{"title":"Pt-Mn2O3/CN 纳米复合催化剂对甲苯的光热催化氧化作用","authors":"Xiao Yu, Chuang Zhao, Lixia Yang, Jian Zhang and Chunlin Chen","doi":"10.1039/D3EY00298E","DOIUrl":null,"url":null,"abstract":"<p >The Pt–Mn<small><sub>2</sub></small>O<small><sub>3</sub></small>/CN catalyst formed through synthesis <em>via</em> a solvent-thermal method involves a synergistic combination of polymer CN and Pt nanoparticles loaded on Mn<small><sub>2</sub></small>O<small><sub>3</sub></small> to catalyze the degradation of toluene. The composition incorporates Mn<small><sub>2</sub></small>O<small><sub>3</sub></small> as the central element for photothermal conversion, CN as a uniformly dispersed matrix for Pt nanoparticles, and Pt as the catalytically active center, demonstrating significant efficacy. Particularly noteworthy is the discernible enhancement in the photothermal catalytic degradation capability of the Pt–Mn<small><sub>2</sub></small>O<small><sub>3</sub></small>/CN composite catalyst, specifically in the context of toluene. When subjected to light intensity of 300 mW cm<small><sup>−2</sup></small> and a toluene concentration of 400 ppm, Pt–Mn<small><sub>2</sub></small>O<small><sub>3</sub></small>/CN achieves toluene conversion and CO<small><sub>2</sub></small> mineralization rates of 99% and 80.9%, respectively. This improvement primarily stems from the Pt nanoparticles inducing a substantial presence of oxygen vacancies within the catalyst structure, thereby increasing the oxygen adsorption capacity and surface mobility. This, in turn, activates adsorbed oxygen species at the catalyst's interface. The adept utilization and conversion of solar irradiance for volatile organic compound (VOC) abatement underscore its potential as an environmentally friendly and renewable energy source.</p>","PeriodicalId":72877,"journal":{"name":"EES catalysis","volume":null,"pages":null},"PeriodicalIF":0.0000,"publicationDate":"2024-01-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://pubs.rsc.org/en/content/articlepdf/2024/ey/d3ey00298e?page=search","citationCount":"0","resultStr":"{\"title\":\"Photothermal catalytic oxidation of toluene over the Pt–Mn2O3/CN nanocomposite catalyst†\",\"authors\":\"Xiao Yu, Chuang Zhao, Lixia Yang, Jian Zhang and Chunlin Chen\",\"doi\":\"10.1039/D3EY00298E\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p >The Pt–Mn<small><sub>2</sub></small>O<small><sub>3</sub></small>/CN catalyst formed through synthesis <em>via</em> a solvent-thermal method involves a synergistic combination of polymer CN and Pt nanoparticles loaded on Mn<small><sub>2</sub></small>O<small><sub>3</sub></small> to catalyze the degradation of toluene. The composition incorporates Mn<small><sub>2</sub></small>O<small><sub>3</sub></small> as the central element for photothermal conversion, CN as a uniformly dispersed matrix for Pt nanoparticles, and Pt as the catalytically active center, demonstrating significant efficacy. Particularly noteworthy is the discernible enhancement in the photothermal catalytic degradation capability of the Pt–Mn<small><sub>2</sub></small>O<small><sub>3</sub></small>/CN composite catalyst, specifically in the context of toluene. When subjected to light intensity of 300 mW cm<small><sup>−2</sup></small> and a toluene concentration of 400 ppm, Pt–Mn<small><sub>2</sub></small>O<small><sub>3</sub></small>/CN achieves toluene conversion and CO<small><sub>2</sub></small> mineralization rates of 99% and 80.9%, respectively. This improvement primarily stems from the Pt nanoparticles inducing a substantial presence of oxygen vacancies within the catalyst structure, thereby increasing the oxygen adsorption capacity and surface mobility. This, in turn, activates adsorbed oxygen species at the catalyst's interface. The adept utilization and conversion of solar irradiance for volatile organic compound (VOC) abatement underscore its potential as an environmentally friendly and renewable energy source.</p>\",\"PeriodicalId\":72877,\"journal\":{\"name\":\"EES catalysis\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2024-01-20\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://pubs.rsc.org/en/content/articlepdf/2024/ey/d3ey00298e?page=search\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"EES catalysis\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://pubs.rsc.org/en/content/articlelanding/2024/ey/d3ey00298e\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"EES catalysis","FirstCategoryId":"1085","ListUrlMain":"https://pubs.rsc.org/en/content/articlelanding/2024/ey/d3ey00298e","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Photothermal catalytic oxidation of toluene over the Pt–Mn2O3/CN nanocomposite catalyst†
The Pt–Mn2O3/CN catalyst formed through synthesis via a solvent-thermal method involves a synergistic combination of polymer CN and Pt nanoparticles loaded on Mn2O3 to catalyze the degradation of toluene. The composition incorporates Mn2O3 as the central element for photothermal conversion, CN as a uniformly dispersed matrix for Pt nanoparticles, and Pt as the catalytically active center, demonstrating significant efficacy. Particularly noteworthy is the discernible enhancement in the photothermal catalytic degradation capability of the Pt–Mn2O3/CN composite catalyst, specifically in the context of toluene. When subjected to light intensity of 300 mW cm−2 and a toluene concentration of 400 ppm, Pt–Mn2O3/CN achieves toluene conversion and CO2 mineralization rates of 99% and 80.9%, respectively. This improvement primarily stems from the Pt nanoparticles inducing a substantial presence of oxygen vacancies within the catalyst structure, thereby increasing the oxygen adsorption capacity and surface mobility. This, in turn, activates adsorbed oxygen species at the catalyst's interface. The adept utilization and conversion of solar irradiance for volatile organic compound (VOC) abatement underscore its potential as an environmentally friendly and renewable energy source.