TY - JOUR
T1 - Effects of solar irradiation on thermally driven CO2 methanation using Ni/CeO2–based catalyst
AU - Golovanova, Viktoria
AU - Spadaro, Maria Chiara
AU - Arbiol, Jordi
AU - Golovanov, Viacheslav
AU - Rantala, Tapio T.
AU - Andreu, Teresa
AU - Morante, Joan Ramón
N1 - Funding Information:
This work has been done in the framework of the doctorate programme in Materials Science of the Autonomous University of Barcelona. V. Golovanova has received funding from the European Union's Horizon 2020 research and innovation programme under the Marie Sk?odowska-Curie grant agreement No 754397. Authors acknowledge Generalitat de Catalunya for financial support through the CERCA Programme, M2E (2017 SGR 1246) and the CSC ? IT Center for Science, Espoo, Finland for provided resources. IREC also acknowledges additional support by the European Regional Development Funds (ERDF, FEDER) and by MINECO coordinated projects MAT2014-59961-C2, ENE2016-80788-C5-5-R and ENE2017-85087-C3. M. C. Spadaro and J. Arbiol acknowledge funding from Generalitat de Catalunya 2017?SGR 327. ICN2 is supported by the Severo Ochoa programme from Spanish MINECO (Grant No. SEV-2017-0706) and is funded by the CERCA Programme / Generalitat de Catalunya. M. C. Spadaro has received funding from the European Union's Horizon 2020 research and innovation programme under the Marie Sk?odowska-Curie grant agreement No. 754510 (PROBIST) and the Severo Ochoa programme.
Publisher Copyright:
© 2021 The Authors
PY - 2021/8/15
Y1 - 2021/8/15
N2 - Utilization of the renewable energy sources is one of the main challenges in the state-of-the-art technologies for CO2 recycling. Here we have taken advantage of the solar light harvesting in the thermocatalytic approach to carbon dioxide methanation. The large-surface-area Ni/CeO2 catalyst produced by a scalable low-cost method was characterized and tested in the dark and under solar light irradiation conditions. Light-assisted CO2 conversion experiments as well as in-situ DRIFT spectrometry, performed at different illumination intensities, have revealed a dual effect of the incident photons on the catalytic properties of the two-component Ni/CeO2 catalyst. On the one hand, absorbed photons induce a localized surface plasmon resonance in the Ni nanoparticles followed by dissipation of the heat to the oxide matrix. On the other hand, the illumination activates the photocatalytic properties of the CeO2 support, which leads to an increase in the concentration of the intermediates being precursor for methane production. Analysis of the methane production at different temperatures and illumination conditions has shown that the methanation reaction in our case is controlled by a photothermally-activated process. The used approach has allowed us to increase the reaction rate up to 2.4 times and consequently to decrease the power consumption by 20 % under solar illumination, thus replacing the conventional thermal activation of the reaction with a green energy source.
AB - Utilization of the renewable energy sources is one of the main challenges in the state-of-the-art technologies for CO2 recycling. Here we have taken advantage of the solar light harvesting in the thermocatalytic approach to carbon dioxide methanation. The large-surface-area Ni/CeO2 catalyst produced by a scalable low-cost method was characterized and tested in the dark and under solar light irradiation conditions. Light-assisted CO2 conversion experiments as well as in-situ DRIFT spectrometry, performed at different illumination intensities, have revealed a dual effect of the incident photons on the catalytic properties of the two-component Ni/CeO2 catalyst. On the one hand, absorbed photons induce a localized surface plasmon resonance in the Ni nanoparticles followed by dissipation of the heat to the oxide matrix. On the other hand, the illumination activates the photocatalytic properties of the CeO2 support, which leads to an increase in the concentration of the intermediates being precursor for methane production. Analysis of the methane production at different temperatures and illumination conditions has shown that the methanation reaction in our case is controlled by a photothermally-activated process. The used approach has allowed us to increase the reaction rate up to 2.4 times and consequently to decrease the power consumption by 20 % under solar illumination, thus replacing the conventional thermal activation of the reaction with a green energy source.
KW - CO methanation
KW - DRIFTS
KW - LSPR
KW - Nickel-ceria catalyst
KW - Photothermal effect
U2 - 10.1016/j.apcatb.2021.120038
DO - 10.1016/j.apcatb.2021.120038
M3 - Article
AN - SCOPUS:85102152277
SN - 0926-3373
VL - 291
JO - Applied Catalysis B: Environmental
JF - Applied Catalysis B: Environmental
M1 - 120038
ER -