Sara El Hakim, T. Chave, A. Nada, S. Roualdès, S. Nikitenko
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引用次数: 7
摘要
本研究为甘油重整过程中光热活性增强的Ti@TiO2光催化剂的设计提供了新的见解。在纯水中对金属钛纳米粒子进行超声水热处理,得到了Ti@TiO2纳米粒子。通过改变水热温度,可以控制Ti0表面的纳米TiO2壳层。在100 < T < 150℃时,TiO2 NPs的形成主要是通过钛(IV)非晶态的结晶和Ti0纳米颗粒表面的亚氧化钛ti30氧化来实现的。在150℃时,TiO2也是由Ti0与过热水氧化而形成的。动力学研究强调了TiO2纳米晶壳对H2生成的重要性。电化学阻抗谱与光催化数据相关,指出Ti@TiO2纳米粒子更有效的电子转移。表观活化能Ea =(25-31)±5 kJ·mol−1,假设光热效应是由甘油氧化中间体扩散或催化剂表面的水动力学引起的。在加热条件下,即使在纯水中也能观察到光催化H2释放现象。
Tailoring Noble Metal-Free Ti@TiO2 Photocatalyst for Boosting Photothermal Hydrogen Production
In this work, we provide new insights into the design of Ti@TiO2 photocatalyst with enhanced photothermal activity in the process of glycerol reforming. Ti@TiO2 nanoparticles have been obtained by sonohydrothermal treatment of titanium metal nanoparticles in pure water. Variation of sonohydrothermal temperature allows controlling nanocrystalline TiO2 shell on Ti0 surface. At 100 < T < 150°C formation of TiO2 NPs occurs mostly by crystallization of Ti(IV) amorphous species and oxidation of titanium suboxide Ti3O presented at the surface of Ti0 nanoparticles. At T > 150°C, TiO2 is also formed by oxidation of Ti0 with overheated water. Kinetic study highlights the importance of TiO2 nanocrystalline shell for H2 generation. Electrochemical impedance spectroscopy points out more efficient electron transfer for Ti@TiO2 nanoparticles in correlation with photocatalytic data. The apparent activation energy, Ea = (25–31) ± 5 kJ·mol−1, assumes that photothermal effect arises from diffusion of glycerol oxidation intermediates or from water dynamics at the surface of catalyst. Under the heating, photocatalytic H2 emission is observed even in pure water.