Defect-surface engineering of La-doped ceria for microwave-assisted hydrogen production

[EN] Hydrogen plays a pivotal role in decarbonizing the energy and chemical sectors, yet current production methods are limited by high temperatures and energy demands. Microwave-assisted thermochemical redox cycles offer a promising low-temperature, contactless alternative by coupling electromagnet...

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Detalhes bibliográficos
Autores: Domínguez-Saldaña, Aitor|||0000-0001-7539-7493, Carrillo-Del Teso, Alfonso Juan, Balaguer Ramirez, Maria|||0000-0002-7098-9235, García-Baños, Beatriz|||0000-0001-7862-3417, Plaza González, Pedro José|||0000-0002-2623-0782, Catalá Civera, José Manuel|||0000-0002-0617-1762, Serra Alfaro, José Manuel|||0000-0002-1515-1106, Navarrete Algaba, Laura, Santos, Joaquin, Catalán-Martínez, David
Tipo de documento: artigo
Data de publicação:2026
País:España
Recursos:Universitat Politècnica de València (UPV)
Repositório:RiuNet. Repositorio Institucional de la Universitat Politécnica de Valéncia
Idioma:inglês
OAI Identifier:oai:dnet:riunet______::ab2eb09b71bf51414de412d587092bb4
Acesso em linha:https://riunet.upv.es/handle/10251/234416
Access Level:Acceso aberto
Palavra-chave:Microwave-assisted thermochemical cycles
Hydrogen production
Lanthanum-doped ceria
Oxygen vacancies
Redox kinetics
Defect engineering
Descrição
Resumo:[EN] Hydrogen plays a pivotal role in decarbonizing the energy and chemical sectors, yet current production methods are limited by high temperatures and energy demands. Microwave-assisted thermochemical redox cycles offer a promising low-temperature, contactless alternative by coupling electromagnetic energy with reducible oxides. In this study, we explore La-doped ceria (Ce1-xLaxO2-delta) as a tunable platform to enhance microwave-driven hydrogen production. We demonstrate that introducing La3+ into the ceria lattice reduces the bandgap and increases dielectric permittivity, enabling Ce4+ to Ce3+ reduction at temperatures as low as 110 degrees C. Among the series, Ce0.9La0.1O1.95 exhibits optimal performance, balancing high ionic mobility and microwave absorption. Combined with tailored surface area, this composition achieves an unprecedented hydrogen production rate of 2.60 mL g-1 per cycle at temperatures below 400 degrees C. Correlations between dopant concentration, polarization behavior, and redox kinetics reveal the key role of band structure breakdown and defect formation in driving non-equilibrium reduction. Our findings uncover mechanistic insights into microwave-material interactions and establish design principles for next-generation redox materials. This approach provides a framework for scalable, electrified hydrogen production via electronic structure and defect engineering in oxide systems.