{"title":"fsp制备Ru/Ti-SiO2 CO2甲烷化催化剂的联合dft -实验研究","authors":"Okorn Mekasuwandumrong , Tinnakorn Saelee , Jakapob Noppakhun , Meena Rittiruam , Patcharaporn Khajondetchairit , Damien P. Debecker , Supareak Praserthdam , Piyasan Praserthdam","doi":"10.1016/j.mcat.2025.115179","DOIUrl":null,"url":null,"abstract":"<div><div>Flame spray pyrolysis (FSP) was employed to synthesize Ti-modified SiO₂ in a single step, serving as the support for Ru-based catalysts in CO₂ methanation reactions. The addition of Ti led to the formation of anatase and rutile TiO₂ phases, enhancing the catalytic activity of Ru/Ti-SiO₂ catalysts. Benchmarking between Ru/Ti-SiO₂ catalysts of various Ti concentrations prepared using one-step FSP techniques indicated significantly higher catalytic activity for the impregnation-made catalysts compared to the FSP-made ones, where diffuse reflectance infrared Fourier transform spectroscopy (DRIFTS) revealed different CH₄ formation mechanisms between two techniques. For FSP-made catalysts, it predominantly occurred through the CO route, whereas the impregnation-made proceed via both the dissociative adsorption of CO₂ (CO route) and through surface formate species formation. To explain the effect of Ti loading on Ru/SiO₂ catalysts, a multiscale analysis combining density functional theory (DFT) and microkinetic modeling was performed to study the adsorption behavior of CO₂ on different catalysts. The results revealed that a high amount of Ti reduced the adsorption strength of CO₂ on Ru/SiO₂ catalysts, indicating a modified interaction between CO₂ and the catalyst surface.</div></div>","PeriodicalId":393,"journal":{"name":"Molecular Catalysis","volume":"582 ","pages":"Article 115179"},"PeriodicalIF":3.9000,"publicationDate":"2025-05-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"A combined DFT-Experimental study on FSP-made Ru/Ti-SiO2 catalysts for CO2 methanation\",\"authors\":\"Okorn Mekasuwandumrong , Tinnakorn Saelee , Jakapob Noppakhun , Meena Rittiruam , Patcharaporn Khajondetchairit , Damien P. Debecker , Supareak Praserthdam , Piyasan Praserthdam\",\"doi\":\"10.1016/j.mcat.2025.115179\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>Flame spray pyrolysis (FSP) was employed to synthesize Ti-modified SiO₂ in a single step, serving as the support for Ru-based catalysts in CO₂ methanation reactions. The addition of Ti led to the formation of anatase and rutile TiO₂ phases, enhancing the catalytic activity of Ru/Ti-SiO₂ catalysts. Benchmarking between Ru/Ti-SiO₂ catalysts of various Ti concentrations prepared using one-step FSP techniques indicated significantly higher catalytic activity for the impregnation-made catalysts compared to the FSP-made ones, where diffuse reflectance infrared Fourier transform spectroscopy (DRIFTS) revealed different CH₄ formation mechanisms between two techniques. For FSP-made catalysts, it predominantly occurred through the CO route, whereas the impregnation-made proceed via both the dissociative adsorption of CO₂ (CO route) and through surface formate species formation. To explain the effect of Ti loading on Ru/SiO₂ catalysts, a multiscale analysis combining density functional theory (DFT) and microkinetic modeling was performed to study the adsorption behavior of CO₂ on different catalysts. The results revealed that a high amount of Ti reduced the adsorption strength of CO₂ on Ru/SiO₂ catalysts, indicating a modified interaction between CO₂ and the catalyst surface.</div></div>\",\"PeriodicalId\":393,\"journal\":{\"name\":\"Molecular Catalysis\",\"volume\":\"582 \",\"pages\":\"Article 115179\"},\"PeriodicalIF\":3.9000,\"publicationDate\":\"2025-05-05\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Molecular Catalysis\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S2468823125003645\",\"RegionNum\":2,\"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":"Molecular Catalysis","FirstCategoryId":"92","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2468823125003645","RegionNum":2,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, PHYSICAL","Score":null,"Total":0}
A combined DFT-Experimental study on FSP-made Ru/Ti-SiO2 catalysts for CO2 methanation
Flame spray pyrolysis (FSP) was employed to synthesize Ti-modified SiO₂ in a single step, serving as the support for Ru-based catalysts in CO₂ methanation reactions. The addition of Ti led to the formation of anatase and rutile TiO₂ phases, enhancing the catalytic activity of Ru/Ti-SiO₂ catalysts. Benchmarking between Ru/Ti-SiO₂ catalysts of various Ti concentrations prepared using one-step FSP techniques indicated significantly higher catalytic activity for the impregnation-made catalysts compared to the FSP-made ones, where diffuse reflectance infrared Fourier transform spectroscopy (DRIFTS) revealed different CH₄ formation mechanisms between two techniques. For FSP-made catalysts, it predominantly occurred through the CO route, whereas the impregnation-made proceed via both the dissociative adsorption of CO₂ (CO route) and through surface formate species formation. To explain the effect of Ti loading on Ru/SiO₂ catalysts, a multiscale analysis combining density functional theory (DFT) and microkinetic modeling was performed to study the adsorption behavior of CO₂ on different catalysts. The results revealed that a high amount of Ti reduced the adsorption strength of CO₂ on Ru/SiO₂ catalysts, indicating a modified interaction between CO₂ and the catalyst surface.
期刊介绍:
Molecular Catalysis publishes full papers that are original, rigorous, and scholarly contributions examining the molecular and atomic aspects of catalytic activation and reaction mechanisms. The fields covered are:
Heterogeneous catalysis including immobilized molecular catalysts
Homogeneous catalysis including organocatalysis, organometallic catalysis and biocatalysis
Photo- and electrochemistry
Theoretical aspects of catalysis analyzed by computational methods