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Modification of the electronic properties of the TiO 2 (1 1 0) surface upon deposition of the ultrathin conjugated organic layers. / Komolov, A. S.; Møller, P. J.; Mortensen, J.; Komolov, S. A.; Lazneva, E. F.

в: Applied Surface Science, Том 253, № 18, 15.07.2007, стр. 7376-7380.

Результаты исследований: Научные публикации в периодических изданияхстатьяРецензирование

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Komolov, A. S. ; Møller, P. J. ; Mortensen, J. ; Komolov, S. A. ; Lazneva, E. F. / Modification of the electronic properties of the TiO 2 (1 1 0) surface upon deposition of the ultrathin conjugated organic layers. в: Applied Surface Science. 2007 ; Том 253, № 18. стр. 7376-7380.

BibTeX

@article{7aedd46e6ab24b778ef12c4e4917e865,
title = "Modification of the electronic properties of the TiO 2 (1 1 0) surface upon deposition of the ultrathin conjugated organic layers",
abstract = " A few nm thick 3,4,9,10-perylenetetracarboxylic acid dianhydride (PTCDA) and Cu-phthalocyanine (CuPc) overlayers were thermally deposited in situ in UHV onto TiO 2 (1 1 0) surface. Atomic composition of the surfaces under study was monitored using Auger electron spectroscopy (AES). The formation of the interfacial potential barrier and the structure of the unoccupied electronic states located 5-25 eV above the Fermi level (E F ) was monitored using a probing beam of low-energy electrons according to the total current electron spectroscopy (TCS) method. The work function values upon the overlayer deposition changed from 4.6 to 4.9 eV at the PTCDA/TiO 2 (1 1 0) interface and from 4.6 to 4.3 eV at the CuPc/TiO 2 (1 1 0) interface. Band bending in the TiO 2 substrate, molecular polarization in the organic film and changes in the work function due to the change in the surface composition were found to contribute to the formation of the interfacial potential barriers. Oxygen admixture related peaks were observed in the AES and in the TCS spectra of the CuPc overlayers. A mechanism of the transformations in the PTCDA and CuPc overlayers on the TiO 2 (1 1 0) upon elevating temperature from 25 to 400 °C was suggested.",
keywords = "Conjugated organic molecules, Metal oxide surfaces, Surface electronic phenomena, Titanium dioxide",
author = "Komolov, {A. S.} and M{\o}ller, {P. J.} and J. Mortensen and Komolov, {S. A.} and Lazneva, {E. F.}",
year = "2007",
month = jul,
day = "15",
doi = "10.1016/j.apsusc.2007.03.024",
language = "English",
volume = "253",
pages = "7376--7380",
journal = "Applied Surface Science",
issn = "0169-4332",
publisher = "Elsevier",
number = "18",

}

RIS

TY - JOUR

T1 - Modification of the electronic properties of the TiO 2 (1 1 0) surface upon deposition of the ultrathin conjugated organic layers

AU - Komolov, A. S.

AU - Møller, P. J.

AU - Mortensen, J.

AU - Komolov, S. A.

AU - Lazneva, E. F.

PY - 2007/7/15

Y1 - 2007/7/15

N2 - A few nm thick 3,4,9,10-perylenetetracarboxylic acid dianhydride (PTCDA) and Cu-phthalocyanine (CuPc) overlayers were thermally deposited in situ in UHV onto TiO 2 (1 1 0) surface. Atomic composition of the surfaces under study was monitored using Auger electron spectroscopy (AES). The formation of the interfacial potential barrier and the structure of the unoccupied electronic states located 5-25 eV above the Fermi level (E F ) was monitored using a probing beam of low-energy electrons according to the total current electron spectroscopy (TCS) method. The work function values upon the overlayer deposition changed from 4.6 to 4.9 eV at the PTCDA/TiO 2 (1 1 0) interface and from 4.6 to 4.3 eV at the CuPc/TiO 2 (1 1 0) interface. Band bending in the TiO 2 substrate, molecular polarization in the organic film and changes in the work function due to the change in the surface composition were found to contribute to the formation of the interfacial potential barriers. Oxygen admixture related peaks were observed in the AES and in the TCS spectra of the CuPc overlayers. A mechanism of the transformations in the PTCDA and CuPc overlayers on the TiO 2 (1 1 0) upon elevating temperature from 25 to 400 °C was suggested.

AB - A few nm thick 3,4,9,10-perylenetetracarboxylic acid dianhydride (PTCDA) and Cu-phthalocyanine (CuPc) overlayers were thermally deposited in situ in UHV onto TiO 2 (1 1 0) surface. Atomic composition of the surfaces under study was monitored using Auger electron spectroscopy (AES). The formation of the interfacial potential barrier and the structure of the unoccupied electronic states located 5-25 eV above the Fermi level (E F ) was monitored using a probing beam of low-energy electrons according to the total current electron spectroscopy (TCS) method. The work function values upon the overlayer deposition changed from 4.6 to 4.9 eV at the PTCDA/TiO 2 (1 1 0) interface and from 4.6 to 4.3 eV at the CuPc/TiO 2 (1 1 0) interface. Band bending in the TiO 2 substrate, molecular polarization in the organic film and changes in the work function due to the change in the surface composition were found to contribute to the formation of the interfacial potential barriers. Oxygen admixture related peaks were observed in the AES and in the TCS spectra of the CuPc overlayers. A mechanism of the transformations in the PTCDA and CuPc overlayers on the TiO 2 (1 1 0) upon elevating temperature from 25 to 400 °C was suggested.

KW - Conjugated organic molecules

KW - Metal oxide surfaces

KW - Surface electronic phenomena

KW - Titanium dioxide

UR - http://www.scopus.com/inward/record.url?scp=34249914797&partnerID=8YFLogxK

U2 - 10.1016/j.apsusc.2007.03.024

DO - 10.1016/j.apsusc.2007.03.024

M3 - Article

VL - 253

SP - 7376

EP - 7380

JO - Applied Surface Science

JF - Applied Surface Science

SN - 0169-4332

IS - 18

ER -

ID: 18880871