Enhanced photocatalytic activity induced by sp 3 to sp 2 transition of carbon dopants in BiOCl crystals
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KAUST DepartmentPhysical Sciences and Engineering (PSE) Division
Permanent link to this recordhttp://hdl.handle.net/10754/625490
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AbstractThe insufficient light absorption and low quantum efficiency limit the photocatalytic performance of wide bandgap semiconductors. Here, we report a facile strategy to engineer the surface disordered defects of BiOCl nanosheets via carbon doping. The surface defects boost the light absorption and also the quantum yields, as the doped carbon atoms exhibit a transition from sp3 to sp2 hybridization at elevated temperature, corresponding to a change of assembly state from 3D cluster to 2D graphite-like structure. This transition results in an effective charge separation and thus one order of enhancement in photocatalytic activity toward phenol degradation under visible light. The current study opens an avenue to introduce sp3 to sp2 transition of carbon dopants for simultaneous increment of light absorption and quantum efficiency for application in photocatalysis and energy conversion.
CitationSun J, Wu S, Yang S-Z, Li Q, Xiong J, et al. (2017) Enhanced photocatalytic activity induced by sp 3 to sp 2 transition of carbon dopants in BiOCl crystals. Applied Catalysis B: Environmental. Available: http://dx.doi.org/10.1016/j.apcatb.2017.09.037.
SponsorsWe gratefully acknowledge the helpful and informative discussion with Prof. Zhipan Li, Dr. Yuan Yuan and Mr. Yuqi Zhang. This work was supported by the National Natural Science Foundation of China (No.51302329, 51501024) and the Fundamental Research Funds for the Central Universities (No.106112015CDJXY130010, 106112016CDJZR135506). The electron microscopy (S.Z.Y.) was supported by the U.S. Department of Energy, Office of Science, Basic Energy Sciences, Materials Science and Engineering Division. This research used resources of the National Energy Research Scientific Computing Center, a DOE Office of Science User Facility supported by the Office of Science of the U.S. Department of Energy under Contract No. DE-AC02-05CH11231. This work used the Extreme Science and Engineering Discovery Environment (XSEDE), which is supported by National Science Foundation Grant No ACI-1053575 and Grant No DMR160118.