4,821 research outputs found

    Elastocaloric response of PbTiO3 predicted from a first-principles effective Hamiltonian

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    A first-principles based effective Hamiltonian is used within a molecular dynamics simulation to study the elastocaloric effect in PbTiO3. It is found that the transition temperature is a linear function of uniaxial tensile stress. Negative temperature change is calculated, when the uniaxial tensile stress is switched off, as a function of initial temperature Delta-T(T_initial). It is predicted that the formation of domain structures under uniaxial tensile stress degrades the effectiveness of the elastocaloric effect.Comment: 6 pages, 7 figures, published in JPS

    Non-Arrhenius ionic conductivities in glasses due to a distribution of activation energies

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    Previously observed non-Arrhenius behavior in fast ion conducting glasses [\textit{Phys.\ Rev.\ Lett.}\ \textbf{76}, 70 (1996)] occurs at temperatures near the glass transition temperature, TgT_{g}, and is attributed to changes in the ion mobility due to ion trapping mechanisms that diminish the conductivity and result in a decreasing conductivity with increasing temperature. It is intuitive that disorder in glass will also result in a distribution of the activation energies (DAE) for ion conduction, which should increase the conductivity with increasing temperature, yet this has not been identified in the literature. In this paper, a series of high precision ionic conductivity measurements are reported for 0.5Na2S+0.5[xGeS2+(1−x)PS5/2]0.5{Na}_{2}{S}+0.5[x{GeS}_{2}+(1-x){PS}_{5/2}] glasses with compositions ranging from 0≤x≤10 \leq x \leq 1. The impact of the cation site disorder on the activation energy is identified and explained using a DAE model. The absence of the non-Arrhenius behavior in other glasses is explained and it is predicted which glasses are expected to accentuate the DAE effect on the ionic conductivity.Comment: 2 figure

    Bromide and other ions in the snow, firn air, and atmospheric boundary layer at Summit during GSHOX

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    Measurements of gas phase soluble bromide in the boundary layer and in firn air, and Br− in aerosol and snow, were made at Summit, Greenland (72.5° N, 38.4° W, 3200 m a.s.l.) as part of a larger investigation into the influence of Br chemistry on HOx cycling. The soluble bromide measurements confirm that photochemical activation of Br− in the snow causes release of active Br to the overlying air despite trace concentrations of Br− in the snow (means 15 and 8 nmol Br− kg−1 of snow in 2007 and 2008, respectively). Mixing ratios of soluble bromide above the snow were also found to be very small (mean \u3c1 ppt both years, with maxima of 3 and 4 ppt in 2007 and 2008, respectively), but these levels clearly oxidize and deposit long-lived gaseous elemental mercury and may perturb HOx partitioning. Concentrations of Br− in surface snow tended to increase/decrease in parallel with the specific activities of the aerosol-associated radionuclides 7Be and 210Pb. Earlier work has shown that ventilation of the boundary layer causes simultaneous increases in 7Be and 210Pb at Summit, suggesting there is a pool of Br in the free troposphere above Summit in summer time. Speciation and the source of this free tropospheric Br− are not well constrained, but we suggest it may be linked to extensive regions of active Br chemistry in the Arctic basin which are known to cause ozone and mercury depletion events shortly after polar sunrise. If this hypothesis is correct, it implies persistence of the free troposphere Br− for several months after peak Br activation in March/April. Alternatively, there may be a ubiquitous pool of Br− in the free troposphere, sustained by currently unknown sources and processes

    Real Space Visualization of Thermomagnetic Irreversibility within Supercooling and Superheating Spinodals in Mn1.85Co0.15SbMn_{1.85}Co_{0.15}Sb using Scanning Hall Probe Microscopy

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    Phase coexistence across disorder-broadened and magnetic-field-induced first order antiferromagnetic to ferrimagnetic transition in polycrystalline Mn1.85Co0.15SbMn_{1.85}Co_{0.15}Sb has been studied mesoscopically by Scanning Hall Probe Microscope at 120K and up to 5 Tesla magnetic fields. We have observed hysteresis with varying magnetic field and the evolution of coexisting antiferromagnetic and ferrimagnetic state on mesoscopic length scale. These studies show that the magnetic state of the system at low field depends on the path followed to reach 120 K. The low field magnetic states are mesoscopically different for virgin and second field increasing cycle when 120 K is reached by warming from 5K, but are the same within measurement accuracy when the measuring temperature of 120K is reached from 300K by cooling
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