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Room-temperature long-range ferromagnetic order in a confined molecular monolayer

  • Yuhua Liu,
  • Haifeng Lv,
  • Bingkai Yuan,
  • Yang Liu,
  • Yuqiao Guo,
  • Yue Lin,
  • Xiaolin Tai,
  • Yongliang Qin,
  • Jing Peng,
  • Jiyin Zhao,
  • Yueqi Su,
  • Kai Chen,
  • Wangsheng Chu,
  • Wensheng Yan,
  • Xiaojun Wu,
  • Changzheng Wu,
  • Yi Xie

摘要

In recent years, research on spin ordering phenomena has broadened to include intermolecular exchange interactions in organic–inorganic crystals and goes beyond the traditional focus on interatomic interactions. However, a crystallized framework used for stabilizing parallel spin alignment through an ordered lattice is indispensable to ferromagnetism. Here we demonstrate room-temperature ferromagnetic order in two-dimensional confined molecule-based monolayers. The confinement effect of the van der Waals interlayer space enables cobaltocene molecules to self-assemble into a monolayer with a honeycomb-like configuration. The spontaneous uniform spin orientation—ferromagnetic coupling—is established by an intermolecular vibronic superexchange interaction, involving a cooperative dynamic Jahn–Teller effect in the confined cobaltocene monolayer. The molecular cobaltocene monolayers exhibit a ferromagnetic transition temperature above room temperature and have a large saturation magnetization.