论文标题

在密集的Gd $^{3+} $双pleovskites中自由旋转主导的磁电效应

Free-spin dominated magnetocaloric effect in dense Gd$^{3+}$ double perovskites

论文作者

Koskelo, EliseAnne C., Liu, Cheng, Mukherjee, Paromita, Kelly, Nicola D., Dutton, Sian E.

论文摘要

具有致密磁性晶格的沮丧的灯笼氧化物具有基本的兴趣,因为由于较大的基态熵并抑制了有序温度,因此在低温制冷中的潜力,但通常可以受到短距离相关性的限制。在这里,我们介绍了沮丧的FCC氧化物的例子,ba $ _2 $ gdsbo $ _6 $和sr $ _2 $ _2 $ gdsbo $ _6 $以及新的站点订购的模拟CA $ _2 $ _2 $ _2 $ gdsbo $ _6 $([cagd] $ _ [casb] $ _ $ _ b $ $ $ o $ $ o $ _6 $ _6 $ _6 $) superexchange($ j_1 \ sim 10 $ mk)。我们通过低场敏感性和等温磁化测量结果报告了使用粉末X射线衍射和大量磁性的晶体结构。 GD化合物的磁性熵更改为-15.8 j/k/mol $ _ \ textrm {gd} $在2 K时为7 t的领域,超过20%的磁性熵,与-13.0 j/k/k/k/mol $ $ $ $ $ _ \ textrm {gd} $相比,gd $ __ $ o o o o。热容量测量表明,缺乏磁性订购至BA $ _2 $ GDSBO $ _6 $和SR $ _2 $ _2 $ GDSBO $ _6 $的磁性订购,这表明通过液体4-HE制度冷却。与其他表现最好的GD基于GD的氧化物相比,使用平均场模型来阐明这些化合物的磁源性能中主要自旋行为的作用。双钙壶的化学柔韧性提高了GD $^{3+} $ fcc lattices中进一步增强磁含量效应的可能性。

Frustrated lanthanide oxides with dense magnetic lattices are of fundamental interest for their potential in cryogenic refrigeration due to a large ground state entropy and suppressed ordering temperatures, but can often be limited by short-range correlations. Here, we present examples of frustrated fcc oxides, Ba$_2$GdSbO$_6$ and Sr$_2$GdSbO$_6$ and the new site-disordered analog Ca$_2$GdSbO$_6$ ([CaGd]$_A$[CaSb]$_B$O$_6$), in which the magnetocaloric effect is influenced by minimal superexchange ($J_1 \sim 10$ mK). We report on the crystal structures using powder x-ray diffraction and the bulk magnetic properties through low-field susceptibility and isothermal magnetization measurements. The Gd compounds exhibit a magnetic entropy change of up to -15.8 J/K/mol$_\textrm{Gd}$ in a field of 7 T at 2 K, a 20 % excess compared to the value of -13.0 J/K/mol$_\textrm{Gd}$ for a standard in magnetic refrigeration, Gd$_3$Ga$_5$O$_{12}$. Heat capacity measurements indicate a lack of magnetic ordering down to 0.4 K for Ba$_2$GdSbO$_6$ and Sr$_2$GdSbO$_6$, suggesting cooling down through the liquid 4-He regime. A mean-field model is used to elucidate the role of primarily free spin behavior in the magnetocaloric performance of these compounds in comparison to other top-performing Gd-based oxides. The chemical flexibility of the double perovskites raises the possibility of further enhancement of the magnetocaloric effect in the Gd$^{3+}$ fcc lattices.

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