丝光沸石
沸石
阳离子聚合
金属
催化氧化
无机化学
傅里叶变换红外光谱
化学工程
化学
催化作用
有机化学
工程类
作者
T.A. Zepeda,Alfredo Solís-García,O.E. Jaime Acuña,Juan C. Fierro‐Gonzalez,Andrey Simakov,Vitalii Petranovskii,O. Raymond
标识
DOI:10.1016/j.apcatb.2023.122855
摘要
The presence of cationic gold species is a key factor for the CO oxidation over the supported gold catalysts based on non-reducible metal oxides. The deactivation of such catalysts is mainly associated with the Au nanoparticles (AuNPs) sintering and the concomitant reduction of cationic Au species. Here we report the high catalytic stability at the CO oxidation of the cationic Au species confined into a mordenite-like zeolite matrix prepared by a one-pot synthesis method. The sample with lowest Au loading (0.32 % wt.) exhibited the higher catalytic performance and stability during CO oxidation. Detailed FTIR analysis showed that the CO oxidation on sample with low Au content (0.32 wt%) occurred preferentially via CO interaction with the cationic interface Au-hydroxyl (Au1+–OH−) species to produce CO2(g) via decarboxylation. In contrast, the sample with a high Au content (1.56 wt%) displayed lower CO oxidation ability, which was associated with a low content and less stability of cationic gold species. Proposed synthesis method permits to obtain in a one-pot way stable cationic gold species highly effectively for the CO oxidation.
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