化学
非阻塞I/O
钙钛矿(结构)
六方晶系
离子
结晶学
无机化学
催化作用
生物化学
有机化学
作者
Zhenhong Tan,Takashi Saito,Fabio Denis Romero,Midori Amano Patiño,Masato Goto,Wei‐Tin Chen,Yu‐Chun Chuang,Hwo‐Shuenn Sheu,Yuichi Shimakawa
出处
期刊:Inorganic Chemistry
[American Chemical Society]
日期:2018-08-01
卷期号:57 (16): 10410-10415
被引量:8
标识
DOI:10.1021/acs.inorgchem.8b01618
摘要
BaFe xNi1- xO3 with end members of BaNiO3 ( x = 0) and BaFeO3 ( x = 1), which, respectively, adopt the 2H and 6H hexagonal perovskite structures, were synthesized, and their crystal structures were investigated. A new single phase, Ba4Fe3NiO12 ( x = 0.75), that adopts the 12R perovskite structure with the space group R3̅ m ( a = 5.66564(7) Å and c = 27.8416(3) Å), was found to be stabilized. Mössbauer spectroscopy results and structure analysis using synchrotron and neutron powder diffraction data revealed that nominal Fe3+ occupies the corner-sharing octahedral site while the unusually high valence Fe4+ and Ni4+ occupy the face-sharing octahedral sites in the trimers, giving a charge formula of Ba4Fe3+Fe4+2Ni4+O11.5. The magnetic properties of the compound are also discussed.
科研通智能强力驱动
Strongly Powered by AbleSci AI