As gradual increases in atmospheric CO2 and depletion of fossil fuels have raised considerable public concern in recent decades, utilizing the unlimited solar energy to convert CO2 to fuels (e.g., formic acid and methanol) apparently could simultaneously resolve these issues for sustainable development. However, due to the complicated characteristics of CO2 reduction, the mechanism has yet to be disclosed. To clarify the postulated pathway as mentioned in the literature, the technique of electron paramagnetic resonance (ESR) was implemented herein to confirm the mechanism and related pathways of CO2 reduction under visible light using graphene-TiO2 as catalyst. The findings indicated that CO(-•) radicals, as the main intermediates, were first detected herein to react with several hydrogen ions and electrons for the formation of CH3OH. For example, the generation of CO(-•) radicals is possibly the vital rate-controlling step for conversion of CO2 to methanol as hypothesized elsewhere. The kinetics behind the proposed mechanism was also determined in this study. The mechanism and kinetics could provide the in-depth understanding to the pathway of CO2 reduction and disclose system optimization of maximal conversion for further application.
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http://dx.doi.org/10.1021/es505301x | DOI Listing |
J Environ Manage
December 2024
College of Petrochemical Engineering, Lanzhou University of Technology, Lanzhou, 730050, China.
Microbially mediated anaerobic oxidation of methane (AOM) regulates methane (CH) fluxes. Increases in the global atmospheric carbon dioxide (CO) concentration and iron oxide rich in paddy soils influence AOM. However, the response and mechanisms between these two processes and AOM remain unclear.
View Article and Find Full Text PDFAdv Mater
December 2024
The Soft2D Lab, State Key Laboratory of Metal Matrix Composites, Shanghai Key Laboratory of Electrical Insulation and Thermal Ageing, School of Chemistry and Chemical Engineering, Shanghai Jiao Tong University, Shanghai, 200240, China.
The electrochemical conversion of carbon dioxide (CO) into hydrocarbon products emerges as a pivotal sustainable strategy for carbon utilization. Cu-based catalysts are currently prioritized as the most effective means for this process, yet it remains a long-term goal to achieve high product selectivity at elevated current densities. This study delved into exploring the influence of a topological poly(2-aminoazulene) with a substantial dipole moment on modulating the Cu surface dipole field to augment the catalytic activity involved in CO reduction.
View Article and Find Full Text PDFHorizontal subsurface flow constructed wetlands (HFCWs) are capable of eliminating organic matter and nitrogen while emitting less methane (CH) and nitrous oxide (NO) than free water surface flow wetlands. However, the simultaneous removal of pollutants and reduction of greenhouse gases (GHG) emissions from high-strength wastewater containing high levels of organic matter and ammonium nitrogen (NH-N) has not get been investigated. The influent COD concentration affected the efficiency of nitrogen removal, GHG emissions and the presence of iron from iron ore, but the COD and TP removal efficiencies remained unaffected.
View Article and Find Full Text PDFGlob Chang Biol
January 2025
University of Nebraska-Lincoln, Lincoln, Nebraska, USA.
Agriculture serves as both a source and a sink of global greenhouse gases (GHGs), with agricultural intensification continuing to contribute to GHG emissions. Climate-smart agriculture, encompassing both nature- and technology-based actions, offers promising solutions to mitigate GHG emissions. We synthesized global data, between 1990 and 2021, from the Food and Agriculture Organization (FAO) of the United Nations to analyze the impacts of agricultural activities on global GHG emissions from agricultural land, using structural equation modeling.
View Article and Find Full Text PDFAngew Chem Int Ed Engl
December 2024
Huazhong University of Science and Technology, School of Chemistry and Chemical Engineering, CHINA.
Porous organic polymers have shown great potential in photocatalytic CO2 reduction due to their unique tunable structure favoring gas adsorption and metal sites integration. However, efficient photocatalysis in porous polymers is greatly limited by the low surface reactivity and electron mobility of bulk structure. Herein, we incorporate TiO2 nanoparticles and Ni(II) sites into a layered cationic imidazolium polymer (IP), in which the imidazolium moieties and free anions can stabilize the key intermediates and enhance the reaction kinetics of CO2 reduction.
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