Orientation dependent ionization potential of In2O3: a natural source for inhomogeneous barrier formation at electrode interfaces in organic electronics

电极 方向(向量空间) 电离 材料科学 数码产品 化学物理 自然(考古学) 光电子学 纳米技术 化学 物理化学 几何学 地质学 离子 有机化学 古生物学 数学
作者
Mareike V. Hohmann,Péter Ágoston,André Wachau,Thorsten J. M. Bayer,Joachim Brötz,Karsten Albe,Andreas Klein
出处
期刊:Journal of Physics: Condensed Matter [IOP Publishing]
卷期号:23 (33): 334203-334203 被引量:46
标识
DOI:10.1088/0953-8984/23/33/334203
摘要

The ionization potentials of In2O3 films grown epitaxially by magnetron sputtering on Y-stabilized ZrO2 substrates with (100) and (111) surface orientation are determined using photoelectron spectroscopy. Epitaxial growth is verified using x-ray diffraction. The observed ionization potentials, which directly affect the work functions, are in good agreement with ab initio calculations using density functional theory. While the (111) surface exhibits a stable surface termination with an ionization potential of ∼ 7.0 eV, the surface termination and the ionization potential of the (100) surface depend strongly on the oxygen chemical potential. With the given deposition conditions an ionization potential of ∼ 7.7 eV is obtained, which is attributed to a surface termination stabilized by oxygen dimers. This orientation dependence also explains the lower ionization potentials observed for In2O3 compared to Sn-doped In2O3 (ITO) (Klein et al 2009 Thin Solid Films 518 1197–203). Due to the orientation dependent ionization potential, a polycrystalline ITO film will exhibit a laterally varying work function, which results in an inhomogeneous charge injection into organic semiconductors when used as electrode material. The variation of work function will become even more pronounced when oxygen plasma or UV–ozone treatments are performed, as an oxidation of the surface is only possible for the (100) surface. The influence of the deposition technique on the formation of stable surface terminations is also discussed.

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