Regulation of d-band center of TiO2 through fluoride doping for enhancing photocatalytic H2O2 production activity

Abstract

Titanium dioxide (TiO2) has received extensive attention for photocatalytic hydrogen peroxide (H2O2) production, with the d-band center related to the adsorption performance, which affects the photocatalytic reaction process. Herein, an ingenious strategy to lower the antibonding-orbital occupancy in the Ti 3d orbital by fluoride ion (F−) doping is proposed, with density functional theory calculations predicting that F-doping into TiO2 induces a non-uniform charge distribution and enables an upshift of the d-band center in F/TiO2. This manipulation provides accessible active centers with favorable d-band energy levels, which can improve the charge-transfer behavior, strengthen the interaction between the adsorbed oxygen and the photocatalyst, and reduce the adsorption energy of oxygen, eventually promoting the photocatalytic H2O2 production rate. The experimental results further confirm that a lower antibonding-orbital occupancy can intensify the adsorption of atomic oxygen at the Ti sites. Electron paramagnetic resonance experiment reveals that the presence of F− ions in the lattice induces the formation of Ti3+ centers that localize the extra electron needed for charge compensation. Femtosecond transient absorption (fs-TA) spectroscopy suggests that photogenerated electrons are transferred from the conduction band of F/TiO2 to the Ti3+ surface states and surface F− ions, expediting the separation of electrons and holes. Consequently, with F− doping in TiO2, the photocatalytic H2O2 production yields improved from 277 to 467 μmol·g−1·h−1, with ethanol as a sacrificial reagent. This study provides a new strategy for regulating the d-band center to optimize the adsorption strength between the photocatalyst and oxygen atoms and achieve enhanced photocatalytic H2O2 production performance.