Electrochemical Reduction of CO2 Using Polycrystalline Phosphorus-Doped Diamond Electrode

In this study, we investigated the electrochemical reduction of carbon dioxide (CO2) using a phosphorus-doped polycrystalline diamond (PDD) electrode and compared it with a conventional boron-doped diamond (BDD) electrode. In the reduction reaction of CO2 in a 0.5 M KCl aqueous solution, the PDD electrode showed high selectivity for formic acid production over a wide potential range. This tendency was particularly evident at potentials below −1.8 V (vs. RHE). Moreover, at more negative potentials of −2.4 V and −2.6 V, formic acid remained the dominant product, while hydrogen evolution was the main reaction on the BDD electrode at the negative potentials. Similarly, in electrochemical reduction using an 0.1 M KClO4 aqueous solution, carbon monoxide was confirmed to be a major product, and hydrogen generation was effectively suppressed in a more negative potential range. In other words, PDD is a promising electrode material that can efficiently convert CO2 into valuable chemicals while suppressing hydrogen evolution, even in negative potential regions.

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Publication Details

Journal
Catalysts
Published
2026-01-02
DOI
https://doi.org/10.3390/catal16010054
Primary Topic
CO2 Reduction Techniques and Catalysts
Type
article
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Electrochemical Reduction of CO2 Using Polycrystalline Phosphorus-Doped Diamond Electrode

Yasuaki. Einaga, Tomokiyo Moriguchi
Catalysts
CO2 Reduction Techniques and Catalysts
article

Electrochemical Reduction of CO2 Using Polycrystalline Phosphorus-Doped Diamond Electrode

Yasuaki. Einaga, Tomokiyo Moriguchi
article en

Abstract

In this study, we investigated the electrochemical reduction of carbon dioxide (CO2) using a phosphorus-doped polycrystalline diamond (PDD) electrode and compared it with a conventional boron-doped diamond (BDD) electrode. In the reduction reaction of CO2 in a 0.5 M KCl aqueous solution, the PDD electrode showed high selectivity for formic acid production over a wide potential range. This tendency was particularly evident at potentials below −1.8 V (vs. RHE). Moreover, at more negative potentials of −2.4 V and −2.6 V, formic acid remained the dominant product, while hydrogen evolution was the main reaction on the BDD electrode at the negative potentials. Similarly, in electrochemical reduction using an 0.1 M KClO4 aqueous solution, carbon monoxide was confirmed to be a major product, and hydrogen generation was effectively suppressed in a more negative potential range. In other words, PDD is a promising electrode material that can efficiently convert CO2 into valuable chemicals while suppressing hydrogen evolution, even in negative potential regions.

CatalystsVol. 16(1)
Suzuki (Japan) (JP), Keio University (JP)
Openalex Percentile: Top 100%
CO2 Reduction Techniques and Catalysts
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