Characterization of powellite-based solid solutions by site-selective time resolved laser fluorescence spectroscopy

Publikation: Beitrag in FachzeitschriftArtikelForschungPeer-Review

Autoren

  • Moritz Schmidt
  • Stephanie Heck
  • Dirk Bosbach
  • Steffen Ganschow
  • Clemens Walther
  • Thorsten Stumpf

Externe Organisationen

  • Karlsruher Institut für Technologie (KIT)
  • Forschungszentrum Jülich
  • Leibniz-Institut für Kristallzüchtung (IKZ)
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Details

OriginalspracheEnglisch
Seiten (von - bis)8387-8393
Seitenumfang7
FachzeitschriftDalton Transactions
Jahrgang42
Ausgabenummer23
PublikationsstatusVeröffentlicht - 4 Apr. 2013

Abstract

We present a comprehensive study of the solid solution system Ca 2(MoO4)2-NaGd(MoO4)2 on the molecular scale, by means of site-selective time resolved laser fluorescence spectroscopy (TRLFS). Eu3+ is used as a trace fluorescent probe, homogeneously substituting for Gd3+ in the solid solution crystal structure. Site-selective TRLFS of a series of polycrystalline samples covering the whole composition range of the solid solution series from 10% substitution of Ca2+ to the NaGd end-member reveals it to be homogeneous throughout the whole range. The trivalent ions are incorporated into the powellite structure in only one coordination environment, which exhibits a very strong ligand-metal interaction. Polarization-dependent measurements of a single crystal of NaGd(Eu)(MoO4)2 identify the coordination geometry to be of C2v point symmetry. The S4 symmetry of the Ca site within the powellite lattice can be transformed into C2v assuming minor motion in the first coordination sphere.

ASJC Scopus Sachgebiete

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Characterization of powellite-based solid solutions by site-selective time resolved laser fluorescence spectroscopy. / Schmidt, Moritz; Heck, Stephanie; Bosbach, Dirk et al.
in: Dalton Transactions, Jahrgang 42, Nr. 23, 04.04.2013, S. 8387-8393.

Publikation: Beitrag in FachzeitschriftArtikelForschungPeer-Review

Schmidt M, Heck S, Bosbach D, Ganschow S, Walther C, Stumpf T. Characterization of powellite-based solid solutions by site-selective time resolved laser fluorescence spectroscopy. Dalton Transactions. 2013 Apr 4;42(23):8387-8393. doi: 10.1039/c3dt50146a
Schmidt, Moritz ; Heck, Stephanie ; Bosbach, Dirk et al. / Characterization of powellite-based solid solutions by site-selective time resolved laser fluorescence spectroscopy. in: Dalton Transactions. 2013 ; Jahrgang 42, Nr. 23. S. 8387-8393.
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abstract = "We present a comprehensive study of the solid solution system Ca 2(MoO4)2-NaGd(MoO4)2 on the molecular scale, by means of site-selective time resolved laser fluorescence spectroscopy (TRLFS). Eu3+ is used as a trace fluorescent probe, homogeneously substituting for Gd3+ in the solid solution crystal structure. Site-selective TRLFS of a series of polycrystalline samples covering the whole composition range of the solid solution series from 10% substitution of Ca2+ to the NaGd end-member reveals it to be homogeneous throughout the whole range. The trivalent ions are incorporated into the powellite structure in only one coordination environment, which exhibits a very strong ligand-metal interaction. Polarization-dependent measurements of a single crystal of NaGd(Eu)(MoO4)2 identify the coordination geometry to be of C2v point symmetry. The S4 symmetry of the Ca site within the powellite lattice can be transformed into C2v assuming minor motion in the first coordination sphere.",
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T1 - Characterization of powellite-based solid solutions by site-selective time resolved laser fluorescence spectroscopy

AU - Schmidt, Moritz

AU - Heck, Stephanie

AU - Bosbach, Dirk

AU - Ganschow, Steffen

AU - Walther, Clemens

AU - Stumpf, Thorsten

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N2 - We present a comprehensive study of the solid solution system Ca 2(MoO4)2-NaGd(MoO4)2 on the molecular scale, by means of site-selective time resolved laser fluorescence spectroscopy (TRLFS). Eu3+ is used as a trace fluorescent probe, homogeneously substituting for Gd3+ in the solid solution crystal structure. Site-selective TRLFS of a series of polycrystalline samples covering the whole composition range of the solid solution series from 10% substitution of Ca2+ to the NaGd end-member reveals it to be homogeneous throughout the whole range. The trivalent ions are incorporated into the powellite structure in only one coordination environment, which exhibits a very strong ligand-metal interaction. Polarization-dependent measurements of a single crystal of NaGd(Eu)(MoO4)2 identify the coordination geometry to be of C2v point symmetry. The S4 symmetry of the Ca site within the powellite lattice can be transformed into C2v assuming minor motion in the first coordination sphere.

AB - We present a comprehensive study of the solid solution system Ca 2(MoO4)2-NaGd(MoO4)2 on the molecular scale, by means of site-selective time resolved laser fluorescence spectroscopy (TRLFS). Eu3+ is used as a trace fluorescent probe, homogeneously substituting for Gd3+ in the solid solution crystal structure. Site-selective TRLFS of a series of polycrystalline samples covering the whole composition range of the solid solution series from 10% substitution of Ca2+ to the NaGd end-member reveals it to be homogeneous throughout the whole range. The trivalent ions are incorporated into the powellite structure in only one coordination environment, which exhibits a very strong ligand-metal interaction. Polarization-dependent measurements of a single crystal of NaGd(Eu)(MoO4)2 identify the coordination geometry to be of C2v point symmetry. The S4 symmetry of the Ca site within the powellite lattice can be transformed into C2v assuming minor motion in the first coordination sphere.

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