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Register a new userHydrostatic pressure to trigger and assist magnetic transitions: baromagnetic refrigeration
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Added by
Mariano H. Quintero Dr
Publication date
2014
fields
Physics
and research's language is
English
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The possible application of the barocaloric effect to produce solid state refrigerators is a topic of interest in the field of applied physics. In this work, we present experimental data about the influence of external pressure on the magnetic properties of a manganite with phase separation. Using the Jahn Teller effect associated with the presence of the charge ordering we were able to follow the transition to the ferromagnetic state induced by pressure. We also demonstrated that external pressure can assist the ferromagnetic state, decreasing the magnetic field necessary to generate the magnetic transition.
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Structural phase transitions in $f$-electron materials have attracted sustained attention both for practical and basic science reasons, including that they offer an environment to directly investigate relationships between structure and the $f$-state. Here we present results for UCr$_2$Si$_2$, where structural (tetragonal $rightarrow$ monoclinic) and antiferromagnetic phase transitions are seen at $T_{rm{S}}$ $=$ 205 K and $T_{rm{N}}$ $=$ 25 K, respectively. We also provide evidence for an additional second order phase transition at $T_{rm{X}}$ = 280 K. We show that $T_{rm{X}}$, $T_{rm{S}}$, and $T_{rm{N}}$ respond in distinct ways to the application of hydrostatic pressure and Cr $rightarrow$ Ru chemical substitution. In particular, hydrostatic compression increases the structural ordering temperature, eventually causes it to merge with $T_{rm{X}}$ and destroys the antiferromagnetism. In contrast, chemical substitution in the series UCr$_{2-x}$Ru$_x$Si$_2$ suppresses both $T_{rm{S}}$ and $T_{rm{N}}$, causing them to approach zero temperature near $x$ $approx$ 0.16 and 0.08, respectively. The distinct $T-P$ and $T-x$ phase diagrams are related to the evolution of the rigid Cr-Si and Si-Si substructures, where applied pressure semi-uniformly compresses the unit cell and Cr $rightarrow$ Ru substitution results in uniaxial lattice compression along the tetragonal $c$-axis and an expansion in the $ab$-plane. These results provide insights into an interesting class of strongly correlated quantum materials where degrees of freedom associated with $f$-electron magnetism, strong electronic correlations, and structural instabilities are readily controlled.
Motivated by recent experimental observation of an hydrostatic pressure induced transition from semiconductor to semimetal in black phosphorus [Chen et al. in arXiv:1504.00125], we present the first principles calculation on the pressure effect of the electronic structures of black phosphorus. It is found that the band crossover and reversal at the Z point occur around the critical pressure Pc1=1.23 Gpa, and the band inversion evolves into 4 twofold-degenerate Dirac cones around the Z point, suggesting a 3D Dirac semimetal. With further increasing pressure the Dirac cones in the Gamma-Z line move toward the Gamma point and evolve into two hole-type Fermi pockets, and those in the Z-M lines move toward the M point and evolve into 2 hole-type Fermi pockets up to P=4.0 Gpa. It demonstrates clearly that the Lifshitz transition occurs at $P_{c1}$ from semiconductor to 3D Dirac semimetal protected by the nonsymmorphic space symmetry of bulk. This suggests the bright perspective of black phosphorus for optoelectronic and electronic devices due to its easy modulation by pressure.
The results of DC magnetization measurements under hydrostatic (helium-gas) pressure are reported for an ambient pressure superconductor Na0.35CoO2.1.4D2O and its precursor compound, the gamma-phase Na0.75CoO2 that is known to combine a metallic conductivity with an unusual magnetic state below ~22K. The obtained data allowed us to present for the first time the pressure dependence of the magnetic transition in a metallic sodium cobaltate system. This dependence appears to be positive, with the magnetic transition rapidly shifting towards higher temperatures when an applied pressure increases. We ascribe the observed effect to the pressure-induced enhancement of the out-of-plane antiferromagnetic coupling mediated by localized spins interactions (of either superexchange or RKKY type), the scenario consistent with the A-type antiferromagnetic state suggested by recent neutron-scattering data. As for the pressure effect on the superconductivity in Na0.35CoO2.1.4D2O, our measurements established negative and linear for the entire pressure range from 1 bar to 8.3 kbar pressure dependence of Tc, the behavior quite different from the reported by previous workers strong non-linearity of the Tc (P) dependence. (Dated September 12, 2005) PACS numbers: 74.62.Fj, 74.70.-b, 75.20. En, 75.50 Ee, 75.30 Kz.
We present a study of the magnetocaloric effect in La5/8-yPryCa3/8MnO3 (y=0.3) and Pr0.5Ca0.09Sr0.41MnO3 manganites. The low temperature state of both ystems is the result of a competition between the antiferromagnetic and ferromagnetic phases. The samples display magnetocaloric effect evidenced in an adiabatic temperature change during a metamagnetic transition from an antiferromagnetic to a ferromagnetic phase . As additional features, La5/8-yPryCa3/8MnO3 exhibits phase separation characterized by the coexistence of antiferromagnetic and ferromagnetic phases and Pr0.5Ca0.09Sr0.41MnO3 displays inverse magnetocaloric effect in which temperature decreases while applying an external magnetic field. In both cases, a significant part of the magnetocaloric effect appears from non-reversible processes. As the traditional thermodynamic description of the effect usually deals with reversible transitions, we developed an alternative way to calculate the adiabatic temperature change in terms of the change of the relative ferromagnetic fraction induced by magnetic field. To evaluate our model, we performed direct measurement of the samples adiabatic temperature change by means of a differential thermal analysis. An excellent agreement has been obtained between experimental and calculated data. These results show that metamagnetic transition in manganites play an important role in the study of magnetic refrigeration.
The sudden decrease in molar volume exhibited by most lanthanides under high pressure is often attributed to changes in the degree of localization of their 4f-electrons. We give evidence, based on electrical resistivity measurements of dilute Y(Gd) and Y(Tb) alloys to 120 GPa, that the volume collapse transitions in Gd and Tb metals have different origins, despite their being neighbors in the periodic table. Remarkably, the change under pressure in the magnetic state of isolated Pr or Tb impurity ions in the nonmagnetic Y host appears to closely mirror corresponding changes in pure Pr or Tb metals. The collapse in Tb appears to be driven by an enhanced negative exchange interaction between 4f and conduction electrons under pressure (Kondo resonance) which, in the case of Y(Tb), dramatically alters the superconducting properties of the Y host, much like previously found for Y(Pr). In Gd our resistivity measurements suggest that a Kondo resonance is not the main driver for its volume collapse. X-ray absorption and emission spectroscopies clearly show that 4f local moments remain largely intact across both volume collapse transitions ruling out 4f band formation (delocalization) and valence transition models as possible drivers. The results highlight the richness of behavior behind the volume collapse transition in lanthanides and demonstrate the stability of the 4f level against band formation to extreme pressure.
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