Chiarello Gian Luca, Tealdi Cristina, Mustarelli Piercarlo, Selli Elena
Dipartimento di Chimica, Università degli Studi di Milano, via Golgi 19, Milano 20133, Italy.
Dipartimento di Chimica, Università degli Studi di Pavia, viale Taramelli 16, Pavia 27100, Italy.
Materials (Basel). 2016 Apr 8;9(4):279. doi: 10.3390/ma9040279.
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.
通过复合Pt/Ti/TiO₂光电极的相对两侧实现了光催化水分解产生纯氢气和氧气。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(UV-vis-NIR)漫反射光谱对其进行表征。通过入射光子到电流效率(IPCE)测量以及在两室电池中的光催化水分解测量来评估光催化活性。通过6小时TiO₂沉积制备的光电极实现了最高的H₂产生速率,这得益于其在金红石多晶型物中的高含量,该多晶型物在可见光下具有活性。相比之下,由于电子转移路径变长导致电子-空穴复合概率增加,较长沉积时间下的光活性下降。