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Slow Surface Charge Trapping Kinetics on Irradiated TiO_2

机译:TiO_2辐照的慢表面电荷俘获动力学

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摘要

Free and trapped charge carriers in polycrystalline TiO_2 following band gap irradiation are characterized by diffuse reflectance IR spectroscopy (DRIFTS). A spectrum-wide absorption signal proportional to λ~(1.7) (λ = wavelength/μm) indicates the presence of free conduction band electrons coupled with acoustic phonons in the lattice. Free electrons appear to decay according to saturation kinetics. The fitted parameters indicate a limited number of trapping states. The concentration of these states appears to be diminished by sequential UV treatments. The free carrier decay lifetime is lengthened as the samples are dehydrated, which suggests an excited-state relaxation event during electron trapping. Photogenerated free electrons are comparable to conduction band electrons injected from surface-bound chromophores, and the lifetime of these electrons can be extended across several orders of magnitude. A broad IR absorption peak centered at 3380 cm~(-1) is attributed to an electronic transition from an occupied surface electron trap 0.42 eV below the conduction band.
机译:带隙辐照后多晶TiO_2中的自由和捕获的电荷载流子通过漫反射红外光谱(DRIFTS)进行表征。与λ〜(1.7)(λ=波长/μm)成正比的宽光谱吸收信号表明晶格中存在与声子耦合的自由导带电子。自由电子似乎根据饱和动力学而衰减。拟合的参数指示有限数量的捕获状态。通过连续的紫外线处理,这些状态的浓度似乎降低了。随着样品的脱水,自由载流子的衰变寿命得以延长,这表明在电子俘获过程中发生了激发态弛豫事件。光生自由电子可与从表面结合的生色团注入的导带电子相媲美,这些电子的寿命可以延长几个数量级。中心在3380 cm〜(-1)处的宽IR吸收峰归因于来自导带以下0.42 eV的表面电子陷阱的电子跃迁。

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