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تسجيل مستخدم جديدTuning the phase transition dynamics by variation of cooling field and metastable phase fraction in Al doped Pr$_{0.5}$Ca$_{0.5}$MnO$_3$
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We report the effect of field, temperature and thermal history on the time dependence in resistivity and magnetization in the phase separated state of Al doped Pr$_{0.5}$Ca$_{0.5}$MnO$_3$. The rate of time dependence in resistivity is much higher than that of magnetization and it exhibits a different cooling field dependence due to percolation effects. Our analysis show that the time dependence in physical properties depends on the phase transition dynamics which can be effectively tuned by variation of temperature, cooling field and metastable phase fraction. The phase transition dynamics can be broadly divided into the arrested and un-arrested regimes, and in the arrested regime, this dynamics is mainly determined by time taken in the growth of critical nuclei. An increase in cooling field and/or temperature shifts this dynamics from arrested to un-arrested regime, and in this regime, this dynamics is determined by thermodynamically allowed rate of formation of critical nuclei which in turn depends on the cooling field and available metastable phase fraction. At a given temperature, a decrease in metastable phase fraction shifts the crossover from arrested to un-arrested regimes towards lower cooling field. It is rather significant that inspite of the metastable phase fraction calculated from resistivity being somewhat off from that of magnetization, their cooling field dependence exhibits a striking similarity which indicate that the dynamics in arrested and un-arrested regimes are so different that it comes out vividly provided that the measurements are done around percolation threshold.
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We studied the charge-orbital ordering in the superlattice of charge-ordered insulating Pr$_{0.5}$Ca$_{0.5}$MnO$_3$ and ferromagnetic metallic La$_{0.5}$Sr$_{0.5}$MnO$_3$ by resonant soft x-ray diffraction. A temperature-dependent incommensurability
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Dc magnetic measurements across the charge ordering (CO) transition temperature (T$_{CO}$) in polycrystalline Pr$_{0.5}$Ca$_{0.5}$Mn$_{0.975}$Al$_{0.025}$O$_3$ have been performed under simultaneous influence of external hydrostatic pressure (P) and
magnetic field (H). We show the first experimental evidence that the melting of charge order instability obey an interesting scaling function, $delta$T$_{CO}$/P$^alpha$ = $f$(H/P$^beta$) in H-P-T landscape, where $delta$T$_{CO}$ is the suppression of T$_{CO}$ by P and H. Corresponding values of the exponents, $alpha$ = 1.63 and $beta$ = 0.33 have been extracted from data collapsing phenomena. Possible origin of such a scaling behavior has been discussed.
We report low temperature specific heat measurements of Pr$_{1-x}$Ca$_{x}$MnO$_{3}$ ($0.3leq x leq 0.5$) and La$_{0.5}$Ca$_{0.5}$MnO$_{3}$ with and without applied magnetic field. An excess specific heat, $C^{prime}(T)$, of non-magnetic origin associ
ated with charge ordering is found for all the samples. A magnetic field sufficient to induce the transition from the charge-ordered state to the ferromagnetic metallic state does not completely remove the $C^{prime}$ contribution. This suggests that the charge ordering is not completely destroyed by a melting magnetic field. In addition, the specific heat of the Pr$_{1-x}$Ca$_{x}$MnO$_{3}$ compounds exhibit a large contribution linear in temperature ($gamma T$) originating from magnetic and charge disorder.
We report the study of magnetic and orbital order in Pr$_{0.5}$Ca$_{0.5}$MnO$_3$ epitaxial thin films grown on (LaAlO$_3$)$_{0.3}$-(SrAl$_{0.5}$Ta$_{0.5}$O$_3$)$_{0.7}$ (LSAT) (011)$_c$. In a new experimental approach, the polarization and energy dep
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