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ZnO/Graphene Oxide on Halloysite Nanotubes as a Superabsorbent Nanocomposite Photocatalyst for the Degradation of Organic Dyesopen access

Authors
Park, JongikLee, HyungwookLee, KeonkuNoh, SieunJin, SoyeongJae, JunghoJeong, YoungdoNoh, Jaegeun
Issue Date
Jul-2023
Publisher
MDPI
Keywords
photocatalyst; halloysite nanotubes; graphene oxide; zinc oxide; nanocomposite; photocatalytic effect; degradation; organic dyes
Citation
NANOMATERIALS, v.13, no.13, pp.1 - 13
Indexed
SCIE
SCOPUS
Journal Title
NANOMATERIALS
Volume
13
Number
13
Start Page
1
End Page
13
URI
https://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/190376
DOI
10.3390/nano13131895
ISSN
2079-4991
Abstract
Using renewable photocatalysts for pollutant degradation represents a promising approach to addressing environmental water challenges by harnessing solar energy without additional energy consumption. However, for the practical use of photocatalysts, it is necessary to improve catalyst efficiency, considering cost and biocompatibility. In this study, we developed a new superabsorbent photocatalyst for the degradation of organic dyes in water. Our photocatalyst comprises halloysite nanotubes (HNTs) with a large outer diameter and Si-O and Al-O groups on the outer and inner surfaces, respectively; graphene oxide (GO) possessing numerous sp2 bonds and light-conductive properties; and ZnO, which can degrade organic molecules via a photon source. By exploiting the superabsorbent properties of GOs for organic dyes and stabilizing ZnO nanoparticles on HNTs to inhibit aggregation, our photocatalysts demonstrated significantly improved degradability compared to ZnO nanoparticles alone and combinations of ZnO with HNTs or GO. The structural characteristics of the nanocomposites were characterized using SEM, EDX, Raman spectroscopy, and XRD. Their enhanced photocatalytic activity was demonstrated by the degradation of rhodamine b in water, showing 95% photodegradation under UV illumination for 60 min, while the ZnO nanoparticles showed only 56% dye degradation under the same condition. Additionally, the degradation rate was enhanced by four times. Furthermore, the catalysts maintained their initial activity with no significant loss after four uses, showing their potential for practical implementation in the mass purification of wastewater.
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