# Effect of A-site ionic radius on metamagnetic transition in charge   ordered $Sm_{0.5}(Ca_{0.5-y}Sr_{y})MnO_3$ compounds

**Authors:** Sanjib Banik, Kalpataru Pradhan, I. Das

arXiv: 1903.11348 · 2019-03-28

## TL;DR

This study explores how increasing the A-site ionic radius via Sr doping affects the metamagnetic transition in charge-ordered Sm-based manganites, revealing a decrease in critical magnetic field and phase separation enhancement.

## Contribution

It provides new insights into the role of A-site ionic radius and Sr doping in controlling metamagnetic transitions and phase separation in Sm-based manganites, supported by experimental and theoretical analysis.

## Key findings

- Critical field decreases with Sr doping.
- Phase separation increases with A-site ionic radius.
- Metamagnetic transition is martensitic in nature.

## Abstract

We investigate the ultra-sharp jump in the isothermal magnetization and the resistivity in the polycrystalline $Sm_{0.5}(Ca_{0.5-y}Sr_{y})MnO_3$ $(y = 0, 0.1, 0.2, 0.25, 0.3, 0.5)$ compounds. The critical field $(H_{cr})$, required for the ultra-sharp jump, decreases with increase of `Sr' concentration, i.e. with increase of average A-site ionic radius $\langle r_A\rangle$. The magnetotransport data indicate that the phase separation increases with the increase of $\langle r_A\rangle$, i.e. with $y$. The dependency of $H_{cr}$ with magnetic field sweep rate reveals that the ultra-sharp jump from antiferromagnetic (AFM) state to the ferromagnetic (FM) state is of martensitic in nature. Our two-band double exchange model Hamiltonian calculations show that the `Sr' doping induces the ferromagnetic clusters in the antiferromagnetic insulating phase and in turn reduces the critical field. In the end we present a phenomenological picture obtained from our combined experimental and theoretical study.

## Full text

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## Figures

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## References

36 references — full list in the complete paper: https://tomesphere.com/paper/1903.11348/full.md

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Source: https://tomesphere.com/paper/1903.11348