Junkai Li, Guanhua Wang*, Xiaoyi Wang, Yutong Zhao, Yuze Zhao, Wenjie Sui, Dingsheng Wang and Chuanling Si*,
{"title":"在温和条件下,在木质素裁剪钴单原子催化剂上通过提高钴负载量定向转化 HMF 为 FDCA","authors":"Junkai Li, Guanhua Wang*, Xiaoyi Wang, Yutong Zhao, Yuze Zhao, Wenjie Sui, Dingsheng Wang and Chuanling Si*, ","doi":"10.1021/acscatal.4c0441910.1021/acscatal.4c04419","DOIUrl":null,"url":null,"abstract":"<p >Heterogeneous catalysis over single-atom catalysts (SACs) has garnered significant attention in biomass-derived platform chemical conversion owing to the high atomic utilization and reliable selectivity/stability. Herein, Co single-atom catalysts (Co–N/F1) derived from fractionated lignin were employed for the oriented oxidation of 5-hydroxymethylfurfural (HMF), a typical platform chemical derived from glucose, into 2,5-furandicarboxylicacid (FDCA) under mild conditions. The Co–N/F1 with enhanced Co content was obtained using the low-molecular-weight lignin fraction (F1) with high functional group contents (e.g., Ph–OH and COOH), and the as-prepared catalyst was demonstrated to present a Co–N<sub>4</sub> configuration. Owing to the absence of colored byproduct formation from HMF at elevated temperatures, Co–N/F1 realized the highly selective conversion of HMF to FDCA (100% HMF conversion, 99.20% FDCA yield) under mild conditions (65 °C, 3 bar O<sub>2</sub>), which outperformed most reported non-noble metal-supported catalysts. Density functional theory calculations indicate that the Co–N<sub>4</sub> site in Co–N/F1 facilitates the dehydrogenation of the α-C position on HMF and its aldehyde intermediates, resulting in a significantly enhanced catalytic efficiency. Furthermore, Co–N/F1 exhibited stable reusability due to the alkaline resistance of the Co–N<sub>4</sub> structure. Our study details the insights into the synthesis of Co-SACs using a lignin fractionation strategy and further demonstrates its good feasibility for the oriented conversion of biomass-derived platform chemicals under mild conditions.</p>","PeriodicalId":9,"journal":{"name":"ACS Catalysis ","volume":"14 21","pages":"16003–16013 16003–16013"},"PeriodicalIF":11.3000,"publicationDate":"2024-10-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Oriented Conversion of HMF to FDCA under Mild Conditions over Lignin-Tailored Co Single-Atom Catalyst with Enhanced Co Loadings\",\"authors\":\"Junkai Li, Guanhua Wang*, Xiaoyi Wang, Yutong Zhao, Yuze Zhao, Wenjie Sui, Dingsheng Wang and Chuanling Si*, \",\"doi\":\"10.1021/acscatal.4c0441910.1021/acscatal.4c04419\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p >Heterogeneous catalysis over single-atom catalysts (SACs) has garnered significant attention in biomass-derived platform chemical conversion owing to the high atomic utilization and reliable selectivity/stability. Herein, Co single-atom catalysts (Co–N/F1) derived from fractionated lignin were employed for the oriented oxidation of 5-hydroxymethylfurfural (HMF), a typical platform chemical derived from glucose, into 2,5-furandicarboxylicacid (FDCA) under mild conditions. The Co–N/F1 with enhanced Co content was obtained using the low-molecular-weight lignin fraction (F1) with high functional group contents (e.g., Ph–OH and COOH), and the as-prepared catalyst was demonstrated to present a Co–N<sub>4</sub> configuration. Owing to the absence of colored byproduct formation from HMF at elevated temperatures, Co–N/F1 realized the highly selective conversion of HMF to FDCA (100% HMF conversion, 99.20% FDCA yield) under mild conditions (65 °C, 3 bar O<sub>2</sub>), which outperformed most reported non-noble metal-supported catalysts. Density functional theory calculations indicate that the Co–N<sub>4</sub> site in Co–N/F1 facilitates the dehydrogenation of the α-C position on HMF and its aldehyde intermediates, resulting in a significantly enhanced catalytic efficiency. Furthermore, Co–N/F1 exhibited stable reusability due to the alkaline resistance of the Co–N<sub>4</sub> structure. Our study details the insights into the synthesis of Co-SACs using a lignin fractionation strategy and further demonstrates its good feasibility for the oriented conversion of biomass-derived platform chemicals under mild conditions.</p>\",\"PeriodicalId\":9,\"journal\":{\"name\":\"ACS Catalysis \",\"volume\":\"14 21\",\"pages\":\"16003–16013 16003–16013\"},\"PeriodicalIF\":11.3000,\"publicationDate\":\"2024-10-16\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"ACS Catalysis \",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://pubs.acs.org/doi/10.1021/acscatal.4c04419\",\"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://pubs.acs.org/doi/10.1021/acscatal.4c04419","RegionNum":1,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, PHYSICAL","Score":null,"Total":0}
Oriented Conversion of HMF to FDCA under Mild Conditions over Lignin-Tailored Co Single-Atom Catalyst with Enhanced Co Loadings
Heterogeneous catalysis over single-atom catalysts (SACs) has garnered significant attention in biomass-derived platform chemical conversion owing to the high atomic utilization and reliable selectivity/stability. Herein, Co single-atom catalysts (Co–N/F1) derived from fractionated lignin were employed for the oriented oxidation of 5-hydroxymethylfurfural (HMF), a typical platform chemical derived from glucose, into 2,5-furandicarboxylicacid (FDCA) under mild conditions. The Co–N/F1 with enhanced Co content was obtained using the low-molecular-weight lignin fraction (F1) with high functional group contents (e.g., Ph–OH and COOH), and the as-prepared catalyst was demonstrated to present a Co–N4 configuration. Owing to the absence of colored byproduct formation from HMF at elevated temperatures, Co–N/F1 realized the highly selective conversion of HMF to FDCA (100% HMF conversion, 99.20% FDCA yield) under mild conditions (65 °C, 3 bar O2), which outperformed most reported non-noble metal-supported catalysts. Density functional theory calculations indicate that the Co–N4 site in Co–N/F1 facilitates the dehydrogenation of the α-C position on HMF and its aldehyde intermediates, resulting in a significantly enhanced catalytic efficiency. Furthermore, Co–N/F1 exhibited stable reusability due to the alkaline resistance of the Co–N4 structure. Our study details the insights into the synthesis of Co-SACs using a lignin fractionation strategy and further demonstrates its good feasibility for the oriented conversion of biomass-derived platform chemicals under mild conditions.
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.