Carbon capture and valorization is a new route increasingly discussed to reduce greenhouse gas emissions. One of the paths foreseen for CO2 valorization is its transformation into fuels by electrochemical reduction of carbon dioxide. In this approach, molten carbonates are of particular interest since they can be used to capture CO2 molecule because of its high solubility; hence, valorization by electrolysis is possible in molten carbonate media. To better understand CO2 reduction, chronopotentiometric and chronoamperometric techniques were used at gold and graphite electrodes immersed in four alkali carbonate eutectics, Li-Na, Li-K, Li-Na-K and Na-K. The results complemented a previous work based on cyclic voltammetry and confirmed the existence of a main CO2 reduction phenomena around -1.2 V vs Ag/Ag+ that involves two one-electron steps or a two-electron unique step. Transition time analysis showed that the reduction mechanism is either simultaneous reduction of CO2 adsorbed and diffusion species or rapid equilibrium between adsorbed and diffusing species. Furthermore, we identified another electrochemical system involving adsorbed CO2 and CO at higher potentials. In summary, we have succeeded in proving and precising some previous results, as well as identifying reduction mechanisms. (C) The Author(s) 2017. Published by ECS. All rights reserved.
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PSL Res Univ, CNRS, Inst Rech Chim Paris, Chim ParisTech, 11 Rue Pierre & Marie Cone, F-75005 Paris, FrancePSL Res Univ, CNRS, Inst Rech Chim Paris, Chim ParisTech, 11 Rue Pierre & Marie Cone, F-75005 Paris, France
Chery, Deborah
Lair, Virginie
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PSL Res Univ, CNRS, Inst Rech Chim Paris, Chim ParisTech, 11 Rue Pierre & Marie Cone, F-75005 Paris, FrancePSL Res Univ, CNRS, Inst Rech Chim Paris, Chim ParisTech, 11 Rue Pierre & Marie Cone, F-75005 Paris, France
Lair, Virginie
Cassir, Michel
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PSL Res Univ, CNRS, Inst Rech Chim Paris, Chim ParisTech, 11 Rue Pierre & Marie Cone, F-75005 Paris, FrancePSL Res Univ, CNRS, Inst Rech Chim Paris, Chim ParisTech, 11 Rue Pierre & Marie Cone, F-75005 Paris, France
机构:Nagoya Univ, Res Ctr Adv Energy Convers, Chikusa Ku, Nagoya, Aichi 4648603, Japan
Iwaki, H
Ye, SF
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Nagoya Univ, Res Ctr Adv Energy Convers, Chikusa Ku, Nagoya, Aichi 4648603, JapanNagoya Univ, Res Ctr Adv Energy Convers, Chikusa Ku, Nagoya, Aichi 4648603, Japan
Ye, SF
Katagiri, H
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机构:Nagoya Univ, Res Ctr Adv Energy Convers, Chikusa Ku, Nagoya, Aichi 4648603, Japan
Katagiri, H
Kitagawa, K
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机构:Nagoya Univ, Res Ctr Adv Energy Convers, Chikusa Ku, Nagoya, Aichi 4648603, Japan
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Wuhan Univ, Sch Resource & Environm Sci, Hubei Int Sci & Technol Cooperat Base Sustainable, Wuhan 430072, Hubei, Peoples R ChinaWuhan Univ, Sch Resource & Environm Sci, Hubei Int Sci & Technol Cooperat Base Sustainable, Wuhan 430072, Hubei, Peoples R China
Gao, Muxing
Deng, Bowen
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Wuhan Univ, Sch Resource & Environm Sci, Hubei Int Sci & Technol Cooperat Base Sustainable, Wuhan 430072, Hubei, Peoples R ChinaWuhan Univ, Sch Resource & Environm Sci, Hubei Int Sci & Technol Cooperat Base Sustainable, Wuhan 430072, Hubei, Peoples R China
Deng, Bowen
Chen, Zhigang
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Wuhan Univ, Sch Resource & Environm Sci, Hubei Int Sci & Technol Cooperat Base Sustainable, Wuhan 430072, Hubei, Peoples R ChinaWuhan Univ, Sch Resource & Environm Sci, Hubei Int Sci & Technol Cooperat Base Sustainable, Wuhan 430072, Hubei, Peoples R China
Chen, Zhigang
Tao, Meng
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Arizona State Univ, Sch Elect Comp & Energy Engn, Tempe, AZ 85287 USAWuhan Univ, Sch Resource & Environm Sci, Hubei Int Sci & Technol Cooperat Base Sustainable, Wuhan 430072, Hubei, Peoples R China
Tao, Meng
Wang, Dihua
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Wuhan Univ, Sch Resource & Environm Sci, Hubei Int Sci & Technol Cooperat Base Sustainable, Wuhan 430072, Hubei, Peoples R ChinaWuhan Univ, Sch Resource & Environm Sci, Hubei Int Sci & Technol Cooperat Base Sustainable, Wuhan 430072, Hubei, Peoples R China