| Literature DB >> 27960353 |
Yoshinori Kuno1, Cédric Tassel1,2, Koji Fujita1, Dmitry Batuk3, Artem M Abakumov3,4, Kazuki Shitara5, Akihide Kuwabara5, Hiroki Moriwake5, Daichi Watabe1, Clemens Ritter6, Craig M Brown7, Takafumi Yamamoto1, Fumitaka Takeiri1, Ryu Abe1, Yoji Kobayashi1, Katsuhisa Tanaka1, Hiroshi Kageyama1,8.
Abstract
By using a high-pressure reaction, we prepared a new oxynitride ZnTaO2N that crystallizes in a centrosymmetric (R3̅c) high-temperature LiNbO3-type structure (HTLN-type). The stabilization of the HTLN-type structure down to low temperatures (at least 20 K) makes it possible to investigate not only the stability of this phase, but also the phase transition to a noncentrosymmetric (R3c) LiNbO3-type structure (LN-type) which is yet to be clarified. Synchrotron and neutron diffraction studies in combination with transmission electron microscopy show that Zn is located at a disordered 12c site instead of 6a, implying an order-disorder mechanism of the phase transition. It is found that the closed d-shell of Zn2+, as well as the high-valent Ta5+ ion, is responsible for the stabilization of the HTLN-type structure, affording a novel quasitriangular ZnO2N coordination. Interestingly, only 3% Zn substitution for MnTaO2N induces a phase transition from LN- to HTLN-type structure, implying the proximity in energy between the two structural types, which is supported by the first-principles calculations.Entities:
Year: 2016 PMID: 27960353 DOI: 10.1021/jacs.6b08635
Source DB: PubMed Journal: J Am Chem Soc ISSN: 0002-7863 Impact factor: 15.419