Related Experiment Video
Updated: Mar 28, 2026

Measuring Magnetically-Tuned Ferroelectric Polarization in Liquid Crystals
Published on: August 15, 2018
Magnetic Ordering-Induced Multiferroic Behavior in [CH3NH3][Co(HCOO)3] Metal-Organic Framework
L Claudia Gómez-Aguirre1, Breogán Pato-Doldán1, J Mira2
1Department of Fundamental Chemistry, Faculty of Sciences, University of A Coruña , 15071 A Coruña, Spain.
We discovered multiferroic behavior in a metal-organic framework magnet. This spin canted antiferromagnet exhibits coupled magnetic and electric properties, showing memory effects under magnetic fields.
Area of Science:
- Materials Science
- Solid State Physics
- Chemistry
Background:
- Metal-organic frameworks (MOFs) offer tunable structures for novel properties.
- Multiferroic materials exhibit coupled magnetic and electric ordering.
- Investigating MOFs for multiferroic behavior is an emerging research area.
Purpose of the Study:
- To report the first instance of magnetic ordering-induced multiferroic behavior in a MOF.
- To characterize the magnetic and electric properties of [CH3NH3][Co(HCOO)3].
- To elucidate the mechanism behind the observed multiferroic coupling.
Main Methods:
- Synthesis and structural analysis of the [CH3NH3][Co(HCOO)3] compound.
- Magnetic susceptibility and magnetization measurements.
- Electric polarization measurements under applied magnetic fields.
Main Results:
- The compound [CH3NH3][Co(HCOO)3] exhibits multiferroic behavior below 15.9 K.
- Magnetic ordering is spin canted antiferromagnetic with a weak ferromagnetic component due to Dzyaloshinskii-Moriya (DM) interactions.
- Coupled magnetic and electric switching observed along specific crystallographic directions, with an unusual electric polarization memory effect.
Conclusions:
- The metal-organic framework [CH3NH3][Co(HCOO)3] is a novel multiferroic material.
- The observed multiferroic behavior is attributed to an inverse-DM mechanism.
- The findings open new avenues for MOF-based multiferroic applications.
More Related Videos
06:53Author Spotlight: Magnetometric Characterization of Intermediates in the Solid-State Electrochemistry of Redox-Active Metal-Organic Frameworks
Published on: June 9, 2023
08:55Methods of Ex Situ and In Situ Investigations of Structural Transformations: The Case of Crystallization of Metallic Glasses
Published on: June 7, 2018
Related Concept Videos
Colors and Magnetism
When atoms or molecules absorb light at the proper frequency, their electrons are excited to higher-energy orbitals. For many main group atoms and molecules, the absorbed photons are in the ultraviolet range of the electromagnetic spectrum, which cannot be detected by the human eye. For coordination compounds, the energy difference between the d orbitals often allows photons in the visible range to be absorbed and emitted, which is seen as colors by the human...
Valence Bond Theory
Ferromagnetism
Crystal Field Theory - Octahedral Complexes
To explain the observed behavior of transition metal complexes (such as colors), a model involving electrostatic interactions between the electrons from the ligands and the electrons in the unhybridized d orbitals of the central metal atom has been developed. This electrostatic model is crystal field theory (CFT). It helps to understand, interpret, and predict the colors, magnetic behavior, and some structures of coordination compounds of transition metals.
CFT focuses on...
Metallic Solids
All metallic solids exhibit high thermal and electrical conductivity, metallic luster, and malleability....
Structural Isomerism
Isomers are different chemical species that have the same chemical formula. Structural isomerism of coordination compounds can be divided into two subcategories, the linkage isomers and coordination-sphere isomers.
Linkage isomers occur when the coordination compound contains a ligand that can bind to the transition metal center through two different atoms. For example, the CN− ligand can bind through the carbon atom or through the nitrogen atom. Similarly, SCN− can...