Electrocatalytic reduction of CO2 to formate using particulate Sn electrodes: Effect of metal loading and particle size

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Título: Electrocatalytic reduction of CO2 to formate using particulate Sn electrodes: Effect of metal loading and particle size
Autor/es: Castillo, Andrés del | Alvarez-Guerra, Manuel | Solla-Gullón, José | Sáez, Alfonso | Montiel, Vicente | Irabien, Ángel
Grupo/s de investigación o GITE: Electroquímica Aplicada y Electrocatálisis
Centro, Departamento o Servicio: Universidad de Alicante. Departamento de Química Física | Universidad de Alicante. Instituto Universitario de Electroquímica
Palabras clave: Carbon dioxide | Formate | Tin particles | Electroreduction | Valorization
Área/s de conocimiento: Química Física
Fecha de publicación: 1-nov-2015
Editor: Elsevier
Cita bibliográfica: Applied Energy. 2015, 157: 165-173. doi:10.1016/j.apenergy.2015.08.012
Resumen: The development of electrochemical processes for the conversion of CO2 into value-added products allows innovative carbon capture & utilization (CCU) instead of carbon capture & storage (CCS). In addition, coupling this conversion with renewable energy sources would make it possible to chemically store electricity from these intermittent renewable sources. The electroreduction of CO2 to formate in aqueous solution has been performed using Sn particles deposited over a carbon support. The effect of the particle size and Sn metal loading has been evaluated using cyclic voltammetry and chronoamperometry. The selected electrode has been tested on an experimental filter-press type cell system for continuous and single pass CO2 electroreduction to obtain formate as main product at ambient pressure and temperature. Experimental results show that using electrodes with 0.75 mg Sn cm−2, 150 nm Sn particles, and working at a current density of 90 mA cm−2, it is possible to achieve rates of formate production over 3.2 mmol m−2 s−1 and faradaic efficiencies around 70% for 90 min of continuous operation. These experimental conditions allow formate concentrations of about 1.5 g L−1 to be obtained on a continuous mode and with a single pass of catholyte through the cell.
Patrocinador/es: This work was conducted under the framework of the Spanish Ministry of Science and Innovation Projects ENE2010-14828 and Spanish Ministry of Economy Competitiveness CTQ2013-48280-C3-1-R and CTQ2013-48280-C3-3-R. Andrés Del Castillo also acknowledges the research grant from University of Cantabria, co-financed by the Regional Government of Cantabria.
URI: http://hdl.handle.net/10045/53154
ISSN: 0306-2619 (Print) | 1872-9118 (Online)
DOI: 10.1016/j.apenergy.2015.08.012
Idioma: eng
Tipo: info:eu-repo/semantics/article
Derechos: © 2015 Elsevier Ltd.
Revisión científica: si
Versión del editor: http://dx.doi.org/10.1016/j.apenergy.2015.08.012
Aparece en las colecciones:INV - LEQA - Artículos de Revistas

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