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Title: Synthesis, structures and magnetic properties of n=3 Ruddlesden-Popper compounds Ca{sub 4}Mn{sub 3-x}Ta{sub x}O{sub 10} (0<=x<=0.3)

Journal Article · · Journal of Solid State Chemistry
 [1];  [1];  [1];  [1]
  1. State Key Laboratory of Rare Earth Resources Utilization, Changchun Institute of Applied Chemistry, Chinese Academy of Sciences, Changchun 130022 (China)

The structural and magnetic properties of Ta-doped Ca{sub 4}Mn{sub 3-x}Ta{sub x}O{sub 10} (0<=x<=0.3) compounds have been investigated. Structural refinement indicates that the Ta doping maintains the orthorhombic layered perovskite structure with space group Pbca as Ca{sub 4}Mn{sub 3}O{sub 10} but induces an increase in both unit cell volume and octahedral distortion. The magnetization measurements reveal that the magnetization first increases and reaches to maximum for the x=0.1 sample and then gradually decreases with the increase of Ta content. There appear short-range ferromagnetic (FM) clusters in all the doped samples, which are caused by the double-exchange interaction between Mn{sup 4+} and Mn{sup 3+} that is induced by the charge compensation effect. As x is higher than 0.1, the overall results show evidence for the gradual appearance of a cluster glass behavior. When x increases to 0.3, the long-range antiferromagnetic (AFM) ground state is melted into the short-range magnetically ordered regions due to the increase of Ta{sup 5+} and Mn{sup 3+} at the expense of Mn{sup 4+}. The competition between AFM regions and FM clusters makes the short-range magnetic components frustrate when the temperature falls to a frustrating point, and thus cluster glass transition occurs. - Graphical Abstract: The magnetic structures of Ca{sub 4}Mn{sub 3-x}Ta{sub x}O{sub 10} transit from G-type AFM to cluster glass state with the intermediate state of FM clusters exhibited in AFM matrix as Ta increasing.

OSTI ID:
21372538
Journal Information:
Journal of Solid State Chemistry, Vol. 183, Issue 3; Other Information: DOI: 10.1016/j.jssc.2009.12.001; PII: S0022-4596(09)00564-7; Copyright (c) 2010 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.; ISSN 0022-4596
Country of Publication:
United States
Language:
English