Ru exsolution in substituted La0.75Sr0.25Cr0.5Mn0.5O3-δ compound as anode material for an IT-SOFCs
- 1. Institut des Matériaux Jean Rouxel (IMN), Université de Nantes, 2, rue de la Houssinière, BP 32229, 44322, Nantes (France)
- 2. Laboratory of Interaction Materials and Environment (LIME), University of Jijel (Algeria)
- 3. Department of Electroceramics, Instituto de Cerámica y Vidrio (CSIC), C/Kelsen 5. Campus de Cantoblanco, 28049, Madrid (Spain)
- 4. Department of Oxides and Fluorides, Institute of Molecules and Materials Le Mans (IMMM) Université du Maine, Avenue Olivier Messiaen, 72085, Le Mans (France)
Description
Highlights: • Synthesis of a Ru substituted La0.75Sr0.25Cr0.5Mn0.5O3-δ compound is presented and its total conductivity is measured. • The total conductivity of LSC0.4MRu0.1 is mainly electronic and is much higher than that of LSCM0.3Ni0.2 and LSCM. • LSC0.4MRu0.1 presents a dispersion of Ru particles on the surface of its grain after reduction at 1000 °C. • LSC0.4MRu0.1 symmetrical cell exhibits the lowest Rp, 0.087 Ω cm2 under Ar/H2 5% and 0.04 Ω cm2 under methane at 600 °C. In this study, the synthesis of La0.75Sr0.25Cr0.4Mn0.5Ru0.1O3-δ a (LSC0.4MRu0.1) compound is presented and its total conductivity is measured and compared with that of La0.75Sr0.25Cr0.5Mn0.5O3-δ (LSCM) and the Ni-substituted compound La0.75Sr0.25Cr0.5Mn0.3Ni0.2O3-δ (LSCM0.3Ni0.2). While the substitution of Ni decreased LSCM conductivity under a reducing atmosphere, an increase of the total conductivity of Ru substituted phase is evidenced. The reduction of Ni and Ru-substituted LSCM under Ar/H2 5% up to 800 °C or 1000 °C respectively leads to the exsolution of nanoparticles, but also to a slight decomposition for the Ru-substituted compound. However, the use of these reduced materials as anode for solid oxide fuel cell (SOFC) in symmetrical cells based on Ce0.9Gd0.1O1.95 (CGO) electrolyte implies not reducing the total system at a temperature higher than 600 °C to avoid ceria reduction. The solution consists of pre-reducing the electrode materials at their exsolution temperature before casting them on CGO thin disk. Under reductive atmospheres, Electrochemical impedance spectroscopy study of symmetrical cells suggests that the exsolution approach improves the adsorption of gaseous species compared to LSCM. LSC0.4MRu0.1 symmetrical cell exhibits the lowest polarization resistance, 0.087 Ω cm2 under Ar/H2 (5%) and 0.044 Ω cm2 under methane at 600 °C.
Availability note (English)
Available from http://dx.doi.org/10.1016/j.matchemphys.2021.124724Additional details
Identifiers
- DOI
- 10.1016/j.matchemphys.2021.124724;
- PII
- S0254058421005071;
Publishing Information
- Journal Title
- Materials Chemistry and Physics (Print)
- Journal Volume
- 268
- Journal Page Range
- vp.
- ISSN
- 0254-0584
- CODEN
- MCHPDR
INIS
- Country of Publication
- Switzerland
- Country of Input or Organization
- International Atomic Energy Agency (IAEA)
- INIS RN
- 54028088
- Subject category
- S36: MATERIALS SCIENCE;
- Descriptors DEI
- ADSORPTION; CERIUM OXIDES; COMPARATIVE EVALUATIONS; DECOMPOSITION; ELECTROCHEMISTRY; ELECTROLYTES; METHANE; NANOPARTICLES; POLARIZATION; SOLID OXIDE FUEL CELLS; SOLUTIONS; SPECTROSCOPY; SURFACES; SYNTHESIS
- Descriptors DEC
- ALKANES; CERIUM COMPOUNDS; CHALCOGENIDES; CHEMICAL REACTIONS; CHEMISTRY; DIRECT ENERGY CONVERTERS; DISPERSIONS; ELECTROCHEMICAL CELLS; EVALUATION; FUEL CELLS; HIGH-TEMPERATURE FUEL CELLS; HOMOGENEOUS MIXTURES; HYDROCARBONS; MIXTURES; ORGANIC COMPOUNDS; OXIDES; OXYGEN COMPOUNDS; PARTICLES; RARE EARTH COMPOUNDS; SOLID ELECTROLYTE FUEL CELLS; SORPTION
Optional Information
- Copyright
- Copyright (c) 2021 Elsevier B.V. All rights reserved.