The conversion of carbon dioxide into value-added products is progressively gaining momentum. Several strategies have been used to develop technologies that reduce the net emissions of CO2. The utilisation of CO2 could either contribute to carbon recycling. In this paper, the transformation of CO2 was investigated in a co-electrolysis cell constituted by a solid polymer electrolyte, a car-bon-supported CuO-Ag composite cathode and NiFeOx anode. Non-critical raw materials were synthesised according to the oxalate method and investigated in an alkaline environment. Low-carbon alcohols were obtained with a specific selectivity for ethanol and methanol over the CuO-Ag/KB cathode. The reaction rates at 1.6V and 1.8V cell voltages have been determined in steady-state experiments using NaHCO3 supporting electrolyte recirculated at the anode.
Bifunctional CuO-Ag/KB catalyst for the electrochemical re-duction of CO2 in an alkaline solid-state electrolysis cell
Sabrina Campagna Zignani
;Massimiliano Lo Faro;Alessandra Palella;Lorenzo Spadaro;Stefano Trocino;Carmelo Lo Vecchio;Antonino Salvatore Arico
2022
Abstract
The conversion of carbon dioxide into value-added products is progressively gaining momentum. Several strategies have been used to develop technologies that reduce the net emissions of CO2. The utilisation of CO2 could either contribute to carbon recycling. In this paper, the transformation of CO2 was investigated in a co-electrolysis cell constituted by a solid polymer electrolyte, a car-bon-supported CuO-Ag composite cathode and NiFeOx anode. Non-critical raw materials were synthesised according to the oxalate method and investigated in an alkaline environment. Low-carbon alcohols were obtained with a specific selectivity for ethanol and methanol over the CuO-Ag/KB cathode. The reaction rates at 1.6V and 1.8V cell voltages have been determined in steady-state experiments using NaHCO3 supporting electrolyte recirculated at the anode.File | Dimensione | Formato | |
---|---|---|---|
catalysts-12-00293.pdf
accesso aperto
Tipologia:
Versione Editoriale (PDF)
Licenza:
Creative commons
Dimensione
5.6 MB
Formato
Adobe PDF
|
5.6 MB | Adobe PDF | Visualizza/Apri |
I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.