首页> 外文期刊>Journal of Photochemistry and Photobiology, A. Chemistry >Interfacial charge transfer in Pt-loaded TiO2 P25 photocatalysts studied by in-situ diffuse reflectance FTIR spectroscopy of adsorbed CO
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Interfacial charge transfer in Pt-loaded TiO2 P25 photocatalysts studied by in-situ diffuse reflectance FTIR spectroscopy of adsorbed CO

机译:通过原位漫射反射率的Pt-Loaded TiO2 P25光催化剂中的界面电荷转移反射粘附性FTIR光谱法的吸附CO

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摘要

The efficiency of photocatalytic systems is strongly depending on the charge carrier transfer from the excited semiconductor to co-catalyst particles attached on its surface. In this study, we investigated the influence of photo-induced charge transfer in photoplatinized TiO2 P25 photocatalysts by diffuse reflectance FTIR spectros-copy of CO molecules adsorbed on the Pt co-catalyst under well-defined gas phase conditions. In contrast to aqueous conditions, where shifts of the CO stretching vibration of up to 50 cm(-1) have been reported, the observed shifts under gas phase conditions are very small ( 1 cm(-1)). This demonstrates that the difference in dielectric properties between aqueous electrolytes and vacuum are critical for the development of prominent shifts of adsorbed CO bands upon trapping of photogenerated charge carriers on co-catalyst particles. The experimental findings are discussed in terms of an electrostatic Stark effect, charge screening, co-adsorption, coverage-dependent shifts of the vibrational bands of adsorbed CO and photocatalytic surface reactions.
机译:光催化系统的效率根据来自激发半导体的电荷载体转移到附着在其表面上的助催化剂颗粒。在这项研究中,我们研究了在明确限定的气相条件下在Pt助催化剂上吸附在Pt助催化剂上的CO分子的弥散反射率FTIR光谱催化剂在光塑性的TiO 2 P25光催化剂中的影响。与含水条件相比,报道了高达50cm(-1)的CO拉伸振动的偏移,在气相条件下观察到的偏移非常小(& 1cm(-1))。这表明含水电解质和真空之间的介电性质之间的差异对于在助催化剂颗粒上捕获光生电荷载体时突出的吸附CO带突出的发展至关重要。在静电颗粒效应,电荷筛选,共吸收,振动带的振动带的振动带的振动带的振动带的覆盖率依赖性差异讨论了实验结果。

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