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A non-isothermal water formation cell for electrochemical heat recovery

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dc.contributor.author MONDAL, RITWIK en_US
dc.contributor.author YUVARAJ, SHYAAM SRIRANGADHAMU en_US
dc.contributor.author NAYAK, BHOJKUMAR en_US
dc.contributor.author PRADHAN, HEMANGA en_US
dc.contributor.author THOTIYL, MUSTHAFA OTTAKAM en_US
dc.date.accessioned 2025-04-22T04:03:51Z
dc.date.available 2025-04-22T04:03:51Z
dc.date.issued 2025-04 en_US
dc.identifier.citation Chemical Science. en_US
dc.identifier.issn 2041-6520 en_US
dc.identifier.issn 2041-6539 en_US
dc.identifier.uri https://doi.org/10.1039/D5SC00892A en_US
dc.identifier.uri http://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/9661
dc.description.abstract Low-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.iso en en_US
dc.publisher Royal Society of Chemistry en_US
dc.subject State en_US
dc.subject Ions en_US
dc.subject 2025 en_US
dc.subject 2025-APR-WEEK3 en_US
dc.subject TOC-APR-2025 en_US
dc.title A non-isothermal water formation cell for electrochemical heat recovery en_US
dc.type Article en_US
dc.contributor.department Dept. of Chemistry en_US
dc.identifier.sourcetitle Chemical Science en_US
dc.publication.originofpublisher Foreign en_US


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