Enhanced photocatalytic activity by the construction of a TiO2/carbon nitride nanosheets heterostructure with high surface area via direct interfacial assembly
),
Tianyou Peng2(
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A TiO2 heterostructure modified with carbon nitride nanosheets (CN-NSs) has been synthesized via a direct interfacial assembly strategy. The CN-NSs, which have a unique two-dimensional structure, were favorable for supporting TiO2 nanoparticles (NPs). The uniform dispersion of TiO2 NPs on the surface of the CN-NSs creates sufficient interfacial contact at their nanojunctions, as was confirmed by electron microscopy analyses. In comparison with other reported metal oxide/CN composites, the strong interactions of the ultrathin CN-NSs layers with the TiO2 nanoparticles restrain their re-stacking, which results in a large specific surface area of 234.0 m2·g-1. The results indicate that the optimized TiO2/CN-NSs hybrid exhibits remarkably enhanced photocatalytic efficiency for dye degradation (with k of 0.167 min-1 under full spectrum) and H2 production (with apparent quantum yield = 38.4% for λ = 400 ± 15 nm monochromatic light). This can be ascribed to the improved surface area and quantum efficiency of the hybrid, with a controlled ratio that reaches the appropriate balance between producing sufficient nanojunctions and absorbing enough photons. Furthermore, based on the identification of the main active species for photodegradation, and the confirmation of active sites for H2 evolution, the charge transfer pathway across the TiO2/CN-NSs interface under simulated solar light is proposed.
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Enhanced photocatalytic activity by the construction of a TiO2/carbon nitride nanosheets heterostructure with high surface area via direct interfacial assembly
), Tianyou Peng2(
)
Abstract
A TiO2 heterostructure modified with carbon nitride nanosheets (CN-NSs) has been synthesized via a direct interfacial assembly strategy. The CN-NSs, which have a unique two-dimensional structure, were favorable for supporting TiO2 nanoparticles (NPs). The uniform dispersion of TiO2 NPs on the surface of the CN-NSs creates sufficient interfacial contact at their nanojunctions, as was confirmed by electron microscopy analyses. In comparison with other reported metal oxide/CN composites, the strong interactions of the ultrathin CN-NSs layers with the TiO2 nanoparticles restrain their re-stacking, which results in a large specific surface area of 234.0 m2·g-1. The results indicate that the optimized TiO2/CN-NSs hybrid exhibits remarkably enhanced photocatalytic efficiency for dye degradation (with k of 0.167 min-1 under full spectrum) and H2 production (with apparent quantum yield = 38.4% for λ = 400 ± 15 nm monochromatic light). This can be ascribed to the improved surface area and quantum efficiency of the hybrid, with a controlled ratio that reaches the appropriate balance between producing sufficient nanojunctions and absorbing enough photons. Furthermore, based on the identification of the main active species for photodegradation, and the confirmation of active sites for H2 evolution, the charge transfer pathway across the TiO2/CN-NSs interface under simulated solar light is proposed.
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Acknowledgements
We thank the Analysis and Testing Center, Huazhong University of Science and Technology for their assistance in characterization of materials. This work is supported by the National Natural Science Foundation of China (No. 21571071), Hubei Provincial Natural Science Foundation of China (No. 2015CFB313), and the Fundamental Research Funds for the Central Universities (No. 2015QN183).
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