材料科学
四方晶系
价(化学)
凝聚态物理
外延
结晶学
大气温度范围
晶体结构
物理
纳米技术
热力学
化学
量子力学
图层(电子)
作者
Sebastian Kölsch,Alfons Georg Schuck,Michael Huth,O. Fedchenko,D. Vasilyev,Sergeij Chernov,Olena Tkach,H. J. Elmers,G. Schönhense,Christoph Schlüter,T. R. F. Peixoto,Andrii Gloskowski,C. Krellner
标识
DOI:10.1103/physrevmaterials.6.115003
摘要
Bulk ${\mathrm{EuPd}}_{2}{\mathrm{Si}}_{2}$ show a temperature-driven valence transition of europium from $\ensuremath{\sim}+2$ above 200 K to $\ensuremath{\sim}+3$ below 100 K, which is correlated with a shrinking by approximately 2% of the tetragonal crystal lattice along the two $a$-axes. Due to this interconnection between lattice and electronic degrees of freedom the influence of strain in epitaxial thin films is particularly interesting. Ambient x-ray diffraction (XRD) confirms an epitaxial relationship of tetragonal ${\mathrm{EuPd}}_{2}{\mathrm{Si}}_{2}$ on MgO(001) with an out-of plane $c$-axis orientation for the thin film, whereby the $a$-axes of both lattices align. XRD at low temperatures reveals a strong coupling of the thin film lattice to the substrate, showing no abrupt compression over the temperature range from 300 to 10 K. Hard x-ray photoelectron spectroscopy at 300 and 20 K reveals a temperature-independent valence of $+2.0$ for Eu. The evolving biaxial tensile strain upon cooling is suggested to suppress the valence transition. Instead temperature-dependent transport measurements of the resistivity and the Hall effect in a magnetic field up to 5 T point to a film thickness independent phase transition at 16 to 20 K, indicating magnetic ordering.
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