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Energy level alignment at interfaces between 3-(4-biphenylyl)-4-phenyl-5-(4-tert-butyl phenyl)-1, 2, 4-triazole (TAZ) and metals (Ca, Mg, Ag, and Au): experiment and theory

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Abstract

We have performed ultraviolet photoelectron spectroscopy measurements and density functional theory calculations to study the electronic structure at the interface between organic semiconductor (3-(4-biphenylyl)-4-phenyl-5-(4-tert-butyl phenyl)-1,2,4-triazole (TAZ)) and metals (Ca, Mg, Ag, and Au). The basic mechanism of interface states at organic–metal interfaces can be understood by controlling the injection of charge carriers at these interfaces. The position of highest occupied molecular orbital relative to the Fermi level and the magnitude of the interface dipole are measured for each organic–metal interface. For TAZ on Ca, Mg, and Ag, interface states are observed near the Fermi level. However, no interface state is observed for TAZ on Au. It is analyzed qualitatively that the interface state is formed due to interaction of TAZ lowest unoccupied molecular orbital composed of C2p and metal s levels. It is suggested that the interface state plays an important role in charge transport at the interface. The mechanism of formation of interface states and electrical properties are discussed.

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Authors and Affiliations

  1. Institute of Applied Physics, University of Tsukuba, Tsukuba, Ibaraki, 305-8577, Japan

    Akihisa Baba, Takeaki Sakurai & Katsuhiro Akimoto

  2. WCU Multiscale Engineering Division, School of Mechanical and Aerospace Engineering, Seoul National University, Seoul, 151-742, South Korea

    Mahesh Datt Bhatt

Authors
  1. Mahesh Datt Bhatt
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  2. Akihisa Baba
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  3. Takeaki Sakurai
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  4. Katsuhiro Akimoto
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Correspondence to Mahesh Datt Bhatt.

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Bhatt, M.D., Baba, A., Sakurai, T. et al. Energy level alignment at interfaces between 3-(4-biphenylyl)-4-phenyl-5-(4-tert-butyl phenyl)-1, 2, 4-triazole (TAZ) and metals (Ca, Mg, Ag, and Au): experiment and theory. J Solid State Electrochem 16, 1141–1149 (2012). https://doi.org/10.1007/s10008-011-1497-2

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  • DOI: https://doi.org/10.1007/s10008-011-1497-2

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