Wei Zhishun, Rosa Lorenzo, Wang Kunlei, Endo Maya, Juodkazis Saulius, Ohtani Bunsho, Kowalska Ewa
Institute for Catalysis, Hokkaido University, N21 W10, 001-0021 Sapporo, Japan.
Centre for Micro-Photonics, Swinburne University of Technology, PO Box 218, Hawthorn, 3122 Australia.
Appl Catal B. 2017 Jun 5;206:393-405. doi: 10.1016/j.apcatb.2017.01.043.
Octahedral anatase particles (OAPs), prepared by ultrasonication-hydrothermal reaction (US-HT), were modified with 2 wt% of gold by photodeposition. Conditions of US-HT process such as durations of US and durations of HT were varied to obtain OAPs products different by physicochemical and morphological properties. Au/OAPs samples were characterized by X-ray diffraction (XRD), scanning transmission electron microscopy (STEM), X-ray photoelectron spectroscopy (XPS) and diffuse reflectance spectroscopy (DRS). The photocatalytic activity was tested under UV irradiation for decomposition of acetic acid (CO system) and dehydrogenation of methanol (H system) under aerobic and anaerobic conditions, respectively, and for oxidation of 2-propanol under visible light irradiation. Photodeposition of gold was very fast for all OAPs samples (0.5-10 min) under Ar atmosphere, and the clear correlation between the content of electron traps (ETs) and the induction period, during which nanoparticles (NPs) of gold are formed, indicates that ETs in titania samples are a key-factor for rapidity of gold photodeposition on titania surface. It was found that better morphology of titania (larger content of faceted particles) resulted in formation of larger gold NPs, while small gold NPs were deposited on structural defects. Modification of OAPs with gold NPs resulted in significant enhancement of photocatalytic activity, being e.g., 1.5 (CO system), 7.7 (H system), and even more than 40 under vis irradiation. It was found that both the properties of titania and gold are crucial for resultant photocatalytic activity, but a direct correlation between one structural/physical property and photocatalytic activity could not be obtained since all structural properties changed simultaneously when conditions of photocatalyst preparation (US-HT) were changed. Therefore, gold NPs of controlled sizes were deposited on OAPs product with the best morphology by modified photodeposition method. Clear correlation between photocatalytic activity under visible light and the size of gold NPs indicates that gold properties are decisive for visible light activity rather than titania properties. 3D-FDTD simulations confirm that an increase in the size of gold NPs results in extended surface areas with field enhancement.
通过超声-水热反应(US-HT)制备的八面体锐钛矿颗粒(OAPs),采用光沉积法用2 wt%的金进行改性。改变US-HT过程的条件,如超声持续时间和水热持续时间,以获得物理化学和形态性质不同的OAPs产物。通过X射线衍射(XRD)、扫描透射电子显微镜(STEM)、X射线光电子能谱(XPS)和漫反射光谱(DRS)对Au/OAPs样品进行表征。分别在有氧和无氧条件下,在紫外光照射下测试了光催化活性,用于乙酸分解(CO体系)和甲醇脱氢(H体系),以及在可见光照射下对2-丙醇的氧化。在氩气气氛下,所有OAPs样品(0.5-10分钟)的金光沉积都非常快,电子陷阱(ETs)含量与金纳米颗粒(NPs)形成的诱导期之间的明显相关性表明,二氧化钛样品中的ETs是金在二氧化钛表面光沉积速度的关键因素。发现二氧化钛更好的形态(多面颗粒含量更高)导致形成更大的金NPs,而小金NPs沉积在结构缺陷上。用金NPs对OAPs进行改性导致光催化活性显著增强,例如在CO体系中为1.5,在H体系中为7.7,在可见光照射下甚至超过40。发现二氧化钛和金的性质对所得光催化活性都至关重要,但由于当光催化剂制备条件(US-HT)改变时所有结构性质同时改变,因此无法获得一种结构/物理性质与光催化活性之间的直接相关性。因此,通过改进的光沉积方法将尺寸可控的金NPs沉积在形态最佳的OAPs产物上。可见光下光催化活性与金NPs尺寸之间的明显相关性表明,金的性质对可见光活性起决定性作用,而不是二氧化钛的性质。三维有限时域差分(3D-FDTD)模拟证实,金NPs尺寸的增加导致具有场增强的表面积扩大。