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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)

Date: 2018
Abstract: 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.
Note: Número d'acord de subvenció MINECO/MAT2016-77100-C2-1-P
Note: Número d'acord de subvenció EC/H2020/645658
Note: Número d'acord de subvenció MINECO/SEV-2013-0295
Rights: Tots els drets reservats.
Language: Anglès
Document: article ; recerca ; acceptedVersion
Subject: 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
Published in: Journal of materials chemistry, Vol. 6, Issue 26 (July 2018) , p. 12430-12439, ISSN 2050-7496

DOI: 10.1039/c8ta02790k


Postprint
30 p, 1.4 MB

The record appears in these collections:
Research literature > UAB research groups literature > Research Centres and Groups (scientific output) > Experimental sciences > Catalan Institute of Nanoscience and Nanotechnology (ICN2)
Articles > Research articles
Articles > Published articles

 Record created 2020-06-03, last modified 2020-11-07



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