Substrate-Independent Magnetic Bistability in Monolayers of the Single-Molecule Magnet Dy2ScN@C80 on Metals and Insulators

Research output: Contribution to journalArticle

Abstract

Magnetic hysteresis is demonstrated for monolayers of the single-molecule magnet (SMM) Dy2ScN@C80 deposited on Au(111), Ag(100), and MgO|Ag(100) surfaces by vacuum sublimation. The topography and electronic structure of Dy2ScN@C80 adsorbed on Au(111) were studied by STM. X-ray magnetic CD studies show that the Dy2ScN@C80 monolayers exhibit similarly broad magnetic hysteresis independent on the substrate used, but the orientation of the Dy2ScN cluster depends strongly on the surface. DFT calculations show that the extent of the electronic interaction of the fullerene molecules with the surface is increasing dramatically from MgO to Au(111) and Ag(100). However, the charge redistribution at the fullerene-surface interface is fully absorbed by the carbon cage, leaving the state of the endohedral cluster intact. This Faraday cage effect of the fullerene preserves the magnetic bistability of fullerene-SMMs on conducting substrates and facilitates their application in molecular spintronics.

Details

Authors
  • Denis S. Krylov
  • Sebastian Schimmel
  • Vasilii Dubrovin
  • Fupin Liu
  • T. T.Nhung Nguyen
  • Lukas Spree
  • Chia Hsiang Chen
  • Georgios Velkos
  • Claudiu Bulbucan
  • Rasmus Westerström
  • Michał Studniarek
  • Jan Dreiser
  • Christian Hess
  • Bernd Büchner
  • Stanislav M. Avdoshenko
  • Alexey A. Popov
Organisations
External organisations
  • Leibniz Institute for Solid State and Materials Research
  • Institute for Basic Science, Korea
  • Kaohsiung Medical University
  • Paul Scherrer Institute
Research areas and keywords

Subject classification (UKÄ) – MANDATORY

  • Materials Chemistry

Keywords

  • endohedral metallofullerenes, monolayers, scanning probe microscopy, single-molecule magnets, XMCD
Original languageEnglish
JournalAngewandte Chemie - International Edition
Publication statusE-pub ahead of print - 2020
Publication categoryResearch
Peer-reviewedYes