Please use this identifier to cite or link to this item: http://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/9661
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dc.contributor.authorMONDAL, RITWIKen_US
dc.contributor.authorYUVARAJ, SHYAAM SRIRANGADHAMUen_US
dc.contributor.authorNAYAK, BHOJKUMARen_US
dc.contributor.authorPRADHAN, HEMANGAen_US
dc.contributor.authorTHOTIYL, MUSTHAFA OTTAKAMen_US
dc.date.accessioned2025-04-22T04:03:51Z-
dc.date.available2025-04-22T04:03:51Z-
dc.date.issued2025-04en_US
dc.identifier.citationChemical Science.en_US
dc.identifier.issn2041-6520en_US
dc.identifier.issn2041-6539en_US
dc.identifier.urihttps://doi.org/10.1039/D5SC00892Aen_US
dc.identifier.urihttp://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/9661-
dc.description.abstractLow-grade heat harvesting has emerged as a promising strategy to recover waste heat into usable energy. However, most of the thermo-electrochemical approaches are limited to redox reactions involving metal ion complexes and halide species, which often exhibit low heat-to-electricity conversion efficiencies. We demonstrate a heat harvesting approach based on a non-redox reaction; water formation driven by a net-zero hydrogen redox process. Under standard conditions, its positive entropy change enables the interconversion of nearly 30% of surrounding heat into electrical energy, resulting in a thermodynamic efficiency greater than unity. This water formation-based galvanic-thermogalvanic device demonstrated a temperature-insensitive maximum power density as high as similar to 33.55 mW m-2 K-2. Notably, this figure of merit is similar to 70 times higher than the state-of-the-art ferrocyanide-ferricyanide-based thermogalvanic devices, thereby extending the scope of electrochemical heat harvesting beyond conventional redox processes.en_US
dc.language.isoenen_US
dc.publisherRoyal Society of Chemistryen_US
dc.subjectStateen_US
dc.subjectIonsen_US
dc.subject2025en_US
dc.subject2025-APR-WEEK3en_US
dc.subjectTOC-APR-2025en_US
dc.titleA non-isothermal water formation cell for electrochemical heat recoveryen_US
dc.typeArticleen_US
dc.contributor.departmentDept. of Chemistryen_US
dc.identifier.sourcetitleChemical Scienceen_US
dc.publication.originofpublisherForeignen_US
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