This study presents a highly sustainable nanocomposite platform for dual applications in both photocatalysis and sensing. The nanomaterial is synthesized via a green process using natural, readily available components, including halloysite nanotubes (HNTs), glutathione (GSH), and xanthopterin, utilizing copper ions (Cu1+) as the catalytically active species. The synthesis, which exclusively uses green solvents like tetrahydropyran (THP) and water, involves functionalizing HNTs with (3-aminopropyl)triethoxysilane (APTES), followed by the attachment of GSH as a chelating agent for Cu1+. Finally, xanthopterin is loaded to act as a light-harvesting antenna. Fourier-transform infrared (FT-IR) spectroscopy and thermogravimetric analysis (TGA) confirmed the successful functionalization and composition. Scanning electron microscopy (SEM) and energy-dispersive X-ray (EDX) analysis validated the material’s morphology and elemental composition. The resulting nanocomposite, HNT-NH2-GSH-Cu1+-X, demonstrated a remarkable synergistic effect, achieving a CO2 conversion of 42.2% and a high (86.1%) CH4 selectivity. Furthermore, the HNT-GSH-Cu2+ nanocomposite exhibited excellent electrochemical sensing capabilities for bisphenol A, with a low limit of detection (LOD) of 0.022 μM and a high sensitivity of 5.098 μA μM–1·cm–2. The work successfully demonstrates the creation of a sustainable, multifunctional nanomaterial that addresses critical environmental challenges by combining efficient solar fuel production with highly sensitive pollutant detection.

Multifunctional Halloysite-Glutathione Nanocomposite for Solar CO2 Conversion and Pollutant Sensing

Saccullo, Erika
Primo
;
Ferlazzo, Angelo
Secondo
;
Dativo, Giusy;Fiorenza, Roberto;Sambataro, Giulia;Bruno, Elena;Gulino, Antonino;Rescifina, Antonio;Patamia, Vincenzo
Penultimo
Conceptualization
;
Floresta, Giuseppe
Ultimo
Conceptualization
2026-01-01

Abstract

This study presents a highly sustainable nanocomposite platform for dual applications in both photocatalysis and sensing. The nanomaterial is synthesized via a green process using natural, readily available components, including halloysite nanotubes (HNTs), glutathione (GSH), and xanthopterin, utilizing copper ions (Cu1+) as the catalytically active species. The synthesis, which exclusively uses green solvents like tetrahydropyran (THP) and water, involves functionalizing HNTs with (3-aminopropyl)triethoxysilane (APTES), followed by the attachment of GSH as a chelating agent for Cu1+. Finally, xanthopterin is loaded to act as a light-harvesting antenna. Fourier-transform infrared (FT-IR) spectroscopy and thermogravimetric analysis (TGA) confirmed the successful functionalization and composition. Scanning electron microscopy (SEM) and energy-dispersive X-ray (EDX) analysis validated the material’s morphology and elemental composition. The resulting nanocomposite, HNT-NH2-GSH-Cu1+-X, demonstrated a remarkable synergistic effect, achieving a CO2 conversion of 42.2% and a high (86.1%) CH4 selectivity. Furthermore, the HNT-GSH-Cu2+ nanocomposite exhibited excellent electrochemical sensing capabilities for bisphenol A, with a low limit of detection (LOD) of 0.022 μM and a high sensitivity of 5.098 μA μM–1·cm–2. The work successfully demonstrates the creation of a sustainable, multifunctional nanomaterial that addresses critical environmental challenges by combining efficient solar fuel production with highly sensitive pollutant detection.
2026
bisphenol A
chelating agent
CO2
photoconversion
electrochemical nanosensor
HNT
nanotube
File in questo prodotto:
File Dimensione Formato  
Multifunctional Halloysite-Glutathione Nanocomposite.pdf

accesso aperto

Tipologia: Versione Editoriale (PDF)
Licenza: Creative commons
Dimensione 8.09 MB
Formato Adobe PDF
8.09 MB Adobe PDF Visualizza/Apri

I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.

Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/20.500.11769/704973
Citazioni
  • ???jsp.display-item.citation.pmc??? ND
  • Scopus 0
  • ???jsp.display-item.citation.isi??? 0
social impact