Hyperfine Interactions

, Volume 158, Issue 1, pp 353–359

Experimental Verification of Calculated Lattice Relaxations Around Impurities in CdTE


    • Hahn-Meitner-Institut Berlin GmbHBereich Strukturforschung
  • H. Haas
    • Hahn-Meitner-Institut Berlin GmbHBereich Strukturforschung
  • V. Koteski
    • Hahn-Meitner-Institut Berlin GmbHBereich Strukturforschung
    • VINĈA
  • N. Novakovic
    • Hahn-Meitner-Institut Berlin GmbHBereich Strukturforschung
    • VINĈA
  • P. Fochuk
    • University of Chernivtsi
  • O. Panchuk
    • University of Chernivtsi
HFI Probes in Semiconductors, Metals and Insulators

DOI: 10.1007/s10751-005-9053-z

Cite this article as:
Mahnke, H., Haas, H., Koteski, V. et al. Hyperfine Interact (2004) 158: 353. doi:10.1007/s10751-005-9053-z


We have measured the lattice distortion around As (acceptor) and Br (donor) in CdTe with fluorescence detected X-ray absorption spectroscopy. We could experimentally verify the lattice relaxation with a bond length reduction of 8% around the As atom as inferred indirectly from ab initio calculations of the electric field gradient performed with the WIEN97 package in comparison with the measured value in a Perturbed Angular Correlation experiment as recently reported. We have complemented our own calculations of relaxation with WIEN97 with calculations using the FHI96md pseudo-potential program, which allows the use of larger super-cell sizes. Encouraged by the good agreement between experiment and model calculation for As in CdTe as well as similarly for the isovalent Se in CdTe, we extended our investigation to Br in CdTe, where the electric field gradient has also been measured, and could not only verify the derived lattice expansion around Br with our EXAFS analysis but additionally observe fractions of Br in the A-center as well as in a DX-center configuration.

Key Words

calculations with DFT theories with LAPW and pseudo-potential methodsdopants in CdTefluorescence detected X-ray absorptionlattice relaxationlocal structure

PACS codes


Copyright information

© Springer Science+Business Media, Inc. 2005