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dc.contributor.authorChoi, Hyeonuk-
dc.contributor.authorHa, Min Gwan-
dc.contributor.authorSuh, Jungwon-
dc.contributor.authorLim, Chulwan-
dc.contributor.authorKim, Beomil-
dc.contributor.authorWang, Sun Eon-
dc.contributor.authorLee, Jang Yong-
dc.contributor.authorOh, Hyung-Suk-
dc.contributor.authorOh, Jihun-
dc.date.accessioned2024-11-20T07:00:10Z-
dc.date.available2024-11-20T07:00:10Z-
dc.date.created2024-11-20-
dc.date.issued2024-10-
dc.identifier.issn0926-3373-
dc.identifier.urihttps://pubs.kist.re.kr/handle/201004/151118-
dc.description.abstractSimple, large-scale synthesis of metal single-atom catalysts (SACs) is limited by the aggregation of metal atoms on the support material surface. The N atoms in small organic ligands (SOLs) can anchor single metal atoms, affording abundant surface-active sites. In this study, we investigated the effect of the nitrogen/carbon ratio (N/C) in SOLs on the properties of the resultant Ni single-atom confined nitrogen-doped carbon black (Ni-NCB). The N/C ratio affected the thermal stability of Ni-NCB_N/Cs during carbonization, and the optimal Ni-NCB (Ni-NCB_0.5) was synthesized with the SOL 2-methylimidazole. Ni-NCB_0.5 achieved a CO partial current density of >?500?mA?cm?2 and high CO Faradaic efficiency (96.4?%) in the CO2 reduction reaction. The 3- and 4-cell stack systems with Ni-NCB_0.5 (25?cm2 area per unit cell) exhibited an overall current of 10?A, high CO selectivity (>?96.0?%), and long-term stability (50?h). This synthetic strategy for SACs can be commercialized and even extended to other industrial electrocatalysts.-
dc.languageEnglish-
dc.publisherElsevier BV-
dc.titleEffect of the nitrogen/carbon ratio in the organic ligand of a nickel single-atom catalyst on its electrochemical activity in CO2 reduction-
dc.typeArticle-
dc.identifier.doi10.1016/j.apcatb.2024.124192-
dc.description.journalClass1-
dc.identifier.bibliographicCitationApplied Catalysis B: Environment and Energy, v.355-
dc.citation.titleApplied Catalysis B: Environment and Energy-
dc.citation.volume355-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
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