# Giant Ferrimagnetism and Polarization in a Mixed Metal Perovskite   Metal-Organic Framework

**Authors:** Paresh Chandra Rout, Varadharajan Srinivasan

arXiv: 1703.10853 · 2018-01-24

## TL;DR

This study computationally designs a mixed metal perovskite MOF with giant ferrimagnetism, high polarization, and elevated transition temperature, advancing the potential for multiferroic applications.

## Contribution

It introduces a novel mixed metal perovskite MOF with significantly enhanced magnetic and electric properties, demonstrating a new approach for designing multiferroic materials.

## Key findings

- Magnetization increased by two orders of magnitude
- Polarization of 9.9 μC/cm2 achieved
- Transition temperature up to 56 K predicted

## Abstract

Perovskite metal-organic frameworks (MOFs) have recently emerged as potential candidates for multiferroicity. However, the compounds synthesized so far possess only weak ferromagnetism and low polarization. Additionally, the very low magnetic transition temperatures ($T_c$) also pose a challenge to the application of the materials. We have computationally designed a mixed metal perovskite MOF -[C(NH2)3][(Cu0.5Mn0.5)(HCOO)3]- that is predicted to have magnetization two orders of magnitude larger than its parent ([C(NH2)3][Cu(HCOO)3]), a significantly larger polarization (9.9 {\mu}C/cm2), and an enhanced $T_c$ of up to 56 K, unprecedented in perovskite MOFs. A detailed study of the magnetic interactions revealed a novel mechanism leading to the large moments as well as the increase in the $T_c$. Mixing a non-Jahn-Teller ion (Mn$^{2+}$) into a Jahn-Teller host (Cu$^{2+}$) leads to competing lattice distortions which are possibly responsible for the enhanced polarization. The MOF is thermodynamically stable as evidenced by the computed enthalpy of formation, and can likely be synthesized. Our work represents a first step towards rational design of multiferroic perovskite MOFs through the largely unexlpored mixed metal approach.

## Full text

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## Figures

13 figures with captions in the complete paper: https://tomesphere.com/paper/1703.10853/full.md

## References

50 references — full list in the complete paper: https://tomesphere.com/paper/1703.10853/full.md

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Source: https://tomesphere.com/paper/1703.10853