The porous NiO nanoplates modified with rGO nanosheets and SnO_(2)nanoparticles are developed for accurate and rapid ppb-level NO_(2)detection.The developed SnO_(2)/NiO/rGO sensor towards 50 ppm NO_(2)gas demonstrates...The porous NiO nanoplates modified with rGO nanosheets and SnO_(2)nanoparticles are developed for accurate and rapid ppb-level NO_(2)detection.The developed SnO_(2)/NiO/rGO sensor towards 50 ppm NO_(2)gas demonstrates an excellent gas-sensing response of 14.8 at 23℃,which is 3.03 times that of Ni O/rGO sensor(4.89)and 6.49 times that of NiO sensor(2.28),respectively.The developed SnO_(2)/NiO/rGO sensor exhibits faster response/recovery speed(12.7/32.8 s@5 ppm),with extra-low theoretical detection limit of 0.15 ppb at room temperature.More fascinatingly,our sensors indicate great sensitivity,outstanding repeatability and long-term stability for longer than 7 weeks.Additionally,it also suggests that 1℃and 1%relative humidity have the same effect on the SnO_(2)/NiO/rGO sensor signal as approximately 13 ppb and 7.0 ppb NO_(2)gas change,respectively.Such excellent properties are mainly attributed to the large surface-to-volume ratio,which provides active sites to NO_(2)gas spread,adsorption and diffusion on material surface in redox reaction.Moreover,the ternary heterojunctions formed by NiO,rGO and SnO_(2)may serve as highly conductive channels to accelerate carrier transfer and abundant oxygen vacancies to reduce the adsorption energy for O_(2)and NO_(2)gas,thus further improving performance of the sensors.展开更多
The limited redox capability of photocatalysts often leads to harmful NO_(2) byproduct formation during photocatalytic NO oxidation.Herein,Bi_(4)Ti_(3)O_(12) nanosheets modified with plasmonic metallic bismuth and abu...The limited redox capability of photocatalysts often leads to harmful NO_(2) byproduct formation during photocatalytic NO oxidation.Herein,Bi_(4)Ti_(3)O_(12) nanosheets modified with plasmonic metallic bismuth and abundant oxygen vacancies were synthesized via an in-situ reduction method.The optimized catalyst(BTOR2,with a molar ratio of 40%NaBH_(4) to Bi_(4)Ti_(3)O_(12))achieved a maximum NO removal efficiency of 62.3%,significantly higher than pristine Bi_(4)Ti_(3)O_(12)(40.5%) while minimizing NO_(2) production.The results reveal that the synergistic effects of Bi’s plasmonic resonance and oxygen vacancies enhanced visible light absorption and charge separation.The density functional theory(DFT)analysis showed electrons can transfer from Bi_(4)Ti_(3)O_(12)to Bi,promoting O_(2)activation to·O_(2)^(-)radicals.In-situ diffuse reflectance infrared Fourier transform spectroscopy(DRIFTS)confirmed that light-induced H2O adsorption was strengthened,improving·OH radical generation.These radicals promoted the selective conversion of activated NO^(-) to NO_(3)^(-),rather than NO_(2).This work provides valuable insights for advancing research into efficient photocatalysts for air pollution control.展开更多
基金funded by the National Natural Science Foundation of China(No.62364002)Key Scientific Research Projects of Universities in Henan Province(No.24A510014)+5 种基金Xinjiang-Changji Vocational Education Alliance Special Project(No.2050305)National Laboratory of Solid State Microstructures,Nanjing University(No.M36001)Jiangsu Key Laboratory of Optoelectronic Information Functional Materials,Nanjing University(No.ndgd2024005)Henan Province Higher Education College Student Innovation Training Program Project(No.202410478019)the Doctoral Research Initiation Fund Project,Zhoukou Normal University(No.ZKNUC2022018)the Natural Science Foundation Project of Xinjiang Uygur Autonomous Region(No.2022D01C006)。
文摘The porous NiO nanoplates modified with rGO nanosheets and SnO_(2)nanoparticles are developed for accurate and rapid ppb-level NO_(2)detection.The developed SnO_(2)/NiO/rGO sensor towards 50 ppm NO_(2)gas demonstrates an excellent gas-sensing response of 14.8 at 23℃,which is 3.03 times that of Ni O/rGO sensor(4.89)and 6.49 times that of NiO sensor(2.28),respectively.The developed SnO_(2)/NiO/rGO sensor exhibits faster response/recovery speed(12.7/32.8 s@5 ppm),with extra-low theoretical detection limit of 0.15 ppb at room temperature.More fascinatingly,our sensors indicate great sensitivity,outstanding repeatability and long-term stability for longer than 7 weeks.Additionally,it also suggests that 1℃and 1%relative humidity have the same effect on the SnO_(2)/NiO/rGO sensor signal as approximately 13 ppb and 7.0 ppb NO_(2)gas change,respectively.Such excellent properties are mainly attributed to the large surface-to-volume ratio,which provides active sites to NO_(2)gas spread,adsorption and diffusion on material surface in redox reaction.Moreover,the ternary heterojunctions formed by NiO,rGO and SnO_(2)may serve as highly conductive channels to accelerate carrier transfer and abundant oxygen vacancies to reduce the adsorption energy for O_(2)and NO_(2)gas,thus further improving performance of the sensors.
基金supported by the Natural Science Foundation of Chongqing(Nos.CSTB2024NSCQ-MSX1278,CSTB2023NSCQ-MSX0006)Technology Innovation Project of Shapingba District,Chongqing(No.2024004)+2 种基金Science and Technology Research Program of Chongqing Municipal Education Commission(Nos.KJZD-K202403102,KJQN202103110,KJQN202400512,KJQN202403107)National Natural Science Foundation of China(No.22406014)China Postdoctoral Science Foundation(No.2023MD744137).
文摘The limited redox capability of photocatalysts often leads to harmful NO_(2) byproduct formation during photocatalytic NO oxidation.Herein,Bi_(4)Ti_(3)O_(12) nanosheets modified with plasmonic metallic bismuth and abundant oxygen vacancies were synthesized via an in-situ reduction method.The optimized catalyst(BTOR2,with a molar ratio of 40%NaBH_(4) to Bi_(4)Ti_(3)O_(12))achieved a maximum NO removal efficiency of 62.3%,significantly higher than pristine Bi_(4)Ti_(3)O_(12)(40.5%) while minimizing NO_(2) production.The results reveal that the synergistic effects of Bi’s plasmonic resonance and oxygen vacancies enhanced visible light absorption and charge separation.The density functional theory(DFT)analysis showed electrons can transfer from Bi_(4)Ti_(3)O_(12)to Bi,promoting O_(2)activation to·O_(2)^(-)radicals.In-situ diffuse reflectance infrared Fourier transform spectroscopy(DRIFTS)confirmed that light-induced H2O adsorption was strengthened,improving·OH radical generation.These radicals promoted the selective conversion of activated NO^(-) to NO_(3)^(-),rather than NO_(2).This work provides valuable insights for advancing research into efficient photocatalysts for air pollution control.
