{"title":"CO2 Hydrogenation Using Size-dependent Ru Particles Supported on g-C3N4","authors":"Rasmeet Singh, Lizhuo Wang, Haoyue Sun, Jun Huang","doi":"10.1016/j.ccst.2024.100248","DOIUrl":null,"url":null,"abstract":"<div><p>Efficient catalysis of CO<sub>2</sub> hydrogenation holds significant promise for addressing environmental concerns and advancing sustainable energy solutions. In this study, we report the synthesis of a novel series of Ru-supported on graphitic carbon nitride (g-C<sub>3</sub>N<sub>4</sub>) catalysts, with a focus on the impact of ruthenium (Ru) loading on the thermocatalytic performance. Varying Ru concentrations were introduced, including 0.2, 0.5, 1.0, 2.0, and 5.0 wt%, resulting in different Ru particle sizes on g-C<sub>3</sub>N<sub>4</sub> support. Through a multifaceted characterization approach, it was observed that the catalyst containing 1 wt% Ru loading displayed superior performance, with a high density of active sites, indicated by an enhanced CO<sub>2</sub> conversion rate of 36.8 % at 450 °C and a CO yield of 25 %. This catalyst also exhibited remarkable CO selectivity of 83 % at 375 °C. Conversely, lower loadings of 0.2 and 0.5 wt % Ru were found to be less effective, yielding minimal CO<sub>2</sub> conversion. Loadings above 1 wt% Ru, while achieving high CO<sub>2</sub> conversion, demonstrated a preference for CH<sub>4</sub> production over CO, indicating lower selectivity for the desired product. This study elucidates the critical role of Ru nanocluster size in the catalytic activity and selectivity, with 1 wt % Ru-supported g-C<sub>3</sub>N<sub>4</sub> emerging as a promising candidate for selective CO generation from CO<sub>2</sub> hydrogenation, offering a pathway for the valorization of CO<sub>2</sub> as a raw material in the chemical industry.</p></div>","PeriodicalId":9387,"journal":{"name":"Carbon Capture Science & Technology","volume":null,"pages":null},"PeriodicalIF":0.0000,"publicationDate":"2024-06-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S2772656824000605/pdfft?md5=bba456e443c3eb656e41644a6c53e4c3&pid=1-s2.0-S2772656824000605-main.pdf","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Carbon Capture Science & Technology","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2772656824000605","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
Efficient catalysis of CO2 hydrogenation holds significant promise for addressing environmental concerns and advancing sustainable energy solutions. In this study, we report the synthesis of a novel series of Ru-supported on graphitic carbon nitride (g-C3N4) catalysts, with a focus on the impact of ruthenium (Ru) loading on the thermocatalytic performance. Varying Ru concentrations were introduced, including 0.2, 0.5, 1.0, 2.0, and 5.0 wt%, resulting in different Ru particle sizes on g-C3N4 support. Through a multifaceted characterization approach, it was observed that the catalyst containing 1 wt% Ru loading displayed superior performance, with a high density of active sites, indicated by an enhanced CO2 conversion rate of 36.8 % at 450 °C and a CO yield of 25 %. This catalyst also exhibited remarkable CO selectivity of 83 % at 375 °C. Conversely, lower loadings of 0.2 and 0.5 wt % Ru were found to be less effective, yielding minimal CO2 conversion. Loadings above 1 wt% Ru, while achieving high CO2 conversion, demonstrated a preference for CH4 production over CO, indicating lower selectivity for the desired product. This study elucidates the critical role of Ru nanocluster size in the catalytic activity and selectivity, with 1 wt % Ru-supported g-C3N4 emerging as a promising candidate for selective CO generation from CO2 hydrogenation, offering a pathway for the valorization of CO2 as a raw material in the chemical industry.