Infrared analysis showed that the characteristics bands for the bare nanoparticles are still exhibited in the vitamins@P25TiO2NPs spectra, such as a wide peak in 450–1028 cm−1 related to the stretching vibration of Ti-O-Ti and other peaks in 1630 cm−1 and 3400 cm−1, which represent the surface OH groups stretching. The IR spectrum of vitaminB2@P25TiO2NPs showed signs of binding between compounds. The OH bending peak (1634 cm−1) corresponding to bare nanoparticles disappeared, and the NH2 bending band characteristic of vitamin B2 appeared (1650 cm−1). The IR spectrum of vitaminC@P25TiO2NPs also showed signs of successful functionalization. Bands at 1075 cm−1; 1120 cm−1; 1141 cm−1 were observed, which are originated by C
O-C vibrations present in the vitamin C. The intense band at 1672 cm−1 is attributed to the C = O stretching in the lactone ring while the peak at 1026 cm−1 is ascribed to the stretching vibration Ti-O-C. Wide bands at 3880–3600 cm−1 are related to stretching vibration OH groups, but those disappear in the modified nanoparticles spectrum. These observations confirm the interactions between the P25TiO2NPs and the vitamins [35].
O-C vibrations present in the vitamin C. The intense band at 1672 cm−1 is attributed to the C = O stretching in the lactone ring while the peak at 1026 cm−1 is ascribed to the stretching vibration Ti-O-C. Wide bands at 3880–3600 cm−1 are related to stretching vibration OH groups, but those disappear in the modified nanoparticles spectrum. These observations confirm the interactions between the P25TiO2NPs and the vitamins [35].
