Chinnabathini Vana Chinnappa, Dingenen Fons, Borah Rituraj, Abbas Imran, van der Tol Johan, Zarkua Zviadi, D'Acapito Francesco, Nguyen Thi Hong Trang, Lievens Peter, Grandjean Didier, Verbruggen Sammy W, Janssens Ewald
Quantum Solid-State Physics, Department of Physics and Astronomy, KU Leuven, Belgium.
Sustainable Energy, Air & Water Technology (DuEL), University of Antwerp, Belgium.
Nanoscale. 2023 Apr 6;15(14):6696-6708. doi: 10.1039/d2nr07287d.
Cluster beam deposition is employed for fabricating well-defined bimetallic plasmonic photocatalysts to enhance their activity while facilitating a more fundamental understanding of their properties. AuAg clusters with compositions ( = 0, 0.1, 0.3, 0.5, 0.7, 0.9 and 1) spanning the metals' miscibility range were produced in the gas-phase and soft-landed on TiO P25-coated silicon wafers with an optimal coverage of 4 atomic monolayer equivalents. Electron microscopy images show that at this coverage most clusters remain well dispersed whereas EXAFS data are in agreement with the finding that the deposited clusters have an average size of . 5 nm and feature the same composition as the ablated alloy targets. A composition-dependant electron transfer from Au to Ag that is likely to impart chemical stability to the bimetallic clusters and protect Ag atoms against oxidation is additionally evidenced by XPS and XANES. Under simulated solar light, AuAg clusters show a remarkable composition-dependent volcano-type enhancement of their photocatalytic activity towards degradation of stearic acid, a model compound for organic fouling on surfaces. The Formal Quantum Efficiency (FQE) is peaking at the AuAg composition with a value that is twice as high as that of the pristine TiO P25 under solar simulator. Under UV the FQE of all compositions remains similar to that of pristine TiO. A classical electromagnetic simulation study confirms that among all compositions AuAg features the largest near-field enhancement in the wavelength range of maximal solar light intensity, as well as sufficient individual photon energy resulting in a better photocatalytic self-cleaning activity. This allows ascribing the mechanism for photocatalysis mostly to the plasmonic effect of the bimetallic clusters through direct electron injection and near-field enhancement from the resonant cluster towards the conduction band of TiO. These results not only demonstrate the added value of using well-defined bimetallic nanocatalysts to enhance their photocatalytic activity but also highlights the potential of the cluster beam deposition to design tailored noble metal modified photocatalytic surfaces with controlled compositions and sizes without involving potentially hazardous chemical agents.
采用簇束沉积法制备结构明确的双金属等离子体光催化剂,以提高其活性,同时有助于更深入地了解其性质。在气相中制备了组成((x = 0)、(0.1)、(0.3)、(0.5)、(0.7)、(0.9)和(1))跨越两种金属混溶范围的金银簇,并软着陆在涂覆有二氧化钛P25的硅片上,最佳覆盖量为4个原子单层当量。电子显微镜图像显示,在此覆盖量下,大多数簇保持良好分散,而扩展X射线吸收精细结构(EXAFS)数据与以下发现一致:沉积的簇平均尺寸为(2.5)纳米,且与烧蚀合金靶具有相同的组成。X射线光电子能谱(XPS)和X射线吸收近边结构(XANES)还证明了从金到银的成分依赖性电子转移,这可能赋予双金属簇化学稳定性并保护银原子不被氧化。在模拟太阳光下,金银簇对硬脂酸(一种表面有机污垢的模型化合物)的光催化降解活性呈现出显著的成分依赖性火山型增强。在太阳模拟器下,形式量子效率(FQE)在金银组成处达到峰值,其值是原始二氧化钛P25的两倍。在紫外光下,所有组成的FQE与原始二氧化钛的FQE保持相似。一项经典电磁模拟研究证实,在所有组成中,金银在最大太阳光强度的波长范围内具有最大的近场增强,以及足够的单个光子能量,从而产生更好的光催化自清洁活性。这使得光催化机制主要归因于双金属簇的等离子体效应,即通过直接电子注入以及从共振簇到二氧化钛导带的近场增强。这些结果不仅证明了使用结构明确的双金属纳米催化剂提高其光催化活性的附加价值,还突出了簇束沉积在设计具有可控组成和尺寸的定制贵金属修饰光催化表面方面的潜力,而无需使用潜在危险的化学试剂。