The synthesis of transition metal heterostructures is currently one of the most vivid fields in the design of novel functional materials. In this paper we propose a simple scheme to predict \emph{band alignment }and \emph{charge transfer} in complex oxide interfaces. For semiconductor heterostructures band alignment rules like the well known Anderson or Schottky-Mott rule are based on comparison of the work function or electron affinity of the bulk components. This scheme breaks down for oxides due to the invalidity of a single workfunction approximation as recently shown (Phys. Rev. B 93, 235116; Adv. Funct. Mater. 26, 5471). Here we propose a new scheme which is built on a continuity condition of valence states originating in the compounds' shared network of oxygen. It allows for the prediction of sign and relative amplitude of the intrinsic charge transfer, taking as input only information about the bulk properties of the components. We support our claims by numerical density functional theory simulations as well as (where available) experimental evidence. Specific applications include i) controlled doping of SrTiO3 layers with the use of 4d and 5d transition metal oxides and ii) the control of magnetic ordering in manganites through tuned charge transfer.
@article{arxiv.1611.08689,
title = {Band alignment and charge transfer in complex oxide interfaces},
author = {Zhicheng Zhong and Philipp Hansmann},
journal= {arXiv preprint arXiv:1611.08689},
year = {2017}
}