Nd0.7-xLaxSr0.3MnO3 (x = 0.0 - 0.3) 锰矿的磁焦效应研究和临界磁场分析

Sudarsan Vadnala, T. D. Rao, S. Asthana, M. Pal
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摘要

本研究探讨了通过固态反应路线合成的 Nd0.7-xLaxSr0.3MnO3(x = 0.0、0.1、0.2 和 0.3)锰矿样品的磁化温度依赖性、磁致效应和临界磁场分析。将 La3+ 置换到 Nd3+ 位点后,A 位点的平均离子半径 ( ) 从 1.321 Å(x = 0.0 时)增加到 1.348 Å(x = 0.3 时)。x = 0.0 时,A 位的平均离子半径 ( ) 从 1.321 Å 增加到 1.348 Å(x = 0.3 时),从而降低了晶格内部的化学压力,使 Mn-O-Mn 键角接近 180°。此外,Mn-O-Mn 键角的增加抑制了自旋-晶格相互作用,从而降低了磁转变温度下最大磁熵的变化。这意味着A位平均离子半径的变化会影响最大磁熵的变化。根据过渡温度 TC 附近的磁化测量数据,研究了锰矿样品的临界行为。利用改良 Arrott 图、Kouvel-Fisher 法和临界等温线分析等多种技术测量了铁磁转变温度 TC 值以及临界指数 β、γ 和 δ。
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Investigation of Magnetocaloric Effect and Critical Field Analysis of Nd0.7-xLaxSr0.3MnO3 (x = 0.0 - 0.3) Manganites
This research explored the temperature dependence magnetization, magnetocaloric effect, and critical field analysis of Nd0.7-xLaxSr0.3MnO3 (x = 0.0, 0.1, 0.2 and 0.3) manganites samples synthesized through solid state reaction route. The substitution of La3+ at Nd3+ site enhances the A-site average ionic radius ( ) from 1.321 Å (for x = 0.0) to 1.348 Å (for x = 0.3). An increase in reduced the internal chemical pressure inside the lattice such that the Mn-O-Mn bond angle approached 180°. In addition, an increase in Mn-O-Mn bond angle supresses the spin-lattice interaction, which consequently reduces the change in maximum magnetic entropy at the magnetic transition temperature. This implies that variation of A-site average ionic radius influences the change in maximum magnetic entropy. The critical behavior of the manganite samples was addressed based on the data of magnetization measurements around the transition temperature TC. Various techniques such as modified Arrott plot, a Kouvel–Fisher method, and critical isotherm analysis were used to measure the values of the ferromagnetic transition temperature TC, as well as the critical exponents of β, γ, and δ. The magnetic order parameter is very well obeyed with scaling relation with change in magnetic entropy.
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