Please use this identifier to cite or link to this item: http://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/8716
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dc.contributor.authorMENDHE, RAHUL MAHADEOen_US
dc.contributor.authorMONDAL, RITWIKen_US
dc.contributor.authorKOTTAICHAMY, ALAGAR RAJAen_US
dc.contributor.authorHARIDAS, AKSHAYen_US
dc.contributor.authorKotresh, Harish Makri Nimbegondien_US
dc.contributor.authorPrabhakaran, Vinoden_US
dc.contributor.authorTHIMMAPPA, RAVIKUMARen_US
dc.contributor.authorTHOTIYL, MUSTHAFA OTTAKAMen_US
dc.date.accessioned2024-04-24T05:45:27Z
dc.date.available2024-04-24T05:45:27Z
dc.date.issued2024-04en_US
dc.identifier.citationGreen Chemistryen_US
dc.identifier.issn1463-9270en_US
dc.identifier.urihttps://doi.org/10.1039/D4GC00740Aen_US
dc.identifier.urihttp://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/8716
dc.description.abstractWe demonstrate that the catalytic metal centre for ammonia production can be selectively activated with only a slight alteration in ligand isomerization (α and β isomers), making it practical and effective even for agricultural effluents. With almost 90 % Faradaic efficiency, the β isomer generates approximately 0.64 mg h-1 cm-2 of ammonia. Energy-efficient ammonia recovery is made possible by the interfacial proton charge assembly that β-isomerization creates, which attracts the reacting nitrate and repels the competing hydronium ions. With minimal energy consumption, this isomerization approach can interconvert agricultural effluents into ammonia fuel, reaching up to 84 % of its theoretical yield and maintaining stability over 100 hours of continuous electrolysis.en_US
dc.language.isoenen_US
dc.publisherRoyal Society of Chemistryen_US
dc.subjectChemistryen_US
dc.subjectTOC-APR-2024en_US
dc.subject2024en_US
dc.subject2024-APR-WEEK2en_US
dc.subjectTOC-APR-2024en_US
dc.titleFuel from Waste: Electrosynthesizing Ammonia Directly from Agricultural Digestate through Ligand Isomerizationen_US
dc.typeArticleen_US
dc.contributor.departmentDept. of Chemistryen_US
dc.identifier.sourcetitleGreen Chemistryen_US
dc.publication.originofpublisherForeignen_US
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