Liang Zhang, Yilong Yang, Yao Xiao and Xiazhang Li
{"title":"Construction of perovskite oxide/modified biochar for photothermal synergistic catalytic degradation of VOCs†","authors":"Liang Zhang, Yilong Yang, Yao Xiao and Xiazhang Li","doi":"10.1039/D4NJ05408C","DOIUrl":null,"url":null,"abstract":"<p >Photothermal catalytic degradation of volatile organic compounds (VOCs) has been deemed as a promising strategy for air purification. In this work, LaMnO<small><sub>3</sub></small>/N-doped biochar (NBC) composites with rich oxygen defects and nitrogen-containing functional groups were successfully synthesized by co-pyrolysis of soybean dregs and Mn/La salts, and they were employed for photo-thermal catalytic decomposition of <em>p</em>-xylene. N atoms from soybean dregs were successfully embedded into the biochar framework by the La<small><sup>3+</sup></small> and Mn<small><sup>2+</sup></small> modification. The abundant nitrogen-containing functional groups promoted the adsorption and enrichment of <em>p</em>-xylene on the catalyst surface. The carbon doping from soybean dregs increased oxygen defects of LaMnO<small><sub>3</sub></small>, which acted as the active center for <em>p</em>-xylene degradation. The <em>p</em>-xylene degradation rate reached as high as 99.6% for the LaMnO<small><sub>3</sub></small>/NBC-1.5 composite, which was significantly higher than that of pristine LaMnO<small><sub>3</sub></small> (65.2%). The biochar introduction enhanced the visible light absorption of LaMnO<small><sub>3</sub></small>/NBC composites, which then converted light energy into thermal energy, serving as the extra heat source for <em>p</em>-xylene degradation. Moreover, the photogenerated electron–hole pairs of LaMnO<small><sub>3</sub></small>/NBC composites further generated active radicals such as ˙OH and ˙O<small><sub>2</sub></small><small><sup>−</sup></small> with strong oxidative properties on the catalyst surface, which participated in and enhanced the oxidative degradation of <em>p</em>-xylene.</p>","PeriodicalId":95,"journal":{"name":"New Journal of Chemistry","volume":" 10","pages":" 4099-4107"},"PeriodicalIF":2.7000,"publicationDate":"2025-02-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"New Journal of Chemistry","FirstCategoryId":"92","ListUrlMain":"https://pubs.rsc.org/en/content/articlelanding/2025/nj/d4nj05408c","RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
引用次数: 0
Abstract
Photothermal catalytic degradation of volatile organic compounds (VOCs) has been deemed as a promising strategy for air purification. In this work, LaMnO3/N-doped biochar (NBC) composites with rich oxygen defects and nitrogen-containing functional groups were successfully synthesized by co-pyrolysis of soybean dregs and Mn/La salts, and they were employed for photo-thermal catalytic decomposition of p-xylene. N atoms from soybean dregs were successfully embedded into the biochar framework by the La3+ and Mn2+ modification. The abundant nitrogen-containing functional groups promoted the adsorption and enrichment of p-xylene on the catalyst surface. The carbon doping from soybean dregs increased oxygen defects of LaMnO3, which acted as the active center for p-xylene degradation. The p-xylene degradation rate reached as high as 99.6% for the LaMnO3/NBC-1.5 composite, which was significantly higher than that of pristine LaMnO3 (65.2%). The biochar introduction enhanced the visible light absorption of LaMnO3/NBC composites, which then converted light energy into thermal energy, serving as the extra heat source for p-xylene degradation. Moreover, the photogenerated electron–hole pairs of LaMnO3/NBC composites further generated active radicals such as ˙OH and ˙O2− with strong oxidative properties on the catalyst surface, which participated in and enhanced the oxidative degradation of p-xylene.