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Enhanced visible-light photocatalytic performance of Fe3O4 nanopyramids for water splitting and dye degradation
Iron oxide (Fe 3 O 4 ) pyramid nanostructures were synthesized via a co-precipitation method, without using surfactants or template, for photocatalytic and photoelectrocatalytic activities. The as-made Fe 3 O 4 was characterized via X-ray diffraction (XRD), scanning electron microscopy (SEM), energy...
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Published in: | Journal of solid state electrochemistry 2018-11, Vol.22 (11), p.3535-3546 |
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Main Authors: | , , , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | Iron oxide (Fe
3
O
4
) pyramid nanostructures were synthesized via a co-precipitation method, without using surfactants or template, for photocatalytic and photoelectrocatalytic activities. The as-made Fe
3
O
4
was characterized via X-ray diffraction (XRD), scanning electron microscopy (SEM), energy-dispersive X-ray spectroscopy (EDS), transmission electron microscopy (TEM), UV–vis spectroscopy, photoluminescence spectroscopy, N
2
adsorption–desorption analysis, and X-ray photoelectron spectroscopy (XPS). The data clearly demonstrate that the Fe
3
O
4
nanostructures display excellent crystallinity, uniform morphology with a Brunauer–Emmett–Teller (BET) surface area of 52.95 m
2
g
−1
, and an optical bandgap of 2.17 eV, which allows them to serve as outstanding catalysts under visible irradiation. The highest photocatalytic activity of ~ 97% was achieved in the degradation of rhodamine B under visible irradiation, with a degradation rate constant of 0.0322 min
−1
at room temperature. Further, electrochemical studies demonstrated that the Fe
3
O
4
electrode possesses good electrocatalytic activity in 0.1 M KOH electrolyte. The highest photocurrent density of 1.2 × 10
−4
mA cm
−2
was observed in the water splitting reaction. The Fe
3
O
4
nanostructures exhibited superior performance in terms of both dye degradation and photoelectrochemical activity. |
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ISSN: | 1432-8488 1433-0768 |
DOI: | 10.1007/s10008-018-4054-4 |