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Dimensional Transformation of Molecular Magnetic Materials

  • Yulong Huang
  • , Weiyi Gong
  • , Gengyi Zhang
  • , Zheng Li
  • , Haiqing Lin
  • , Qimin Yan
  • , Shenqiang Ren
  • SUNY Buffalo
  • Northeastern University

Research output: Contribution to journalArticlepeer-review

2 Scopus citations

Abstract

Two-dimensional (2D) magnetic layered materials have revolutionized size dependent magnetism to manipulate spin-based devices. However, it has been challenging to artificially create 2D magnetic materials from three-dimensional (3D) crystal structures with a variety of material groups. Here, we present the dimensionality manipulation via cation exchange of a 3D Prussian blue analogue [RbMnFe(CN)6] toward a 2D magnetic sheet [(K,Rb)(V,Mn)(Cr,Fe)(CN)6] with the magnetic ordering temperature rising from 12 to 330 K. Such a 2D magnetic sheet achieves crystalline V-Cr coordination in the Prussian blue lattice with pronounced anisotropy and stimuli responsiveness. The pressure dependent magnetic tunability of such 2D networks is predicted using first-principles calculations and demonstrated using the phase transitions of the hydrogel. This previously unobserved phenomenon of dimensional manipulation of a bulk crystal structure provides a rational strategy to expand the diversity and chemical compositions of 2D molecular magnetic material libraries.

Original languageEnglish
Pages (from-to)13232-13240
Number of pages9
JournalACS Nano
Volume16
Issue number8
DOIs
StatePublished - Aug 23 2022

Keywords

  • 2D
  • cation exchange
  • dimensional transformation
  • Prussian blue analogue
  • room-temperature magnetic order

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