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ZnO decorated Sn3O4 nanosheet nano-heterostructure: a stable photocatalyst for water splitting and dye degradation under natural sunlight

Herein, a facile hydrothermally-assisted sonochemical approach for the synthesis of a ZnO decorated Sn 3 O 4 nano-heterostructure is reported. The phase purity of the nano-heterostructure was confirmed by X-ray diffraction and Raman spectroscopy. The morphological analysis demonstrated a nanosheet-l...

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Bibliographic Details
Published in:RSC advances 2019-01, Vol.9 (18), p.1289-1296
Main Authors: Balgude, Sagar D, Sethi, Yogesh A, Kale, Bharat B, Amalnerkar, Dinesh P, Adhyapak, Parag V
Format: Article
Language:English
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Summary:Herein, a facile hydrothermally-assisted sonochemical approach for the synthesis of a ZnO decorated Sn 3 O 4 nano-heterostructure is reported. The phase purity of the nano-heterostructure was confirmed by X-ray diffraction and Raman spectroscopy. The morphological analysis demonstrated a nanosheet-like structure of Sn 3 O 4 with a thickness of 20 nm, decorated with ZnO. The optical band gap was found to be 2.60 eV for the ZnO@Sn 3 O 4 nano-heterostructure. Photoluminescence studies revealed the suppression of electron-hole recombination in the ZnO@Sn 3 O 4 nano-heterostructure. The potential efficiency of ZnO@Sn 3 O 4 was further evaluated towards photocatalytic hydrogen production via H 2 O splitting and degradation of methylene blue (MB) dye. Interestingly, it showed significantly superior photocatalytic activity compared to ZnO and Sn 3 O 4 . The complete degradation of MB dye solution was achieved within 40 min. The nano-heterostructure also exhibited enhanced photocatalytic activity towards hydrogen evolution (98.2 μmol h −1 /0.1 g) via water splitting under natural sunlight. The superior photocatalytic activity of ZnO@Sn 3 O 4 was attributed to vacancy defects created due to its nano-heterostructure. Herein, a facile hydrothermally-assisted sonochemical approach for the synthesis of a ZnO decorated Sn 3 O 4 nano-heterostructure is reported.
ISSN:2046-2069
DOI:10.1039/c9ra00788a