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Structure, wettability and photocatalytic activity of graphene doped multi-walled carbon nanotubes/titanium dioxide hybrid coatings.

Authors :
Arslanhan, Melike
Devrim Şam Parmak, Ebru
Source :
Thin Solid Films. Jan2024, Vol. 788, pN.PAG-N.PAG. 1p.
Publication Year :
2024

Abstract

• G-MWCNTs/TiO 2 hybrid coated surfaces showed super hydrophilic properties. • 0.2 and 0.3 wt.% G-MWCNTs improved the optical transmission in the visible region. • According to the ISO 10,678:2010, hybrid coated samples showed photonic efficiency. This paper presents the findings of the structure, wettability and photocatalytic activity of 32 wt % graphene-doped multi-walled carbon nanotubes (G-MWCNTs) / titanium dioxide (TiO 2) hybrid coatings under three different ratios. The hybrid coatings of G-MWCNTs/TiO 2 were compared with the pure (undoped) TiO 2 coating. Pure TiO 2 and G-MWCNTs/TiO 2 hybrid coatings were prepared by sol-gel method and deposited on soda-lime-silica (SLS) glass substrates using a dip coater. The samples were heat-treated in the air at 500 °C for 1 h. The nano-sized G and MWCNTs used as dopants in the resulting hybrid solution were mixed without agglomeration by the sonication method based on the DLVO theory, without any surfactants. To prevent the migration of Na+ ions contained in the structure of SLS glass to TiO 2 -based coatings, a SiO 2 -based sol-gel coating was first deposited on the SLS glass surface using the dip coating method. This was done before applying the pure TiO 2 coating and G-MWCNTs/TiO 2 hybrid coating process. All samples were crystallized in the anatase form and exhibited superhydrophilic behavior. The G-MWCNTs/TiO 2 hybrid coated samples' photoactivity was determined using the ISO 10678 MB degradation standard. According to the ISO 10678:2010 MB degradation standard, G-MWCNTs/TiO 2 hybrid coated samples exhibited photonic efficiency. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
00406090
Volume :
788
Database :
Academic Search Index
Journal :
Thin Solid Films
Publication Type :
Academic Journal
Accession number :
174496663
Full Text :
https://doi.org/10.1016/j.tsf.2023.140149