Please use this identifier to cite or link to this item: http://hdl.handle.net/10397/93033
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dc.contributorDepartment of Mechanical Engineeringen_US
dc.creatorSun, Xen_US
dc.creatorLi, Yen_US
dc.creatorAn, Len_US
dc.creatorLv, Xen_US
dc.date.accessioned2022-05-30T07:40:12Z-
dc.date.available2022-05-30T07:40:12Z-
dc.identifier.issn0013-4651en_US
dc.identifier.urihttp://hdl.handle.net/10397/93033-
dc.language.isoenen_US
dc.publisherElectrochemical Societyen_US
dc.rights© 2019 The Electrochemical Society.en_US
dc.rightsThis manuscript version is made available under the CC-BY-NC-ND 4.0 license (https://creativecommons.org/licenses/by-nc-nd/4.0/)en_US
dc.rightsThe following publication Sun, X., Li, Y., An, L., & Lv, X. (2019). Comparative performance evaluation of self-basifying direct formate fuel cells. Journal of The Electrochemical Society, 166(12), F768 is available at https://doi.org/10.1149/2.0751912jes.en_US
dc.titleComparative performance evaluation of self-basifying direct formate fuel cellsen_US
dc.typeJournal/Magazine Articleen_US
dc.identifier.spageF768en_US
dc.identifier.epageF773en_US
dc.identifier.volume166en_US
dc.identifier.issue12en_US
dc.identifier.doi10.1149/2.0751912jesen_US
dcterms.abstractFormate that is capable of synthesizing from electrochemical conversion of CO2 efficiently is emerging as one of promising fuels for direct liquid fuel cells. In this work, a comparative study on performance of self-basifying direct formate fuel cell that contains non-platinum catalysts, neutral polymer and anion-exchange membrane is reported. Experimental result shows that the peak power density (PPD) of self-basifying direct formate fuel cell reaches 47 mW cm-2 at 60°C without additional base. It is found that the competition between the quickened electrokinetics and increased mass and charge transport resistances induces an optimal anode and cathode Pd loading of 3.0 mg cm-2. The PPD first improves and then decreases with PTFE content in cathode, resulting in an optimal content of 10 wt%. In contrast, it decreases monotonically with anode PTFE content. In addition, the cell performance varies slightly with formate concentration due to the competitive adsorption between HCOO- and OH-. A moderate oxygen flow rate of 100 sccm is required for the highest performance. Moreover, elevating operating temperature quickens electrokinetics and facilitates mass and charge transfer, improving cell performance significantly.en_US
dcterms.accessRightsopen accessen_US
dcterms.bibliographicCitationJournal of the Electrochemical Society, Jan. 2019, v. 166, no. 12, p. F768-F773en_US
dcterms.isPartOfJournal of the Electrochemical Societyen_US
dcterms.issued2019-01-
dc.identifier.scopus2-s2.0-85072910771-
dc.identifier.eissn1945-7111en_US
dc.description.validate202205 bchyen_US
dc.description.oaAccepted Manuscripten_US
dc.identifier.FolderNumberME-0522-
dc.description.fundingSourceOthersen_US
dc.description.fundingTextNational Natural Science Foundation of China; Shenzhen Science and Technology Foundation; Natural Science Basic Research Plan in Shaanxi Province of Chinaen_US
dc.description.pubStatusPublisheden_US
dc.identifier.OPUS20432166-
dc.description.oaCategoryGreen (AAM)en_US
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