{"title":"Construction of Mn2O3/SmMn2O5 interface with tuned Mn coordination environment for efficient air pollutant elimination","authors":"Ruichang Xu, Qi Guo, Yun Long, Zijian Zhou, Minghou Xu","doi":"10.1016/j.jece.2025.119254","DOIUrl":null,"url":null,"abstract":"<div><div>Gaseous pollutants can be efficiently removed by the mullite-type oxides. However, the enhancement effect is greatly limited due to the introduction of disordered defects and univariate regulation of conventional modification methods. Here, through interface engineering, we have successfully constructed the interface between Mn<sub>2</sub>O<sub>3</sub> and SmMn<sub>2</sub>O<sub>5</sub>. The interface is formed during the in-situ calcination process. Various pollutants can be efficiently removed on Mn<sub>2</sub>O<sub>3</sub>/SmMn<sub>2</sub>O<sub>5</sub> due to the interfacial effect. It has been demonstrated that the Mn-O bonds on the interface are stretched and easier to break due to the interfacial effect, thereby improving the redox ability and generating active oxygen species. The interfacial effect is effective in tuning the Mn coordination environment, which is the intrinsic reason for the efficient various pollutant removal ability of Mn<sub>2</sub>O<sub>3</sub>/SmMn<sub>2</sub>O<sub>5</sub>. Specifically, Mn<sub>2</sub>O<sub>3</sub>/SmMn<sub>2</sub>O<sub>5</sub> shows one of the most promising Hg<sup>0</sup> catalytic performances compared with reported catalysts, with a 75 % and 100 % Hg<sup>0</sup> conversion rate under a space velocity of 1000000 h<sup>−1</sup> and 500000 h<sup>−1</sup>, respectively. Mn<sub>2</sub>O<sub>3</sub>/SMO also exhibits a stable Hg<sup>0</sup> conversion rate (100 %) at 100℃ for 50 h under a GHSV of 100000 h<sup>−1</sup>. This work provides guidance for the rational design of efficient catalysts for various pollutant catalytic oxidations and other environmental applications.</div></div>","PeriodicalId":15759,"journal":{"name":"Journal of Environmental Chemical Engineering","volume":"13 6","pages":"Article 119254"},"PeriodicalIF":7.2000,"publicationDate":"2025-09-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Environmental Chemical Engineering","FirstCategoryId":"5","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2213343725039508","RegionNum":2,"RegionCategory":"工程技术","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"ENGINEERING, CHEMICAL","Score":null,"Total":0}
引用次数: 0
Abstract
Gaseous pollutants can be efficiently removed by the mullite-type oxides. However, the enhancement effect is greatly limited due to the introduction of disordered defects and univariate regulation of conventional modification methods. Here, through interface engineering, we have successfully constructed the interface between Mn2O3 and SmMn2O5. The interface is formed during the in-situ calcination process. Various pollutants can be efficiently removed on Mn2O3/SmMn2O5 due to the interfacial effect. It has been demonstrated that the Mn-O bonds on the interface are stretched and easier to break due to the interfacial effect, thereby improving the redox ability and generating active oxygen species. The interfacial effect is effective in tuning the Mn coordination environment, which is the intrinsic reason for the efficient various pollutant removal ability of Mn2O3/SmMn2O5. Specifically, Mn2O3/SmMn2O5 shows one of the most promising Hg0 catalytic performances compared with reported catalysts, with a 75 % and 100 % Hg0 conversion rate under a space velocity of 1000000 h−1 and 500000 h−1, respectively. Mn2O3/SMO also exhibits a stable Hg0 conversion rate (100 %) at 100℃ for 50 h under a GHSV of 100000 h−1. This work provides guidance for the rational design of efficient catalysts for various pollutant catalytic oxidations and other environmental applications.
期刊介绍:
The Journal of Environmental Chemical Engineering (JECE) serves as a platform for the dissemination of original and innovative research focusing on the advancement of environmentally-friendly, sustainable technologies. JECE emphasizes the transition towards a carbon-neutral circular economy and a self-sufficient bio-based economy. Topics covered include soil, water, wastewater, and air decontamination; pollution monitoring, prevention, and control; advanced analytics, sensors, impact and risk assessment methodologies in environmental chemical engineering; resource recovery (water, nutrients, materials, energy); industrial ecology; valorization of waste streams; waste management (including e-waste); climate-water-energy-food nexus; novel materials for environmental, chemical, and energy applications; sustainability and environmental safety; water digitalization, water data science, and machine learning; process integration and intensification; recent developments in green chemistry for synthesis, catalysis, and energy; and original research on contaminants of emerging concern, persistent chemicals, and priority substances, including microplastics, nanoplastics, nanomaterials, micropollutants, antimicrobial resistance genes, and emerging pathogens (viruses, bacteria, parasites) of environmental significance.