Unoccupied Electron States and the Formation of Interface between Films of Dimethyl-Substituted Thiophene–Phenylene Coolygomers and Oxidized Silicon Surface
- 作者: Ponomarenko S.A.1,2, Handke B.3, Komolov A.S.4, Lazneva E.F.4, Gerasimova N.B.4, Panina Y.A.4, Zashikhin G.D.4, Pshenichnyuk S.A.5, Borshchev O.V.1
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隶属关系:
- Enikopolov Institute of Synthetic Polymeric Materials
- Moscow State University
- Faculty of Material Science and Ceramics
- St. Petersburg State University
- Institute of Molecules and Crystals
- 期: 卷 60, 编号 5 (2018)
- 页面: 1029-1034
- 栏目: Polymers
- URL: https://bakhtiniada.ru/1063-7834/article/view/202991
- DOI: https://doi.org/10.1134/S1063783418050128
- ID: 202991
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详细
The unoccupied electron states and the boundary potential barrier during deposition of ultrathin films of dimethyl-substituted thiophene–phenylene coolygomers of the type of CH3–phenylene–thiophene–thiophene–phenylene–CH3 (CH3–PTTP–CH3) on an oxidized silicon surface have been studied. The electronic characteristics have been measured in the energy range from 5 to 20 eV above the Fermi level using total current spectroscopy (TCS). The structure of the CH3–PTTP–CH3 film surfaces has been studied by atomic force microscopy (AFM), and the atomic compositions of the films have been studied by X-ray photoelectron spectroscopy (XPS). The changes in the maximum intensities measured by the TCS method obtained from the deposited CH3–PTTP–CH3 film and from the substrate during increasing in the organic coating thickness to 6 nm is discussed. The formation of the boundary potential barrier in the n-Si/SiO2/CH3–PTTP–CH3 is accompanied by the decrease in the surface work function from 4.2 ± 0.1 to 4.0 ± 0.1 eV as the organic coating thickness increases to 3 nm. The ratio of atomic concentrations C: S in the CH3–PTTP–CH3 films well corresponds to the chemical formula of CH3–PTTP–CH3 molecules. The roughness of the CH3–PTTP–CH3 coating surface was not higher than 10 nm on the ~10 × 10 μm areas as the total CH3–PTTP–CH3-layer thickness was about 100 nm.
作者简介
S. Ponomarenko
Enikopolov Institute of Synthetic Polymeric Materials; Moscow State University
Email: a.komolov@spbu.ru
俄罗斯联邦, Moscow, 117393; Moscow, 119991
B. Handke
Faculty of Material Science and Ceramics
Email: a.komolov@spbu.ru
波兰, Kraków
A. Komolov
St. Petersburg State University
编辑信件的主要联系方式.
Email: a.komolov@spbu.ru
俄罗斯联邦, St. Petersburg, 199034
E. Lazneva
St. Petersburg State University
Email: a.komolov@spbu.ru
俄罗斯联邦, St. Petersburg, 199034
N. Gerasimova
St. Petersburg State University
Email: a.komolov@spbu.ru
俄罗斯联邦, St. Petersburg, 199034
Yu. Panina
St. Petersburg State University
Email: a.komolov@spbu.ru
俄罗斯联邦, St. Petersburg, 199034
G. Zashikhin
St. Petersburg State University
Email: a.komolov@spbu.ru
俄罗斯联邦, St. Petersburg, 199034
S. Pshenichnyuk
Institute of Molecules and Crystals
Email: a.komolov@spbu.ru
俄罗斯联邦, pr. Oktyabrya 151, Ufa, Bashkortostan, 450075
O. Borshchev
Enikopolov Institute of Synthetic Polymeric Materials
Email: a.komolov@spbu.ru
俄罗斯联邦, Moscow, 117393
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