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  •   University of Thessaly Institutional Repository
  • Επιστημονικές Δημοσιεύσεις Μελών ΠΘ (ΕΔΠΘ)
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  •   University of Thessaly Institutional Repository
  • Επιστημονικές Δημοσιεύσεις Μελών ΠΘ (ΕΔΠΘ)
  • Δημοσιεύσεις σε περιοδικά, συνέδρια, κεφάλαια βιβλίων κλπ.
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Electrochemical reduction of carbon dioxide at nanostructured SnO2/carbon aerogels: The effect of tin oxide content on the catalytic activity and formate selectivity

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Author
Yu J., Liu H., Song S., Wang Y., Tsiakaras P.
Date
2017
Language
en
DOI
10.1016/j.apcata.2017.07.043
Keyword
Aerogels
Carbon dioxide
Catalysts
Efficiency
Electrolytic reduction
Nanocrystals
Reduction
Tin
Tin dioxide
Tin oxides
Active ingredients
Control potential
Electrochemical reductions
Faradaic efficiencies
Hydrothermal methods
Oxide contents
Tin oxide nanocrystals
Value-added chemicals
Catalyst activity
Elsevier B.V.
Metadata display
Abstract
Electrochemical reduction of CO2 has been considered as a promising method for the production of value-added chemicals. In this work, the electrochemical reduction of CO2 to formate is carried out over novel carbon aerogel supported SnO2 nanocrystals prepared by a facile hydrothermal method. The as prepared materials exhibit good catalytic activity and high formate selectivity. It is found that the content of SnO2 plays an important role in the whole process, in which the formate is the exclusive product. At low SnO2 content the catalyst shows poor activity due to the lack of active ingredients, while at high SnO2 content it results in a dramatic decrease of the faradaic efficiency for the formate because of the blockage of part of active sites due to the agglomeration and poor conductivity of SnO2. It is also found that the optimized SnO2/CA-80 with 28.1 wt.% SnO2 leads to the best performance, offering a relatively high faradaic efficiency of ∼76% for the formate formation in 1.0 mol/L KHCO3 at −0.96 V (vs. RHE). Moreover, the above catalyst exhibits excellent stability during the control potential electrolysis for 12 h. © 2017 Elsevier B.V.
URI
http://hdl.handle.net/11615/80901
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