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...
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Published in | Zeitschrift für anorganische und allgemeine Chemie (1950) Vol. 649; no. 5 |
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Main Authors | , , , |
Format | Journal Article |
Language | English |
Published |
01.03.2023
|
Online Access | Get full text |
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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. |
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ISSN: | 0044-2313 1521-3749 |
DOI: | 10.1002/zaac.202200324 |