Chronopotentiometric Approach of CO2 Reduction in Molten Carbonates

被引:6
|
作者
Melendez-Ceballos, A. [1 ]
Brouzgou, A. [1 ,2 ]
Crapart, C. [1 ]
Albin, V. [1 ]
Lair, V. [1 ]
Cassir, M. [1 ]
机构
[1] PSL Res Univ, Chim Paristech CNRS, Inst Rech Chim Paris, F-75231 Paris 05, France
[2] Univ Thessaly, Thessaly, Greece
关键词
ELECTROCHEMICAL REDUCTION; ELECTRODE-REACTIONS; OXYGEN REDUCTION; FUEL-CELLS; DIOXIDE; CAPTURE; CONVERSION;
D O I
10.1149/2.0241708jes
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
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.
引用
收藏
页码:H5175 / H5182
页数:8
相关论文
共 50 条
  • [1] Thermodynamic and experimental approach of electrochemical reduction of CO2 in molten carbonates
    Chery, D.
    Albin, V.
    Lair, V.
    Cassir, M.
    [J]. INTERNATIONAL JOURNAL OF HYDROGEN ENERGY, 2014, 39 (23) : 12330 - 12339
  • [2] Mechanistic approach of the electrochemical reduction of CO2 into CO at a gold electrode in molten carbonates by cyclic voltammetry
    Chery, D.
    Albin, V.
    Melendez-Ceballos, A.
    Lair, V.
    Cassir, M.
    [J]. INTERNATIONAL JOURNAL OF HYDROGEN ENERGY, 2016, 41 (41) : 18706 - 18712
  • [3] CO2 electrochemical reduction into CO or C in molten carbonates: a thermodynamic point of view
    Chery, D.
    Lair, V.
    Cassir, M.
    [J]. ELECTROCHIMICA ACTA, 2015, 160 : 74 - 81
  • [4] Overview on CO2 valorization: challenge of molten carbonates
    Chery, Deborah
    Lair, Virginie
    Cassir, Michel
    [J]. FRONTIERS IN ENERGY RESEARCH, 2015,
  • [5] Electrochemical investigations on CO2 reduction mechanism in molten carbonates in view of H2O/CO2 co-electrolysis
    Meskine, H.
    Albin, V
    Cassir, M.
    Ringuede, A.
    Lair, V
    [J]. INTERNATIONAL JOURNAL OF HYDROGEN ENERGY, 2021, 46 (28) : 14944 - 14952
  • [6] Reactivity of CO2 in molten alkali carbonates: A DFT study
    Corradini, Dario
    Coudert, Francois-Xavier
    Vuilleumier, Rodolphe
    [J]. ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY, 2015, 250
  • [7] Wastepaper gasification with CO2 or steam using catalysts of molten carbonates
    Iwaki, H
    Ye, SF
    Katagiri, H
    Kitagawa, K
    [J]. APPLIED CATALYSIS A-GENERAL, 2004, 270 (1-2) : 237 - 243
  • [8] Study on the removal of CO2 by Electrochemical Cell with Molten Carbonates as Electrolyte
    陆岗
    陈晓勇
    路琼华
    李盘生
    [J]. 华东理工大学学报(自然科学版), 1996, (04) : 383 - 387
  • [9] DETERMINATION OF CO2 DISSOCIATION PRESSURES OF MOLTEN CARBONATES BY AN EMF TECHNIQUE
    LORENZ, PK
    JANZ, GJ
    [J]. ELECTROCHIMICA ACTA, 1970, 15 (12) : 2001 - &
  • [10] Enhanced kinetics of CO2 electro-reduction on a hollow gas bubbling electrode in molten ternary carbonates
    Gao, Muxing
    Deng, Bowen
    Chen, Zhigang
    Tao, Meng
    Wang, Dihua
    [J]. ELECTROCHEMISTRY COMMUNICATIONS, 2019, 100 : 81 - 84