First Cu-nanostar as a sustainable catalyst realized through synergistic effects of bowl-shaped features and surface activation of sporopollenin exine

Recently, nanostar-shaped structures, including gold nanostars (NS), have drawn much attention for their potential use in surface-enhanced Raman spectroscopy (SERS) and catalysis. Yet, very few studies have been conducted on Cu-Au hybrid NS, and there are none for Cu-based NS. Herein, we describe an...

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Veröffentlicht in:Nanoscale 2024-10, Vol.16 (39), p.18356-18364
Hauptverfasser: Gowri, Vijayendran, Kumari, Sarita, Sharma, Raina, Selim, Abdul, Jayamurugan, Govindasamy
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Sprache:eng
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Zusammenfassung:Recently, nanostar-shaped structures, including gold nanostars (NS), have drawn much attention for their potential use in surface-enhanced Raman spectroscopy (SERS) and catalysis. Yet, very few studies have been conducted on Cu-Au hybrid NS, and there are none for Cu-based NS. Herein, we describe an effective method for controlling copper-oxide nanostar (ESP-PEI-Cu I/II O-NS) growth using sporopollenin as a sustainable template material. However, ESP-PEI-Cu I/II O-NS growth depends on sporopollenin surface functionalization. Sporopollenin surface activation was done by amine functionalization with polyethyleneimine (PEI), without which ESP-PEI-Cu I/II O-NS growth was not observed. The sporopollenin's exine (outer wall) has a bowl-like structure, which mediates the growth of Cu nanorods, resulting in an NS morphology. Furthermore, due to their increased surface area, ESP-PEI-Cu I/II O-NS showed excellent catalytic activity for Huisgen 1,3-dipolar cycloadditions even when used in H 2 O and without additives under green conditions. This approach utilising biomass as a sustainable template would pave the way for developing controlled growth of nanostructures for SERS-related and catalytic applications. The bowl-shaped outer surface of biomass-derived sporopollenin has been combined with polyethyleneimine functionalization to develop CuO nanostars for the first time that show efficient triazole formation under sustainable conditions.
ISSN:2040-3364
2040-3372
2040-3372
DOI:10.1039/d4nr00390j