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Article: Synergistic electroreduction of carbon dioxide to carbon monoxide on bimetallic layered conjugated metal-organic frameworks

TitleSynergistic electroreduction of carbon dioxide to carbon monoxide on bimetallic layered conjugated metal-organic frameworks
Authors
Issue Date2020
Citation
Nature Communications, 2020, v. 11, n. 1, article no. 1409 How to Cite?
AbstractHighly effective electrocatalysts promoting CO2 reduction reaction (CO2RR) is extremely desirable to produce value-added chemicals/fuels while addressing current environmental challenges. Herein, we develop a layer-stacked, bimetallic two-dimensional conjugated metal-organic framework (2D c-MOF) with copper-phthalocyanine as ligand (CuN4) and zinc-bis(dihydroxy) complex (ZnO4) as linkage (PcCu-O8-Zn). The PcCu-O8-Zn exhibits high CO selectivity of 88%, turnover frequency of 0.39 s−1 and long-term durability (>10 h), surpassing thus by far reported MOF-based electrocatalysts. The molar H2/CO ratio (1:7 to 4:1) can be tuned by varying metal centers and applied potential, making 2D c-MOFs highly relevant for syngas industry applications. The contrast experiments combined with operando spectroelectrochemistry and theoretical calculation unveil a synergistic catalytic mechanism; ZnO4 complexes act as CO2RR catalytic sites while CuN4 centers promote the protonation of adsorbed CO2 during CO2RR. This work offers a strategy on developing bimetallic MOF electrocatalysts for synergistically catalyzing CO2RR toward syngas synthesis.
Persistent Identifierhttp://hdl.handle.net/10722/349415

 

DC FieldValueLanguage
dc.contributor.authorZhong, Haixia-
dc.contributor.authorGhorbani-Asl, Mahdi-
dc.contributor.authorLy, Khoa Hoang-
dc.contributor.authorZhang, Jichao-
dc.contributor.authorGe, Jin-
dc.contributor.authorWang, Mingchao-
dc.contributor.authorLiao, Zhongquan-
dc.contributor.authorMakarov, Denys-
dc.contributor.authorZschech, Ehrenfried-
dc.contributor.authorBrunner, Eike-
dc.contributor.authorWeidinger, Inez M.-
dc.contributor.authorZhang, Jian-
dc.contributor.authorKrasheninnikov, Arkady V.-
dc.contributor.authorKaskel, Stefan-
dc.contributor.authorDong, Renhao-
dc.contributor.authorFeng, Xinliang-
dc.date.accessioned2024-10-17T06:58:23Z-
dc.date.available2024-10-17T06:58:23Z-
dc.date.issued2020-
dc.identifier.citationNature Communications, 2020, v. 11, n. 1, article no. 1409-
dc.identifier.urihttp://hdl.handle.net/10722/349415-
dc.description.abstractHighly effective electrocatalysts promoting CO2 reduction reaction (CO2RR) is extremely desirable to produce value-added chemicals/fuels while addressing current environmental challenges. Herein, we develop a layer-stacked, bimetallic two-dimensional conjugated metal-organic framework (2D c-MOF) with copper-phthalocyanine as ligand (CuN4) and zinc-bis(dihydroxy) complex (ZnO4) as linkage (PcCu-O8-Zn). The PcCu-O8-Zn exhibits high CO selectivity of 88%, turnover frequency of 0.39 s−1 and long-term durability (>10 h), surpassing thus by far reported MOF-based electrocatalysts. The molar H2/CO ratio (1:7 to 4:1) can be tuned by varying metal centers and applied potential, making 2D c-MOFs highly relevant for syngas industry applications. The contrast experiments combined with operando spectroelectrochemistry and theoretical calculation unveil a synergistic catalytic mechanism; ZnO4 complexes act as CO2RR catalytic sites while CuN4 centers promote the protonation of adsorbed CO2 during CO2RR. This work offers a strategy on developing bimetallic MOF electrocatalysts for synergistically catalyzing CO2RR toward syngas synthesis.-
dc.languageeng-
dc.relation.ispartofNature Communications-
dc.titleSynergistic electroreduction of carbon dioxide to carbon monoxide on bimetallic layered conjugated metal-organic frameworks-
dc.typeArticle-
dc.description.naturelink_to_subscribed_fulltext-
dc.identifier.doi10.1038/s41467-020-15141-y-
dc.identifier.pmid32179738-
dc.identifier.scopuseid_2-s2.0-85081993209-
dc.identifier.volume11-
dc.identifier.issue1-
dc.identifier.spagearticle no. 1409-
dc.identifier.epagearticle no. 1409-
dc.identifier.eissn2041-1723-

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