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用于高效催化臭氧分解的受限空间锰氧化物纳米片。

Space-confined manganese oxides nanosheets for efficient catalytic decomposition of ozone.

机构信息

Guangdong Key Laboratory of Environmental Pollution and Health, College of Environment and Climate, Jinan University, Guangzhou, 511443, PR China.

College of Environment and Resource, Research Center of Environment and Health, Shanxi University, Taiyuan, Shanxi, 030006, PR China.

出版信息

Chemosphere. 2024 Jun;358:142113. doi: 10.1016/j.chemosphere.2024.142113. Epub 2024 Apr 22.

DOI:10.1016/j.chemosphere.2024.142113
PMID:38657694
Abstract

Ground-level ozone has long posed a substantial menace to human well-being and the ecological milieu. The widely reported manganese-based catalysts for ozone decomposition still facing the persisting issues encompass inefficiency and instability. To surmount these challenges, we developed a mesoporous silica thin films with perpendicular nanochannels (SBA(⊥)) confined MnO catalyst (MnO@SBA(⊥)). Under a weight hourly space velocity (WHSV) of 500,000 mL g h, the MnO@SBA(⊥) catalyst exhibited 100% ozone decomposition efficiency in 5 h and stability across a wide humidity range, which exceed the performance of bulk MnO and MnO confine in commonly reported SBA-15. Rapidly decompose 20 ppm O to a safety level below 100 μg m in the presence of dust in smog chamber (60 × 60 × 60 cm) was also realized. This prominent catalytic performance can be attributed to the unique confined structure engenders the highly exposed active sites, facilitate the reactant-active sites contact and impeded the water accumulation on the active sites. This work offers new insights into the design of confined structure catalysts for air purification.

摘要

地面臭氧长期以来对人类健康和生态环境构成了重大威胁。广泛报道的用于臭氧分解的基于锰的催化剂仍然存在效率低和不稳定性的问题。为了克服这些挑战,我们开发了一种具有垂直纳米通道的介孔硅薄膜(SBA(⊥))限域 MnO 催化剂(MnO@SBA(⊥))。在重量时空速度(WHSV)为 500,000 mL g h 的条件下,MnO@SBA(⊥)催化剂在 5 h 内实现了 100%的臭氧分解效率,并且在很宽的湿度范围内具有稳定性,超过了体相 MnO 和通常报道的 SBA-15 中限域 MnO 的性能。在烟雾室(60×60×60 cm)中存在灰尘的情况下,也能迅速将 20 ppm O 分解为安全水平以下的 100μg m。这种突出的催化性能可归因于独特的限域结构产生了高度暴露的活性位点,促进了反应物-活性位点的接触,并阻碍了活性位点上水的积累。这项工作为空气净化用限域结构催化剂的设计提供了新的见解。

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