Fabrication and interfacial electron transfer of ultrathin g-C3N4 nanosheet/TNT@CNTs ternary nanostructure heterojunction for high-efficiency visible-light-driven photocatalysis
The purpose of this research is to design and fabricate a novel ternary hybrid nanostructure heterojunction with high-efficiency visible-light-driven photocatalysis. The porous layered TiO 2 nanotubular structures (TNTs) with high percentage of photocatalytic reactive facets, which were turned into...
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Veröffentlicht in: | Journal of materials science. Materials in electronics 2018-05, Vol.29 (10), p.8673-8687 |
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Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | The purpose of this research is to design and fabricate a novel ternary hybrid nanostructure heterojunction with high-efficiency visible-light-driven photocatalysis. The porous layered TiO
2
nanotubular structures (TNTs) with high percentage of photocatalytic reactive facets, which were turned into by commercially available TiO
2
, were wrapped on the surface of hydroxylation carbon nanotubes (CNTs) through the formation of Ti–O=C and/or Ti–O–C bond between CNTs and TiO
2
. Then the TNT@CNT nanotubular composites were coated by ultrathin g-C
3
N
4
nanosheets with a thickness of 3–4 nm. The ternary nanocomposites owned strong absorption performance, low charge recombination rates and high-efficiency photocatalytic activities, which were all owe to high surface areas and excellent adsorptivity of the CNTs, photocatalytic performance of TiO
2
nanotubes (TNTs) and moderate band gap of g-C
3
N
4
nanosheet. What’s more, the formation of chemical bonds greatly improved visible-light photocatalytic activity with a degradation rate of 98.2 and 97.9% for methylene blue and rhodamine B in 60 min under visible-light irradiation, which showed ~ 10 times enhancement compared to pure TiO
2
. In addition, the existence of h
+
and ·OH and ·O
2−
radicals played main role in the photocatalytic process. The new material was of great significance to environmental protection and energy criss. |
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ISSN: | 0957-4522 1573-482X |
DOI: | 10.1007/s10854-018-8883-9 |