{"title":"在 Co-Ce-Zr 三元金属固溶体上以甲醇和二氧化碳为原料直接合成碳酸二甲酯","authors":"Xin Li, Lele Cao, Dongdong Jia, Yongyue Sun","doi":"10.1016/j.fuproc.2024.108157","DOIUrl":null,"url":null,"abstract":"<div><div>To investigate highly performance catalysts for the direct synthesis of dimethyl carbonate (DMC) from carbon dioxide (CO<sub>2</sub>) and methanol, a Co<sub>0.02</sub>/Ce<sub>0.7</sub>Zr<sub>0.3</sub>O<sub>2</sub> ternary metal solid solution nanoparticle catalyst was synthesized, demonstrating superior performance with a DMC yield of 3.86 mmol g<sup>−1</sup> and selectivity of 100 % at 7 MPa and 140 °C. A series of characterizations further validated the successful incorporation of cobalt and zirconium into the crystal lattice of CeO<sub>2</sub>, resulting in an increased number of acid-base sites on its surface and a rise in oxygen vacancy content from 10.1 % to 28.7 %. The density functional theory (DFT) calculation results further corroborated the experimental findings, indicating that the doping of cobalt and zirconium ions significantly reduced the formation energy of oxygen vacancies on the catalyst surface from 2.53 to −1.38 eV, while concurrently decreasing the adsorption energy of CO<sub>2</sub> from −0.33 to −1.74 eV. Additionally, charge calculation results revealed that oxygen vacancies functioned as Lewis acid sites, whereas lattice oxygen atoms served as Lewis base sites, facilitating the cooperative activation of CO<sub>2</sub>. The results may provide a new approach for designing and improving CeO<sub>2</sub>-based catalysts for CO<sub>2</sub> activation.</div></div>","PeriodicalId":326,"journal":{"name":"Fuel Processing Technology","volume":"266 ","pages":"Article 108157"},"PeriodicalIF":7.2000,"publicationDate":"2024-11-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Direct synthesis of dimethyl carbonate from methanol and carbon dioxide over Co-Ce-Zr ternary metal solid solution\",\"authors\":\"Xin Li, Lele Cao, Dongdong Jia, Yongyue Sun\",\"doi\":\"10.1016/j.fuproc.2024.108157\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>To investigate highly performance catalysts for the direct synthesis of dimethyl carbonate (DMC) from carbon dioxide (CO<sub>2</sub>) and methanol, a Co<sub>0.02</sub>/Ce<sub>0.7</sub>Zr<sub>0.3</sub>O<sub>2</sub> ternary metal solid solution nanoparticle catalyst was synthesized, demonstrating superior performance with a DMC yield of 3.86 mmol g<sup>−1</sup> and selectivity of 100 % at 7 MPa and 140 °C. A series of characterizations further validated the successful incorporation of cobalt and zirconium into the crystal lattice of CeO<sub>2</sub>, resulting in an increased number of acid-base sites on its surface and a rise in oxygen vacancy content from 10.1 % to 28.7 %. The density functional theory (DFT) calculation results further corroborated the experimental findings, indicating that the doping of cobalt and zirconium ions significantly reduced the formation energy of oxygen vacancies on the catalyst surface from 2.53 to −1.38 eV, while concurrently decreasing the adsorption energy of CO<sub>2</sub> from −0.33 to −1.74 eV. Additionally, charge calculation results revealed that oxygen vacancies functioned as Lewis acid sites, whereas lattice oxygen atoms served as Lewis base sites, facilitating the cooperative activation of CO<sub>2</sub>. The results may provide a new approach for designing and improving CeO<sub>2</sub>-based catalysts for CO<sub>2</sub> activation.</div></div>\",\"PeriodicalId\":326,\"journal\":{\"name\":\"Fuel Processing Technology\",\"volume\":\"266 \",\"pages\":\"Article 108157\"},\"PeriodicalIF\":7.2000,\"publicationDate\":\"2024-11-16\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Fuel Processing Technology\",\"FirstCategoryId\":\"5\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S0378382024001279\",\"RegionNum\":2,\"RegionCategory\":\"工程技术\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"CHEMISTRY, APPLIED\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Fuel Processing Technology","FirstCategoryId":"5","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0378382024001279","RegionNum":2,"RegionCategory":"工程技术","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, APPLIED","Score":null,"Total":0}
Direct synthesis of dimethyl carbonate from methanol and carbon dioxide over Co-Ce-Zr ternary metal solid solution
To investigate highly performance catalysts for the direct synthesis of dimethyl carbonate (DMC) from carbon dioxide (CO2) and methanol, a Co0.02/Ce0.7Zr0.3O2 ternary metal solid solution nanoparticle catalyst was synthesized, demonstrating superior performance with a DMC yield of 3.86 mmol g−1 and selectivity of 100 % at 7 MPa and 140 °C. A series of characterizations further validated the successful incorporation of cobalt and zirconium into the crystal lattice of CeO2, resulting in an increased number of acid-base sites on its surface and a rise in oxygen vacancy content from 10.1 % to 28.7 %. The density functional theory (DFT) calculation results further corroborated the experimental findings, indicating that the doping of cobalt and zirconium ions significantly reduced the formation energy of oxygen vacancies on the catalyst surface from 2.53 to −1.38 eV, while concurrently decreasing the adsorption energy of CO2 from −0.33 to −1.74 eV. Additionally, charge calculation results revealed that oxygen vacancies functioned as Lewis acid sites, whereas lattice oxygen atoms served as Lewis base sites, facilitating the cooperative activation of CO2. The results may provide a new approach for designing and improving CeO2-based catalysts for CO2 activation.
期刊介绍:
Fuel Processing Technology (FPT) deals with the scientific and technological aspects of converting fossil and renewable resources to clean fuels, value-added chemicals, fuel-related advanced carbon materials and by-products. In addition to the traditional non-nuclear fossil fuels, biomass and wastes, papers on the integration of renewables such as solar and wind energy and energy storage into the fuel processing processes, as well as papers on the production and conversion of non-carbon-containing fuels such as hydrogen and ammonia, are also welcome. While chemical conversion is emphasized, papers on advanced physical conversion processes are also considered for publication in FPT. Papers on the fundamental aspects of fuel structure and properties will also be considered.