Response surface methodology(RSM) was employed to optimize the control parameters of TiO_2/graphene with exposed {001} facets during synthesis, and its enhanced photocatalytic activities were evaluated in the photodeg...Response surface methodology(RSM) was employed to optimize the control parameters of TiO_2/graphene with exposed {001} facets during synthesis, and its enhanced photocatalytic activities were evaluated in the photodegradation of toluene. Experimental results were in good agreement with the predicted results obtained using RSM with a correlation coefficient(R^2) of 0.9345. When 22.06 mg of graphite oxide(GO) and 2.09 mL of hydrofluoric acid(HF) were added and a hydrothermal time of 28 h was used, a maximum efficiency in the degradation of toluene was achieved. X-ray diffraction(XRD), transmission electron microscopy(TEM), and scanning electron microscopy(SEM) were employed to characterize the obtained hybrid photocatalyst. The electron transferred between Ti and C retarded the combination of electron–hole pairs and hastened the transferring of electrons, which enhanced the photocatalytic activity.展开更多
基金supported by the National Natural Science Foundation of China (Nos. 21406164, 21466035 and 51203111)the National Basic Research Program of China ("973" Program, Nos. 2012CB720100 and 2014CB239300)
文摘Response surface methodology(RSM) was employed to optimize the control parameters of TiO_2/graphene with exposed {001} facets during synthesis, and its enhanced photocatalytic activities were evaluated in the photodegradation of toluene. Experimental results were in good agreement with the predicted results obtained using RSM with a correlation coefficient(R^2) of 0.9345. When 22.06 mg of graphite oxide(GO) and 2.09 mL of hydrofluoric acid(HF) were added and a hydrothermal time of 28 h was used, a maximum efficiency in the degradation of toluene was achieved. X-ray diffraction(XRD), transmission electron microscopy(TEM), and scanning electron microscopy(SEM) were employed to characterize the obtained hybrid photocatalyst. The electron transferred between Ti and C retarded the combination of electron–hole pairs and hastened the transferring of electrons, which enhanced the photocatalytic activity.
