# Electron-proton Co-doping Induced Metal-insulator Transition in VO2 Film via Surface Self-assembled Ascorbic Acid Molecules

## TL;DR

This paper demonstrates a novel surface self-assembled molecule-driven electron-proton co-doping method to induce and stabilize a metallic phase in VO2 at room temperature, offering a new approach for tuning correlated materials.

## Contribution

It introduces a new co-doping mechanism using self-assembled ascorbic acid molecules to achieve stable metallic VO2 at room temperature, enhancing phase control.

## Key findings

- Stable metallic VO2 achieved at room temperature.
- Surface molecules protect hydrogen dopants within the lattice.
- Charge transfer and structural changes confirmed by synchrotron and simulations.

## Abstract

Charge doping is an effective way to induce metal-insulate transition (MIT) in correlated materials for many important utilizations, which is however practically limited by problem of low stability. In this study, we have achieved pronounced phase modulation and stabilized the metallic state of monoclinic vanadium dioxide (VO2) at room temperature, via a novel electron-proton co-doping mechanism driven by surface absorption of self-assembled L-ascorbic acid (AA) molecules. The ionized AA- species in solution donate effective electrons to the adsorbed VO2 surface, which then electrostatically attract surrounding protons to penetrate, and eventually results in stable hydrogen-doped metallic VO2. The variations of phase and electronic structures as well as the electron occupancy of V-3d/O-2p hybrid orbitals were examined by synchrotron characterizations and first-principle theoretical simulations, which explain the formation of stable metallic state. Importantly, the adsorbed molecules protect hydrogen dopants from escaping out of lattice and thereby stabilize the metallic phase for VO2. Such an electron-proton co-doping mechanism driven by suitable molecules absorption would open a new door for engineering properties of correlated oxide materials.

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Source: https://tomesphere.com/paper/1901.05597