Mehar Vikram, Edström Helen, Shipilin Mikhail, Hejral Uta, Wu Chengjun, Kadiri Aravind, Albertin Stefano, Hagman Benjamin, von Allmen Kim, Wiegmann Tim, Pfaff Sebastian, Drnec Jakub, Zetterberg Johan, Lundgren Edvin, Merte Lindsay R, Gustafson Johan, Weaver Jason F
Department of Chemical Engineering, University of Florida, Gainesville, Florida 32611, United States.
Synchrotron Radiation Research, Lund University, Box 118, SE-221 00 Lund, Sweden.
J Phys Chem Lett. 2023 Sep 28;14(38):8493-8499. doi: 10.1021/acs.jpclett.3c01958. Epub 2023 Sep 18.
The catalytic oxidation of CO and CH can be strongly influenced by the structures of oxide phases that form on metallic catalysts during reaction. Here, we show that an epitaxial PdO(100) structure forms at temperatures above 600 K during the oxidation of Pd(100) by gaseous O atoms as well as exposure to O-rich mixtures at millibar partial pressures. The oxidation of Pd(100) by gaseous O atoms preferentially generates an epitaxial, multilayer PdO(101) structure at 500 K, but initiating Pd(100) oxidation above 600 K causes an epitaxial PdO(100) structure to grow concurrently with PdO(101) and produces a thicker and rougher oxide. We present evidence that this change in the oxidation behavior is caused by a temperature-induced change in the stability of small PdO domains that initiate oxidation. Our discovery of the epitaxial PdO(100) structure may be significant for developing relationships among oxide structure, catalytic activity, and reaction conditions for applications of oxidation catalysis.
CO和CH的催化氧化会受到反应过程中在金属催化剂上形成的氧化物相结构的强烈影响。在此,我们表明,在高于600 K的温度下,气态O原子氧化Pd(100)以及在毫巴分压下暴露于富O混合物时,会形成外延PdO(100)结构。气态O原子氧化Pd(100)在500 K时优先生成外延多层PdO(101)结构,但在600 K以上引发Pd(100)氧化会导致外延PdO(100)结构与PdO(101)同时生长,并产生更厚且更粗糙的氧化物。我们提供的证据表明,这种氧化行为的变化是由引发氧化的小PdO域稳定性的温度诱导变化引起的。我们对外延PdO(100)结构的发现对于建立氧化催化应用中氧化物结构、催化活性和反应条件之间的关系可能具有重要意义。