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Enhanced photodegradation activity of methyl orange over Z-scheme type MoO3–g-C3N4 composite under visible light irradiation
| Content Provider | Semantic Scholar |
|---|---|
| Author | He, Yiming Zhang, Lihong Wang, Xiaoxing Wu, Ying Lin, Hongjun Zhao, Leihong Weng, Weizheng Wan, Huilin Fan, Maohong |
| Copyright Year | 2014 |
| Abstract | Novel Z-scheme type MoO3–g-C3N4 composites photocatalysts were prepared with a simple mixing–calcination method, and evaluated for their photodegradation activities of methyl orange (MO). The optimized MoO3–g-C3N4 photocatalyst shows a good activity with a kinetic constant of 0.0177 min−1, 10.4 times higher than that of g-C3N4. Controlling various factors (MoO3–g-C3N4 amount, initial MO concentration, and pH value of MO solution) can lead to the enhancement of the photocatalytic activity of the composite. Only MoO3 and g-C3N4 are detected with X-ray diffraction (XRD) and Fourier transform infrared spectroscopy (FT-IR) spectra. N2 adsorption and UV-vis diffuse reflectance spectroscopy (DRS) results suggest that the addition of MoO3 slightly affects the specific surface area and the photoabsorption performance. The transmission electron microscopy (TEM) image of MoO3–g-C3N4 indicates a close contact between MoO3 and g-C3N4, which is beneficial to interparticle electron transfer. The high photocatalytic activity of MoO3–g-C3N4 is mainly attributed to the synergetic effect of MoO3 and g-C3N4 in electron–hole pair separation via the charge migration between the two semiconductors. The charge transfer follows direct Z-scheme mechanism, which is proven by the reactive species trapping experiment and the ˙OH-trapping photoluminescence spectra. |
| Starting Page | 13610 |
| Ending Page | 13619 |
| Page Count | 10 |
| File Format | PDF HTM / HTML |
| DOI | 10.1039/C4RA00693C |
| Volume Number | 4 |
| Alternate Webpage(s) | http://www.rsc.org/suppdata/ra/c4/c4ra00693c/c4ra00693c1.pdf |
| Alternate Webpage(s) | https://doi.org/10.1039/C4RA00693C |
| Language | English |
| Access Restriction | Open |
| Content Type | Text |
| Resource Type | Article |