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CaF2-Based Near-Infrared Photocatalyst Using the Multifunctional CaTiO3 Precursors as the Calcium Source

机译:多功能CaTiO3前驱体作为钙源的基于CaF2的近红外光催化剂

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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 "semiconduction" precursors (C-CaTiO3) were used to synthesize the NIR photocatalyst of Er3+/Tm3+/Yb3+-(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+ (CaTiO3/TiO2) (C-ETYCT) and Er3+/Tm3+/Yb3+ (CaTiO3/CaF2) (C-ETYCC), respectively. The degradation rates of MO and salicylic acid over C-ETYCCT with UV-vis-NIR 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 hole pair separation.
机译:由相关半导体前体的多级氟化物上转换剂形成为制造具有高光催化活性的近红外(NIR)光催化剂提供了一条有希望的途径。在此,以棉花为模板的CaTiO3“半导体”前体(C-CaTiO3)合成了Er3 + / Tm3 + / Yb3 +-(CaTiO3 / CaF2 / TiO2)(C-ETYCCT)的近红外光催化剂。 CaF2和异质结构的形成由C-CaTiO3显示。生成的CaF2充当镧系元素离子的主体材料,并且在锐钛矿,金红石和其余CaTiO3之间构建了异质结构。诱导的氧空位和Ti3 +离子使样品能够利用大部分上转换发光进行光催化。 N-IR驱动的甲基橙(MO)在C-ETYCCT上的降解率达到52.34%,分别是Er3 + / Tm3 + / Yb3 +(CaTiO3 / TiO2)(C-ETYCT)和Er3 + / Tm3 + / Yb3 +的1.6和2.5倍(CaTiO3 / CaF2)(C-ETYCC)。 UV-vis-NIR光照射下C-ETYCCT对MO和水杨酸的降解率也比其他样品高得多,这主要是由于其高上转换发光和有效的电子空穴对分离的结果。

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