催化作用
氧化还原
吸附
热重分析
催化氧化
漫反射红外傅里叶变换
傅里叶变换红外光谱
扫描电子显微镜
材料科学
化学工程
降级(电信)
纳米材料基催化剂
无机化学
比表面积
表征(材料科学)
化学
氧气
热解
红外光谱学
漫反射
分解
选择性催化还原
Crystal(编程语言)
晶体结构
原位
作者
Fukun Bi,Yanxuan Wang,Jingyi He,Haoyu Qu,Hong‐Xin Li,Baolin Liu,Yuxin Wang,Xiaodong Zhang
出处
期刊:Catalysts
[Multidisciplinary Digital Publishing Institute]
日期:2025-12-05
卷期号:15 (12): 1145-1145
被引量:2
标识
DOI:10.3390/catal15121145
摘要
The design of efficient catalysts is vital for the application of catalytic oxidation technology in the removal of gaseous pollutants. Herein, a series of MnOx catalysts with the typical Mn2O3 crystal structure was synthesized via the high-temperature pyrolysis method by using Mn-based metal–organic frameworks (Mn-MOFs) with various morphologies as the precursors. The physicochemical properties of these Mn-MOF-derived MnOx samples were investigated by various characterization techniques, including X-ray diffraction (XRD), thermogravimetry (TG), N2 adsorption–desorption, scanning electron microscope (SEM), and H2 temperature-programmed reduction (H2-TPR), and their catalytic activity was evaluated for catalytic CO degradation. The results showed that the Mn-MOF with leaf-like morphology, derived MnOx-Leaf, presented the optimal catalytic CO oxidation performance (T98 = 214 °C), stability, and reusability. Characterization results showed that the different Mn-MOF-derived MnOx catalysts possessed different physical–chemical properties. The superior catalytic activity of MnOx-Leaf for CO degradation was ascribed to its large surface area and pore size, better low-temperature redox properties, and high H2 consumption, which promoted the adsorption and activation of the CO and gaseous oxygen molecules, improving CO oxidation. Finally, the possible CO degradation pathway was evaluated by in situ diffuse reflectance Fourier transform infrared spectroscopy (DRIFTS), which showed that gaseous CO and O2 were adsorbed on the surface of the catalyst and oxidized to form surface carbon-related species (bicarbonate and carbonate), and finally converted to CO2.
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