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Fabrication of Pt/Ti/TiO2 Photoelectrodes by RF-Magnetron Sputtering for Separate Hydrogen and Oxygen Production

机译:射频磁控溅射制备Pt / Ti / TiO2光电电极以分离制氢和制氧

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摘要

Evolution of pure hydrogen and oxygen by photocatalytic water splitting was attained from the opposite sides of a composite Pt/Ti/TiO2 photoelectrode. The TiO2 films were prepared by radio frequency (RF)-Magnetron Sputtering at different deposition time ranging from 1 up to 8 h and then characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM) and ultraviolet-visible-near infrared (UV-vis-NIR) diffuse reflectance spectroscopy. The photocatalytic activity was evaluated by incident photon to current efficiency (IPCE) measurements and by photocatalytic water splitting measurements in a two-compartment cell. The highest H2 production rate was attained with the photoelectrode prepared by 6 h-long TiO2 deposition thanks to its high content in the rutile polymorph, which is active under visible light. By contrast, the photoactivity dropped for longer deposition time, because of the increased probability of electron-hole recombination due to the longer electron transfer path.
机译:从复合Pt / Ti / TiO2光电极的相对两侧,通过光催化水分解可释放出纯氢和氧。通过射频(RF)-磁控溅射在1至8小时的不同沉积时间制备TiO2薄膜,然后通过X射线衍射(XRD),扫描电子显微镜(SEM)和紫外可见近红外光谱对其进行表征(UV-vis-NIR)漫反射光谱。通过在两室电池中通过入射光子电流效率(IPCE)测量和通过光催化水分解测量来评估光催化活性。通过在6 h长的TiO2中沉积制备的光电极,由于其在金红石多晶型物中的含量高,在可见光下具有活性,因此可以实现最高的H2生成率。相比之下,由于更长的电子传输路径导致电子-空穴复合的可能性增加,光活性在更长的沉积时间内下降。

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