Assembly of colloidal Cu nanoparticles and Ni–N–C nanocarbons to electrochemically boost cascade production of ethylene from CO2 reduction
Cu-based tandem catalysis provides an efficient route to boost production of C 2+ products for electrochemical carbon dioxide reduction (CO 2 RR), but colloidally synthesized Cu NPs are still less explored in tandem electrocatalyst design. A Cu-based tandem catalyst was constructed in hexane by asse...
Gespeichert in:
Veröffentlicht in: | Journal of materials science 2023-12, Vol.58 (45), p.17200-17210 |
---|---|
Hauptverfasser: | , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
Zusammenfassung: | Cu-based tandem catalysis provides an efficient route to boost production of C
2+
products for electrochemical carbon dioxide reduction (CO
2
RR), but colloidally synthesized Cu NPs are still less explored in tandem electrocatalyst design. A Cu-based tandem catalyst was constructed in hexane by assembling colloidal Cu NPs and Ni–N–C nanocarbon with tunable Cu NPs/Ni–N–C mass ratios, of which colloidal Cu NPs are homogeneously distributed over Ni–N–C nanocarbon. The Cu NPs/Ni–N–C tandem catalysts have been fully characterized by TEM, PXRD and XPS. In the H-type cell, the CO
2
RR contrast experiments verified that the optimized Cu NPs/Ni–N–C composite produced tandem effect in generating C
2
H
4
, benefiting from which a fourfold promotion in faradaic efficiency, and fivefold enhancement in partial current density were achieved compared to the reference Cu NPs/Vulcan carbon. Finally, the post-CO
2
RR Cu NPs/Ni–N–C catalysts were also measured by CV, EIS, TEM and XPS to further understand the change of tandem catalyst during CO
2
RR.
Graphical abstract
An efficient Cu-based tandem catalyst was designed by compositing colloidal Cu NPs and Ni–N–C nanocarbon, which boosts cascade production of C
2
H
4
from electrochemical carbon dioxide reduction. |
---|---|
ISSN: | 0022-2461 1573-4803 |
DOI: | 10.1007/s10853-023-09140-9 |