Inorganic/organic interfaces (IOI) consist of TiO2/PEDOT (poly 3,4-ethylenedioxythiophene) and [PMo12O40]3- or MoO3/PEDOT were subject to photoelectrochemical studies in both aqueous nanosuspensions and in thin solid ...Inorganic/organic interfaces (IOI) consist of TiO2/PEDOT (poly 3,4-ethylenedioxythiophene) and [PMo12O40]3- or MoO3/PEDOT were subject to photoelectrochemical studies in both aqueous nanosuspensions and in thin solid films. The effects PEDOT modifier caused on the photoelectrochemical behavior of the IOI were investigated using [Fe(CN)6]4- as the photoactive hydrated electron donor agent. Results show that native PEDOT or PEDOT doped with MoO3 thin films increased charge storage capability evident by the high capacitive current. In the case of nano suspensions composed of TiO2/PEDOT the adsorption process of [Fe(CN)6]3- (photolysis product) control of the photoactivity outcome of the IOI assemblies. TiO2/PEDOT shows a lower heterogeneous photochemical response than native TiO2 in short term photolysis times. At longer photolysis times the IOI shows photoactivity greater than that of native TiO2. The interface activities were explained by analyzing the IOI junction characteristics, such as electron affinity, work function and hole/electrons barrier heights. The aqueous nano-systems retained moderate stability as indicated by the reproducibility of their photocatalytic activities. Both [Fe(CN)6]4-and PEDT contributed to the stability of native TiO2 surfaces.展开更多
Photoelectrochemical studies on TiO2 doped with Ce2O3 or CeO2 took place in aqueous solutions of [Fe(CN)6]4- as the source of hydrated electrons. Our studies show that doping TiO2 with CeO2 gave better photocatalytic ...Photoelectrochemical studies on TiO2 doped with Ce2O3 or CeO2 took place in aqueous solutions of [Fe(CN)6]4- as the source of hydrated electrons. Our studies show that doping TiO2 with CeO2 gave better photocatalytic reduction of [Fe(CN)6]3- than TiO2 doped with Ce2O3. However the TiO2 assemblies doped with either Ce(III) or Ce(IV) oxides give less photochemical reduction of [Fe(CN)6]3- that the oxides of pure metals (Ti or Ce). In both cases a lowering of the band gaps of TiO2 was noticed. Immobilized TiO2 doped with Ce oxides on a FTO (Fluorine Ten Oxide) surface gave greater photocurrent with I2/I3– than that recorded for [Fe(CN)6]3-/4- redox systems. Our studies indicate that the TiO2 doped with Ce2O3 or CeO2 maintained photoactivity after being immobilized in thin solid sheets and can be used in all solid state photoelectron-chemical cells.展开更多
文摘Inorganic/organic interfaces (IOI) consist of TiO2/PEDOT (poly 3,4-ethylenedioxythiophene) and [PMo12O40]3- or MoO3/PEDOT were subject to photoelectrochemical studies in both aqueous nanosuspensions and in thin solid films. The effects PEDOT modifier caused on the photoelectrochemical behavior of the IOI were investigated using [Fe(CN)6]4- as the photoactive hydrated electron donor agent. Results show that native PEDOT or PEDOT doped with MoO3 thin films increased charge storage capability evident by the high capacitive current. In the case of nano suspensions composed of TiO2/PEDOT the adsorption process of [Fe(CN)6]3- (photolysis product) control of the photoactivity outcome of the IOI assemblies. TiO2/PEDOT shows a lower heterogeneous photochemical response than native TiO2 in short term photolysis times. At longer photolysis times the IOI shows photoactivity greater than that of native TiO2. The interface activities were explained by analyzing the IOI junction characteristics, such as electron affinity, work function and hole/electrons barrier heights. The aqueous nano-systems retained moderate stability as indicated by the reproducibility of their photocatalytic activities. Both [Fe(CN)6]4-and PEDT contributed to the stability of native TiO2 surfaces.
文摘Photoelectrochemical studies on TiO2 doped with Ce2O3 or CeO2 took place in aqueous solutions of [Fe(CN)6]4- as the source of hydrated electrons. Our studies show that doping TiO2 with CeO2 gave better photocatalytic reduction of [Fe(CN)6]3- than TiO2 doped with Ce2O3. However the TiO2 assemblies doped with either Ce(III) or Ce(IV) oxides give less photochemical reduction of [Fe(CN)6]3- that the oxides of pure metals (Ti or Ce). In both cases a lowering of the band gaps of TiO2 was noticed. Immobilized TiO2 doped with Ce oxides on a FTO (Fluorine Ten Oxide) surface gave greater photocurrent with I2/I3– than that recorded for [Fe(CN)6]3-/4- redox systems. Our studies indicate that the TiO2 doped with Ce2O3 or CeO2 maintained photoactivity after being immobilized in thin solid sheets and can be used in all solid state photoelectron-chemical cells.
