Yanglin Chen, Mei Zheng, Jiajun Sun, Jianzhong Xu, Chao Wu, Jiyuan Liu, Limo He, Shibo Xi, Shuzhou Li, Can Xue
{"title":"木质纤维素在单原子铁分散的有序/无序聚合物氮化碳均相结上光复生成一氧化碳和乳酸","authors":"Yanglin Chen, Mei Zheng, Jiajun Sun, Jianzhong Xu, Chao Wu, Jiyuan Liu, Limo He, Shibo Xi, Shuzhou Li, Can Xue","doi":"10.1021/acscatal.4c05510","DOIUrl":null,"url":null,"abstract":"Photoreforming lignocellulose into valuable fuels and chemicals represents an environmentally friendly and energy-saving technology. Herein, a single-atom Fe-dispersed order/disorder polymeric carbon nitride homojunction (Fe-SA/PCN-HJ) is constructed for highly efficient photocatalytic reforming of lignocellulose into CO and lactic acid, wherein Fe single atoms are confined to the surface of the PCN-HJ. Experimental investigations and density functional theory (DFT) calculations reveal that the homojunctions and dispersed Fe atoms on the surface greatly improve the separation efficiency and transport of photogenerated charge carriers. As such, driven by the internal electric field across the entire junction, the photoinduced electrons can rapidly migrate from the bulk to the surface, leading to the enrichment of surface electrons at the dispersed Fe–N<sub>4</sub> sites. In addition, the Fe–N<sub>4</sub> sites optimize the adsorption and activation of molecular oxygen and facilitate electron transfer to the adsorbed molecular oxygen, thereby promoting the formation of reactive oxygen species for lignocellulose photoreforming. Under full spectrum irradiation for 2 h, the Fe-SA/PCN-HJ exhibits an ultrahigh CO generation rate of 92.33 mmol g<sup>–1</sup> and yields 136.21 mg of lactic acid by using 900 mg of fructose as the model substrate. Moreover, we have further demonstrated that the Fe-SA/PCN-HJ photocatalyst presents universally applicable capabilities for the photoreforming of various types of lignocellulosic biomass. This work provides an approach for the production of CO and lactic acid through the photoreforming of lignocellulose, which is promising for the production of fuels and valuable chemicals.","PeriodicalId":9,"journal":{"name":"ACS Catalysis ","volume":null,"pages":null},"PeriodicalIF":11.3000,"publicationDate":"2024-11-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Photoreforming of Lignocellulose into CO and Lactic Acid over a Single-Atom Fe-Dispersed Order/Disorder Polymeric Carbon Nitride Homojunction\",\"authors\":\"Yanglin Chen, Mei Zheng, Jiajun Sun, Jianzhong Xu, Chao Wu, Jiyuan Liu, Limo He, Shibo Xi, Shuzhou Li, Can Xue\",\"doi\":\"10.1021/acscatal.4c05510\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Photoreforming lignocellulose into valuable fuels and chemicals represents an environmentally friendly and energy-saving technology. Herein, a single-atom Fe-dispersed order/disorder polymeric carbon nitride homojunction (Fe-SA/PCN-HJ) is constructed for highly efficient photocatalytic reforming of lignocellulose into CO and lactic acid, wherein Fe single atoms are confined to the surface of the PCN-HJ. Experimental investigations and density functional theory (DFT) calculations reveal that the homojunctions and dispersed Fe atoms on the surface greatly improve the separation efficiency and transport of photogenerated charge carriers. As such, driven by the internal electric field across the entire junction, the photoinduced electrons can rapidly migrate from the bulk to the surface, leading to the enrichment of surface electrons at the dispersed Fe–N<sub>4</sub> sites. In addition, the Fe–N<sub>4</sub> sites optimize the adsorption and activation of molecular oxygen and facilitate electron transfer to the adsorbed molecular oxygen, thereby promoting the formation of reactive oxygen species for lignocellulose photoreforming. Under full spectrum irradiation for 2 h, the Fe-SA/PCN-HJ exhibits an ultrahigh CO generation rate of 92.33 mmol g<sup>–1</sup> and yields 136.21 mg of lactic acid by using 900 mg of fructose as the model substrate. Moreover, we have further demonstrated that the Fe-SA/PCN-HJ photocatalyst presents universally applicable capabilities for the photoreforming of various types of lignocellulosic biomass. This work provides an approach for the production of CO and lactic acid through the photoreforming of lignocellulose, which is promising for the production of fuels and valuable chemicals.\",\"PeriodicalId\":9,\"journal\":{\"name\":\"ACS Catalysis \",\"volume\":null,\"pages\":null},\"PeriodicalIF\":11.3000,\"publicationDate\":\"2024-11-11\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"ACS Catalysis \",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://doi.org/10.1021/acscatal.4c05510\",\"RegionNum\":1,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"CHEMISTRY, PHYSICAL\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"ACS Catalysis ","FirstCategoryId":"92","ListUrlMain":"https://doi.org/10.1021/acscatal.4c05510","RegionNum":1,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, PHYSICAL","Score":null,"Total":0}
Photoreforming of Lignocellulose into CO and Lactic Acid over a Single-Atom Fe-Dispersed Order/Disorder Polymeric Carbon Nitride Homojunction
Photoreforming lignocellulose into valuable fuels and chemicals represents an environmentally friendly and energy-saving technology. Herein, a single-atom Fe-dispersed order/disorder polymeric carbon nitride homojunction (Fe-SA/PCN-HJ) is constructed for highly efficient photocatalytic reforming of lignocellulose into CO and lactic acid, wherein Fe single atoms are confined to the surface of the PCN-HJ. Experimental investigations and density functional theory (DFT) calculations reveal that the homojunctions and dispersed Fe atoms on the surface greatly improve the separation efficiency and transport of photogenerated charge carriers. As such, driven by the internal electric field across the entire junction, the photoinduced electrons can rapidly migrate from the bulk to the surface, leading to the enrichment of surface electrons at the dispersed Fe–N4 sites. In addition, the Fe–N4 sites optimize the adsorption and activation of molecular oxygen and facilitate electron transfer to the adsorbed molecular oxygen, thereby promoting the formation of reactive oxygen species for lignocellulose photoreforming. Under full spectrum irradiation for 2 h, the Fe-SA/PCN-HJ exhibits an ultrahigh CO generation rate of 92.33 mmol g–1 and yields 136.21 mg of lactic acid by using 900 mg of fructose as the model substrate. Moreover, we have further demonstrated that the Fe-SA/PCN-HJ photocatalyst presents universally applicable capabilities for the photoreforming of various types of lignocellulosic biomass. This work provides an approach for the production of CO and lactic acid through the photoreforming of lignocellulose, which is promising for the production of fuels and valuable chemicals.
期刊介绍:
ACS Catalysis is an esteemed journal that publishes original research in the fields of heterogeneous catalysis, molecular catalysis, and biocatalysis. It offers broad coverage across diverse areas such as life sciences, organometallics and synthesis, photochemistry and electrochemistry, drug discovery and synthesis, materials science, environmental protection, polymer discovery and synthesis, and energy and fuels.
The scope of the journal is to showcase innovative work in various aspects of catalysis. This includes new reactions and novel synthetic approaches utilizing known catalysts, the discovery or modification of new catalysts, elucidation of catalytic mechanisms through cutting-edge investigations, practical enhancements of existing processes, as well as conceptual advances in the field. Contributions to ACS Catalysis can encompass both experimental and theoretical research focused on catalytic molecules, macromolecules, and materials that exhibit catalytic turnover.