Subrahmanyam A, Rajakumar A, Rakibuddin Md, Paul Ramesh T, Raveendra Kiran M, Shankari D, Chandrasekhar K
Department of Physics, IIT Madras, Chennai 600036, India.
Phys Chem Chem Phys. 2014 Dec 7;16(45):24790-9. doi: 10.1039/c4cp02819h.
The present work describes in detail the photocatalytic properties of controlled titanium doped indium tin oxide (Ti/TiO2-ITO) composite thin films prepared by DC magnetron sputtering and their applicability to developing a bio-medical lung assistive device. The catalytic films of various thicknesses (namely, C1, C2, C3 and C4) were characterized using surface imaging (SEM), X-ray analyses (XRD and EDX), and Raman studies. The optical band gaps of the prepared films are ∼3.72-3.77 eV. Photocatalytic efficiencies of the film catalysts were investigated with the aid of a model organic molecule (Rhodamine B dye). The overall photodegradation capacity of the films was found to be slow kinetically, and the catalyst C1 was identified as having a better degradation efficiency (RhB 5 ppm, at pH 6.5) over 5 h under irradiation at 254 nm. The distinctive features of these composite films lie in their oxygen accumulation capacity and unique electron-hole pair separation ability. Investigations on oxygen species revealed the formation of superoxide radicals in aqueous systems (pH 6.5). The prepared films have TiO2 in the anatase phase in the surfaces, and possess the desired photocatalytic efficiency, compatibility to the heme system (are not involved in harmful hydroxyl radical production), and appreciable reusability. Especially, the thin films have a significant ability for mobilization of oxygen rapidly and continuously in aqueous medium under the irradiation conditions. Hence, these films may be a suitable choice for the photo-aided lung assistive design under development.
本工作详细描述了通过直流磁控溅射制备的可控钛掺杂氧化铟锡(Ti/TiO₂-ITO)复合薄膜的光催化性能及其在开发生物医学肺辅助装置中的适用性。使用表面成像(SEM)、X射线分析(XRD和EDX)以及拉曼研究对各种厚度的催化薄膜(即C1、C2、C3和C4)进行了表征。制备薄膜的光学带隙约为3.72 - 3.77 eV。借助模型有机分子(罗丹明B染料)研究了薄膜催化剂的光催化效率。发现薄膜的整体光降解能力在动力学上较慢,并且在254 nm光照下5小时内,催化剂C1被确定在pH 6.5时对5 ppm的RhB具有更好的降解效率。这些复合薄膜的独特之处在于它们的氧积累能力和独特的电子 - 空穴对分离能力。对氧物种的研究揭示了在水体系(pH 6.5)中形成超氧自由基。制备的薄膜在表面具有锐钛矿相的TiO₂,并且具有所需的光催化效率、与血红素系统的相容性(不参与有害羟基自由基的产生)以及可观的可重复使用性。特别是,这些薄膜在光照条件下在水介质中具有快速且持续地迁移氧的显著能力。因此,这些薄膜可能是正在开发的光辅助肺辅助设计的合适选择。