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We report low-temperature absorption, time-integrated photoluminescence, and resonant-Raman-scattering spectra near the fundamental band gap of TiO₂ single crystals. The photoluminescence spectrum comprises a first peak at =3. 031 eV, followed by several peaks at lower energies. A polarization study of the emission spectrum indicates that the highest energy peak corresponds to 2pₗₘ dipole-allowed second-class excitonic transitions while the lower-energy peaks are phonon replicas of the 1s quadrupolar exciton. This result is corroborated by time-resolved photoluminescence measurements. The near-band-gap optical response of TiO₂ is thus controlled by two distinct exciton states. The Raman-scattering intensity is found to increase slowly for excitation energies in the range 2. 7--3 eV. This indicates that the Raman cross-section enhancement is dominated by virtual transitions involving the first dipole-allowed direct gap at 4. 2 eV.
Amtout et al. (Wed,) studied this question.