Enhanced visible light photocatalytic hydrogen evolution via cubic CeO2 hybridized g-C3N4 composite
[Display omitted] •Nanocubic CeO2 {100} plane hybridized g-C3N4 composites were synthesized.•cCN5 had superior photocatalytic performance, for advantageous interfacial effects.•The interfacial effects of cCN catalysts were via hydrogen bond and p-π hybrid.•The possible photocatalytic mechanism was p...
Saved in:
Published in | Applied catalysis. B, Environmental Vol. 218; pp. 51 - 59 |
---|---|
Main Authors | , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
Elsevier B.V
05.12.2017
|
Subjects | |
Online Access | Get full text |
Cover
Loading…
Summary: | [Display omitted]
•Nanocubic CeO2 {100} plane hybridized g-C3N4 composites were synthesized.•cCN5 had superior photocatalytic performance, for advantageous interfacial effects.•The interfacial effects of cCN catalysts were via hydrogen bond and p-π hybrid.•The possible photocatalytic mechanism was proposed.
In this work, CeO2 nanocubes hybridized g-C3N4 composites had been facilely synthesized to investigate the interfacial effects on photocatalytic water splitting. The c-CeO2/g-C3N4 composites exhibited the superior photocatalytic hydrogen evolution under visible light irradiation. The optimal c-CeO2 loading content was 5wt%, with the H2 evolution of 4300μmolg−1 for 5h illumination, higher than that of pristine CeO2, g-C3N4 and irregular CeO2 nanoparticles/g-C3N4. Moreover, UV–vis DRS, PL spectra and photoelectrochemical measurements demonstrated that 5wt% c-CeO2/g-C3N4 composite possessed more visible light adsorption and faster charge transfer, which was attributed to the stronger interfacial effects through the presence of the hydrogen bond and p-π hybrid between c-CeO2 {100} and g-C3N4, revealed by the FT-IR and XPS results. The work suggested that engineering the structures of the CeO2 and g-C3N4 interface could be an effective strategy to obtain excellent photocatalysts. |
---|---|
ISSN: | 0926-3373 1873-3883 |
DOI: | 10.1016/j.apcatb.2017.03.085 |