The (1x1)→hexagonal structural transition on Pt(100) studied by high-energy resolution core level photoemission

被引:11
作者
Baraldi, Alessandro
Vesselli, Erik
Bianchettin, Laura
Comelli, Giovanni
Lizzit, Silvano
Petaccia, Luca
de Gironcoli, Stefano
Locatelli, Andrea
Mentes, T. Onur
Aballe, Lucia
Weissenrieder, Jonas
Andersen, Jesper N.
机构
[1] Univ Trieste, Dept Phys, I-34127 Trieste, Italy
[2] Univ Trieste, Ctr Excellence Nanostructured Mat, I-34127 Trieste, Italy
[3] CNR, INFM, TASC, Italy Lab, I-34012 Trieste, Italy
[4] Sincrotrone Trieste SCpA, I-34012 Trieste, Italy
[5] SISSA, I-34014 Trieste, Italy
[6] Natl Simulat Ctr, INFM CNR DEMOCRITOS, I-34014 Trieste, Italy
[7] Lund Univ, Max Lab, SE-22100 Lund, Sweden
[8] Lund Univ, Dept Synchrotron Radiat Res, S-22100 Lund, Sweden
关键词
D O I
10.1063/1.2794344
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 (1 x 1)-> quasihexagonal (HEX) phase transition on a clean Pt(100) surface was investigated by monitoring the time evolution of the Pt4f(7/2) core level photoemission spectra. The spectral component originating from the atoms forming the (1 x .1) metastable unreconstructed surface was found at -570 +/- 20 meV with respect to the bulk peak. Ab initio calculations based on density functional theory confirmed the experimental assignment. At temperatures above 370 K, the (1 x 1) phase irreversibly reverts to the more stable HEX phase, characterized by a surface core level shifted component at -185 +/- 40 meV. By analyzing the intensity evolution of the core level components, measured at different temperatures in the range of 393-475 K, we determined the activation energy of the phase transformation, E=0.76 +/- 0.04 eV. This value is considerably lower than the one previously determined by means of low energy electron diffraction. Possible reasons for this discrepancy are discussed. (C) 2007 American Institute of Physics.
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页数:7
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