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Tuning the Spin State in LaCoO3 Thin Films for Enhanced High-Temperature Oxygen Electrocatalysis.
Hong, Wesley T; Gadre, Milind; Lee, Yueh-Lin; Biegalski, Michael D; Christen, Hans M; Morgan, Dane; Shao-Horn, Yang.
Afiliação
  • Gadre M; Department of Materials Science & Engineering, University of Wisconsin-Madison , 1509 University Avenue, Madison, Wisconsin 53706, United States.
  • Biegalski MD; Center for Nanophase Materials Sciences, Oak Ridge National Laboratory , Oak Ridge, Tennessee 37831, United States.
  • Christen HM; Center for Nanophase Materials Sciences, Oak Ridge National Laboratory , Oak Ridge, Tennessee 37831, United States.
  • Morgan D; Department of Materials Science & Engineering, University of Wisconsin-Madison , 1509 University Avenue, Madison, Wisconsin 53706, United States.
J Phys Chem Lett ; 4(15): 2493-2499, 2013 Aug 01.
Article em En | MEDLINE | ID: mdl-28803480
ABSTRACT
The slow kinetics of oxygen surface exchange hinders the efficiency of high-temperature oxygen electrocatalytic devices such as solid oxide fuel cells and oxygen separation membranes. Systematic investigations of material properties that link to catalytic activity can aid in the rational design of highly active cathode materials. Here, we explore LaCoO3 thin films as a model system for tuning catalytic activity through strain-induced changes in the Co spin state. We demonstrate that Raman spectroscopy can be used to probe the Co-O bond strength at different temperatures to determine the relative spin occupancies of LaCoO3. We find that strain can be used to reduce the spin transition temperature and promote the occupation of higher spin states that weaken the Co-O bond. The decrease in Co-O bond strength and increased spin moment of the thin films result in significant enhancements of the oxygen surface exchange kinetics by up to 2 orders of magnitude.
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Texto completo: 1 Bases de dados: MEDLINE Idioma: En Revista: J Phys Chem Lett Ano de publicação: 2013 Tipo de documento: Article

Texto completo: 1 Bases de dados: MEDLINE Idioma: En Revista: J Phys Chem Lett Ano de publicação: 2013 Tipo de documento: Article