| Literature DB >> 27355695 |
Cedric Tassel1, Yoshinori Goto1, Daichi Watabe1, Ya Tang, Honcheng Lu1, Yoshinori Kuno1, Fumitaka Takeiri1, Takafumi Yamamoto1, Craig M Brown2, James Hester3, Yoji Kobayashi1, Hiroshi Kageyama4.
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.Entities:
Keywords: Ruddlesden-Popper perovskites; anion order; mixed-anion compounds; oxyhydrides; solid-state structures
Year: 2016 PMID: 27355695 DOI: 10.1002/anie.201605123
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336