Mossbauer spectroscopy investigation of mn-substituted co-ferrite (CoMnxFe2-xO4) -: art. no. 10F101

被引:90
作者
Krieble, K [1 ]
Schaeffer, T
Paulsen, JA
Ring, AP
Lo, CCH
Snyder, JE
机构
[1] Moravian Coll, Bethlehem, PA 18018 USA
[2] Iowa State Univ, Ctr Nondestruct Evaluat, Ames, IA 50011 USA
[3] Iowa State Univ, Mat & Engn Phys Program, Ames Lab, US Dept Energy, Ames, IA 50011 USA
[4] Iowa State Univ, Dept Mat Sci & Engn, Ames, IA 50011 USA
关键词
D O I
10.1063/1.1846271
中图分类号
O59 [应用物理学];
学科分类号
摘要
Understanding the effect of Mn substitution for Fe in Co ferrite presents a challenge because there are three different transition-metal ions distributed among two distinct crystallographic and magnetic sublattices with complicated superexchange and anisotropic interactions. In this study, a series of six powder samples with compositions Co1.0MnxFe2-xO4 were investigated using transmission Mossbauer spectroscopy. Mossbauer spectroscopy provides an excellent tool for probing the local environment of the Fe atoms present in such materials. Results show two sets of six-line hyperfine patterns for all samples, indicating the presence of Fe in both A and B sites. Identification of sites is accomplished by evidence from hyperfine distribution width, integrated intensity, and isomer-shift data. Increasing Mn concentration was found to decrease the hyperfine field strength at both sites, but at unequal rates, and to increase the distribution width. This effect is due to the relative strengths of Fe-O-X superexchange (X=Fe, Co, or Mn) and the different numbers of the next-nearest neighbors of A and B sites. Results are consistent with a model of Mn substituting into B sites and displacing Co ions onto A sites. (c) 2005 American Institute of Physics.
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