X射线光电子能谱
密度泛函理论
光电发射光谱学
工作职能
分析化学(期刊)
化学
价(化学)
光谱学
结晶学
材料科学
分子物理学
金属
计算化学
核磁共振
有机化学
量子力学
物理
色谱法
作者
Angelo Stummo,Monica Montecchi,Francesca Parenti,Davide Vanossi,Claudio Fontanesi,Raffaella Capelli,Luca Pasquali
出处
期刊:Langmuir
[American Chemical Society]
日期:2023-04-07
卷期号:39 (15): 5602-5609
被引量:1
标识
DOI:10.1021/acs.langmuir.3c00572
摘要
Ultrathin films of a stereoisomeric mixture of benzo[1,2-b:4,5-b']dithiophene derivatives were grown by thermal evaporation in vacuum on Au(111), and they were studied in situ by photoelectron spectroscopy. X-ray photons from a non-monochromatic Mg Kα conventional X-ray source and UV photons from a He I discharge lamp equipped with a linear polarizer were used. He I photoemission results were compared with density functional theory (DFT) calculations: density of states (DOS) and 3D molecular orbital density distribution. Au 4f, C 1s, O 1s, and S 2p core-level components suggest a surface rearrangement as a function of film nominal thickness, with the variation of the molecular orientation, from flat-laying at the initial deposition to tilted toward the surface normal at coverages exceeding 2 nm. Eventually, the DFT results were exploited in assigning of the valence band experimental structures. Moreover, polarization-dependent photoemission confirmed the tilted arrangement of the molecules, starting at 2 nm. A variation of the work function of 1.4 eV with respect to the clean substrate was measured, together with a valence band offset of 1.3 eV between the organic layer and gold.
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