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<title>Publications</title>
<copyright>Copyright (c) 2013 Southern Illinois University Carbondale All rights reserved.</copyright>
<link>http://opensiuc.lib.siu.edu/phys_pubs</link>
<description>Recent documents in Publications</description>
<language>en-us</language>
<lastBuildDate>Sat, 26 Jan 2013 23:56:24 PST</lastBuildDate>
<ttl>3600</ttl>








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<title>The Comparison of Direct and Indirect Methods for Determining the Magnetocaloric Parameters in the Heusler Alloy Ni50Mn34.8In14.2B</title>
<link>http://opensiuc.lib.siu.edu/phys_pubs/66</link>
<guid isPermaLink="true">http://opensiuc.lib.siu.edu/phys_pubs/66</guid>
<pubDate>Fri, 02 Nov 2012 12:05:46 PDT</pubDate>
<description>
	<![CDATA[
	<p>The magnetocaloric properties of the Ni<sub>50</sub>Mn<sub>34.8</sub>In<sub>14.2</sub>B Heusler alloy have been studied by direct measurements of the adiabatic temperature change (ΔT<sub>AD</sub>(T,H)) and indirectly by magnetization (M(T,H)), differential scanning calorimetry, and specific heat (C(T,H)) measurements. The presence of a first-order ferromagnetic-paramagnetic transition has been detected for Ni<sub>50</sub>Mn<sub>34.8</sub>In<sub>14.2</sub>B at 320 K. The magnetocaloric parameters, i.e., the magnetic entropy change (ΔS<sub>M</sub> = (2.9-3.2) J/kgK) and the adiabatic temperature change (ΔT<sub>AD</sub> = (1.3-1.52) K), have been evaluated for ΔH = 1.8 T from C<sub>P</sub>(T,H) and M(T,H) data and from direct ΔT<sub>AD</sub>(T,H) measurements. The extracted magnetocaloric parameters are comparable to those of Gd.</p>

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</description>

<author>Igor Dubenko et al.</author>


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<title>The Role of Ni-Mn Hybridization on the Martensitic Phase Transitions in Mn-rich Heusler Alloys</title>
<link>http://opensiuc.lib.siu.edu/phys_pubs/65</link>
<guid isPermaLink="true">http://opensiuc.lib.siu.edu/phys_pubs/65</guid>
<pubDate>Fri, 02 Nov 2012 12:05:45 PDT</pubDate>
<description>
	<![CDATA[
	<p>Room temperature x-ray diffraction, dc magnetization, and ac susceptibility measurements have been performed on a series of Mn rich Ni<sub>50</sub>Mn<sub>37-<em>x</em></sub>Cr<sub><em>x</em></sub>Sb<sub>13</sub> and Ni<sub>50+<em>x</em></sub>Mn<sub>37-<em>x</em></sub>Sb<sub>13</sub> Heusler alloys. Depending on the value of <em>x</em>, the room temperature crystal structures of the samples are either L2<sub>1</sub> cubic or orthorhombic. It is a commonly accepted idea that the martensitic transition temperatures in Ni-Mn-Z (Z = Ga, In, Sb, Sn) based Heusler alloys decrease (increase) with decreasing (increasing) valence electron concentration, <em>e/a</em>. However, the present work shows that regardless of the change in <em>e/a</em>, the martensitic transition temperature (T<sub><em>M</em></sub>) decreases with increasing Cr or Ni concentration. These results support the model where, in the case of Mn rich Heusler alloys, it is the hybridization between the Ni atoms and the Mn atoms in the Z sites that plays the dominant role in driving the martensitic transformation.</p>

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</description>

<author>Mahmud Khan et al.</author>


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<title>Magnetostructural Phase Transitions and Magnetocaloric Effects in MnNiGe1-xAlx</title>
<link>http://opensiuc.lib.siu.edu/phys_pubs/64</link>
<guid isPermaLink="true">http://opensiuc.lib.siu.edu/phys_pubs/64</guid>
<pubDate>Fri, 02 Nov 2012 12:05:44 PDT</pubDate>
<description>
	<![CDATA[
	<p>The thermomagnetic and magnetocaloric properties of the MnNiGe<sub>1−x</sub>Al<sub>x</sub> system have been investigated by magnetization and differential scanning calorimetry (DSC) measurements. The presence of first-order magnetostructural transitions (MSTs) from hexagonal ferromagnetic to orthorhombic antiferromagnetic phases has been detected for x = 0.085 and 0.09 at 193 K and 186 K, respectively. The values of latent heat (L = 6.6 J/g) and corresponding total entropy changes (ΔS<sub>T</sub> = 35 J/kg K) have been evaluated for the MST (x = 0.09) from DSC measurements. The magnetic entropy change for x = 0.09 (ΔS<sub>M</sub> = 17.6 J/kg K for 5 T) was found to be comparable with well-known giant magnetocaloric materials, such as Gd<sub>5</sub>Si<sub>2</sub>Ge<sub>2</sub>, MnFeP<sub>0.45</sub>As<sub>0.55</sub>, and Ni<sub>50</sub>Mn<sub>37</sub>Sn<sub>13</sub>.</p>

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</description>

<author>Tampas Samanta et al.</author>


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<title>Direct Measurements of Field-Induced Adiabatic Temperature Changes Near Compound Phase Transitions in Ni–Mn–In Based Heusler Alloys</title>
<link>http://opensiuc.lib.siu.edu/phys_pubs/63</link>
<guid isPermaLink="true">http://opensiuc.lib.siu.edu/phys_pubs/63</guid>
<pubDate>Fri, 02 Nov 2012 12:05:43 PDT</pubDate>
<description>
	<![CDATA[
	<p>The adiabatic temperature changes (ΔT<sub>ad</sub>) in the vicinity of the Curie and martensitic transition temperatures of Ni<sub>50</sub>Mn<sub>35</sub>In<sub>15</sub> and Ni<sub>50</sub>Mn<sub>35</sub>In<sub>14</sub>Z (Z = Al and Ge) Heusler alloys have been studied using an adiabatic magnetocalorimeter of 250–350 K temperature interval for applied magnetic field changes up to ΔH = 1.8 T. The largest measured changes were ΔT<sub>ad</sub> = −2 and 2 K near the martensitic (first-order) and ferromagnetic (second-order) transitions for ΔH = 1.8 T, respectively. It was observed that |ΔT<sub>ad</sub>| ≈ 1 K for relatively small field changes (ΔH = 1 T) for both types of transitions. The results indicate that these materials should be further explored as potential working materials in magnetic refrigeration applications.</p>

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</description>

<author>A. P. Kazakov et al.</author>


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<title>Magnetic and Magnetocaloric Properties of the New Rare-Earth-Transition-Metal Intermetallic Compound Gd3Co29Ge4B10</title>
<link>http://opensiuc.lib.siu.edu/phys_pubs/62</link>
<guid isPermaLink="true">http://opensiuc.lib.siu.edu/phys_pubs/62</guid>
<pubDate>Fri, 02 Nov 2012 12:05:42 PDT</pubDate>
<description>
	<![CDATA[
	<p>The compounds Gd<sub>3-<em>x</em></sub>Y<sub><em>x</em></sub>Co<sub>29</sub>Ge<sub>4</sub>B<sub>10</sub> (<em>x</em> = 0, 0.5, 1.0, 1.5, and 3.0), Gd<sub>3</sub>Co<sub>29</sub>Al<sub>4</sub>B<sub>10</sub>, and Gd<sub>3</sub>Co<sub>29</sub>Al<sub>4</sub>B<sub>10</sub> were synthesized by arc melting, and their magnetic properties investigated as a function of temperature and applied magnetic field. X-ray measurements showed primarily single-phase samples with the tetragonal crystal structure <em>P4</em>/<em>nmm</em>. It was found that Gd<sub>3</sub>Co<sub>29</sub>Ge<sub>4</sub>B<sub>10</sub> orders ferromagnetically at <em>T</em><sub><em>C</em></sub>  = 212 K and shows a compensation point at 128 K, indicating a ferrimagnetic ordering of the Co and Gd moments. An entropy change of −Δ<em>S</em> = 0.5 J/kgK was observed in a 5-T field at <em>T</em><sub><em>C</em></sub> for this sample, while a change in sign for this quantity was observed both at the maximum value of magnetization (around 200 K) and then again at the compensation point. Substitution of Y for Gd in Gd<sub>3</sub>Co<sub>29</sub>Ge<sub>4</sub>B<sub>10</sub> does not affect the Curie temperature, but shifts the compensation point to lower temperatures. This indicates that a decrease in Gd concentration does not affect the <em>d</em>-<em>d</em> exchange interaction, but has a pronounced effect on the <em>f</em>-<em>d</em> exchange interaction.</p>

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</description>

<author>P. Hill et al.</author>


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<title>Induced Magnetic Anisotropy and Spin Polarization in Pulsed Laser-Deposited Co2MnSb Thin Films</title>
<link>http://opensiuc.lib.siu.edu/phys_pubs/61</link>
<guid isPermaLink="true">http://opensiuc.lib.siu.edu/phys_pubs/61</guid>
<pubDate>Fri, 02 Nov 2012 12:05:41 PDT</pubDate>
<description>
	<![CDATA[
	<p>Co<sub>2</sub>MnSb thin films were grown on glass and GaAs (001) substrates using pulsed laser deposition. The films were grown in magnetic fields (H<sub>G</sub> = 500 Oe and 0 Oe) that were applied in the plane of the substrate during the deposition process. Angle-dependent magneto-optic Kerr effect measurements for films grown on glass revealed a uniaxial magnetic anisotropy in the direction of the applied growth field. Films grown on GaAs (001) exhibited more complicated magnetic anisotropy behavior, due to additional contributions from the substrate. Point contact Andreév reflection spectroscopy measurements indicated that the spin polarizations of the films were about P~ 50%, with negligible difference between films grown in zero and non-zero applied fields.</p>

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</description>

<author>Moti R. Paudel et al.</author>


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<title>Ferromagnetic ZnO Nanocrystals and Al-induced Defects</title>
<link>http://opensiuc.lib.siu.edu/phys_pubs/60</link>
<guid isPermaLink="true">http://opensiuc.lib.siu.edu/phys_pubs/60</guid>
<pubDate>Fri, 02 Nov 2012 12:05:40 PDT</pubDate>
<description>
	<![CDATA[
	<p>ZnO nanocrystals (NCs) capped with polyvinyl pyrrolidone reveal room temperature ferromagnetism. Incorporation of Al<sup>3+</sup>-ions induce defects in ZnO NCs leading to quenching of excitonic luminescence of ZnO at the cost of an increase in the intensity of oxygen vacancy related emission. Photoluminescence excitation spectra exhibit an additional hump like feature attributed to Al-doping. Saturation magnetization of Al<sup>3+</sup>-doped ZnO NCs is the same as that of the undoped ZnO NCs. However, a remarkable decrease in the coercivity associated with change in the nature of M (T) curve and electron paramagnetic resonance signal with g = 1.96 is observed consequent to Al doping. The results provide direct evidence of the defects within the core of NCs that are responsible for the ferromagnetic ordering in the Al<sup>3+</sup>-doped ZnO. The M(T) curve unravels a typical exchange mechanism.</p>

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</description>

<author>Chinmay Phadnis et al.</author>


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<title>Electronic Transport Imaging in a Multiwire SnO2 Chemical Field-Effect Transistor Device</title>
<link>http://opensiuc.lib.siu.edu/phys_pubs/59</link>
<guid isPermaLink="true">http://opensiuc.lib.siu.edu/phys_pubs/59</guid>
<pubDate>Fri, 02 Nov 2012 12:05:39 PDT</pubDate>
<description>
	<![CDATA[
	<p>The electronic transport and the sensing performance of an individual SnO<sub>2</sub> crossed-nanowires device in a three-terminal field-effect transistor configuration were investigated using a combination of macroscopic transport measurements and scanning surface-potential microscopy (SSPM). The structure of the device was determined using both scanning electron- and atomic force microscopy data. The SSPM images of two crossed one-dimensional nanostructures, simulating a prototypical nanowire network sensors, exhibit large dc potential drops at the crossed-wire junction and at the contacts, identifying them as the primary electroactive elements in the circuit. The gas sensitivity of this device was comparable to those of sensors formed by individual homogeneous nanostructures of similar dimensions. Under ambient conditions, the dc transport measurements were found to be strongly affected by field-induced surface charges on the nanostructure and the gate oxide. These charges result in a memory effect in transport measurements and charge dynamics which are visualized by SSPM. Finally, scanning probe microscopy is used to measure the current-voltage characteristics of individual active circuit elements, paving the way to a detailed understanding of chemical functionality at the level of an individual electroactive element in an individual nanowire.</p>

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</description>

<author>Sergei V. Kalinin et al.</author>


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<title>Grain Boundary Sliding Mechanisms in ZrN-Ag, ZrN-Au, and ZrN-Pd Nanocomposite Films</title>
<link>http://opensiuc.lib.siu.edu/phys_pubs/58</link>
<guid isPermaLink="true">http://opensiuc.lib.siu.edu/phys_pubs/58</guid>
<pubDate>Fri, 02 Nov 2012 12:05:38 PDT</pubDate>
<description>
	<![CDATA[
	<p>Nanocomposite films of ZrN-Me (Me = Ag, Au, or Pd) were produced by reactive unbalanced magnetron sputtering and were found to form a dense and homogeneous microstructure whereby nanocrystals of Me are distributed evenly throughout the ZrN matrix. Interestingly, the Young’s modulus was found to decrease much more dramatically with the increase in metal content for the ZrN-Ag system. A systematic <em>ab initio</em> study was undertaken to understand the mechanism of grain boundary sliding in these nanostructures. The maximum energy variation during the sliding was found to be the largest and the smallest for ZrN-Pd and ZrN-Ag, respectively.</p>

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</description>

<author>S. M. Aouadi et al.</author>


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<title>Correlation Between Interfacial Electronic Structure and Mechanical Properties of ZrN–Me (Me=Ag, Au, or Pd) Nanocomposite Films</title>
<link>http://opensiuc.lib.siu.edu/phys_pubs/57</link>
<guid isPermaLink="true">http://opensiuc.lib.siu.edu/phys_pubs/57</guid>
<pubDate>Fri, 02 Nov 2012 12:05:37 PDT</pubDate>
<description>
	<![CDATA[
	<p>Nanocomposite films of ZrN–Me (Me=Ag, Au, or Pd) were prepared using reactive unbalanced magnetron sputtering. The hardness and elastic modulus were measured by nanoindention and were found to vary differently with composition for the three nanocomposite structures. Young’s modulus was found to decrease much more dramatically with the increase in Me content for the ZrN–Ag system. These findings were attributed to the weaker bonding mechanism at the interface between the ceramic and the metallic phases, which is more prone to grain-boundary sliding as shown using first-principles calculations of the electronic structure at the interface for the three systems.</p>

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</description>

<author>S. M. Aouadi et al.</author>


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<title>Coupling Nanowire Chemiresistors with MEMS Microhotplate Gas Sensing Platforms</title>
<link>http://opensiuc.lib.siu.edu/phys_pubs/56</link>
<guid isPermaLink="true">http://opensiuc.lib.siu.edu/phys_pubs/56</guid>
<pubDate>Fri, 02 Nov 2012 12:05:36 PDT</pubDate>
<description>
	<![CDATA[
	<p>Recent advances in nanotechnology have yielded materials and structures that offer great potential for improving the sensitivity, selectivity, stability, and speed of next-generation chemical gas sensors. To fabricate practical devices, the “bottom-up” approach of producing nanoscale sensing elements must be integrated with the “top-down” methodology currently dominating microtechnology. In this letter, the authors illustrate this approach by coupling a single-crystal SnO<sub>2</sub> nanowire sensing element with a microhotplate gas sensor platform. The sensing results obtained using this prototype sensor demonstrate encouraging performance aspects including reduced operating temperature, reduced power consumption, good stability, and enhanced sensitivity.</p>

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</description>

<author>Douglas C. Meier et al.</author>


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<title>Direct Measurements of Field-Induced Adiabatic Temperature Changes Near Compound Phase Transitions in Ni–Mn–In Based Heusler Alloys</title>
<link>http://opensiuc.lib.siu.edu/phys_pubs/55</link>
<guid isPermaLink="true">http://opensiuc.lib.siu.edu/phys_pubs/55</guid>
<pubDate>Fri, 02 Nov 2012 11:43:52 PDT</pubDate>
<description>
	<![CDATA[
	<p>The adiabatic temperature changes (ΔT<sub>ad</sub>) in the vicinity of the Curie and martensitic transition temperatures of Ni<sub>50</sub>Mn<sub>35</sub>In<sub>15</sub> and Ni<sub>50</sub>Mn<sub>35</sub>In<sub>14</sub>Z (Z = Al  and Ge) Heusler alloys have been studied using an adiabatic  magnetocalorimeter of 250–350 K temperature interval for applied  magnetic field changes up to ΔH = 1.8 T. The largest measured changes were ΔT<sub>ad</sub> = −2 and 2 K near the martensitic (first-order) and ferromagnetic (second-order) transitions for ΔH = 1.8 T, respectively. It was observed that |ΔT<sub>ad</sub>| ≈ 1 K for relatively small field changes (ΔH = 1 T)  for both types of transitions. The results indicate that these  materials should be further explored as potential working materials in  magnetic refrigeration applications.</p>

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</description>

<author>A. P. Kazakov et al.</author>


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<title>Large Inverse Magnetic Entropy Changes and Magnetoresistance in the Vicinity of a Field-Induced Martensitic Transformation in Ni50−xCoxMn32−yFeyGa18</title>
<link>http://opensiuc.lib.siu.edu/phys_pubs/54</link>
<guid isPermaLink="true">http://opensiuc.lib.siu.edu/phys_pubs/54</guid>
<pubDate>Tue, 31 Jan 2012 16:15:00 PST</pubDate>
<description>
	<![CDATA[
	<p>Significantly large inverse magnetic entropy changes (ΔS<sub>M</sub>)  and magnetoresistance (MR) were observed at the inverse martensitic  phase transitions of the Ga-based magnetic shape memory Heusler alloys: Ni<sub>50−x</sub>Co<sub>x</sub>Mn<sub>32−y</sub>Fe<sub>y</sub>Ga<sub>18</sub>.  The crystal structures of alloys were tetragonal at 300 K and the phase  transition temperatures and magnetic properties were found to be  correlated with the degree of tetragonal distortion. The maximum peak  values of the ΔS<sub>M</sub> and MR at H = 5 T were determined as  ≈ (+)31 J Kg<sup>−1</sup> K<sup>−1</sup> and ≈−21%, respectively, for x = 8 and y = 2.  The relatively small hysteretic loss and large refrigeration capacity  observed in this system make these compounds promising materials for  applications.</p>

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</description>

<author>Arjun K. Pathak et al.</author>


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<title>Magnetoresistance and Magnetocaloric Effect at a Structural Phase Transition from a Paramagnetic Martensitic State to a Paramagnetic Austenitic State in Ni50Mn36.5In13.5 Heusler Alloys</title>
<link>http://opensiuc.lib.siu.edu/phys_pubs/53</link>
<guid isPermaLink="true">http://opensiuc.lib.siu.edu/phys_pubs/53</guid>
<pubDate>Tue, 31 Jan 2012 16:14:58 PST</pubDate>
<description>
	<![CDATA[
	<p>It is established, using magnetization measurements, that Ni<sub>50</sub>Mn<sub>36.5</sub>In<sub>13.5</sub> is in a paramagnetic state (PS) above and below the martensitic transition temperature (T<sub>M</sub>). Magnetoresistance (MR) and magnetic entropy changes (ΔS<sub>M</sub>) in the vicinity of T<sub>M</sub> were studied. MR and ΔS<sub>M</sub> at T<sub>M</sub> were found to be ≈−8% and  ≈ +24 J Kg<sup>−1</sup> K<sup>−1</sup>, respectively, at ΔH = 5 T. Although MR and ΔS<sub>M</sub> values were lower than compared to those found in other Heusler systems, the significantly smaller hysteresis observed in Ni<sub>50</sub>Mn<sub>36.5</sub>In<sub>13.5</sub> makes this compound, and other such compounds that undergo a  martensitic transition in a PS, promising for the study and applications  of magnetocaloric magnetic materials.</p>

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</description>

<author>Arjun K. Pathak et al.</author>


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<title>Exchange Bias Behavior in Ni–Mn–Sb Heusler Alloys</title>
<link>http://opensiuc.lib.siu.edu/phys_pubs/52</link>
<guid isPermaLink="true">http://opensiuc.lib.siu.edu/phys_pubs/52</guid>
<pubDate>Tue, 31 Jan 2012 16:14:57 PST</pubDate>
<description>
	<![CDATA[
	<p>The authors report the observation of exchange bias in bulk polycrystalline Ni<sub>50</sub>Mn<sub>25+<em>x</em></sub>Sb<sub>25−<em>x</em></sub> Heusler alloys. Shifts in hysteresis loops of up to 248 Oe were observed in the 5 T field cooled samples. The observed exchange bias behavior in Ni<sub>50</sub>Mn<sub>25+<em>x</em></sub>Sb<sub>25−<em>x</em></sub> is attributed to the coexistence of antiferromagnetic and ferromagnetic  exchange interactions in the system. Such behavior is an addition to  the multifunctional properties of the Ni<sub>50</sub>Mn<sub>25+<em>x</em></sub>Sb<sub>25−<em>x</em></sub> Heusler alloy system.</p>

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</description>

<author>Mahmud Khan et al.</author>


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<title>Large Magnetic Entropy Change in Ni50Mn50−xInx Heusler Alloys</title>
<link>http://opensiuc.lib.siu.edu/phys_pubs/51</link>
<guid isPermaLink="true">http://opensiuc.lib.siu.edu/phys_pubs/51</guid>
<pubDate>Tue, 31 Jan 2012 16:13:30 PST</pubDate>
<description>
	<![CDATA[
	<p>The magnetocaloric properties of polycrystalline Ni<sub>50</sub>Mn<sub>50−<em>x</em></sub>In<sub><em>x</em></sub> (15 ⩽ <em>x</em> ⩽ 16)  associated with the second order magnetic transition at the Curie  temperature and the first order martensitic transition were studied  using magnetization measurements. The refrigeration capacity and  magnetic entropy change were found to depend on the In concentration and  reach a maximum value of refrigeration capacity of 280 J/kg with a magnetic entropy change of −6.8 J/kg K at 318 K for a magnetic field change of 5 T.  These values of the magnetocaloric parameters are comparable to that of  the largest values reported near the second order transition of  metallic magnets near room temperature.</p>

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</description>

<author>Arjun Kumar Pathak et al.</author>


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<title>Magnetocaloric Properties of Ni2Mn1−xCuxGa</title>
<link>http://opensiuc.lib.siu.edu/phys_pubs/50</link>
<guid isPermaLink="true">http://opensiuc.lib.siu.edu/phys_pubs/50</guid>
<pubDate>Tue, 31 Jan 2012 15:56:16 PST</pubDate>
<description>
	<![CDATA[
	<p>We present the magnetocaloric properties of the substituted Heusler alloy Ni<sub>2</sub>Mn<sub>1−<em>x</em></sub>Cu<sub><em>x</em></sub>Ga, which shows a maximum magnetic entropy change of Δ<em>S</em><sub><em>M</em></sub> ≈ −64 J/Kg K = −532 mJ/cm<sup>3</sup> K at 308 K for a magnetic field change Δ<em>H</em> = 5 T. The dependence of Δ<em>S</em><sub><em>M</em></sub> on Δ<em>H</em> is approximately linear and does not reach saturation at 5 T. It is demonstrated that the temperature at which Δ<em>S</em><sub><em>M</em></sub> occurs can be tuned through subtle variations in composition.</p>

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</description>

<author>Shane Stadler et al.</author>


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<title>Magnetic Phase Diagrams of Erbium</title>
<link>http://opensiuc.lib.siu.edu/phys_pubs/49</link>
<guid isPermaLink="true">http://opensiuc.lib.siu.edu/phys_pubs/49</guid>
<pubDate>Wed, 11 Jan 2012 15:19:14 PST</pubDate>
<description>
	<![CDATA[
	<p>The magnetic phase diagrams of erbium in the magnetic field–temperature  plane have been constructed for applied magnetic fields along the <em>a</em> and <em>b</em> axes. For an <em>a</em>-axis applied field our <em>H</em>–<em>T</em> phase diagrams determined from magnetization and magnetoresistance data  are in good agreement and consistent with that of Jehan et al. for  temperatures below 50 K. A splitting of the basal plane Néel temperature  (<em>T</em><sub><em>N</em>⊥</sub>)  above 3.75 T introduces two new magnetic phases. Also a transition from  a fan to a canted fan phase as suggested by Jehan et al. is observed in  an increasing field below <em>T</em><sub><em>C</em></sub>. Our phase diagram for a <em>b</em>-axis  applied field constructed from magnetization data is very similar to  the phase diagram of Watson and Ali using magnetoresistance  measurements. However, the anomaly at 42 K reported by Watson and Ali is  not observed in the present study. No splitting of the <em>T</em><sub><em>N</em>⊥</sub> transition is observed in either work for a field applied along the <em>b</em> axis.</p>

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</description>

<author>B. H. Frazer et al.</author>


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<title>Colossal Magnetoresistance in Ce Doped Manganese Oxides</title>
<link>http://opensiuc.lib.siu.edu/phys_pubs/48</link>
<guid isPermaLink="true">http://opensiuc.lib.siu.edu/phys_pubs/48</guid>
<pubDate>Wed, 11 Jan 2012 15:11:13 PST</pubDate>
<description>
	<![CDATA[
	<p>In this study we investigate the effects of Ce doping in R<sub>1−<em>x</em></sub>A<sub><em>x</em></sub>MnO<sub>3</sub> (R = La, Ce, and A = Sr, Ce) on the magnetic and transport properties of this system. For La<sub>1−<em>x</em></sub>Ce<sub><em>x</em></sub>MnO<sub>3</sub> (LCMO), an increase in Ce concentration is accompanied by an increase in <em>T</em><sub><em>C</em></sub> from 225 to 236 K, as well as an increase in the electrical  resistivity. An extremely high resistivity is observed in the new system  Ce<sub>1−<em>x</em></sub>Sr<sub><em>x</em></sub>MnO<sub>3</sub> (CSMO) which becomes insulating below its Curie temperature of 43 K. A  maximum magnetoresistance (MR) ratio of 40% for CSMO and 53% for LCMO is  observed. A larger change in resistivity is seen to correspond to an  increase in the Ce concentration, however this is offset by an overall  resistivity increase which keeps the MR ratio low. The high resistivity  may be due to unreacted oxides in the samples. If true, the amount of  impurity appears to be proportional to the Ce doping. If this impurity  level can be reduced, a significant colossal magnetoresistance effect  could be exhibited by these systems.</p>

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<author>J. R. Gebhardt et al.</author>


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<title>Magnetic Properties of RTSb3</title>
<link>http://opensiuc.lib.siu.edu/phys_pubs/47</link>
<guid isPermaLink="true">http://opensiuc.lib.siu.edu/phys_pubs/47</guid>
<pubDate>Wed, 11 Jan 2012 12:54:41 PST</pubDate>
<description>
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	<p>Magnetization, electrical resistivity, and thermal expansion measurements have been performed on polycrystalline RTSb<sub>3</sub> (R=La, Ce, Pr, Nd, Gd, Tb, and Dy; T=Cr, V) samples in order to study  their magnetic properties. Depending on the rare-earth element, RTSb<sub>3</sub> has been found to have either a purely ferromagnetic (or  antiferromagnetic) phase or combination of antiferromagnetic  (lower-temperature) and ferromagnetic (higher-temperature) phases. The  antiferromagnetic order evolves from the ferromagnetic order as a result  of the competition between R<sup>3+</sup> and Cr<sup>3+</sup> ions. As R is changed from La to Dy, the antiferromagnetic ordering of the R<sup>3+</sup> ions becomes more prominent and predominate over the ferromagnetic ordering of Cr<sup>3+</sup> for R=Gd, Tb, and Dy. Thermal expansion measurements show that the  antiferromagnetic transition accompanies a drop in the sample dimension.  The order of the ferromagnetic transition is found to be of the second  order.</p>

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<author>Michael Leonard et al.</author>


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