Wei Zhishun, Kowalska Ewa, Ohtani Bunsho
Catalysis Research Center, Hokkaido University, Sapporo 001-0021, Japan.
Molecules. 2014 Nov 26;19(12):19573-87. doi: 10.3390/molecules191219573.
The influence of changes in structural and physical properties on the photocatalytic activity of octahedral anatase particles (OAPs), exposing eight equivalent {101} facets, caused by calcination (2 h) in air or grinding (1 h) in an agate mortar was studied with samples prepared by ultrasonication (US; 1 h)-hydrothermal reaction (HT; 24 h, 433 K). Calcination in air at temperatures up to 1173 K induced particle shape changes, evaluated by aspect ratio (AR; d001/d101 = depth vertical to anatase {001} and {101} facets estimated by the Scherrer equation with data obtained from X-ray diffraction (XRD) patterns) and content of OAP and semi-OAP particles, without transformation into rutile. AR and OAP content, as well as specific surface area (SSA), were almost unchanged by calcination at temperatures up to 673 K and were then decreased by elevating the calcination temperature, suggesting that calcination at a higher temperature caused dull-edging and particle sintering, the latter also being supported by the analysis of particle size using XRD patterns and scanning electron microscopic (SEM) images. Time-resolved microwave conductivity (TRMC) showed that the maximum signal intensity (Imax), corresponding to a product of charge-carrier density and mobility, and signal-decay rate, presumably corresponding to reactivity of charge carriers, were increased with increase in AR, suggesting higher photocatalytic activity of OAPs than that of dull-edged particles. Grinding also decreased the AR, indicating the formation of dull-edged particles. The original non-treated samples showed activities in the oxidative decomposition of acetic acid (CO2 system) and dehydrogenation of methanol (H2 system) comparable to and lower than those of a commercial anatase titania (Showa Denko Ceramics FP-6), respectively. The activities of calcined and ground samples for the CO2 system and H2 system showed almost linear relations with AR and Imax, respectively, suggesting that those activities may depend on different properties.
研究了通过超声处理(US;1小时)-水热反应(HT;24小时,433K)制备的样品,在空气中煅烧(2小时)或在玛瑙研钵中研磨(1小时)对暴露八个等效{101}面的八面体锐钛矿颗粒(OAPs)光催化活性的影响,这些影响由结构和物理性质的变化引起。在高达1173K的温度下于空气中煅烧会导致颗粒形状发生变化,通过长宽比(AR;d001/d101 = 垂直于锐钛矿{001}和{101}面的深度,由谢乐方程根据从X射线衍射(XRD)图谱获得的数据估算)以及OAP和半OAP颗粒的含量来评估,且不会转化为金红石。在高达673K的温度下煅烧,AR和OAP含量以及比表面积(SSA)几乎不变,然后随着煅烧温度升高而降低,这表明在较高温度下煅烧会导致颗粒边缘变钝和颗粒烧结,通过使用XRD图谱和扫描电子显微镜(SEM)图像进行的粒度分析也支持了后者。时间分辨微波电导率(TRMC)表明,对应于电荷载流子密度和迁移率乘积的确最大信号强度(Imax)以及大概对应于电荷载流子反应性的信号衰减率,会随着AR的增加而增加,这表明OAPs的光催化活性高于边缘变钝的颗粒。研磨也会降低AR,表明形成了边缘变钝的颗粒。原始未处理的样品在乙酸氧化分解(CO2体系)和甲醇脱氢(H2体系)中的活性分别与商用锐钛矿二氧化钛(昭和电工陶瓷FP - 6)相当或低于它。煅烧和研磨样品在CO2体系和H2体系中的活性分别与AR和Imax呈现几乎线性的关系,这表明这些活性可能取决于不同的性质。