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Effect of conjugation degree and delocalized π-system on the photocatalytic activity of single layer g-C3N4
[Display omitted] Because of the superiority on conjugation degree and delocalized π-system, single layer g-C3N4-PAM exhibits excellent photocatalytic activity not only on organic degradation but also on H2 evolution. •Chemical exfoliation changes the surface electricity of g-C3N4.•The partial destr...
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Published in: | Applied catalysis. B, Environmental Environmental, 2017-12, Vol.218, p.137-146 |
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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: | [Display omitted]
Because of the superiority on conjugation degree and delocalized π-system, single layer g-C3N4-PAM exhibits excellent photocatalytic activity not only on organic degradation but also on H2 evolution.
•Chemical exfoliation changes the surface electricity of g-C3N4.•The partial destruction occurred during acid exfoliation.•High conjugation degree was kept in g-C3N4-PAM.•Delocalized π-system was extended in g-C3N4-PAM.•g-C3N4-PAM exhibits higher photocatalytic activity.
Single layer g-C3N4 could be obtained from a protonic acid treatment of g-C3N4 or a new sandwich-like orientation growth of melamine. Through the self-assembly of melamine and polyacrylamide by hydrogen bonds and electrostatic interactions, g-C3N4, with extended planarized atomic single layer, exhibits superiority in both photocatalytic hydrogen evolution and photocatalytic degradation under visible light irradiation. Besides low efficiency, the acid exfoliation will destroy the delocalized π-system by inducing O atoms. The decrease of conjugation degree increases the optical gaps, making it hard for g-C3N4 to capture photons. On the contrary, the facile sandwich-like orientation growth of melamine highly keeps the conjugation degree of g-C3N4 and extends its delocalized π-system. Such single layer g-C3N4 is more active even better than N-doped TiO2 under visible light irradiation. |
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ISSN: | 0926-3373 1873-3883 |
DOI: | 10.1016/j.apcatb.2017.06.017 |