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Title: EXAFS Analysis of the Local Structure of Cd(1-x)MxTe (M=Cr, Fe, Ni)

Journal Article · · AIP Conference Proceedings
DOI:https://doi.org/10.1063/1.2644589· OSTI ID:21054678
 [1];  [2];  [3]
  1. Beamline Research Division, Pohang Accelerator Laboratory, Pohang 790-784 (Korea, Republic of)
  2. Department of Semiconductor Applications, Ulsan College, Ulsan, 680-749 (Korea, Republic of)
  3. Research Center Dielect and Advanced Material Physics, Pusan National University, Pusan, 609-735 (Korea, Republic of)

CdTe, doped with transition metals, has received much attention for decades as promising II-VI dilute magnetic semiconductor materials. High purity Cd(1-x)MxTe (M=Cr, Fe, Ni) monocrystals have been prepared by the Bridgman method. Because the solubility of transition metals in CdTe is rather small, the zinc-blende phases were prepared in the limit of x {<=} 0.1. The local structural relaxation and effects of metal ion substitution on CdTe have been studied by measuring the fluorescence detected X-ray absorption fine structure (XAFS) spectra of the M K-edges and Te L1-edges. While II-VI compounds show significant variations of band structures, carrier densities and mobilities depending on the amount of donor or acceptor, XANES and EXAFS analysis of the M K-edge spectra reveal that only slight variations of oxidation states and bond lengths appear in no connection with atomic number of substituting metals, On the other hand, Te L1-edge spectra, for example of Cd(1-x)FexTe, exhibit rather a strong distortion around the central atom as a function of x. This distortion is attributed to the redistribution of Cd atoms from their original locations as the Fe concentration increases.

OSTI ID:
21054678
Journal Information:
AIP Conference Proceedings, Vol. 882, Issue 1; Conference: XAFS13: 13. international conference on X-ray absorption fine structure, Stanford, CA (United States), 9-14 Jul 2006; Other Information: DOI: 10.1063/1.2644589; (c) 2007 American Institute of Physics; Country of input: International Atomic Energy Agency (IAEA); ISSN 0094-243X
Country of Publication:
United States
Language:
English