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dc.contributor.authorKong, Jimin-
dc.contributor.authorKim, Min-Seok-
dc.contributor.authorAkbar, Ramavi-
dc.contributor.authorPark, Hee Young-
dc.contributor.authorJang, Jong Hyun-
dc.contributor.authorKim, Hansung-
dc.contributor.authorHur, Kahyun-
dc.contributor.authorPark, Hyun S.-
dc.date.accessioned2024-01-19T14:32:28Z-
dc.date.available2024-01-19T14:32:28Z-
dc.date.created2021-10-21-
dc.date.issued2021-06-
dc.identifier.issn1944-8244-
dc.identifier.urihttps://pubs.kist.re.kr/handle/201004/116919-
dc.description.abstractWe studied the electrochemical synthesis of NH3 on Fe-CuS/C catalysts in an alkaline aqueous solution under ambient conditions. The metal chalcogenide catalyst is active in the nitrogen reduction reaction (NRR) for approximately 45 min with an NH3 production yield of 16 mu g h(-1) cm(-2) at -0.4 V-RHE, while it decomposes to CuO. The rapid degradation of the catalyst hinders the precise investigation of the NH3 production activity in longer time measurements. Herein, the electrochemical NH3 production rate is enhanced with increased overpotentials when the degradation effect is mitigated in the measurement, which was difficult to observe in the NRR reports. In the Tafel analysis, the exchange current density, heterogeneous rate constant, and transfer coefficient of the Fe-CuS/C catalyst on the NRR were estimated. When the electrode degradation is mitigated, one of the best NH3 production activities among the reported metal sulfide electrochemical NRR catalysts is obtained, which is 42 mu g h(-1) cm(-2) at -0.6 V-RHE.-
dc.languageEnglish-
dc.publisherAmerican Chemical Society-
dc.titleElectrochemical Nitrogen Reduction Kinetics on a Copper Sulfide Catalyst for NH3 Synthesis at Low Temperature and Atmospheric Pressure-
dc.typeArticle-
dc.identifier.doi10.1021/acsami.1c00850-
dc.description.journalClass1-
dc.identifier.bibliographicCitationACS Applied Materials & Interfaces, v.13, no.21, pp.24593 - 24603-
dc.citation.titleACS Applied Materials & Interfaces-
dc.citation.volume13-
dc.citation.number21-
dc.citation.startPage24593-
dc.citation.endPage24603-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.identifier.wosid000659315800022-
dc.identifier.scopusid2-s2.0-85105034106-
dc.relation.journalWebOfScienceCategoryNanoscience & Nanotechnology-
dc.relation.journalWebOfScienceCategoryMaterials Science, Multidisciplinary-
dc.relation.journalResearchAreaScience & Technology - Other Topics-
dc.relation.journalResearchAreaMaterials Science-
dc.type.docTypeArticle-
dc.subject.keywordPlusELECTROCATALYTIC N-2 FIXATION-
dc.subject.keywordPlusCARBON-
dc.subject.keywordPlusCO2-
dc.subject.keywordPlusAMMONIA-
dc.subject.keywordPlusFUNDAMENTALS-
dc.subject.keywordPlusPERFORMANCE-
dc.subject.keywordPlusSOLUBILITY-
dc.subject.keywordPlusACTIVATION-
dc.subject.keywordPlusSTRATEGY-
dc.subject.keywordAuthorammonia-
dc.subject.keywordAuthorelectrocatalyst-
dc.subject.keywordAuthornitrogen reduction-
dc.subject.keywordAuthorcopper sulfide-
dc.subject.keywordAuthorTafel analysis-
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