Reversible photostructural changes in a binary As2Se3 glass have been
studied by high-precision in-situ EXAFS. We demonstrate that the coord
ination number of selenium species increases reversibly in the photoex
cited state while the coordination number for arsenic species remains
unchanged, which is attributable to the creation of dynamic Se-Se inte
rlayer bonds. Photoexcitation increases disorder near selenium and ars
enic species and gives rise to bond breaking which restores the initia
l coordination number of both constituents and creates ''wrong'' As-As
and Se-Se bonds. (C) 1997 American Institute of Physics.