煅烧
X射线光电子能谱
催化作用
纳米颗粒
粒径
降水
粒子(生态学)
沉积(地质)
化学
化学工程
材料科学
纳米技术
物理
工程类
有机化学
地质学
古生物学
气象学
海洋学
生物
沉积物
作者
Shuo Zhang,Wenxia Zhao,Ailing Ren,Bin Guo,Ying Dong,Xiaoqing Deng
标识
DOI:10.1016/j.cattod.2019.04.020
摘要
Abstract Driven by excellent CO oxidation capability of gold nanoparticles at room temperature, a TiO2 supported Au nanoparticles (Au/TiO2) is synthesized by deposition-precipitation with urea (DPU). To solve the sintering issue of gold nanoparticles during activation process, atmospheric-pressure cold O2 plasma is employed to activate the Au/TiO2 catalysts and compared with the conventional calcination. The plasma activated one (S-P) shows poorer activity compared to the calcined one (S-C). However, S-P with further TPD treatment (S-PT) shows the best catalytic activity among above-mentioned samples. To elucidate the plasma effect, TEM, XPS, UV–vis spectroscopy and in situ DRIFTS techniques are used for catalyst characterization. Based on TEM results, S-P sample has smaller particle size and narrower size distribution compared to S-C sample, while the high content of low-coordinated Au atoms and the poisoning nitrate species over S-P are revealed by in situ DRIFTS. Upon further TPD treatment, the poisoning species occupying the active sites is desorbed from catalyst surface and the improvements in Au particle size and size distribution are maintained. The mechanism for plasma effect on activation of Au/TiO2 prepared by DPU is also discussed.
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