Pure and highly crystallized gold nanoparticles-doped-TiO2(B) nanofibers (Au-T(B)NFs), with thickness of 50-200 nm and length of several microns, were successfully synthesized by combination of low-temperature (150 degrees C) hydrothermal reaction of titanium (IV) isopropoxide (Ti[OC3H7](4)) and sonication of the ensued precipitate with gold nanoparticles followed by post-heat treatment at 300 degrees C. Formation of pure TiO2(B) was confirmed by X-ray diffraction, high resolution transmission electron microscopy and Raman spectroscopy. The UV-vis diffuse reflectance spectra (DRS) of Au-TiO2(B) nanofibers exhibited surface-state absorption beyond 400 nm with band gap energy at 2.94 eV and broad gold plasma resonance band around 550 nm. The photoluminescence (PL) emission spectra of the Au-T(B)NFs exhibited structural emission band around 410 nm with shoulders around 464 nm and 540 am. Analysis of these optical properties revealed that the surface state absorption is attributed to the indirect transition. These results suggest that coupling of the surface charge carriers with the lattice phonon of Au-T(B)NFs is so strong that the charge recombination is mostly nonradiative as supported by the significantly quenched emission of Au-T(B)NFs as compared to that of free T(B)NFs. These optoelectronic properties were well correlated with highly efficient solar photocatalytic activities of Au-T(B)NFs for oxidation of methylene blue (MB). (C) 2011 Elsevier B.V. All rights reserved.