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carbon dioxide
M.D. González-Hernández 1,2*, Eileen Yu2, A.P. de los Ríos1
1 School of Chemical Engineering and Advanced Materials, University of Newcastle Upon Tyne, Newcastle NE1 7RU, United Kingdom
2 Department of Chemical Engineering, Faculty of Chemistry, University of Murcia, Campus de Espinardo, E-30100, Murcia, Spain
*Corresponding author. Tel.: +34 868 889 112; fax: +34 968 364 148. E-mail address: mariadelia.gonzalez@um.es
Introduction
The CO2 could be considered as an almost infinite source of carbon for chemical industry in the production of alcohols, aldehydes, hydrocarbons
or carboxylic acids. However, only 1% of entire atmospheric CO2 is used for chemical synthesis. Mainly this is due to its high chemical
inertness and the difficulties associated with its capture. Despite these, many scientists are working to convert greenhouse gasses into
commercially valuable compounds since this could make removal of excess CO2 from the atmosphere into a profitable industry.
For that reason the electrocatalytic reduction of CO2 to liquid fuels, chemical feedstock and valuable chemicals has attracted growing
interest in CO2 capture in the past several years. These electrochemical processes offer good reaction selectivity and reduced cost because of
possibility of direct control of electrode surface free energy through electrode potential.
For this research project we studied the synthesis of catalysts for CO2 electroreduction to methanol, all of them based on cuprous oxide (Cu2O)
modified surface because this compound has previously shown specific catalytic activity for this electrochemical reaction. The same project also
focused on developing a catalyst for CO2 electroreduction to formic acid. For this purpose a metallic complex was synthesized belonging to the
aminoftalocianes group which contain metals known to have good catalytic activity for CO2 electroreduction [2,3].