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在光致变色反应的辅助下,通过尺寸控制在氧化铝上沉积 Ag 纳米粒子,并研究其催化性能。

Size-controlled deposition of Ag nanoparticles on alumina with the assistance of a photo-induced chromic reaction, and study of their catalytic properties.

机构信息

Division of Materials and Manufacturing Science, Graduate School of Engineering, Osaka University, 2-1 Yamada-oka, Suita, Osaka 565-0871.

出版信息

Phys Chem Chem Phys. 2011 Sep 21;13(35):15821-4. doi: 10.1039/c1cp21508f. Epub 2011 Aug 8.

Abstract

This paper describes a promising method to synthesize supported metal catalysts based on a photochromic reaction. Highly dispersed Ag nanoparticles (NPs) with a mean diameter of ca. 10 nm stabilized by 3-mercaptopropionic acid (3-MPA) were prepared as a colloidal precursor solution. The zeta electric potential was found to be negatively charged in the region of pH higher than 5 due to the presence of dissociated carboxylate ions (-COO(-)), which led to electric repulsion between Ag NPs and kept the solution in a highly dispersed colloidal state. In the presence of photochromic molecules, trans-2-hydroxychalcone, the photo-irradiation gradually decreased the electric charge on the nanoparticles owing to the formation of flavylium cations, which induced the assembly of Ag NPs. Such photo-induced assembly-dispersion control of Ag NPs enables size selective deposition on a catalyst support, which is controlled by varying the photo-irradiation time.

摘要

本文描述了一种基于光致变色反应合成负载型金属催化剂的有前途的方法。以 3-巯基丙酸(3-MPA)稳定的平均直径约为 10nm 的高度分散的 Ag 纳米颗粒(NPs)被制备为胶体前体溶液。由于存在离解的羧酸根离子(-COO(-)),在 pH 值高于 5 的区域中,zeta 电动电势呈现负电性,这导致 Ag NPs 之间的电排斥,使溶液保持在高度分散的胶体状态。在光致变色分子,反式-2-羟基查耳酮存在下,光照射逐渐由于形成黄烷酮阳离子而降低纳米颗粒上的电荷,这诱导了 Ag NPs 的组装。这种 Ag NPs 的光诱导组装-分散控制能够实现对催化剂载体的尺寸选择性沉积,这可以通过改变光照射时间来控制。

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