Web of Science: 2 cites, Scopus: 2 cites, Google Scholar: cites,
An in operando study of chemical expansion and oxygen surface exchange rates in epitaxial GdBaCo2O5.5 electrodes in a solid-state electrochemical cell by time-resolved X-ray diffraction
Chatterjee, Arindom (Institut Català de Nanociència i Nanotecnologia)
Caicedo Roque, José Manuel (Institut Català de Nanociència i Nanotecnologia)
Ballesteros, Belén (Institut Català de Nanociència i Nanotecnologia)
Santiso, José (Institut Català de Nanociència i Nanotecnologia)

Data: 2018
Resum: This report explores the fundamental characteristics of epitaxial thin films of a mixed ionic electronic conducting GdBaCoO (GBCO) material with a layered perovskite structure, relevant for use as an active electrode for the oxygen reduction and evolution reactions in electrochemical devices. Time-resolved X-ray diffraction in combination with voltage step chrono-amperometric measurements in a solid state electrochemical cell provides a deeper insight into the chemical expansion mechanism in the GBCO electrode. The chemical expansion coefficient along the c-axis, α, shows a negative value upon the compound oxidation contrary to standard perovskite materials with disordered oxygen vacancies. Chemical expansion also shows a remarkable asymmetry from α = -0. 037 to -0. 014 at δ < 0 and δ > 0, respectively. This change in chemical expansion is an indication of a different mechanism of the structural changes associated with the variable Co cation oxidation state from Co → Co → Co. Since redox reactions are dominated by oxygen surface exchange between the GBCO electrode and gas atmosphere, monitoring the time response of the structural changes allows for direct determination of oxygen reduction and evolution reaction kinetics. The reaction kinetics are progressively slowed down upon reduction in the δ < 0 oxygen stoichiometry region, while they maintain a high catalytic activity in the δ > 0 region, in agreement with the structural changes and the electronic carrier delocalization when crossing δ = 0. This work validates the time-resolved XRD technique for fast and reversible measurements of electrode activity in a wide range of oxygen non-stoichiometry in a solid-state electrochemical cell operating under realistic working conditions.
Nota: Número d'acord de subvenció MINECO/MAT2016-77100-C2-1-P
Nota: Número d'acord de subvenció EC/H2020/645658
Nota: Número d'acord de subvenció MINECO/SEV-2013-0295
Drets: Tots els drets reservats.
Llengua: Anglès
Document: article ; recerca ; acceptedVersion
Matèria: Amperometric measurements ; Electrochemical devices ; Fundamental characteristics ; Layered perovskite structure ; Oxygen non-stoichiometries ; Oxygen reduction and evolution reactions ; Solid-state electrochemical cells ; Time resolved x-ray diffractions
Publicat a: Journal of materials chemistry, Vol. 6, Issue 26 (July 2018) , p. 12430-12439, ISSN 2050-7496

DOI: 10.1039/c8ta02790k

30 p, 1.4 MB

El registre apareix a les col·leccions:
Documents de recerca > Documents dels grups de recerca de la UAB > Centres i grups de recerca (producció científica) > Ciències > Institut Català de Nanociència i Nanotecnologia (ICN2)
Articles > Articles de recerca
Articles > Articles publicats

 Registre creat el 2020-06-03, darrera modificació el 2020-09-18

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