High-pressure X-ray photoelectron spectroscopy of palladium model hydrogenation catalysts.: Part 1:: Effect of gas ambient and temperature

被引:89
作者
Teschner, D
Pestryakov, A
Kleimenov, E
Hävecker, M
Bluhm, H
Sauer, H
Knop-Gericke, A
Schlögl, R
机构
[1] Max Planck Gesell, Fritz Haber Inst, D-14195 Berlin, Germany
[2] Hungarian Acad Sci, CRC, Inst Isotope & Surface Chem, H-1525 Budapest, Hungary
关键词
high-pressure XPS; palladium; hydrogen; carbonaceous deposits; surface oxide; palladium hydride;
D O I
10.1016/j.jcat.2004.11.036
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
In light of accumulating evidence highlighting the major effect of operational conditions (gas composition, pressure, temperature) on the surface/bulk structure of catalytic materials, their characterization should involve more and more in situ methods. We constructed a synchrotron-based high-pressure X-ray photoelectron spectroscopic (XPS) instrument, allowing us to investigate the surface and near-surface state of a catalyst in the mbar pressure range. We discuss here the surface characteristics of palladium samples as a function of gas phase (hydrogen, oxygen) and temperature. We demonstrate that the surface region of catalytic materials behaves dynamically in its composition, always reflecting its environment. For example, surface oxide can be formed on Pd(111) in oxygen, which decomposes rapidly when the gas supply is switched off. The chemical nature of carbonaceous deposits also depends strongly on the operational conditions (gas-phase hydrogen, temperature). This is the first time that an XPS investigation of palladium beta-hydride was performed at RT. The possible drawbacks Of using a non-UHV setup (e.g., fast carbon accumulation) are also discussed. (C) 2004 Elsevier Inc. All rights reserved.
引用
收藏
页码:186 / 194
页数:9
相关论文
共 76 条
[1]   SURFACE CORE-LEVEL SHIFTS OF SOME 4D-METAL SINGLE-CRYSTAL SURFACES - EXPERIMENTS AND AB-INITIO CALCULATIONS [J].
ANDERSEN, JN ;
HENNIG, D ;
LUNDGREN, E ;
METHFESSEL, M ;
NYHOLM, R ;
SCHEFFLER, M .
PHYSICAL REVIEW B, 1994, 50 (23) :17525-17533
[2]   CATALYTIC OXIDATION OF METHANE [J].
ANDERSON, RB ;
STEIN, KC ;
FEENAN, JJ ;
HOFER, LJE .
INDUSTRIAL AND ENGINEERING CHEMISTRY, 1961, 53 (10) :809-812
[3]   XPS LINE-SHAPE ASYMMETRY IN PD-H SYSTEM - ROLE OF ELECTRON SCREENING [J].
ANTONANGELI, F ;
BALZAROTTI, A ;
BIANCONI, A ;
PERFETTI, P ;
ASCARELLI, P ;
NISTICO, N .
SOLID STATE COMMUNICATIONS, 1977, 21 (02) :201-204
[4]   ELECTRONIC-STRUCTURE AND SURFACE KINETICS OF PALLADIUM HYDRIDE STUDIED WITH X-RAY PHOTOELECTRON-SPECTROSCOPY AND ELECTRON-ENERGY-LOSS SPECTROSCOPY [J].
BENNETT, PA ;
FUGGLE, JC .
PHYSICAL REVIEW B, 1982, 26 (11) :6030-6039
[5]  
BLUHM H, IN PRESS J PHYS CH B
[6]  
BOND GC, 1964, ADV CATAL, V15, P91
[7]   The study of the nature of adsorbed species to build a bridge between surface science and catalysis: Problems of pressure and material gap [J].
Bukhtiyarov, VI .
KINETICS AND CATALYSIS, 2003, 44 (03) :420-431
[8]   In situ study of selective oxidation of methanol to formaldehyde over copper [J].
Bukhtiyarov, VI ;
Prosvirin, IP ;
Tikhomirov, EP ;
Kaichev, VV ;
Sorokin, AM ;
Evstigneev, VV .
REACTION KINETICS AND CATALYSIS LETTERS, 2003, 79 (01) :181-188
[9]  
CHAUVEL A, 1989, PETROCHEMICAL PROCES, V2, P36
[10]   OXIDATION OF METHANE OVER SUPPORTED PRECIOUS METAL-CATALYSTS [J].
CULLIS, CF ;
WILLATT, BM .
JOURNAL OF CATALYSIS, 1983, 83 (02) :267-285