Please use this identifier to cite or link to this item: http://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/10671
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dc.contributor.authorNAYAK, BHOJKUMARen_US
dc.contributor.authorThodika, Abdul Raafik Arattuen_US
dc.contributor.authorPRADHAN, HEMANGAen_US
dc.contributor.authorMENDHE, RAHUL MAHADEOen_US
dc.contributor.authorTHOTIYL, MUSTHAFA OTTAKAMen_US
dc.date.accessioned2026-01-30T06:35:07Z-
dc.date.available2026-01-30T06:35:07Z-
dc.date.issued2026-01en_US
dc.identifier.citationChemical Scienceen_US
dc.identifier.issn2041-6539en_US
dc.identifier.urihttps://doi.org/10.1039/D5SC08236Fen_US
dc.identifier.urihttp://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/10671-
dc.description.abstractWe demonstrate electrostatic decatalysis, where long-range Coulomb interactions selectively screen parasitic chemistry, leading to distinct catalytic selectivity outcomes. By reconfiguring interfacial electrostatic landscapes, this approach achieves site and flux selective screening of competing reactions while promoting ammonia electrosynthesis. Molecular dynamics simulations reveal a near sevenfold enhancement in substrate enrichment factors, arising from optimized electrostatic screening and strategic charge distribution. Experimentally, we observe more than a twofold increase in ammonia Faradaic efficiency at practically relevant current densities, suggesting electrostatic contributes to reaction selectivity with energy savings exceeding 50% relative to conventional benchmarks. Importantly, the Coulombic screening strategy exhibits pH-insensitive universality, enabling broad applicability for electrochemical process modulations.en_US
dc.language.isoenen_US
dc.publisherRoyal Society of Chemistryen_US
dc.subjectChemistryen_US
dc.subject2026-JAN-WEEK1en_US
dc.subjectTOC-JAN-2026en_US
dc.subject2026en_US
dc.titleElectrostatic Decatalysis through Coulombic Screeningen_US
dc.typeArticleen_US
dc.contributor.departmentDept. of Chemistryen_US
dc.identifier.sourcetitleChemical Scienceen_US
dc.publication.originofpublisherForeignen_US
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