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dc.contributor.authorGu, Mingyao
dc.date.accessioned2025-04-09T01:28:14Z
dc.date.available2025-04-09T01:28:14Z
dc.date.issued2025en
dc.identifier.urihttps://hdl.handle.net/2123/33806
dc.description.abstractAmmonia is a key industrial chemical with diverse applications. However, the traditional Haber-Bosch process is energy-intensive and environmentally taxing. Electrochemical nitrate reduction reaction presents a sustainable alternative for NH3 synthesis, leveraging nitrate's high solubility and abundant availability. This study evaluates carbon nanotube-supported metal phthalocyanine catalysts, focusing on FePc, CoPc, NiPc, CuPc, and MnPc. CuPc/CNT exhibits the highest Faradaic efficiency and catalytic activity in alkaline conditions, but its performance significantly drops in neutral environments due to competition with the hydrogen evolution reaction. It requires precise pH control, limiting its applicability in diverse conditions. CoPc/CNT and NiPc/CNT show balanced performance in both alkaline and neutral environments, with moderate NH3 selectivity and catalytic activity. They are suitable for a wide range of applications but do not achieve the highest efficiency. MnPc/CNT demonstrates the lowest NH3 selectivity, primarily stabilizing early intermediates like NO2-. It is less effective for deep reduction to NH3 but may be useful in applications requiring selective intermediate generation. In contrast, while not the most active catalyst, FePc/CNT shows remarkable stability and adaptability in both alkaline and neutral conditions. Its strong binding with intermediates like NO2 and NO ensures consistent NH3 selectivity, making it a promising candidate for industrial applications where stability is prioritized. The study highlighted that the stable performance of FePc/CNT under different conditions highlights its potential for practical applications. Future research directions include tuning CNT oxygen surface groups and MPc side groups to enhance catalytic activity and selectivity and exploring magnetization strategies to regulate metal center electronic structures. This work provides insights for advancing NO3RR catalysts toward sustainable ammonia production.en
dc.language.isoenen
dc.rightsThe author retains copyright of this thesis
dc.subjectM-N-C catalysten
dc.subjectNitrate reduction reaction (NO3RR)en
dc.subjectAmmonia (NH3) selectivityen
dc.titleIron-Based Metal-Nitrogen-Carbon Catalyst for Electrochemical Nitrogen Reduction Reactionen
dc.typeThesis
dc.type.thesisMasters by Researchen
dc.rights.otherThe author retains copyright of this thesis. It may only be used for the purposes of research and study. It must not be used for any other purposes and may not be transmitted or shared with others without prior permission.en
usyd.facultySeS faculties schools::Faculty of Engineering::School of Chemical and Biomolecular Engineeringen
usyd.degreeMaster of Philosophy M.Philen
usyd.awardinginstThe University of Sydneyen
usyd.advisorWei, Li


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