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Vacuum-Level Shift at Al/LiF/Alq(3) Interfaces: A First-Principles Study

[Image: see text] Work function changes, or vacuum-level shifts (Δ(VLS)), in Al(001) surfaces by the adsorption of thin layers composed of tris(8-hydroxyquinolinato)aluminum (Alq(3)) and/or LiF are theoretically investigated. First-principles calculations reasonably reproduce experimentally obtained...

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Detalles Bibliográficos
Autores principales: Kondo, Masakazu, Matsushita, Takeshi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2019
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6705215/
https://www.ncbi.nlm.nih.gov/pubmed/31460471
http://dx.doi.org/10.1021/acsomega.9b01667
Descripción
Sumario:[Image: see text] Work function changes, or vacuum-level shifts (Δ(VLS)), in Al(001) surfaces by the adsorption of thin layers composed of tris(8-hydroxyquinolinato)aluminum (Alq(3)) and/or LiF are theoretically investigated. First-principles calculations reasonably reproduce experimentally obtained Δ(VLS) values, enabling us to discuss the underlying mechanism. Dipole moment of Alq(3) and interfacial charge rearrangement (Pauli push-back effect) are the main reasons for Δ(VLS) at Al(001)–Alq(3) and Al(001)–LiF interfaces, respectively. For a stacked Al(001)–LiF–Alq(3) layer configuration, theory suggests a more complicated picture, which takes charge rearrangement between LiF and Alq(3) layers into account, than a simple sum rule of dipole contributions from the two layers.