Ordered mesoporous Fe/TiO2 was prepared by an evaporation-induced self-assembly method. The iron ions were in situ embedded in the pore wall of the TiO2 framework. The catalyst has excellent light-assisted Fenton cata...Ordered mesoporous Fe/TiO2 was prepared by an evaporation-induced self-assembly method. The iron ions were in situ embedded in the pore wall of the TiO2 framework. The catalyst has excellent light-assisted Fenton catalytic performance under UV and visible light irradiation. X-ray diffraction and transmission electron microscopy results showed that the TiO2 samples have an ordered two-dimensional hexagonal pore structure and an anatase phase structure with high crystallinity. The ordered pore structure of the TiO2 photocatalyst with a large specific surface area is beneficial to mass transfer and light harvesting. Furthermore, iron ions can be controlled by embedding them into the TiO2 framework to prevent iron ion loss and inactivation. After five cycles, the reaction rate of the ordered mesoporous Fe/TiO2 remained unchanged, indicating that the material has stable performance and broad application prospects for the purification of environmental pollutants.展开更多
Although the traditional Fenton reaction is considered an effective strategy for solving problems caused by environmental pollution,construction of an efficient photocatalytic system by coordinating the Fenton reactio...Although the traditional Fenton reaction is considered an effective strategy for solving problems caused by environmental pollution,construction of an efficient photocatalytic system by coordinating the Fenton reaction is challenging.In this study,2D/2D step-schemeα-Fe2O3/Bi2WO6(FO/BWO)heterostructure photo-Fenton catalysts were successfully fabricated by a facile hydrothermal method.The as-prepared materials were characterized by XRD,FT-IR,TEM,XPS,UV-vis DRS,PL,I-t,EIS,and BET analyses.Under visible light irradiation,FO/BWO exhibited remarkably high and stable photo-Fenton catalytic activity for the degradation of methyl blue(MB)at low concentrations of H2O2.It was noted that FO/BWO(0.5)displayed a significantly enhanced photo-Fenton catalytic activity,which was 11.06 and 3.29 times those of FO nanosheets and BWO nanosheets,respectively.The notably improved photo-Fenton catalytic activity of FO/BWO was mainly due to the combination of H2O2 and FO under light illumination and the presence of the 2D/2D S-scheme heterostructure,with the large contact surface,abundant active sites,and efficient separation rate of photogenerated carriers playing contributory roles.Additionally,a possible catalytic mechanism for the FO/BWO composite was preliminarily proposed via active species trapping experiments.In summary,this study provided new insights into the synthesis of an effectively heterogeneous 2D/2D S-scheme photo-Fenton catalyst for degradation of organic pollutants in wastewater.展开更多
In this work,a set of novel Cu2ZnSnS4/Bi2WO6(CZTS/BWO)two-dimensional(2 D)/two-dimensional(2 D)type-Ⅱheterojunctions with different CZTS weight ratios(1%,2%,and 5%)were successfully synthesized via a brief secondary ...In this work,a set of novel Cu2ZnSnS4/Bi2WO6(CZTS/BWO)two-dimensional(2 D)/two-dimensional(2 D)type-Ⅱheterojunctions with different CZTS weight ratios(1%,2%,and 5%)were successfully synthesized via a brief secondary solvothermal process.The successful formation of the heterojunctions was affirmed by characterization methods such as X-ray photoelectron spectroscopy and high-resolution transmission electron microscopy.The photocatalytic activity results showed that the prepared CZTS/BWO heterojunctions had excellent photocatalytic behaviors for organic degradation,especially when the mass fraction of CZTS with respect to BWO in the composite was 2%.Moreover,the addition of hydrogen peroxide(H2O2)could further improve the dye and antibiotic degradation efficiencies.The reinforced photocatalytic and photo-Fenton degradation performance were primarily attributable to the introduction of BWO,which afforded increased active sites,expanded the solar spectral response range,and accelerated the cycle of Cu(Ⅱ)/Cu(Ⅰ);after four cycling times,its catalytic activity did not decrease significantly.In addition,reasonable hypotheses of the photocatalytic and photo-Fenton catalytic mechanisms were formulated.This study is expected to provide a visual approach for designing a novel photo-Fenton catalyst to jointly utilize the photocatalytic and Fenton activities,which can be better applied to the purification of residual organics in wastewater.展开更多
Iron oxide（Fe2O3） was doped onto fullerene[60]（C（60）） to form a C（60）‐Fe2O3 composite using an easy and scalable impregnation method. The as‐prepared C（60）‐Fe2O3 samples were characterized by powder X‐ra...Iron oxide（Fe2O3） was doped onto fullerene[60]（C（60）） to form a C（60）‐Fe2O3 composite using an easy and scalable impregnation method. The as‐prepared C（60）‐Fe2O3 samples were characterized by powder X‐ray diffraction, X‐ray photoelectron spectroscopy, scanning electron microscopy, high‐resolution transmission electron microscopy, UV‐vis absorption spectroscopy, Raman spec‐troscopy, and Fourier transform infrared spectroscopy. The photocatalytic activity of the C（60）‐Fe2O3 catalyst was evaluated by examining the degradation of methylene blue（MB）, rhodamine B（RhB）, methyl orange（MO）, and phenol under visible light（λ 420 nm） in the presence of hydrogen per‐oxide. The results showed that the catalyst exhibited excellent catalytic properties over a wide pH range 3.06–10.34. Under optimal conditions, 98.9% discoloration and 71% mineralization of MB were achieved in 80 min. Leaching test results indicated that the leaching of iron from the catalyst was negligible and that the catalyst had a high photocatalytic activity after five reaction cycles. The catalyst was also efficient in the degradation of RhB, MO, and phenol. These findings could be at‐tributed to the synergetic effects of C（60） and Fe2O3. We used active species trapping experiments to determine the main active oxidant in the photocatalytic reaction process and found that hydroxyl radicals played a major role in the entire process.展开更多
基金supported by the National Natural Science Foundation of China(21347006)Natural Science Foundation of Jiangsu Province,China(BK20141178)+2 种基金Opening Project of Key Laboratory of Green Chemistry of Sichuan Institutes of Higher Education,China(LZJ1304)Natural Science Foundation of the Jiangsu Higher School of China(12KJA430005)Earmarked Nanotechnology Fund of the Bureau of Science and Technology of Suzhou,China(ZXG201429)~~
基金supported by the National Natural Science Foundation of China(21876114,21761142011,51572174)Shanghai Government(17SG44)+2 种基金International Joint Laboratory on Resource Chemistry(IJLRC)Ministry of Education of China(PCSIRT_IRT_16R49)supported by The Program for Professor of Special Appointment(Eastern Scholar)at Shanghai Institutions of Higher Learning and Shuguang Research Program of Shanghai Education Committee~~
文摘Ordered mesoporous Fe/TiO2 was prepared by an evaporation-induced self-assembly method. The iron ions were in situ embedded in the pore wall of the TiO2 framework. The catalyst has excellent light-assisted Fenton catalytic performance under UV and visible light irradiation. X-ray diffraction and transmission electron microscopy results showed that the TiO2 samples have an ordered two-dimensional hexagonal pore structure and an anatase phase structure with high crystallinity. The ordered pore structure of the TiO2 photocatalyst with a large specific surface area is beneficial to mass transfer and light harvesting. Furthermore, iron ions can be controlled by embedding them into the TiO2 framework to prevent iron ion loss and inactivation. After five cycles, the reaction rate of the ordered mesoporous Fe/TiO2 remained unchanged, indicating that the material has stable performance and broad application prospects for the purification of environmental pollutants.
文摘Although the traditional Fenton reaction is considered an effective strategy for solving problems caused by environmental pollution,construction of an efficient photocatalytic system by coordinating the Fenton reaction is challenging.In this study,2D/2D step-schemeα-Fe2O3/Bi2WO6(FO/BWO)heterostructure photo-Fenton catalysts were successfully fabricated by a facile hydrothermal method.The as-prepared materials were characterized by XRD,FT-IR,TEM,XPS,UV-vis DRS,PL,I-t,EIS,and BET analyses.Under visible light irradiation,FO/BWO exhibited remarkably high and stable photo-Fenton catalytic activity for the degradation of methyl blue(MB)at low concentrations of H2O2.It was noted that FO/BWO(0.5)displayed a significantly enhanced photo-Fenton catalytic activity,which was 11.06 and 3.29 times those of FO nanosheets and BWO nanosheets,respectively.The notably improved photo-Fenton catalytic activity of FO/BWO was mainly due to the combination of H2O2 and FO under light illumination and the presence of the 2D/2D S-scheme heterostructure,with the large contact surface,abundant active sites,and efficient separation rate of photogenerated carriers playing contributory roles.Additionally,a possible catalytic mechanism for the FO/BWO composite was preliminarily proposed via active species trapping experiments.In summary,this study provided new insights into the synthesis of an effectively heterogeneous 2D/2D S-scheme photo-Fenton catalyst for degradation of organic pollutants in wastewater.
基金supported by the National Natural Science Foundation of China(21663030,21666039)the Open Project of State Key Laboratory of Organic-Inorganic Composites Beijing Key Laboratory,Beijing University of Chemical Technology(oic-201901009)+2 种基金the Project of Science&Technology Office of Shannxi Province(2018TSCXL-NY-02-01,2013K11-08,2013SZS20-P01)Industrial Key Project of Yan’an Science and Technology Bureau(2018KG-04)the Project of Yan’an Science Graduate Innovation Project of Yan’an University(YCX201988)~~
文摘In this work,a set of novel Cu2ZnSnS4/Bi2WO6(CZTS/BWO)two-dimensional(2 D)/two-dimensional(2 D)type-Ⅱheterojunctions with different CZTS weight ratios(1%,2%,and 5%)were successfully synthesized via a brief secondary solvothermal process.The successful formation of the heterojunctions was affirmed by characterization methods such as X-ray photoelectron spectroscopy and high-resolution transmission electron microscopy.The photocatalytic activity results showed that the prepared CZTS/BWO heterojunctions had excellent photocatalytic behaviors for organic degradation,especially when the mass fraction of CZTS with respect to BWO in the composite was 2%.Moreover,the addition of hydrogen peroxide(H2O2)could further improve the dye and antibiotic degradation efficiencies.The reinforced photocatalytic and photo-Fenton degradation performance were primarily attributable to the introduction of BWO,which afforded increased active sites,expanded the solar spectral response range,and accelerated the cycle of Cu(Ⅱ)/Cu(Ⅰ);after four cycling times,its catalytic activity did not decrease significantly.In addition,reasonable hypotheses of the photocatalytic and photo-Fenton catalytic mechanisms were formulated.This study is expected to provide a visual approach for designing a novel photo-Fenton catalyst to jointly utilize the photocatalytic and Fenton activities,which can be better applied to the purification of residual organics in wastewater.
基金supported by the National Natural Science Foundation of China (21347006, 21576175, 51478285, 51403148)the Opening Project of Key Laboratory of Jiangsu Province environmental science and engineering of Suzhou University of Science and Technology (zd131205)Collabora‐tive Innovation Center of Technology and Material of Water Treatment and Suzhou Key Lab of Separation and Purification Materials & Technologies (SZS201512)~~
文摘Iron oxide（Fe2O3） was doped onto fullerene[60]（C（60）） to form a C（60）‐Fe2O3 composite using an easy and scalable impregnation method. The as‐prepared C（60）‐Fe2O3 samples were characterized by powder X‐ray diffraction, X‐ray photoelectron spectroscopy, scanning electron microscopy, high‐resolution transmission electron microscopy, UV‐vis absorption spectroscopy, Raman spec‐troscopy, and Fourier transform infrared spectroscopy. The photocatalytic activity of the C（60）‐Fe2O3 catalyst was evaluated by examining the degradation of methylene blue（MB）, rhodamine B（RhB）, methyl orange（MO）, and phenol under visible light（λ 420 nm） in the presence of hydrogen per‐oxide. The results showed that the catalyst exhibited excellent catalytic properties over a wide pH range 3.06–10.34. Under optimal conditions, 98.9% discoloration and 71% mineralization of MB were achieved in 80 min. Leaching test results indicated that the leaching of iron from the catalyst was negligible and that the catalyst had a high photocatalytic activity after five reaction cycles. The catalyst was also efficient in the degradation of RhB, MO, and phenol. These findings could be at‐tributed to the synergetic effects of C（60） and Fe2O3. We used active species trapping experiments to determine the main active oxidant in the photocatalytic reaction process and found that hydroxyl radicals played a major role in the entire process.
