文摘
Multistage formation of fluoride upconversion agents from the related-semiconductor precursors provides a promising route for the fabrication of near-infrared (NIR) photocatalysts with high photocatalytic activities. Herein, the cotton templated CaTiO3 鈥渟emiconduction鈥?precursors (C-CaTiO3) were used to synthesize the NIR photocatalyst of Er3+/Tm3+/Yb3+鈥?CaTiO3/CaF2/TiO2) (C-ETYCCT), and the functions of the Ca2+ source for CaF2 and the heterostructure formations were displayed by C-CaTiO3. The generated CaF2 acted as the host material for the lanthanide ions, and the heterostructures were constructed among anatase, rutile, and the remaining CaTiO3. The induced oxygen vacancies and Ti3+ ions enabled the samples to utilize most of the upconversion luminescence for photocatalysis. The NIR driven degradation rate of methyl orange (MO) over C-ETYCCT reached 52.34%, which was 1.6 and 2.5 times higher than those of Er3+/Tm3+/Yb3+鈥?CaTiO3/TiO2) (C-ETYCT) and Er3+/Tm3+/Yb3+鈥?CaTiO3/CaF2) (C-ETYCC), respectively. The degradation rates of MO and salicylic acid over C-ETYCCT with UV鈥搗is鈥揘IR light irradiation were also much higher than those of other samples, which were mainly results of the contributions of its high upconversion luminescence and the efficient electron鈥揾ole pair separation.