Hong Wesley T, Gadre Milind, Lee Yueh-Lin, Biegalski Michael D, Christen Hans M, Morgan Dane, Shao-Horn Yang
Department of Materials Science & Engineering, University of Wisconsin-Madison , 1509 University Avenue, Madison, Wisconsin 53706, United States.
Center for Nanophase Materials Sciences, Oak Ridge National Laboratory , Oak Ridge, Tennessee 37831, United States.
J Phys Chem Lett. 2013 Aug 1;4(15):2493-2499. doi: 10.1021/jz401271m. Epub 2013 Jul 16.
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 LaCoO 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 LaCoO. 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.
氧表面交换的缓慢动力学阻碍了高温氧电催化装置(如固体氧化物燃料电池和氧分离膜)的效率。对与催化活性相关的材料特性进行系统研究有助于合理设计高活性阴极材料。在此,我们探索将LaCoO薄膜作为一种模型体系,通过应变诱导Co自旋态的变化来调节催化活性。我们证明拉曼光谱可用于探测不同温度下的Co-O键强度,以确定LaCoO的相对自旋占有率。我们发现应变可用于降低自旋转变温度,并促进更高自旋态的占据,从而削弱Co-O键。薄膜中Co-O键强度的降低和自旋矩的增加导致氧表面交换动力学显著增强,提高了多达两个数量级。