mohamed Ghaith1; Ahmed Abdelrahim1; Aya Saada2; Mohamed El Saied3; Attia M Attia4; Ahmed El-Sherif5; Mohamed S. El-Deab* 6 | ||
| 1Department of Chemistry, Faculty of Science, Cairo University | ||
| 2Faculty of Energy and Environmental Engineering, The British University in Egypt | ||
| 3Egyptian Petroleum Research Institute, Nasr City, Cairo, Egypt | ||
| 4The British University in Egypt | ||
| 5organometallic Department of Chemistry, Faculty of Science, Cairo University, Cairo, Egypt | ||
| 6Department of Chemistry, Faculty of Science, Cairo University, Cairo, Egypt | ||
| Abstract | ||
| This paper addresses the electrocatalytic reduction of carbon dioxide (CO2ER) to combat the excessive emissions from heavy industries like steel and cement. This is much done with an aim to prepare liquid fuels (e.g., formic acid) by electrochemical reduction of CO2 (CO2 ER) by the in-situ generated hydrogen gas at binary Cu-Fe porous catalysts. The dynamic hydrogen bubble template (DHBT) technique was used to prepare the porous catalyst layer atop a planar Cu electrode. The simultaneous generation of hydrogen gas at the Cu-Fe binary porous catalyst assisted in directing the selectivity of CO2ER towards formic acid. The exhaustive electrolysis (for 5 hr at –1.7 V) of CO2-saturated 0.1 M NaHCO3 resulted in about 0.028 M formic acid as a detectable liquid reduction product of CO2 at Cu60Fe40, compared to about 0.015 M at the Cu electrode, as revealed from electrochemical analysis. The observed enhancement towards formic acid formation was rationalized by DFT calculations. That is the addition of Fe to Cu enhances the affinity of CO2 adsorption on the surface of the Fe-Cu catalyst, together with less adsorptivity (lowering of adsorption energy) of the generated hydrogen radicals (reactive reducing species), allowing for the favorable interaction with CO2•– radical anion on the binary catalyst surface. Thus, it promotes the production of formic acid. | ||
| Keywords | ||
| CO2 electroreduction; formic acid; 3D porous catalysts; electrocatalysts; Cu-based electrocatalysts | ||
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