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Register a new userAn indirect magnetic approach for determining entropy change in first-order magnetocaloric materials
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Taking into account the phase fraction during transition for the first-order magnetocaloric materials, an improved isothermal entropy change determination has been put forward based on the Clausius-Clapeyron (CC) equation. It was found that the isothermal entropy change value evaluated by our method is in excellent agreement with those determined from the Maxwell-relation (MR) for Ni-Mn-Sn Heusler alloys, which usually presents a weak field-induced phase transforming behavior. In comparison with MR, this method could give rise to a favorable result derived from few thermomagnetic measurements. More importantly, we can eliminate the isothermal entropy change overestimation derived from MR, which always exists in the cases of Ni-Co-Mn-In and MnAs systems with a prominent field-induced transition. These results confirmed that such a CC-equation-based method is quite practical and superior to the MR-based ones in eliminating the spurious spike and reducing measuring cost.
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We combine spin polarised density functional theory and thermodynamic mean field theory to describe the phase transitions of antiperovskite manganese nitrides. We find that the inclusion of the localized spin contribution to the entropy, evaluated through mean field theory, lowers the transition temperatures. Furthermore, we show that the electronic entropy leads to first order phase transitions in agreement with experiments whereas the localized spin contribution adds second order character to the transition. We compare our predictions to available experimental data to assess the validity of the assumptions underpinning our multilevel modelling.
We report the fabrication of ErAl2 magnetocaloric wires by a powder-in-tube method (PIT) and the evaluation of magnetic entropy change through magnetization measurements. The magnetic entropy change of ErAl2 PIT wires exhibits similar behavior to the bulk counterpart, while its magnitude is reduced by the decrease in the volume fraction of ErAl2 due to the surrounding non-magnetic sheaths. We find that another effect reduces the magnetic entropy change of the ErAl2 PIT wires around the Curie temperature, and discuss its possible origin in terms of a correlation between magnetic properties of ErAl2 and mechanical properties of sheath material.
The crystal structure and magnetic properties of MnCoxFe1-xSi (x=0-0.5) compounds were investigated. With increasing Fe content, the unit cell changes anisotropically and the magnetic property evolves gradually: Curie temperature decreases continuously, the first-order metamagnetic transition from a low-temperature helical antiferromagnetic state to a high-temperature ferromagnetic state disappears gradually and then a spin-glass-like state and another antiferromagnetic state emerge in the low temperature region. The Curie transition leads to a moderate conventional entropy change. The metamagnetic transition not only yields a larger negative magnetocaloric effect at lower applied fields than in MnCoSi but also produces a very large temperature span (103 K for H=5 T) of delta S(T), which results in a large refrigerant capacity. These phenomena were explained in terms of crystal structure change and magnetoelastic coupling mechanism. The low-cost MnCo1-xFexSi compounds are promising candidates for near room temperature magnetic refrigeration applications because of the large isothermal entropy change and the wide working temperature span.
The compounds FeMnAsxP1-x are very promising as far as commercial applications of the magnetocaloric effect are concerned. However, the theoretical literature on magnetocaloric materials still adopts simple molecular-field models in the description of important properties like the entropy variation that accompanies applied isothermal magnetic field cycling, for instance. We apply a Green function theoretical treatment for such analysis. The advantages of such approach are well-known since the details of the crystal structure are incorporated in the model, as well as a precise description of correlations between spins of the transition metal ions can be obtained. For the sake of simplcity we adopt a simple one-exchange parameter Heisenberg model, and the observed first-order phase transitions are reproduced by the introduction of a biquadratic term in the hamiltonian. Good agreement with experimental magnetocaloric data for FeMnAsxP1-x compounds is obtained, as well as an agreement with the magnetic field dependence for these properties predicted from the Landau theory of continuous phase transitions.
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Meryl D. Stoller
, Rodney S. Ruoff (Department of Mechanicaln Engineering
, the Texas Materials Institute
2010
Ultracapacitors are rapidly being adopted for use for a wide range of electrical energy storage applications. While ultracapacitors are able to deliver high rates of charge and discharge, they are limited in the amount of energy stored. The capacity of ultracapacitors is largely determined by the electrode material and as a result, research to improve the performance of electrode materials has dramatically increased. While test methods for packaged ultracapacitors are well developed, it is often not feasible for the materials scientist to assemble full sized, packaged cells to test electrode materials. Methodology to reliably measure a materials performance for ultracapacitor electrode use is not well standardized with the different techniques currently being used yielding widely varying results. In this manuscript, we review the best practice test methods that accurately predict a materials performance, yet are flexible and quick enough to accommodate a wide range of material sample types and amounts.
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