Huating Huang, Weiqing Li, Xixi Chen*, Zhiming Yang, Minggang Chen, Anhong Zhang, Chun He and Shuanghong Tian*,
{"title":"通过碳插层削弱Mn-O-Si相互作用增强环境基质中难降解污染物的催化臭氧化","authors":"Huating Huang, Weiqing Li, Xixi Chen*, Zhiming Yang, Minggang Chen, Anhong Zhang, Chun He and Shuanghong Tian*, ","doi":"10.1021/acsami.4c2106810.1021/acsami.4c21068","DOIUrl":null,"url":null,"abstract":"<p >The strong metal–support interaction (MSI) has been widely attributed to enhanced catalytic activity. However, this attribution might be wrong in catalytic ozonation, since MSI that is too strong might impede the activation of electron-poor ozone molecules. Herein, we reported a strategy to subtly modulate the Mn–O–Si interaction by intercalating the carbon film between the silica support and active manganese oxide. When using MnO<sub><i>x</i></sub>/0.5C/SiO<sub>2</sub> with the moderate MSI as a catalyst in the catalytic ozonation of refractory paracetamol (PCM), 91.1 ± 2.4% of PCM was removed within 30 min, about 30% higher than that using the catalyst of MnO<sub><i>x</i></sub>/SiO<sub>2</sub> with a strong MSI. Moreover, the reaction rate reached 8.01 × 10<sup>–2</sup> min<sup>–1</sup>, 2.2 and 1.3 times that with MnO<sub><i>x</i></sub>/SiO<sub>2</sub> and MnO<sub><i>x</i></sub>/1C/SiO<sub>2</sub>, respectively. Importantly, further integration of MnO<sub><i>x</i></sub>/0.5C/SiO<sub>2</sub> into membrane filtration achieved high rejections of PCM (>94.3%) under various realistic water scenarios during a continuous 12 h operation, demonstrating strong resistance to environmental matrices interference. Experimental and theoretical evidence revealed that the moderate MSI resulted in the high dispersion of active MnO<sub><i>x</i></sub> nanoclusters in the size of 2.3–4.4 nm and promoted the adsorption of ozone over MnO<sub><i>x</i></sub> and its dissociation into surface *O, <sup>•</sup>OH, <sup>•</sup>O<sub>2</sub><sup>–</sup>, and <sup>1</sup>O<sub>2</sub> for decontamination. As a constructive work, this study revealed the significance of MSI in catalytic ozonation and offered a simple regulation method for constructing active interfaces of metal-supported catalysts.</p>","PeriodicalId":5,"journal":{"name":"ACS Applied Materials & Interfaces","volume":"17 8","pages":"12177–12188 12177–12188"},"PeriodicalIF":8.2000,"publicationDate":"2025-02-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://pubs.acs.org/doi/epdf/10.1021/acsami.4c21068","citationCount":"0","resultStr":"{\"title\":\"Weakening the Mn–O–Si Interaction via Carbon Intercalation for the Enhanced Catalytic Ozonation of Refractory Pollutants in Environmental Matrices\",\"authors\":\"Huating Huang, Weiqing Li, Xixi Chen*, Zhiming Yang, Minggang Chen, Anhong Zhang, Chun He and Shuanghong Tian*, \",\"doi\":\"10.1021/acsami.4c2106810.1021/acsami.4c21068\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p >The strong metal–support interaction (MSI) has been widely attributed to enhanced catalytic activity. However, this attribution might be wrong in catalytic ozonation, since MSI that is too strong might impede the activation of electron-poor ozone molecules. Herein, we reported a strategy to subtly modulate the Mn–O–Si interaction by intercalating the carbon film between the silica support and active manganese oxide. When using MnO<sub><i>x</i></sub>/0.5C/SiO<sub>2</sub> with the moderate MSI as a catalyst in the catalytic ozonation of refractory paracetamol (PCM), 91.1 ± 2.4% of PCM was removed within 30 min, about 30% higher than that using the catalyst of MnO<sub><i>x</i></sub>/SiO<sub>2</sub> with a strong MSI. Moreover, the reaction rate reached 8.01 × 10<sup>–2</sup> min<sup>–1</sup>, 2.2 and 1.3 times that with MnO<sub><i>x</i></sub>/SiO<sub>2</sub> and MnO<sub><i>x</i></sub>/1C/SiO<sub>2</sub>, respectively. Importantly, further integration of MnO<sub><i>x</i></sub>/0.5C/SiO<sub>2</sub> into membrane filtration achieved high rejections of PCM (>94.3%) under various realistic water scenarios during a continuous 12 h operation, demonstrating strong resistance to environmental matrices interference. Experimental and theoretical evidence revealed that the moderate MSI resulted in the high dispersion of active MnO<sub><i>x</i></sub> nanoclusters in the size of 2.3–4.4 nm and promoted the adsorption of ozone over MnO<sub><i>x</i></sub> and its dissociation into surface *O, <sup>•</sup>OH, <sup>•</sup>O<sub>2</sub><sup>–</sup>, and <sup>1</sup>O<sub>2</sub> for decontamination. 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Weakening the Mn–O–Si Interaction via Carbon Intercalation for the Enhanced Catalytic Ozonation of Refractory Pollutants in Environmental Matrices
The strong metal–support interaction (MSI) has been widely attributed to enhanced catalytic activity. However, this attribution might be wrong in catalytic ozonation, since MSI that is too strong might impede the activation of electron-poor ozone molecules. Herein, we reported a strategy to subtly modulate the Mn–O–Si interaction by intercalating the carbon film between the silica support and active manganese oxide. When using MnOx/0.5C/SiO2 with the moderate MSI as a catalyst in the catalytic ozonation of refractory paracetamol (PCM), 91.1 ± 2.4% of PCM was removed within 30 min, about 30% higher than that using the catalyst of MnOx/SiO2 with a strong MSI. Moreover, the reaction rate reached 8.01 × 10–2 min–1, 2.2 and 1.3 times that with MnOx/SiO2 and MnOx/1C/SiO2, respectively. Importantly, further integration of MnOx/0.5C/SiO2 into membrane filtration achieved high rejections of PCM (>94.3%) under various realistic water scenarios during a continuous 12 h operation, demonstrating strong resistance to environmental matrices interference. Experimental and theoretical evidence revealed that the moderate MSI resulted in the high dispersion of active MnOx nanoclusters in the size of 2.3–4.4 nm and promoted the adsorption of ozone over MnOx and its dissociation into surface *O, •OH, •O2–, and 1O2 for decontamination. As a constructive work, this study revealed the significance of MSI in catalytic ozonation and offered a simple regulation method for constructing active interfaces of metal-supported catalysts.
期刊介绍:
ACS Applied Materials & Interfaces is a leading interdisciplinary journal that brings together chemists, engineers, physicists, and biologists to explore the development and utilization of newly-discovered materials and interfacial processes for specific applications. Our journal has experienced remarkable growth since its establishment in 2009, both in terms of the number of articles published and the impact of the research showcased. We are proud to foster a truly global community, with the majority of published articles originating from outside the United States, reflecting the rapid growth of applied research worldwide.