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Ag-TiO 纳米异质结构中的纯可见光诱导光致变色。

Purely Visible-Light-Induced Photochromism in Ag-TiO Nanoheterostructures.

机构信息

Department of Materials and Ceramic Engineering/CICECO-Aveiro Institute of Materials and ‡Center for Mechanical Technology and Automation-TEMA, Department of Mechanical Engineering, University of Aveiro , Campus Universitário de Santiago, 3810-193 Aveiro, Portugal.

出版信息

Langmuir. 2017 May 23;33(20):4890-4902. doi: 10.1021/acs.langmuir.6b04474. Epub 2017 May 10.

Abstract

We report titania nanoheterostructures decorated with silver, exhibiting tuneable photochromic properties for the first time when stimulated only by visible white light (domestic indoor lamp), with no UV wavelengths. Photochromic materials show reversible color changes under light exposure. However, all inorganic photochromic nanoparticles (NPs) require UV light to operate. Conventionally, multicolor photochromism in Ag-TiO films involves a change in color to brownish-gray during UV-light irradiation (i.e., reduction of Ag to Ag) and a (re)bleaching (i.e., (re)oxidation of Ag to colorless Ag) upon visible-light exposure. In this work, on the contrary, we demonstrate visible-light-induced photochromism (ranging from yellow to violet) of 1-10 mol % Ag-modified titania NPs using both spectroscopic and colorimetric CIELab* analyses. This is not a bleaching of the UV-induced color but a change in color itself under exposure to visible light, and it is shown to be a completely different mechanism-driven by the interfacial charge transfer of an electron from the valence band of TiO to that of the AgO clusters that surround the titania-to the usual UV-triggered photochromism reported in titania-based materials. The quantity of Ag or irradiation time dictated the magnitude and degree of tuneability of the color change, from pale yellow to dark blue, with a rapid change visible only after a few seconds, and the intensity and red shift of surface plasmon resonance induced under visible light also increased. This effect was reversible after annealing in the dark at 100 °C/15 min. Photocatalytic activity under visible light was also assessed against the abatement of nitrogen oxide pollutants, for interior use, therefore showing the coexistence of photochromism and photocatalysis-both triggered by the same wavelength-in the same material, making it a multifunctional material. Moreover, we also demonstrate and explain why X-ray photoelectron spectroscopy is an unreliable technique with such materials.

摘要

我们首次报道了负载银的二氧化钛纳米杂化结构,在仅受可见白光(室内照明用)刺激时表现出可调谐的光致变色性能,而无需使用紫外光。光致变色材料在光照下显示出可逆的颜色变化。然而,所有无机光致变色纳米粒子(NPs)都需要紫外光才能工作。传统上,Ag-TiO 薄膜的多色光致变色涉及在紫外光照射下颜色变为棕灰色(即 Ag 被还原为 Ag),以及在可见光照射下(即 Ag 被氧化为无色 Ag)的漂白(即再氧化)。在这项工作中,相反,我们使用光谱和比色 CIELab*分析证明了 1-10 mol% Ag 修饰的二氧化钛 NPs 的可见光诱导光致变色(从黄色到紫色)。这不是紫外光诱导颜色的漂白,而是暴露于可见光时光致变色本身的颜色变化,并且它被证明是一种完全不同的机制,由 TiO 价带中的电子向围绕 TiO 的 AgO 簇的界面电荷转移驱动,而不是通常在基于 TiO 的材料中报道的紫外光触发的光致变色。Ag 的数量或辐照时间决定了颜色变化的幅度和可调谐性程度,从浅黄色到深蓝色,仅在几秒钟后就可以看到快速变化,并且在可见光下诱导的表面等离子体共振的强度和红移也增加了。这种效应在 100°C/15 分钟的黑暗退火后是可逆的。还评估了可见光下的光催化活性,以去除室内用氮氧化物污染物,因此表明光致变色和光催化在同一材料中共存,两者都由相同波长触发,使其成为一种多功能材料。此外,我们还解释了为什么 X 射线光电子能谱是一种不可靠的技术。

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