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Surfactant-free pH-assisted facile engineering of hierarchical rutile TiO 2 nanostructures by a single step hydrothermal method for water splitting application
A photoanode of distinct hierarchical pure rutile phase TiO 2 nanostructures was successfully prepared by a surfactant and template-free, single-step hydrothermal route. Tuning of the morphology from compact broccoli-like structures of ∼4 μm in diameter to outsized round bottle brush flower-like str...
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Published in: | CrystEngComm 2020-04, Vol.22 (14), p.2462-2471 |
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Main Authors: | , , , , , |
Format: | Article |
Language: | English |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | A photoanode of distinct hierarchical pure rutile phase TiO
2
nanostructures was successfully prepared by a surfactant and template-free, single-step hydrothermal route. Tuning of the morphology from compact broccoli-like structures of ∼4 μm in diameter to outsized round bottle brush flower-like structures of ∼12 μm in diameter was achieved only by varying the pH (concentration of HCl) of the solvent. The subsequent growth mechanism of the different hierarchical structures was thoroughly illustrated using appropriate schematics. The structural, optical and morphological properties of all the rutile TiO
2
photoanodes have been studied by using an X-ray diffractometer, X-ray photoelectron spectrometer, UV-vis spectrophotometer, scanning electron microscope and transmission electron microscope. The deposited TiO
2
nanostructures were directly used as a photoanode in a photoelectrochemical cell. The photocurrent showed an increasing trend with decreasing theoretical pH up to −0.76 (corresponding to a HCl concentration of 5.7 M) of the solvent used for preparing the nanostructures. However, further decrement in the pH resulted in lowering of the photocurrent. The best photoelectrochemical performance is observed for the rutile TiO
2
photoanode with a well-arranged microflower-like structure corresponding to pH −0.76. |
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ISSN: | 1466-8033 1466-8033 |
DOI: | 10.1039/D0CE00202J |