Electrochemical Synthesis of Urea at Gas‐Diffusion Electrodes: IV. Simultaneous Reduction of Carbon Dioxide and Nitrate Ions with Various Metal Catalysts
Source abstract
Abstract
Simultaneous reduction of carbon dioxide and nitrate ions was examined at gas‐diffusion electrodes with various catalysts (Cr, Mo, Mn, Ru, Co, Rh, Ir, Ni, Pd, Pt, Cu, Ag, Au, Zn, Cd, In, Tl, Sn, and Pb). The formation of urea, CO, formic acid, nitrite ions, and ammonia at the gas‐diffusion electrodes with group 11–14 catalysts, except for Au, was found in the simultaneous reduction. The maximum faradaic efficiency of urea formation on Zn catalysts is approximately 35% at −1.75 V. The formation of urea at the gas‐diffusion electrodes with groups 6–10 catalysts was not found in the simultaneous reduction of and nitrate. Relationship of the ability for urea formation to the ability for CO and formation was investigated with various catalysts. The ability for urea formation with the catalysts depends on the ability for CO and formation. The catalysts with high ability for CO and formation could form large amounts of CO‐like and ammonia‐like precursors. The faradaic efficiency of urea formation for simultaneous reduction with nitrate ions is lower than that with nitrite ions. This result seems to be related to the ability for ammonia‐like precursor formation.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: CO2 Reduction Techniques and Catalysts · Ammonia Synthesis and Nitrogen Reduction · Electrocatalysts for Energy Conversion
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Affiliations
Department of Applied Chemistry, Faculty of Engineering, Yamanashi University, 4‐3‐11 Takeda, Kofu 400‐8511, Japan
References
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