Abstract

Electron-phonon coupling in Se species confined in the nanoporous matrix has been investigated by using resonant Raman spectra performed with several different laser lines from deep blue to near infrared. The spectra strongly depend on the energies of the excitation laser lines. The one-phonon symmetric A1 modes for Se single helix and Se8 rings are enhanced in the vicinity of their absorption bands. Detailed analysis shows that the Raman band in the high-frequency range of 450–550cm−1 is composed of three individual second-order Raman bands for the confined Se species. These two-phonon Raman shifts occur at twice the frequency shift of the first-order Raman lines, and their intensities are also enhanced when the excitation laser energy matches an electronic transition in Se nanospecies.

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