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Significant enhancement of photocatalytic activity of rutile TiO2 compared with anatase TiO2 upon Pt nanoparticle deposition studied by far-ultraviolet spectroscopy

机译:远紫外分光光度法研究Pt纳米颗粒沉积时,金红石型TiO2与锐钛矿型TiO2的光催化活性显着提高

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Absorption spectra of anatase and rutile TiO2 in the 150-300 nm region before and after the deposition of Pt nanoparticles were measured. For anatase TiO2, the spectral intensity in the longer wavelength region decreased (> ~210 nm), while that in the shorter wavelength region increased (< ~210 nm). In particular, spectral band intensity in the far-ultraviolet (FUV) region (~160 nm) was increased. In contrast, the spectral intensity of rutile TiO2 increased over the entire wavelength region under investigation. Rutile TiO2 showed a spectral band at a longer wavelength region (~170 nm) than anatase TiO2, and the difference in the band wavelengths in the FUV region was due to the differences in the electronic structures of their phase. The decrease and increase in the intensity upon the Pt nanoparticle deposition suggest electron transfer from the TiO2 to Pt nanoparticles and enhancement of charge-separation, respectively. The photocatalytic activity of rutile TiO2, as evaluated by a photo-degradation reaction of methylene blue, increased more than that of anatase TiO2 upon the deposition of Pt nanoparticles. Thus, we concluded that the charge-separation efficiency of rutile TiO2 is enhanced relative to that of anatase TiO2 upon the deposition of Pt nanoparticles.
机译:测量了Pt纳米粒子沉积前后150-300 nm区域内的锐钛矿和金红石型TiO2的吸收光谱。对于锐钛矿型TiO2,较长波长区域的光谱强度降低(>〜210 nm),而较短波长区域的光谱强度增加(<〜210 nm)。特别是,远紫外(FUV)区域(〜160 nm)的光谱带强度增加了。相反,金红石型TiO2的光谱强度在所研究的整个波长范围内增加。金红石型TiO2比锐钛矿型TiO2在更长的波长范围内(〜170 nm)显示光谱带,而FUV范围内的带波长的差异是由于其相的电子结构的差异。在Pt纳米颗粒沉积时强度的降低和增加分别表明电子从TiO2转移到Pt纳米颗粒和电荷分离增强。通过亚甲基蓝的光降解反应评估,金红石型TiO2的光催化活性比Pt纳米粒子沉积时的锐钛矿型TiO2增强。因此,我们得出结论,在沉积Pt纳米粒子时,金红石型TiO2的电荷分离效率相对于锐钛型TiO2有所提高。

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