FeO x Derived from an Iron-Containing Polyoxometalate Boosting the Photocatalytic Water Oxidation Activity of Ti 3+ -Doped TiO 2
The development of efficient and stable catalyst systems using low-cost, abundant, and nontoxic materials is the primary demand for photocatalytic water oxidation. Distinguishing the true active species in a heterogeneous catalytic system is important for construction of efficient catalytic systems....
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Veröffentlicht in: | ACS applied materials & interfaces 2019-07, Vol.11 (26), p.23135-23143 |
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Hauptverfasser: | , , , , , , , |
Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | The development of efficient and stable catalyst systems using low-cost, abundant, and nontoxic materials is the primary demand for photocatalytic water oxidation. Distinguishing the true active species in a heterogeneous catalytic system is important for construction of efficient catalytic systems. Herein, hydrothermally synthesized Ti
self-doped TiO
, labeled as Ti
/TiO
, was first used as a light absorber in a powder visible light-driven photocatalytic water oxidation reaction. When an iron-containing polyoxometalate Na
[Fe
(H
O)
(OH)
(W
O
)
(α-SbW
O
)
] (Fe11) was used as a cocatalyst, an amorphous layer of active species was wrapped outside the initial Ti
/TiO
nanorod and the in situ formed composite was labeled as F/Ti
/TiO
. When the composite F/Ti
/TiO
was tested as a photocatalytic water oxidation catalyst, dramatically improved oxygen evolution performance was achieved. The composite F/Ti
/TiO
showed an oxygen evolution rate of 410 μmol/g/h, which was about 11-fold higher than that of prism Ti
/TiO
. After 24 h of illumination, an O
yield of 36.4% was achieved. The contrast experiments, high-resolution transmission electron microscopy, and X-ray photoelectron spectroscopy characterization demonstrated that FeO
is the true cocatalyst that enhanced the oxygen evolution activity of TiO
. A recycling experiment proved that the composite F/Ti
/TiO
has favorable stability in the oxygen production process. |
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ISSN: | 1944-8244 1944-8252 |
DOI: | 10.1021/acsami.9b03714 |