One-step thermal synthesis of Ag-modified g-C3N4/N-doped TiO2 hybrids with enhanced visible-light photocatalytic activity
A series of silver nanoparticle-modified graphitic carbon nitride/N-doped TiO 2 hybrids (Ag/g-C 3 N 4 /N-TiO 2 or ACTs) were prepared by one-step in situ calcination process at 550 °C for 3 h in air atmosphere. The morphology, structure, and optical properties of ACTs with different Ag contents were...
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Veröffentlicht in: | Journal of materials science 2017, Vol.52 (2), p.1183-1193 |
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Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | A series of silver nanoparticle-modified graphitic carbon nitride/N-doped TiO
2
hybrids (Ag/g-C
3
N
4
/N-TiO
2
or ACTs) were prepared by one-step in situ calcination process at 550 °C for 3 h in air atmosphere. The morphology, structure, and optical properties of ACTs with different Ag contents were characterized by X-ray diffraction, scanning electron microscopy, transmission electron microscopy, X-ray photoelectron spectroscopy, photoluminescence spectra, and UV–vis diffuse reflectance spectroscopy. Ag nanoparticles with grain size of about 5 nm are anchored on the surface of ACTs. In UV–vis absorption test, a red-shift of light absorption edge and more visible light absorption (compared to N-TiO
2
and g-C
3
N
4
/N-TiO
2
) are observed for ACTs. Moreover, the dependence of photocatalytic activity on Ag contents was investigated, and ACTs-3 presents the highest photocatalytic activity as the optimal Ag content under visible light irradiation. Remarkably enhanced UV–visible light photoelectrochemical response was also confirmed for ACTs compared with TiO
2
, N-TiO
2
, and g-C
3
N
4
/N-TiO
2
. Ag-decorated g-C
3
N
4
/N-TiO
2
composites result in enhanced light absorption capacity and improved transfer of charge carriers, which prominently contribute to the improvement of photoactivity. This work demonstrates that Ag/g-C
3
N
4
/N-TiO
2
is a promising photocatalytic material for organic pollutant degradation under visible light irradiation. |
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ISSN: | 0022-2461 1573-4803 |
DOI: | 10.1007/s10853-016-0414-6 |