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Optical floating zone growth of high-quality Cu2MnAl single crystals

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 Added by Andreas Neubauer
 Publication date 2012
  fields Physics
and research's language is English




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We report the growth of large single-crystals of Cu2MnAl, a ferromagnetic Heusler compound suitable for polarizing neutron monochromators, by means of optical floating zone under ultra-high vacuum compatible conditions. Unlike Bridgman or Czochralsky grown Cu2MnAl, our floating zone grown single-crystals show highly reproducible magnetic properties and an excellent crystal quality with a narrow and homogeneous mosaic spread as examined by neutron diffraction. An investigation of the polarizing properties in neutron scattering suggests a high polarization efficiency, limited by the relatively small sample dimensions studied. Our study identifies optical floating zone under ultra-high vacuum compatible conditions as a highly reproducible method to grow high-quality single-crystals of Cu2MnAl.



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The perovskite SrVO$_3$ is of interest for a variety of applications due to its simple metallic character and stability in reducing environments. Here we report the preparation of single-crystal SrVO$_3$ using the laser floating zone technique. Laue diffraction implies single domains ca. 30 mm in length. The stoichiometry of optimized crystals was found to be Sr$_{0.985}$VO$_{2.91}$ using inductively coupled plasma optical emission spectrometry and neutron powder diffraction analysis, with compositions adjustable depending on the crystal pulling rate. Heat capacity measurements from 2 to 300 K show variations with composition, attributable to a combination of impurity scattering and changes in phonon dynamics.Our results demonstrate the utility of the laser floating zone technique in preparing a range of materials, and our advances with SrVO$_3$ may help lead to applications including catalysis, transparent conducting oxides, thermionic emitters, and other electronic devices.
122 - H. B. Cao , Z. Y. Zhao , M. Lee 2015
High quality single crystals of BaFe$_{12}$O$_{19}$ were grown using the floating zone technique in flowing oxygen pressurized to 100 atm. Single crystal neutron diffraction was used to determine the nuclear and magnetic structure of BaFe$_{12}$O$_{19}$ at 4 K and 295 K. At both temperatures, there exist local electric dipoles formed by the off-mirror-plane displacements of magnetic Fe$^{3+}$ ions at the bipyramidal sites. The displacement at 4 K is about half of that at room temperature. The temperature dependence of the specific heat shows no anomaly associated with long range polar ordering in the temperature range from 1.90-300 K. The inverse dielectric permittivity, $1/varepsilon$, along the c-axis shows a $T^2$ temperature dependence between 10 K and 20 K, with a significantly reduced temperature dependence displayed below 10 K. Moreover, as the sample is cooled below 1.4 K there is an anomalous sharp upturn in $1/varepsilon$. These features resemble those of classic quantum paraelectrics such as SrTiO$_3$. The presence of the upturn in $1/varepsilon$ indicates that BaFe$_{12}$O$_{19}$ is a critical quantum paraelectric system with Fe$^{3+}$ ions involved in both magnetic and electric dipole formation.
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351 - J. S. Wen , Z. J. Xu , G. Y. Xu 2008
Effects of the growth velocity on the crystal growth behavior of Bi_2Sr_2Ca_1Cu_2O_x (Bi-2212) have been studied by floating zone technique. The results show that a necessary condition for obtaining large single crystals along the c-axis is that the solid-liquid interface of a growing rod maintains a stable planar growth front. The planar liquid-solid growth interface tends to break down into a cellular interface, while the growth velocity is higher than 0.25 mm/h. Single crystals of up to 50x7.2x7 mm3 along the a-, b- and caxes have been cut in a 7.2 mm diameter rod with optimum growth conditions. Tconset is 91 K measured by magnetic properties measurement system (MPMS) for as-grown crystals. Optical polarization microscope and neutron diffraction show that the quality of the single crystals is good.
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