Klaysri Rachan, Ratova Marina, Praserthdam Piyasan, Kelly Peter J
Center of Excellence on Catalysis and Catalytic Reaction Engineering, Department of Chemical Engineering, Faculty of Engineering, Chulalongkorn University, Bangkok 10330, Thailand.
Surface Engineering Group, School of Engineering, Manchester Metropolitan University, Manchester M1 5GD, UK.
Nanomaterials (Basel). 2017 May 16;7(5):113. doi: 10.3390/nano7050113.
Doping of titanium dioxide with p-block elements is typically described as an efficient pathway for the enhancement of photocatalytic activity. However, the properties of the doped titania films depend greatly on the production method, source of doping, type of substrate, etc. The present work describes the use of pulsed direct current (pDC) magnetron sputtering for the deposition of carbon-doped titania coatings, using CO₂ as the source of carbon; ratios of O₂/CO₂ were varied through variations of CO₂ flow rates and oxygen flow control setpoints. Additionally, undoped Titanium dioxide (TiO₂) coatings were prepared under identical deposition conditions for comparison purposes. Coatings were post-deposition annealed at 873 K and analysed with scanning electron microscopy (SEM), X-ray diffreaction (XRD), atomic force microscopy (AFM), and X-ray photoelectron spectroscopy (XPS). The photocatalytic properties of the thin films were evaluated under ultraviolet (UV) and visible light irradiation using methylene blue and stearic acid decomposition tests. Photoinduced hydrophilicity was assessed through measurements of the water contact angle under UV and visible light irradiation. It was found that, though C-doping resulted in improved dye degradation compared to undoped TiO₂, the UV-induced photoactivity of Carbon-doped (C-doped) photocatalysts was lower for both model pollutants used.
用p区元素掺杂二氧化钛通常被描述为提高光催化活性的有效途径。然而,掺杂二氧化钛薄膜的性能在很大程度上取决于制备方法、掺杂源、基底类型等。本工作描述了使用脉冲直流(pDC)磁控溅射以二氧化碳作为碳源来沉积碳掺杂二氧化钛涂层;通过改变二氧化碳流速和氧气流量控制设定点来改变氧气/二氧化碳的比例。此外,为了进行比较,在相同的沉积条件下制备了未掺杂的二氧化钛(TiO₂)涂层。涂层在873K下进行沉积后退火,并通过扫描电子显微镜(SEM)、X射线衍射(XRD)、原子力显微镜(AFM)和X射线光电子能谱(XPS)进行分析。使用亚甲基蓝和硬脂酸分解试验在紫外(UV)和可见光照射下评估薄膜的光催化性能。通过测量紫外和可见光照射下的水接触角来评估光致亲水性。结果发现,尽管与未掺杂的TiO₂相比,碳掺杂提高了染料降解率,但对于所使用的两种模型污染物,碳掺杂(C掺杂)光催化剂的紫外诱导光活性较低。