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High-Pressure Synthesis of Manganese Oxyhydride with Partial Anion Order.
Tassel, Cedric; Goto, Yoshinori; Watabe, Daichi; Tang, Ya; Lu, Honcheng; Kuno, Yoshinori; Takeiri, Fumitaka; Yamamoto, Takafumi; Brown, Craig M; Hester, James; Kobayashi, Yoji; Kageyama, Hiroshi.
  • Tassel C; Graduate School of Engineering, Kyoto University, 615-8510, Kyoto, Japan.
  • Goto Y; Graduate School of Engineering, Kyoto University, 615-8510, Kyoto, Japan.
  • Watabe D; Graduate School of Engineering, Kyoto University, 615-8510, Kyoto, Japan.
  • Lu H; Graduate School of Engineering, Kyoto University, 615-8510, Kyoto, Japan.
  • Kuno Y; Graduate School of Engineering, Kyoto University, 615-8510, Kyoto, Japan.
  • Takeiri F; Graduate School of Engineering, Kyoto University, 615-8510, Kyoto, Japan.
  • Yamamoto T; Graduate School of Engineering, Kyoto University, 615-8510, Kyoto, Japan.
  • Brown CM; Center for Neutron Research, National Institute of Standards and Technology (NIST), Gaithersburg, MD, 20899, USA.
  • Hester J; Bragg Institute, Australian Nuclear Science and Technology Organization (ANSTO), Locked Bag 2001, Kirrawee, DC NSW, 2232, Australia.
  • Kobayashi Y; Graduate School of Engineering, Kyoto University, 615-8510, Kyoto, Japan.
  • Kageyama H; Graduate School of Engineering, Kyoto University, 615-8510, Kyoto, Japan. kage@scl.kyoto-u.ac.jp.
Angew Chem Int Ed Engl ; 55(33): 9667-70, 2016 08 08.
Article en En | MEDLINE | ID: mdl-27355695
ABSTRACT
The high-pressure synthesis of a manganese oxyhydride LaSrMnO3.3 H0.7 is reported. Neutron and X-ray Rietveld analyses showed that this compound adopts the K2 NiF4 structure with hydride ions positioned exclusively at the equatorial site. This result makes a striking contrast to topochemical reductions of LaSrMnO4 that result in only oxygen-deficient phases down to LaSrMnO3.5 . This suggests that high H2 pressure plays a key role in stabilizing the oxyhydride phase, offering an opportunity to synthesize other transition-metal oxyhydrides. Magnetic susceptibility revealed a spin-glass transition at 24 K that is due to competing ferromagnetic (Mn(2+) -Mn(3+) ) and antiferromagnetic (Mn(2+) -Mn(2) , Mn(3+) -Mn(3+) ) interactions.
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Texto completo: 1 Banco de datos: MEDLINE Idioma: En Año: 2016 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Idioma: En Año: 2016 Tipo del documento: Article