High-resolution fast X-ray photoelectron spectroscopy study of ethylene interaction with Ir(111): From chemisorption to dissociation and graphene formation

被引:36
作者
Lizzit, Silvano [3 ]
Baraldi, Alessandro [1 ,2 ,4 ]
机构
[1] Univ Trieste, Dept Phys, I-34127 Trieste, Italy
[2] Univ Trieste, Ctr Excellence Nanostruct Mat, I-34127 Trieste, Italy
[3] Sincrotrone Trieste SCpA, I-34149 Trieste, Italy
[4] CNR Lab TASC, IOM, I-34012 Trieste, Italy
关键词
High-energy resolution core level; spectroscopy; Iridium; Chemical reactivity; Graphene; VIBRATIONAL FINE-STRUCTURE; CORE-LEVEL PHOTOEMISSION; ADSORPTION; ETHYLIDYNE; HYDROGEN; PT(111); SURFACE; GENERATION; REACTIVITY; ACETYLENE;
D O I
10.1016/j.cattod.2010.05.028
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
High-energy resolution fast X-ray photoelectron spectroscopy was used to study the thermal evolution of ethylene on Ir(1 1 1). Temperature programmed photoemission spectra of the C 1s and Ir 4f(7/2) core levels were measured in 400 ms/spectrum while ramping the temperature from 170 to 1120K. The C 1s spectra display a large variety of components, assigned to different carbon containing species present on the surface at increasing temperature, namely ethylene, ethylidene, ethylidyne, ethynyl, adsorbed carbon and finally graphene. Components due to the C-H stretch vibration excitation are clearly resolved for C2H4, CHCH3 and C2H3. The C 1s spectra of the last two species display also shifted components that belong to non-equivalent carbon atoms. At temperatures higher than 900 K the narrowing of C 1s spectra is caused by graphene formation. Also the It 4f(7/2) spectra are strongly affected by the presence of the different species. The clean surface component moves initially towards the bulk peak and shifts back and forth along the series, to recover the binding energy position corresponding to the clean surface when the graphene layer is completely formed. A comparison of ethylene interaction with Ir(1 1 1) and Pt(1 1 1) is presented. (C) 2010 Elsevier B.V. All rights reserved.
引用
收藏
页码:68 / 74
页数:7
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