The polystyrene（PS） microspheres were prepared from free radical polymerization of styrene by a sol-gel method combined with centrifugal sedimentation. And the ordered macroporous titania was prepared from Ti（BuO）...The polystyrene（PS） microspheres were prepared from free radical polymerization of styrene by a sol-gel method combined with centrifugal sedimentation. And the ordered macroporous titania was prepared from Ti（BuO）4 in ethanol solution using the mentioned PS microspheres as a template, which was removed from titania by calcination at 450 ℃. SEM images revealed the PS template has a three-dimentional ordered structure with particle diameter of ca. 450 nm and the macroporous titania thus obtained has a pore size of ca. 300 nm. XRD showed the macroporous titania has anatase structure.展开更多
An immobilized Cu2O/g-C3N4 heterojunction film was successfully made on an FTO substrate by electrophoretic deposition of g-C3N4 on a Cu2O thin film.The photoelectrochemical（PEC） performance for water splitting by t...An immobilized Cu2O/g-C3N4 heterojunction film was successfully made on an FTO substrate by electrophoretic deposition of g-C3N4 on a Cu2O thin film.The photoelectrochemical（PEC） performance for water splitting by the Cu2O/g-C3N4 film was better than pure g-C3N4 and pure Cu2O film.Under-0.4 V external bias and visible light irradiation,the photocurrent density and PEC hydrogen evolution efficiency of the optimized Cu2O/g-C3N4 film was-1.38 mA/cm^2 and 0.48 mL h^-1 cm^-2,respectively.The enhanced PEC performance of Cu2O/g-C3N4 was attributed to the synergistic effect of light coupling and a matching energy band structure between g-C3N4 and Cu2O as well as the external bias.展开更多
As a green and sustainable technology,heterogeneous photocatalysis using semiconductors has received much attention during the past decades because of its potential to address energy and environmental problems. Among ...As a green and sustainable technology,heterogeneous photocatalysis using semiconductors has received much attention during the past decades because of its potential to address energy and environmental problems. Among various semiconductors,TiO2 has been regarded as the best and most widely investigated photocatalyst in the past 10 years. Based on the fundamentals of photocatalysis and surface chemistry of TiO2 nanomaterials,we herein summarize and discuss the achievements in the different surface modification strategies employed to date such as surface doping and sensitization,construction of surface heterojunctions,loading of nano-sized co-catalysts,increase in the accessible surface areas,and usage of surface F effects and exposure of highly reactive facets. Especially,the interesting synergistic effects of these different surface modification strategies deserve more attention in the near future. Studying these important advances in photocatalysis fundamentals,and surface chemistry and modification may offer new opportunities for designing highly efficient TiO2-based and non-TiO2-based photocatalysts for solar fuel production,environmental remediation,organic photosynthesis,and other related fields such as solar cell device fabrication,thermal catalysis,and separation and purification.展开更多
Novel WO3/g-C3N4/Ni（OH）x hybrids have been successfully synthesized by a two-step strategy of high temperature calcination and in situ photodeposition.Their photocatalytic performance was investigated using TEOA as ...Novel WO3/g-C3N4/Ni（OH）x hybrids have been successfully synthesized by a two-step strategy of high temperature calcination and in situ photodeposition.Their photocatalytic performance was investigated using TEOA as a hole scavenger under visible light irradiation.The loading of WO3 and Ni（OH）x cocatalysts boosted the photocatalytic H2 evolution efficiency of g-C3N4.WO3/g-C3N4/Ni（OH）x with 20 wt%defective WO3 and 4.8 wt%Ni（OH）x showed the highest hydrogen production rate of 576 μmol/（g·h）,which was 5.7,10.8 and 230 times higher than those of g-C3N4/4.8 wt%Ni（OH）x,20 wt%WO3/C3N4 and g-C3N4 photocatalysts,respectively.The remarkably enhanced H2 evolution performance was ascribed to the combination effects of the Z-scheme heterojunction（WO3/g-C3N4） and loaded cocatalysts（Ni（OH）x）,which effectively inhibited the recombination of the photoexcited electron-hole pairs of g-C3N4 and improved both H2 evolution and TEOA oxidation kinetics.The electron spin resonance spectra of ·O2^- and ·OH radicals provided evidence for the Z-scheme charge separation mechanism.The loading of easily available Ni（OH）x cocatalysts on the Z-scheme WO3/g-C3N4 nanocomposites provided insights into constructing a robust multiple-heterojunction material for photocatalytic applications.展开更多
文摘The polystyrene（PS） microspheres were prepared from free radical polymerization of styrene by a sol-gel method combined with centrifugal sedimentation. And the ordered macroporous titania was prepared from Ti（BuO）4 in ethanol solution using the mentioned PS microspheres as a template, which was removed from titania by calcination at 450 ℃. SEM images revealed the PS template has a three-dimentional ordered structure with particle diameter of ca. 450 nm and the macroporous titania thus obtained has a pore size of ca. 300 nm. XRD showed the macroporous titania has anatase structure.
基金supported by the National Natural Science Foundation of China (21173088)the Science and Technology Project of Guangdong Province (2014A030312007, 2015A050502012, 2016A010104013)+1 种基金the China Postdoctoral Science Foundation (2016M592493)the Open Research Fund of Hunan Key Laboratory of Applied Environmental Photocatalysis (CCSU-XT-06),Changsha University~~
文摘An immobilized Cu2O/g-C3N4 heterojunction film was successfully made on an FTO substrate by electrophoretic deposition of g-C3N4 on a Cu2O thin film.The photoelectrochemical（PEC） performance for water splitting by the Cu2O/g-C3N4 film was better than pure g-C3N4 and pure Cu2O film.Under-0.4 V external bias and visible light irradiation,the photocurrent density and PEC hydrogen evolution efficiency of the optimized Cu2O/g-C3N4 film was-1.38 mA/cm^2 and 0.48 mL h^-1 cm^-2,respectively.The enhanced PEC performance of Cu2O/g-C3N4 was attributed to the synergistic effect of light coupling and a matching energy band structure between g-C3N4 and Cu2O as well as the external bias.
基金supported by the Industry and Research Collaborative Innovation Major Projects Of Guangzhou(201508020098)the National Natural Science Foundation of China(20906034+2 种基金21173088and 21207041)the State Key Laboratory of Advanced Technology for Material Synthesis and Processing,Wuhan University of Technology(2015-KF-7)~~
文摘As a green and sustainable technology,heterogeneous photocatalysis using semiconductors has received much attention during the past decades because of its potential to address energy and environmental problems. Among various semiconductors,TiO2 has been regarded as the best and most widely investigated photocatalyst in the past 10 years. Based on the fundamentals of photocatalysis and surface chemistry of TiO2 nanomaterials,we herein summarize and discuss the achievements in the different surface modification strategies employed to date such as surface doping and sensitization,construction of surface heterojunctions,loading of nano-sized co-catalysts,increase in the accessible surface areas,and usage of surface F effects and exposure of highly reactive facets. Especially,the interesting synergistic effects of these different surface modification strategies deserve more attention in the near future. Studying these important advances in photocatalysis fundamentals,and surface chemistry and modification may offer new opportunities for designing highly efficient TiO2-based and non-TiO2-based photocatalysts for solar fuel production,environmental remediation,organic photosynthesis,and other related fields such as solar cell device fabrication,thermal catalysis,and separation and purification.
基金supported by the National Natural Science Foundation of China (51672089)the Industry and Research Collaborative Innovation Major Projects of Guangzhou (201508020098)+1 种基金the State Key Laboratory of Advanced Technology for Material Synthesis and Processing (Wuhan University of Technology) (2015-KF-7)the Hunan Key Laboratory of Applied Environmental Photocatalysis (Changsha University) (CCSU-XT-04)~~
文摘Novel WO3/g-C3N4/Ni（OH）x hybrids have been successfully synthesized by a two-step strategy of high temperature calcination and in situ photodeposition.Their photocatalytic performance was investigated using TEOA as a hole scavenger under visible light irradiation.The loading of WO3 and Ni（OH）x cocatalysts boosted the photocatalytic H2 evolution efficiency of g-C3N4.WO3/g-C3N4/Ni（OH）x with 20 wt%defective WO3 and 4.8 wt%Ni（OH）x showed the highest hydrogen production rate of 576 μmol/（g·h）,which was 5.7,10.8 and 230 times higher than those of g-C3N4/4.8 wt%Ni（OH）x,20 wt%WO3/C3N4 and g-C3N4 photocatalysts,respectively.The remarkably enhanced H2 evolution performance was ascribed to the combination effects of the Z-scheme heterojunction（WO3/g-C3N4） and loaded cocatalysts（Ni（OH）x）,which effectively inhibited the recombination of the photoexcited electron-hole pairs of g-C3N4 and improved both H2 evolution and TEOA oxidation kinetics.The electron spin resonance spectra of ·O2^- and ·OH radicals provided evidence for the Z-scheme charge separation mechanism.The loading of easily available Ni（OH）x cocatalysts on the Z-scheme WO3/g-C3N4 nanocomposites provided insights into constructing a robust multiple-heterojunction material for photocatalytic applications.
