n‐ to p‐type Sr 2 Fe 1+x Re 1‐x O 6 double perovskites: magnetoresistance and magnetoSeebeck

Abstract The T‐dependent Seebeck (S) of several samples belonging to the Sr 2 Fe 1+x Re 1‐x O 6 series (x≤0.33) has been investigated. All these polycrystalline samples synthesized by solid state reaction in closed vessels crystallize in the I4/m double perovskite structure. Though ferrimagnetic wit...

Full description

Saved in:
Bibliographic Details
Published inZeitschrift für anorganische und allgemeine Chemie (1950) Vol. 649; no. 5
Main Authors Hébert, Sylvie, Carbonio, Raul, Martin, Christine, Maignan, Antoine
Format Journal Article
LanguageEnglish
Published 01.03.2023
Online AccessGet full text

Cover

Loading…
More Information
Summary:Abstract The T‐dependent Seebeck (S) of several samples belonging to the Sr 2 Fe 1+x Re 1‐x O 6 series (x≤0.33) has been investigated. All these polycrystalline samples synthesized by solid state reaction in closed vessels crystallize in the I4/m double perovskite structure. Though ferrimagnetic with T C >400 K, the decrease of their magnetization as x increases from x=0.00 is explained by the cation disorder induced by the deviation from the ideal 1 : 1 Re/Fe ratio for the 2a and 2b crystallographic sites. Interestingly, it is found that at room temperature, the S sign changes from S>0 to S<0 as x increases to about x=0.25. Despite that the magnitude of their magnetoresistance, near −20 % in 9T and at T=5 K, is not very sensitive to x, a positive magneto Seebeck effect is observed only for the samples exhibiting S(300 K)>0. This asymmetry in the magnetothermopower properties of the n‐ and p‐type samples is interpreted in the framework of the spin polarized transport of these magnetoresistive double‐perovskites.
ISSN:0044-2313
1521-3749
DOI:10.1002/zaac.202200324