等结构
反铁磁性
单斜晶系
结晶学
顺磁性
中子衍射
材料科学
X射线晶体学
固溶体
相图
凝聚态物理
晶体结构
相(物质)
衍射
化学
物理
有机化学
冶金
光学
作者
Marius Uv Nagell,Susmit Kumar,Magnus H. Sørby,Helmer Fjellvåg,Anja Olafsen Sjåstad
标识
DOI:10.1080/01411594.2015.1007374
摘要
The Ruddlesden–Popper (RP3) type oxides, La4Co3O10+δ and La4Ni3O10+δ, form a complete solid solution. Powder X-ray and neutron diffraction data show that La4(Co1−xNix)3O10+δ is isostructural to the monoclinic La4Co3O10+δ structure (P21/a) described for all compositions without any further structural distortions as suggested in the literature. A slight elongation of the Co/Ni–O bonds facing the rock salt interlayer occurs for Ni-rich compositions. The magnetic properties of the solid solution series are mapped in the temperature range from 4 to 300 K, and the results are presented in a magnetic phase diagram. Three regimes with antiferromagnetic order (AF) exist at low temperatures, TN < 10 − 30 K. For x = 0.00, the AF is ascribed to Co(II), whereas a broader AF regime around x = 0.50 is ascribed mainly to Ni(II). Pauli paramagnetism is observed close to metallic La4Ni3O10+δ, x > 0.80. The possibility to tune the oxidation state of the transition metal atoms is demonstrated for La4Co3O10+δ, and exemplified by weakening of a temperature-induced spin transition at around 480 K.\n\nThis is an Accepted Manuscript of an article published by Taylor & Francis Group in Phase Transitions: A Multinational Journal, available online: http://www.tandfonline.com
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