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  Red carbon mediated formation of Cu2O clusters dispersed on the oxocarbon framework by Fehling's route and their use for the nitrate electroreduction in acidic conditions

Ba, J., Dong, H., Odziomek, M., Lai, F., Wang, R., Han, Y., et al. (2024). Red carbon mediated formation of Cu2O clusters dispersed on the oxocarbon framework by Fehling's route and their use for the nitrate electroreduction in acidic conditions. Advanced Materials, 2400396. doi:10.1002/adma.202400396.

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Ba, Jingwen, Autor
Dong, Hongliang, Autor
Odziomek, Mateusz1, Autor                 
Lai, Feili, Autor
Wang, Rui, Autor
Han, Yandong, Autor
Shu, Jinfu, Autor
Antonietti, Markus2, Autor                 
Liu, Tianxi, Autor
Yang, Wensheng, Autor
Tian, Zhihong, Autor
Affiliations:
1Mateusz Odziomek, Kolloidchemie, Max Planck Institute of Colloids and Interfaces, Max Planck Society, ou_3505121              
2Markus Antonietti, Kolloidchemie, Max Planck Institute of Colloids and Interfaces, Max Planck Society, ou_1863321              

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Schlagwörter: Cu2 clusters; oxocarbons; Fehling reaction; nitrate electroreduction; carbonaceous materials
 Zusammenfassung: The oligomers of carbon suboxide, known as red carbon, exhibit a highly conjugated structure and semiconducting properties. Upon mild heat treatment, it transforms into a carbonaceous framework rich in oxygen surface terminations, called oxocarbon. In this study, we harness the abundant oxygen functionalities as anchors to create oxocarbon-supported nanohybrid electrocatalysts. Starting with single atomic Cu (II) strongly coordinated to oxygen atoms on red carbon, the Fehling reaction leads to the formation of Cu2O clusters. Simultaneously, a covalent oxocarbon framework emerges via cross-linking, providing a robust support for Cu2O clusters. Notably, the oxocarbon support effectively stabilizes Cu2O clusters of very small size, ensuring their high durability in acidic conditions and the presence of ammonia. The synthesized material exhibits a superior electrocatalytic activity for nitrate reduction under acidic electrolyte conditions, with a high yield rate of NH4+ at 3.31 mmol h−1 mgcat−1 and a Faradaic efficiency of 92.5% achieved at a potential of -0.4 V (vs. RHE).

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Sprache(n): eng - English
 Datum: 2024-03-25
 Publikationsstatus: Online veröffentlicht
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 Ort, Verlag, Ausgabe: -
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 Identifikatoren: DOI: 10.1002/adma.202400396
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Titel: Advanced Materials
  Kurztitel : Adv. Mater.
Genre der Quelle: Zeitschrift
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Ort, Verlag, Ausgabe: Weinheim : Wiley-VCH
Seiten: - Band / Heft: - Artikelnummer: 2400396 Start- / Endseite: - Identifikator: ISSN: 0935-9648