Energy Level Alignment at Metal−Octaethylporphyrin Interfaces
We studied the electronic structure of copper−octaethylporphyrin (CuEOP) adsorbed on three metal surfacesAg(001), Ag(111), and Cu(111)by means of ultraviolet photoelectron spectroscopy (UPS). The adsorption-induced work function shifts saturate roughly beyond two monolayers. The saturation values...
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Published in | The journal of physical chemistry. B Vol. 109; no. 49; pp. 23558 - 23563 |
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Main Authors | , , , , , , |
Format | Journal Article |
Language | English |
Published |
United States
American Chemical Society
15.12.2005
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Online Access | Get full text |
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Summary: | We studied the electronic structure of copper−octaethylporphyrin (CuEOP) adsorbed on three metal surfacesAg(001), Ag(111), and Cu(111)by means of ultraviolet photoelectron spectroscopy (UPS). The adsorption-induced work function shifts saturate roughly beyond two monolayers. The saturation values are substrate dependent, negative, and range from −1.30 to −0.85 eV. This shift is larger than that for tetraphenylporphyrins. The two highest occupied molecular orbitals (HOMO and HOMO-1) of the organic are clearly resolved in the UPS spectra. The origin of the negative work function shift is discussed. |
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Bibliography: | istex:660D193E2E725819321767FBB1C78CBB5FABC773 ark:/67375/TPS-D0JZPW1H-9 ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
ISSN: | 1520-6106 1520-5207 |
DOI: | 10.1021/jp054325j |