TY - JOUR
T1 - Half-Metallicity and Magnetic Anisotropy in Double-Perovskite GdBaCo2O6 Films Prepared via Topotactic Oxidation
AU - Katayama, Tsukasa
AU - Mo, Shishin
AU - Chikamatsu, Akira
AU - Kurauchi, Yuji
AU - Kumigashira, Hiroshi
AU - Hasegawa, Tetsuya
N1 - Funding Information:
This work was supported by JST, PRESTO Grant Number JPMJPR21Q3, Japan, JSPS KAKENHI (20H02614), and Kao Foundation for Arts and Sciences.
Publisher Copyright:
© 2023 American Chemical Society.
PY - 2023/2/14
Y1 - 2023/2/14
N2 - Double-perovskite GdBaCo2Ox is a promising material owing to its fascinating electronic and magnetic features, such as spin crossover, charge and spin-state ordering, magnetic-field or photo-induced antiferromagnetic-to-ferromagnetic phase transition, and large magnetoresistance (MR). These properties can be controlled by changing the oxygen content (x), and an increase of x is effective for stabilizing ferromagnetic order. However, a stoichiometric phase (x = 6) has not yet been obtained because the distorted coordination geometry prefers oxygen vacancies. In this study, we report the successful synthesis of GdBaCo2O6 epitaxial films via the topotactic oxidation of a film with x = 5.5. The transformation between x = 5.5 and 6 phases was reversible via low-temperature redox reactions. The x = 6 film exhibited ferromagnetic and metallic behavior below the Curie temperature (TC) of 110 K and semiconducting behavior above TC. The spontaneous magnetization of the x = 6 film was 4.8 μB/f.u., which is the largest in the double-perovskite cobaltite system owing to the ferromagnetic interaction between Co3.5+ and Gd3+. It also exhibited strong magnetic anisotropy along the a axis (1.7 × 107 erg/cm3) and anisotropic MR behavior associated with the Gd/Ba ordering along the c axis.
AB - Double-perovskite GdBaCo2Ox is a promising material owing to its fascinating electronic and magnetic features, such as spin crossover, charge and spin-state ordering, magnetic-field or photo-induced antiferromagnetic-to-ferromagnetic phase transition, and large magnetoresistance (MR). These properties can be controlled by changing the oxygen content (x), and an increase of x is effective for stabilizing ferromagnetic order. However, a stoichiometric phase (x = 6) has not yet been obtained because the distorted coordination geometry prefers oxygen vacancies. In this study, we report the successful synthesis of GdBaCo2O6 epitaxial films via the topotactic oxidation of a film with x = 5.5. The transformation between x = 5.5 and 6 phases was reversible via low-temperature redox reactions. The x = 6 film exhibited ferromagnetic and metallic behavior below the Curie temperature (TC) of 110 K and semiconducting behavior above TC. The spontaneous magnetization of the x = 6 film was 4.8 μB/f.u., which is the largest in the double-perovskite cobaltite system owing to the ferromagnetic interaction between Co3.5+ and Gd3+. It also exhibited strong magnetic anisotropy along the a axis (1.7 × 107 erg/cm3) and anisotropic MR behavior associated with the Gd/Ba ordering along the c axis.
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U2 - 10.1021/acs.chemmater.2c03335
DO - 10.1021/acs.chemmater.2c03335
M3 - Article
AN - SCOPUS:85146630054
SN - 0897-4756
VL - 35
SP - 1295
EP - 1300
JO - Chemistry of Materials
JF - Chemistry of Materials
IS - 3
ER -