Immobilized TiO 2 was prepared by adding a small composition of polyethylene glycol (PEG) as a binder, and this paper reported for the very first time the formation of C=O from oxidized PEG, which acted as an electron injector in enhancing photoactivity. Water-based TiO 2 with PEG formulation was deposited by using a brush technique onto double-sided adhesive tape (DSAT) as a support binder to increase the adhesiveness of immobilized TiO 2 . The photocatalytic activity of immobilized TiO 2 -PEG was measured by photodegradation of 12 mg·L −1 methylene blue (MB) dye. The optimum condition of immobilized TiO 2 -PEG was observed at TiO 2 /PEG-2 (TP2) with 10:0.1 for the TiO 2 /PEG ratio, which resulted in a 1.8-times higher photodegradation rate as compared to the suspension mode of pristine TiO 2 . The high photodegradation rate was due to the formation of the active C=O bond from oxidized PEG binder in immobilized TiO 2 -PEG as observed by Fourier transform infrared and X-ray photoelectron spectroscopy analyses. The presence of C=O has escalated the photoactivity by forming an electron injector to a conduction band of TiO 2 as proven by higher photoluminescence intensity obtained for TP2 as compared to pristine TiO 2 . The TP2 sample has also increased its adhesiveness when DSAT is applied as a support binder where it can be recycled up to eight times and comparable to recent photocatalysis cycle developments.