THE ADSORBATE-INDUCED REMOVAL OF THE PT(100) SURFACE RECONSTRUCTION .2. CO

被引:79
作者
MARTIN, R [1 ]
GARDNER, P [1 ]
BRADSHAW, AM [1 ]
机构
[1] MAX PLANCK GESELL,FRITZ HABER INST,D-14195 BERLIN,GERMANY
关键词
CARBON MONOXIDE; CHEMISORPTION; INFRARED ABSORPTION SPECTROSCOPY; LOW ENERGY ELECTRON DIFFRACTION (LEED); LOW INDEX SINGLE CRYSTAL SURFACES; PLATINUM; SOLID-GAS INTERFACES; SURFACE RELAXATION AND RECONSTRUCTION;
D O I
10.1016/0039-6028(95)00679-6
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
The CO-induced lifting of the pseudo-hexagonal, clean surface reconstruction of Pt{100} has been re-investigated with infrared reflection-absorption spectroscopy (IRAS) and low energy electron diffraction (LEED). In order to remove inconsistencies arising from previous studies, adsorption on both the reconstructed and the metastable unreconstructed surfaces was studied at temperatures between 90 and 300 K. A sequence of ordered overlayers observed for coverages of theta = 0.5 and above on the unreconstructed surface, including the previously unobserved c(5 root 2 X root 2)R45 degrees structure for theta = 0.6, can be interpreted in terms of new structural models involving both atop and bridging CO. During adsorption on the reconstructed surface at 300 K the (hex) <-> (1 x 1) phase transition can be followed using the C-O stretch. in particular, we observe the co-existence of CO adsorbed on (hex) and (1 X 1) regions in a narrow coverage range. The appearance of CO on the (1 X 1) phase is not only accompanied by a small shift in the linear C-O stretch, but also by the development of a bridge band. At temperatures below similar to 250 K, however, the reconstruction is lifted in a significantly different way. These and other results are compared with the corresponding data for NO described in Part 1 of this study.
引用
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页码:69 / 84
页数:16
相关论文
共 49 条
[31]   THE PT(100)(5X20)REVERSIBLE(1X1)PHASE TRANSITION - A STUDY BY RUTHERFORD BACKSCATTERING, NUCLEAR MICROANALYSIS, LEED AND THERMAL-DESORPTION SPECTROSCOPY [J].
NORTON, PR ;
DAVIES, JA ;
CREBER, DK ;
SITTER, CW ;
JACKMAN, TE .
SURFACE SCIENCE, 1981, 108 (02) :205-224
[32]   LEED INTENSITY ANALYSIS OF THE STRUCTURES OF CLEAN PT(111) AND OF CO ADSORBED ON PT(111) IN THE C(4X2) ARRANGEMENT [J].
OGLETREE, DF ;
VANHOVE, MA ;
SOMORJAI, GA .
SURFACE SCIENCE, 1986, 173 (2-3) :351-365
[33]   ON THE NATURE OF DENSE CO ADLAYERS [J].
PERSSON, BNJ ;
TUSHAUS, M ;
BRADSHAW, AM .
JOURNAL OF CHEMICAL PHYSICS, 1990, 92 (08) :5034-5046
[34]  
PIRUG G, 1978, NEDERLANDS TIJDSCHRI, V16, P152
[35]   LEEM AND SELECTED-AREA LEED STUDIES OF REACTION FRONT PROPAGATION [J].
RAUSENBERGER, B ;
SWIECH, W ;
ENGEL, W ;
BRADSHAW, AM ;
ZEITLER, E .
SURFACE SCIENCE, 1993, 287 :235-240
[36]  
RAUSENBERGER B, COMMUNICATION
[37]   DIRECT OBSERVATION OF A NUCLEATION AND GROWTH-PROCESS ON AN ATOMIC SCALE [J].
RITTER, E ;
BEHM, RJ ;
POTSCHKE, G ;
WINTTERLIN, J .
SURFACE SCIENCE, 1987, 181 (1-2) :403-411
[38]   IS THE FREQUENCY OF THE INTERNAL-MODE OF AN ADSORBED DIATOMIC MOLECULE A RELIABLE GUIDE TO ITS LOCAL ADSORPTION SITE [J].
SCHINDLER, KM ;
HOFMANN, P ;
WEISS, KU ;
DIPPEL, R ;
GARDNER, P ;
FRITZSCHE, V ;
BRADSHAW, AM ;
WOODRUFF, DP ;
DAVILA, ME ;
ASENSIO, MC ;
CONESA, JC ;
GONZALEZELIPE, AR .
JOURNAL OF ELECTRON SPECTROSCOPY AND RELATED PHENOMENA, 1993, 64-5 :75-83
[39]   THE NO + CO REACTION ON CLEAN PT(100) - MULTIPLE STEADY-STATES AND OSCILLATIONS [J].
SCHWARTZ, SB ;
SCHMIDT, LD .
SURFACE SCIENCE, 1988, 206 (1-2) :169-186
[40]   IS THERE A SINGLE MECHANISM OF CATALYTIC RATE OSCILLATIONS ON PT [J].
SCHWARTZ, SB ;
SCHMIDT, LD .
SURFACE SCIENCE, 1987, 183 (1-2) :L269-L278