Close-to-ideal spin polarization in zinc-doped Fe-Mo double perovskites at the nanoscale

A high degree of spin polarization in half-metallic double perovskites is a prerequisite for several applications in spintronics, which depends crucially on the cationic order of the systems. This paper reports a study on tailoring the structure and morphology of nano-sized Sr2Fe1-xZnxMoO6 (x = 0.05, 0.1, 0.15) materials to improve their spin polarization. The combined analysis of synchrotron X-ray diffraction and magnetization data shows that Zn replaces Fe in the B sites. Although the majority of particles have lateral dimensions in the range 30-60 nm as observed by scanning electron microscope, the samples with x = 0.1 and 0.15 show finite-size effects with superparamagnetism below room temperature and a reduced Curie temperature (from 410 K for x = 0.05-390 K for x = 0.15). The results are due to the formation of networks of insulating Mo-O-Zn-O-Mo linkages and antiphase boundaries, which divide the particles into smaller domains with a mean diameter of similar to 11 nm as determined via a Langevin fit. The almost perfectly ordered structure in the nanodomains is responsible for a high magnetoresistance ratio. A value of -42% at 5 K in 50 kOe is recorded for the sample x = 0.15. Via fitting the magnetoresistance curve using the Inoue-Mekagawa theory, the spin polarization of 99% is determined.

Automated summary

By tailoring the structure and morphology of nano-sized Sr2Fe1-xZnxMoO6 materials, this study successfully increased their spin polarization. The formation of smaller domains due to the replacement of Fe by Zn led to a higher magnetoresistance ratio in the samples.