The development of quasi-1D Co 3O 4/ZnO nanocomposites by a two-step plasma enhanced-chemical vapor deposition (PE-CVD) process is presented. Arrays of ?001? oriented ZnO nanorods were first grown on Si(100) and subsequently used as templates for the PE-CVD of Co 3O 4, whose amount was tailored as a function of deposition time. The obtained composites were thoroughly characterized by means of a multitechnique approach, involving field emission-scanning electron microscopy (FE-SEM), energy dispersive X-ray spectroscopy (EDXS), micro-Raman and Fourier-transform infrared (FT-IR) spectroscopies, X-ray photoelectron and X-ray excited Auger electron spectroscopies (XPS, XE-AES), glancing incidence X-ray diffraction (GIXRD), and reflection high energy electron diffraction (RHEED). The use of moderate deposition temperatures (<=300 °C), together with the unique activation provided by nonequilibrium plasmas, prevented undesired solid-state reactions between the two oxides and promoted Co 3O 4 growth on the tips of vertically aligned ZnO nanostructures. In particular, the resulting quasi-1D Co 3O 4/ZnO composites were characterized by an interface epitaxial-like relationship, an important issue for the development of semiconductor-based functional nanosystems. Photoinduced hydrophilic (PH) and photocatalytic (PC) performances of the present nanocomposites were preliminarily investigated, showing attractive results toward the possible fabrication of advanced smart materials.

Epitaxial-like growth of Co3O4/ZnO Quasi-1D Nanocomposites

Gasparotto A;Barreca D;MacCato C;Rossi M;
2012

Abstract

The development of quasi-1D Co 3O 4/ZnO nanocomposites by a two-step plasma enhanced-chemical vapor deposition (PE-CVD) process is presented. Arrays of ?001? oriented ZnO nanorods were first grown on Si(100) and subsequently used as templates for the PE-CVD of Co 3O 4, whose amount was tailored as a function of deposition time. The obtained composites were thoroughly characterized by means of a multitechnique approach, involving field emission-scanning electron microscopy (FE-SEM), energy dispersive X-ray spectroscopy (EDXS), micro-Raman and Fourier-transform infrared (FT-IR) spectroscopies, X-ray photoelectron and X-ray excited Auger electron spectroscopies (XPS, XE-AES), glancing incidence X-ray diffraction (GIXRD), and reflection high energy electron diffraction (RHEED). The use of moderate deposition temperatures (<=300 °C), together with the unique activation provided by nonequilibrium plasmas, prevented undesired solid-state reactions between the two oxides and promoted Co 3O 4 growth on the tips of vertically aligned ZnO nanostructures. In particular, the resulting quasi-1D Co 3O 4/ZnO composites were characterized by an interface epitaxial-like relationship, an important issue for the development of semiconductor-based functional nanosystems. Photoinduced hydrophilic (PH) and photocatalytic (PC) performances of the present nanocomposites were preliminarily investigated, showing attractive results toward the possible fabrication of advanced smart materials.
2012
Istituto di Chimica della Materia Condensata e di Tecnologie per l'Energia - ICMATE
Istituto di Scienze e Tecnologie Molecolari - ISTM - Sede Milano
CHEMICAL-VAPOR-DEPOSITION
ZNO NANOROD ARRAYS
NANOWIRE HETEROSTRUCTURES
FILMS
NANOCRYSTALS
File in questo prodotto:
File Dimensione Formato  
prod_194749-doc_47936.pdf

solo utenti autorizzati

Descrizione: paper
Tipologia: Versione Editoriale (PDF)
Licenza: NON PUBBLICO - Accesso privato/ristretto
Dimensione 1.18 MB
Formato Adobe PDF
1.18 MB Adobe PDF   Visualizza/Apri   Richiedi una copia
prod_194749-doc_47937.pdf

solo utenti autorizzati

Descrizione: supplementary information
Licenza: NON PUBBLICO - Accesso privato/ristretto
Dimensione 167.83 kB
Formato Adobe PDF
167.83 kB Adobe PDF   Visualizza/Apri   Richiedi una copia

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/20.500.14243/232587
Citazioni
  • ???jsp.display-item.citation.pmc??? ND
  • Scopus 19
  • ???jsp.display-item.citation.isi??? 20
social impact