# High-temperature superconductivity in one-unit-cell FeSe films

## TL;DR

This paper reviews the discovery and properties of high-temperature superconductivity in one-unit-cell FeSe films on SrTiO3, emphasizing interface effects like charge transfer and phonon coupling as key mechanisms.

## Contribution

It provides a comprehensive overview of experimental evidence and potential mechanisms for high-temperature superconductivity in 1-UC FeSe/STO, highlighting interface engineering as a pathway for new superconductor development.

## Key findings

- Experimental evidence confirms high Tc in 1-UC FeSe/STO.
- Interface effects like charge transfer enhance superconductivity.
- Phonon coupling at the interface plays a significant role.

## Abstract

Since the dramatic interface enhancement of superconducting transition temperature (Tc) was reported in one unit-cell FeSe film grown on SrTiO3 substrate (1-UC FeSe/STO) by molecular beam epitaxy (MBE), related research on this system has become a new frontier in condensed matter physics. In this paper, we present a brief review on this rapidly developing field, mainly focusing on the superconducting properties of 1-UC FeSe/STO. Experimental evidences for the high-temperature superconductivity in 1-UC FeSe/STO, including the direct evidences revealed by transport and diamagnetic measurements, and other evidences from scanning tunneling microscope (STM) and angle-resolved photoemission spectroscopy (ARPES), are overviewed. Potential mechanisms of the enhanced superconductivity are discussed. There are accumulating arguments suggesting that the strengthened Cooper pairing in 1-UC FeSe/STO originates from the interface effects, specifically charge transfer and coupling to phonon modes in TiO2 plane. The study of superconductivity in 1-UC FeSe/STO not only sheds a new light on the mechanism of high-temperature superconductors with layered structures, but also provides the insight to explore new superconductors by interface engineering.

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Source: https://tomesphere.com/paper/1701.06855