A series of nanometer TiO2 photocatalysts co-doped respectively with rare earth Er3+-Ce3+ and La3+-Fe3+ were prepared by sol-gel method,and the photocatalytic activity under ultra-violet light was evaluated by photocatalytic degradation of methyl blue.The crystallographic forms,particles size,and morphology were characterized by XRD and TEM.The results showed that the optimum heat temperature of co-doped TiO2 was 550 ℃,and the co-doped TiO2 kept anatase.The anatase crystal had the average size of 20 nm.The co-doping caused red-shift of the UV-Vis absorption spectra and enhanced the absorption of light.Compared with the spectrum of pure TiO2 photocatalysts,the red-shift of Er3+-Ce3+ co-doping and La3+-Fe3+ co-doping catalysts was 53 nm and 34 nm,respectively.Optimal co-doping amount for Er3+-Ce3+ was n(Er3+):n(TiO2)=0.1%,n(Ce3+):(TiO2)= 0.05% and La3+-Fe3+ was n(La3+):n(TiO2)=0.05%,n(Fe3+):(TiO2)=0.5%.Under the condition the photocatalysis properties of the samples can be enhanced.It was found that the catalytic activity correlated well with the ratio.The degradation rate of methyl blue examined at two hour of the reaction was 92.37%,and the better photocatalysis properties than the non-doped TiO2 were obtained.The co-doped photocatalyst on methyl blue degradation follows the apparent first-order kinetics. A series of nanometer TiO2 photocatalysts co-doped with rare earth Er3 + -Ce3 + and La3 + -Fe3 + were prepared by sol-gel method, and the photocatalytic activity under ultra-violet light was due by photocatalytic degradation of methyl blue. Crystallographic forms, particles size, and morphology were characterized by XRD and TEM. The results showed that the optimum heat temperature of co-doped TiO2 was 550 ° C, and the co-doped TiO2 had an anatase. The anatase crystal had the average size of 20 nm. co-doping caused red-shift of the UV-Vis absorption spectra and enhanced the absorption of light. Compared with the spectrum of pure TiO2 photocatalysts, the red-shift of Er3 + -Ce3 + co-doping and La3 + -Fe3 + co- doping catalysts was 53 nm and 34 nm, respectively.Optimal co-doping amount for Er3 + -Ce3 + was n (Er3 +): n (TiO2) = 0.1% and n (Ce3 +) :( TiO2) = 0.05% and La3 + -Fe3 + wasn (La3 + ): n (TiO2) = 0.05%, n (Fe3 +) :( TiO2) = 0.5% .Under the condition the photocatalysis properties of the samples can be enhanced.It was found that the catalytic activity correlated well with the ratio. degradation rate of methyl blue examined at two hour of the reaction was 92.37%, and the better photocatalysis properties than the non-doped TiO2 were. The co-doped photocatalyst on methyl blue degradation follows the apparent first-order kinetics.