Abstract
In this report, we present structural, electronic, magnetic and transport properties of Co-rich spin gapless semiconductor CoFeCrGa using both theoretical and experimental techniques. The key advantage of Co-rich samples $\mathrm{Co_{1+x}Fe_{1-x}CrGa}$ is the high Curie temperature (T$\mathrm{_C}$) and magnetization, without compromising the SGS nature (up to x = 0.4), and hence our choice. The quaternary Heusler alloys $\mathrm{Co_{1+x}Fe_{1-x}CrGa}$ (x = 0.1 to 0.5) are found to crystallize in LiMgPdSn-type structure having space group $F\bar{4}3m$ (\# 216). The measured Curie temperature increases from 690 K (x = 0) to 870 K (x = 0.5). Observed magnetization values follow the Slater-Pauling rule. Measured electrical resistivity, in the temperature range of 5-350 K, suggests that the alloys retain the SGS behavior up to x = 0.4, beyond which it reflects metallic character. Unlike conventional semiconductors, the conductivity value ($\mathrm{\sigma_{xx}}$) at 300 K lies in the range of 2289 S $\mathrm{cm^{-1}}$ to 3294 S $\mathrm{cm^{-1}}$, which is close to that of other reported SGS materials. The anomalous Hall effect is comparatively low. The intrinsic contribution to the anomalous Hall conductivity increase with x, which can be correlated with the enhancement in chemical order. The anomalous Hall coefficient is found to increase from 38 S/cm for x = 0.1 to 43 S/cm for 0.3. Seebeck coefficients turn out to be vanishingly small below 300 K, another signature for being SGS. All the alloys (for different x) are found to be both chemically and thermally stable. Simulated magnetization agrees fairly with the experiment. As such Co-rich CoFeCrGa is a promising candidate for room temperature spintronic applications, with enhanced T$\mathrm{_C}$, magnetic properties and SGS nature.
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.