Oxygen Isotope Effect on the Spin State Transition in (Pr0.7_{0.7}Sm0.3_{0.3})0.7_{0.7}Ca0.3_{0.3}CoO3{_3}

Oxygen isotope substitution is performed in the perovskite cobalt oxide (Pr$_{0.7}$Sm$_{0.3}$)$_{0.7}$Ca$_{0.3}$CoO${_3}$ which shows a sharp spin state transition from the intermediate spin (IS) state to the low spin (LS) state at a certain temperature. The transition temperature of the spin state up-shifts with the substitution of $^{16}O$ by $^{18}$O from the resistivity and magnetic susceptibility measurements. The up-shift value is 6.8 K and an oxygen isotope exponent ($\alpha_S$) is about -0.8. The large oxygen isotope effect indicates strong electron-phonon coupling in this material. The substitution of $^{16}$O by $^{18}$O leads to a decrease in the frequency of phonon and an increase in the effective mass of electron ($m$$^\ast$), so that the bandwidth W is decreased and the energy difference between the different spin states is increased. This is the reason why the $T_s$ is shifted to high temperature with oxygen isotopic exchange.Comment: 4 pages, 3 figure

Enhanced spin-orbit torques in MnAl/Ta films with improving chemical ordering

We report the enhancement of spin-orbit torques in MnAl/Ta films with improving chemical ordering through annealing. The switching current density is increased due to enhanced saturation magnetization MS and effective anisotropy field HK after annealing. Both damplinglike effective field HD and fieldlike effective field HF have been increased in the temperature range of 50 to 300 K. HD varies inversely with MS in both of the films, while the HF becomes liner dependent on 1/MS in the annealed film. We infer that the improved chemical ordering has enhanced the interfacial spin transparency and the transmitting of the spin current in MnAl layer