Yuting Wang , Mengxiang Wang , Xuya Zhang , Xinru Pan , Yongpeng Cui , Daoqing Liu , Yajun Wang , Wenqing Yao
{"title":"磷和钠掺杂对 g-C3N4 带状结构的协同调控可提高光催化产生过氧化氢的效率","authors":"Yuting Wang , Mengxiang Wang , Xuya Zhang , Xinru Pan , Yongpeng Cui , Daoqing Liu , Yajun Wang , Wenqing Yao","doi":"10.1016/j.jcat.2024.115807","DOIUrl":null,"url":null,"abstract":"<div><div>In addressing the industrial need for a simple, equipment-minimal, and non-toxic method of in-situ hydrogen peroxide (H<sub>2</sub>O<sub>2</sub>) production, this paper presents a cost-effective, environmentally friendly photocatalyst. Our design strategy focuses on the dual-element doping of phosphorus and sodium into graphitic carbon nitride (g-C<sub>3</sub>N<sub>4</sub>), chosen to synergistically enhance photocatalytic performance. This approach yields a notable H<sub>2</sub>O<sub>2</sub> production concentration of 3001.64 μmol·g<sup>−1</sup>·L<sup>-1</sup> within 100 min, using isopropanol as a sacrificial agent, which was 61-fold increase compared to bulk g-C<sub>3</sub>N<sub>4</sub>. Density Functional Theory (DFT) calculations were performed to elucidate the alterations in the band structure of the catalyst induced by dual-element doping, which consequentially engendered an asymmetric intrinsic electric field. Additionally, oxygen’s transition state affinity due to phosphorus doping was also investigated to reveal the mechanisms of synergistic catalysis. This development contributes to meeting industrial demands for pollutant degradation via Fenton processes and presents a sustainable alternative to traditional H<sub>2</sub>O<sub>2</sub> production methods.</div></div>","PeriodicalId":346,"journal":{"name":"Journal of Catalysis","volume":"440 ","pages":"Article 115807"},"PeriodicalIF":6.5000,"publicationDate":"2024-10-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Synergistic regulation of g-C3N4 band structure by phosphorus and sodium doping to enhance photocatalytic hydrogen peroxide production efficiency\",\"authors\":\"Yuting Wang , Mengxiang Wang , Xuya Zhang , Xinru Pan , Yongpeng Cui , Daoqing Liu , Yajun Wang , Wenqing Yao\",\"doi\":\"10.1016/j.jcat.2024.115807\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>In addressing the industrial need for a simple, equipment-minimal, and non-toxic method of in-situ hydrogen peroxide (H<sub>2</sub>O<sub>2</sub>) production, this paper presents a cost-effective, environmentally friendly photocatalyst. Our design strategy focuses on the dual-element doping of phosphorus and sodium into graphitic carbon nitride (g-C<sub>3</sub>N<sub>4</sub>), chosen to synergistically enhance photocatalytic performance. This approach yields a notable H<sub>2</sub>O<sub>2</sub> production concentration of 3001.64 μmol·g<sup>−1</sup>·L<sup>-1</sup> within 100 min, using isopropanol as a sacrificial agent, which was 61-fold increase compared to bulk g-C<sub>3</sub>N<sub>4</sub>. Density Functional Theory (DFT) calculations were performed to elucidate the alterations in the band structure of the catalyst induced by dual-element doping, which consequentially engendered an asymmetric intrinsic electric field. Additionally, oxygen’s transition state affinity due to phosphorus doping was also investigated to reveal the mechanisms of synergistic catalysis. This development contributes to meeting industrial demands for pollutant degradation via Fenton processes and presents a sustainable alternative to traditional H<sub>2</sub>O<sub>2</sub> production methods.</div></div>\",\"PeriodicalId\":346,\"journal\":{\"name\":\"Journal of Catalysis\",\"volume\":\"440 \",\"pages\":\"Article 115807\"},\"PeriodicalIF\":6.5000,\"publicationDate\":\"2024-10-18\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of Catalysis\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S0021951724005207\",\"RegionNum\":1,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"CHEMISTRY, PHYSICAL\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Catalysis","FirstCategoryId":"92","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0021951724005207","RegionNum":1,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, PHYSICAL","Score":null,"Total":0}
Synergistic regulation of g-C3N4 band structure by phosphorus and sodium doping to enhance photocatalytic hydrogen peroxide production efficiency
In addressing the industrial need for a simple, equipment-minimal, and non-toxic method of in-situ hydrogen peroxide (H2O2) production, this paper presents a cost-effective, environmentally friendly photocatalyst. Our design strategy focuses on the dual-element doping of phosphorus and sodium into graphitic carbon nitride (g-C3N4), chosen to synergistically enhance photocatalytic performance. This approach yields a notable H2O2 production concentration of 3001.64 μmol·g−1·L-1 within 100 min, using isopropanol as a sacrificial agent, which was 61-fold increase compared to bulk g-C3N4. Density Functional Theory (DFT) calculations were performed to elucidate the alterations in the band structure of the catalyst induced by dual-element doping, which consequentially engendered an asymmetric intrinsic electric field. Additionally, oxygen’s transition state affinity due to phosphorus doping was also investigated to reveal the mechanisms of synergistic catalysis. This development contributes to meeting industrial demands for pollutant degradation via Fenton processes and presents a sustainable alternative to traditional H2O2 production methods.
期刊介绍:
The Journal of Catalysis publishes scholarly articles on both heterogeneous and homogeneous catalysis, covering a wide range of chemical transformations. These include various types of catalysis, such as those mediated by photons, plasmons, and electrons. The focus of the studies is to understand the relationship between catalytic function and the underlying chemical properties of surfaces and metal complexes.
The articles in the journal offer innovative concepts and explore the synthesis and kinetics of inorganic solids and homogeneous complexes. Furthermore, they discuss spectroscopic techniques for characterizing catalysts, investigate the interaction of probes and reacting species with catalysts, and employ theoretical methods.
The research presented in the journal should have direct relevance to the field of catalytic processes, addressing either fundamental aspects or applications of catalysis.