Properties of Pt on Cu(111) revealed by AES, LEED, and DEPES

被引:8
作者
Miszczuk, A. [1 ]
Morawski, I. [1 ]
Jurczyszyn, M. [1 ]
Nowicki, M. [1 ]
机构
[1] Univ Wroclaw, Inst Expt Phys, Pl M Borna 9, PL-50204 Wroclaw, Poland
关键词
Electron spectroscopies; Crystalline structure; Growth mode; Adsorbate domains; Superficial alloy; Multiple scattering; ELECTRON-SPECTROSCOPY DEPES; SURFACE ALLOY; BIMETALLIC SYSTEMS; CU; PT/CU(111); GROWTH; REACTIVITY; CU/PT(111); ADSORPTION; PT(111);
D O I
10.1016/j.elspec.2017.12.004
中图分类号
O433 [光谱学];
学科分类号
0703 ; 070302 ;
摘要
The investigations of Pt on Cu(111) were carried out to reveal the growth mode and crystalline structure of the adsorbate with the use of Auger electron spectroscopy (AES), low energy electron diffraction (LEED), and directional elastic peak electron spectroscopy (DEPES). Auger signal recorded during the continuous Pt adsorption on Cu(111) at 330 K confirms the layer by layer growth mode. LEED patterns observed at 1ML of Pt show the formation of the compressed adlayer. At higher coverages such as 3ML and 6ML the increase of the lattice constant of the topmost Pt layer, which approaches the bulk value of Pt(111), is noted. DEPES investigations performed for 1ML of platinum indicate the nucleation of adsorbate domains characterized by A/CBA and B/CBA stacking sequences at the Pt/Cu interface, which at higher coverages lead to the nucleation of mutually rotated by 180 Pt islands. Experimental DEPES data were compared to theoretical results obtained with the use of the multiple scattering (MS) calculations for different adsorption geometries including the Pt and Cu intermixing at the interface. The quantitative analysis of the data made by R-factor calculations enabled the determination of Pt domain populations already at 1 ML and 6ML. (C) 2017 Elsevier B.V. All rights reserved.
引用
收藏
页码:29 / 36
页数:8
相关论文
共 27 条
[1]  
[Anonymous], 1958, Constitution of Binary Alloys
[2]   A CORE-LEVEL PHOTOEMISSION SPECTROSCOPY STUDY OF THE FORMATION OF SURFACE ALLOY CU/PT(111) - COMPARISON WITH PT/CU(111) [J].
BARRETT, NT ;
BELKHOU, R ;
THIELE, J ;
GUILLOT, C .
SURFACE SCIENCE, 1995, 331 :776-781
[3]   GROWTH OF PT/CU(111) CHARACTERIZED BY AUGER-ELECTRON SPECTROSCOPY, CORE LEVEL PHOTOEMISSION AND X-RAY PHOTOELECTRON DIFFRACTION [J].
BELKHOU, R ;
BARRETT, NT ;
GUILLOT, C ;
BARBIER, A ;
EUGENE, J ;
CARRIERE, B ;
NAUMOVIC, D ;
OSTERWALDER, J .
APPLIED SURFACE SCIENCE, 1993, 65-6 :63-70
[4]   FORMATION OF A SURFACE ALLOY BY ANNEALING OF PT/CU(111) [J].
BELKHOU, R ;
BARRETT, NT ;
GUILLOT, C ;
FANG, M ;
BARBIER, A ;
EUGENE, J ;
CARRIERE, B ;
NAUMOVIC, D ;
OSTERWALDER, J .
SURFACE SCIENCE, 1993, 297 (01) :40-56
[5]  
CAMPBELL CT, 1990, ANNU REV PHYS CHEM, V41, P775
[6]   Atomistic modeling of Pt deposition on Cu(111) and Cu deposition on Pt(111) [J].
Canzian, A ;
Mosca, HO ;
Bozzolo, G .
SURFACE REVIEW AND LETTERS, 2004, 11 (02) :235-243
[7]   Phase diagrams for surface alloys [J].
Christensen, A ;
Ruban, AV ;
Stoltze, P ;
Jacobsen, KW ;
Skriver, HL ;
Norskov, JK ;
Besenbacher, F .
PHYSICAL REVIEW B, 1997, 56 (10) :5822-5834
[8]   Step mediated surface alloy formation of Pt/Cu(111) [J].
Dastoor, PC ;
O'Connor, DJ ;
MacLaren, DA ;
Allison, W ;
Noakes, TCQ ;
Bailey, P .
SURFACE SCIENCE, 2005, 588 (1-3) :101-107
[9]   INFLUENCE OF ALLOYING PT WITH CU ON THE REACTION-MECHANISMS OF HYDROCARBON REFORMING REACTIONS [J].
DEJONGSTE, HC ;
PONEC, V ;
GAULT, FG .
JOURNAL OF CATALYSIS, 1980, 63 (02) :395-403
[10]   ROLE OF CU IN THE HYDROGENOLYSIS OF PENTANE ON CU ALLOY CATALYSTS [J].
DEJONGSTE, HC ;
PONEC, V .
JOURNAL OF CATALYSIS, 1980, 63 (02) :389-394