Three way electron transfer of a C–N–S tri doped two-phase junction of TiO2 nanoparticles for efficient visible light photocatalytic dye degradation†
Abstract
C–N–S tridoped TiO2 nanoparticles were synthesized by a sol–gel method using thiourea as a compound source of carbon (C), nitrogen (N) and sulphur (S). 15 wt% of thiourea has been used for effective dopants with different annealing temperatures (300, 400, 500 and 600 °C). X-ray diffraction results show that tridoping with C–N–S could effectively restrain the phase transformation of anatase to rutile at a higher annealing temperature (600 °C). The size–strain plot method indicates that the crystallite size decreases from 32 to 9 nm with the addition of dopants. Fourier transform infrared analysis shows that the peaks observed at 1384, 1128 and 1051 cm−1 are attributed to the N–H bond, bidentate S–O coordination to Ti4+ and the Ti– O– C bond. A UV-Vis study reveals that C–N–S tridoped TiO2 is redshifted compared to pure TiO2. From the photoluminescence spectra the band edge emission is redshifted with different excitation wavelengths (280–320 nm). Enhancement of Rhodamine B dye degradation is observed for C–N–S tridoped TiO2 nanoparticles (99% at 180 minutes) compared with undoped TiO2 under visible light irradiation.