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Vibrational spectroscopy of arsenic-hydrogen complexes in ZnSe

Journal Article · · Applied Physics Letters
DOI:https://doi.org/10.1063/1.116799· OSTI ID:284638
;  [1]; ;  [2]
  1. Lawrence Berkeley National Laboratory and University of California, Berkeley, California 94720 (United States)
  2. Center for Advanced Materials, Materials Sciences Division, Lawrence Berkeley National Laboratory, Berkeley, California 94720 (United States)

Using infrared absorption spectroscopy, we have observed hydrogen local vibrational modes (LVMs) in arsenic-doped ZnSe grown by metalorganic chemical vapor deposition (MOCVD). When hydrogen is used as a carrier gas, we find an absorption peak at 2165.6 cm{sup {minus}1}, which we attribute to a bond-stretching mode of a hydrogen attached to an arsenic acceptor in a bond-centered orientation. With deuterium substituting the hydrogen carrier gas, we find an additional peak at 1557.1 cm{sup {minus}1} with 1/3 the intensity of the hydrogen peak. The isotopic frequency ratio is {ital r}={ital v}{sub H}/{ital v}{sub D}=1.3908, similar to values found in many hydrogen/deuterium-related complexes. The larger area of the hydrogen peak indicates that most of the hydrogen comes from decomposition reactions involving the metalorganic molecules. The temperature dependent shift of the ZnSe:As,H mode is proportional to the lattice thermal energy {ital U}({ital T}), a consequence of the anharmonic coupling between the LVMs and the lattice phonons.

Research Organization:
Lawrence Berkeley National Laboratory
DOE Contract Number:
AC03-76SF00098
OSTI ID:
284638
Journal Information:
Applied Physics Letters, Journal Name: Applied Physics Letters Journal Issue: 24 Vol. 68; ISSN 0003-6951; ISSN APPLAB
Country of Publication:
United States
Language:
English

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