ZnO–TiO2/rGO heterostructure for enhanced photodegradation of IC dye under natural solar light and role of rGO in surface hydroxylation

To overcome the limitations of ZnO as a photocatalyst, the present work reports a ternary nanocomposite (ZnO–TiO 2 /rGO) with a high photocatalytic activity under direct natural solar light irradiation. Reduced graphene oxide (rGO) was obtained after bio-reduction of GO using pomegranate peels. Tech...

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Published inBulletin of materials science Vol. 46; no. 2; p. 83
Main Authors Kacem, Khaoula, Casanova-Chafer, Juan, Hamrouni, Abdessalem, Ameur, Sami, Güell, Frank, Nsib, Mohamed Faouzi, Llobet, Eduard
Format Journal Article
LanguageEnglish
Published Bangalore Indian Academy of Sciences 20.04.2023
Springer Nature B.V
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Summary:To overcome the limitations of ZnO as a photocatalyst, the present work reports a ternary nanocomposite (ZnO–TiO 2 /rGO) with a high photocatalytic activity under direct natural solar light irradiation. Reduced graphene oxide (rGO) was obtained after bio-reduction of GO using pomegranate peels. Techniques of FE-SEM, TEM, XRD, FTIR, UV–Vis DRS, Raman and PL were used for characterization purpose. The ternary nanocomposite exhibited a high photocatalytic activity towards the degradation of indigo carmine dye, resulting in an efficiency of 92% within 150 min under sunlight illumination. Accordingly, the hybridization of ZnO with TiO 2 and rGO improves light absorption, promotes high separation of photogenerated charges, and solves the photocorrosion drawback of ZnO, leading to a better stability and reusability of the nanocomposite. Particularly, the prepared rGO allowed certain hydrophilicity and a better surface hydroxylation. In view of that, a comprehensive photocatalytic mechanism was proposed and discussed, referred to experiments showing the effect of holes and • OH scavengers. The findings revealed that the developed rGO hybridized with ZnO–TiO 2 heterojunction can be a promising candidate for removing environmental contaminations using natural solar light.
ISSN:0973-7669
0250-4707
0973-7669
DOI:10.1007/s12034-023-02913-7