| Literature DB >> 29906092 |
Yogesh Sharma1, Janakiraman Balachandran2, Changhee Sohn1, Jaron T Krogel1, Panchapakesan Ganesh2, Liam Collins2, Anton V Ievlev2, Qian Li2, Xiang Gao1, Nina Balke2, Olga S Ovchinnikova2, Sergei V Kalinin2, Olle Heinonen3, Ho Nyung Lee1.
Abstract
Strongly correlated vanadium dioxide (VO2) is one of the most promising materials that exhibits a temperature-driven, metal-insulator transition (MIT) near room temperature. The ability to manipulate the MIT at nanoscale offers both insight into understanding the energetics of phase transition and a promising potential for nanoelectronic devices. In this work, we study nanoscale electrochemical modifications of the MIT in epitaxial VO2 thin films using a combined approach with scanning probe microscopy (SPM) and theoretical calculations. We find that applying electric voltages of different polarity through an SPM tip locally changes the contact potential difference and conductivity on the surface of VO2 by modulating the oxygen stoichiometry. We observed nearly 2 orders of magnitude change in resistance between positive and negative biased-tip written areas of the film, demonstrating the electric field modulated MIT behavior at the nanoscale. Density functional theory calculations, benchmarked against more accurate many-body quantum Monte Carlo calculations, provide information on the formation energetics of oxygen defects that can be further manipulated by strain. This study highlights the crucial role of oxygen vacancies in controlling the MIT in epitaxial VO2 thin films, useful for developing advanced electronic and iontronic devices.Entities:
Keywords: density functional theory; metal−insulator transition; oxygen vacancy; quantum Monte Carlo; scanning probe microscopy; vanadium dioxide
Year: 2018 PMID: 29906092 DOI: 10.1021/acsnano.8b03031
Source DB: PubMed Journal: ACS Nano ISSN: 1936-0851 Impact factor: 15.881