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Dynamic structural change of Pd particles on LaFeO3 under redox atmosphere and CO/NO catalytic reaction studied by dispersive XAFS

D Matsumura et al 2009 J. Phys.: Conf. Ser. 190 012154 (6pp)   doi: 10.1088/1742-6596/190/1/012154  Help

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D Matsumura1, Y Okajima1, Y Nishihata1, J Mizuki1, M Taniguchi2, M Uenishi2 and H Tanaka2
1 Synchrotron Radiation Research Center, Japan Atomic Energy Agency, Sayo, Hyogo 679–5148, Japan
2 Materials Research and Development Division, Daihatsu Motor Co., Ltd., Gamo, Shiga 520–2593, Japan
E-mail: daiju@spring8.or.jp

Abstract. The local structure of Pd metal fine particles on LaFeO3 which has a high catalytic activity was observed by dispersive XAFS optics from the viewpoint of dynamical structure change of Pd during oxide-metal change and CO/NO catalytic reaction. The oxide-metal change of Pd nanoparticles on LaFeO3 and Al2O3 was investigated by 20–50 Hz rate. It was recognized that, under the reductive atmosphere, Pd atoms show similar speed of movement from oxide to metal state both on the two supports. However, under the oxidative atmosphere, Pd atoms on LaFeO3 show faster movement from metal to oxide state than those on Al2O3. CO/NO catalytic reaction on Pd metal nanoparticles was also observed by 0.2 Hz rate. Slow observation mode made the four EXAFS parameters: coordination number, interatomic distance, Debye-Waller factor and edge shift, precisely determined during catalytic reaction. There are two particular differences between Pd particles on LaFeO3 and Al2O3. Large enhancement of interatomic distance of Pd particle was only observed on Al2O3. Stable surface oxide layer of Pd particle is created on LaFeO3.

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