<p>This work investigates the magnetocaloric effect, characterized by the magnetic entropy change <InlineEquation ID="IEq1"> <EquationSource Format="TEX">\(- \Delta S_{{\text{M}}} \left( {H,T} \right)\)</EquationSource> <EquationSource Format="MATHML"><math> <mrow> <mo>-</mo> <mi mathvariant="normal">Δ</mi> <msub> <mi>S</mi> <mtext>M</mtext> </msub> <mfenced close=")" open="("> <mrow> <mi>H</mi> <mo>,</mo> <mi>T</mi> </mrow> </mfenced> </mrow> </math></EquationSource> </InlineEquation>, using isothermal magnetization data for PrSr<sub>1−<i>x</i></sub>Pb<sub><i>x</i></sub>Mn<sub>2</sub>O<sub>6</sub> (<i>x</i>&#xa0;=&#xa0;0.4, 0.5, and 0.6), denoted as Pb04, Pb05, and Pb06. The analysis was performed using experimental magnetization isotherms, <i>M</i>(<i>H</i>, <i>T</i>), and mean-field theory (MFT). The exchange field, <i>H</i><sub>exch</sub>, spontaneous magnetization, <i>M</i><sub>S</sub>, and saturation magnetization, <InlineEquation ID="IEq2"> <EquationSource Format="TEX">\(M_{0}\)</EquationSource> <EquationSource Format="MATHML"><math> <msub> <mi>M</mi> <mn>0</mn> </msub> </math></EquationSource> </InlineEquation>, were determined through scaling analysis, Arrott plots, and entropy–magnetization correlations. <i>H</i><sub>exch</sub> exhibited a predominantly linear dependence on <i>M</i>, with negligible cubic contribution, yielding exchange parameter λ<sub>1</sub> values of 1.71, 1.97, and 1.73 T·emu<sup>−1</sup>·g for Pb04, Pb05, and Pb06, respectively. Critical exponent <i>β</i> values obtained from both <InlineEquation ID="IEq3"> <EquationSource Format="TEX">\(- \Delta S_{{\text{M}}}\)</EquationSource> <EquationSource Format="MATHML"><math> <mrow> <mo>-</mo> <mi mathvariant="normal">Δ</mi> <msub> <mi>S</mi> <mtext>M</mtext> </msub> </mrow> </math></EquationSource> </InlineEquation> versus <i>M</i><sup>2</sup> and <InlineEquation ID="IEq4"> <EquationSource Format="TEX">\(\frac{H}{M}\)</EquationSource> <EquationSource Format="MATHML"><math> <mfrac> <mi>H</mi> <mi>M</mi> </mfrac> </math></EquationSource> </InlineEquation> versus <i>M</i><sup>2</sup> were close to the MFT prediction (<i>β</i>&#xa0;≈&#xa0;0.5), confirming second-order ferromagnetic–paramagnetic transitions. Numerical solutions of the MFT equation reproduced <i>M</i>(<i>H</i>, <i>T</i>) and <InlineEquation ID="IEq5"> <EquationSource Format="TEX">\(- \Delta S_{{\text{M}}} \left( {H,T} \right)\)</EquationSource> <EquationSource Format="MATHML"><math> <mrow> <mo>-</mo> <mi mathvariant="normal">Δ</mi> <msub> <mi>S</mi> <mtext>M</mtext> </msub> <mfenced close=")" open="("> <mrow> <mi>H</mi> <mo>,</mo> <mi>T</mi> </mrow> </mfenced> </mrow> </math></EquationSource> </InlineEquation> curves in close agreement with experimental results, particularly at higher magnetic fields, validating the model’s applicability to these compounds.</p>

错误:搜索内容不能为空,请输入英文关键词
错误:关键词超出字数限制,请精简
高级检索

Mean-Field Modeling of Magnetocaloric and Magnetic Properties in Pb-Substituted PrSr1−xPbxMn2O6 (x = 0.4, 0.5, 0.6) Double-Perovskite Manganites

  • Beriham Basha,
  • Mohamed Hsini,
  • Fatma Dhaouadi,
  • Fatma Aouaini

摘要

This work investigates the magnetocaloric effect, characterized by the magnetic entropy change \(- \Delta S_{{\text{M}}} \left( {H,T} \right)\) - Δ S M H , T , using isothermal magnetization data for PrSr1−xPbxMn2O6 (x = 0.4, 0.5, and 0.6), denoted as Pb04, Pb05, and Pb06. The analysis was performed using experimental magnetization isotherms, M(H, T), and mean-field theory (MFT). The exchange field, Hexch, spontaneous magnetization, MS, and saturation magnetization, \(M_{0}\) M 0 , were determined through scaling analysis, Arrott plots, and entropy–magnetization correlations. Hexch exhibited a predominantly linear dependence on M, with negligible cubic contribution, yielding exchange parameter λ1 values of 1.71, 1.97, and 1.73 T·emu−1·g for Pb04, Pb05, and Pb06, respectively. Critical exponent β values obtained from both \(- \Delta S_{{\text{M}}}\) - Δ S M versus M2 and \(\frac{H}{M}\) H M versus M2 were close to the MFT prediction (β ≈ 0.5), confirming second-order ferromagnetic–paramagnetic transitions. Numerical solutions of the MFT equation reproduced M(H, T) and \(- \Delta S_{{\text{M}}} \left( {H,T} \right)\) - Δ S M H , T curves in close agreement with experimental results, particularly at higher magnetic fields, validating the model’s applicability to these compounds.