WO2 and TiO2 colMds were synthesized by the hydrolysis technique and part of the TiO2 colloid was treated by means of the hydrothermal method. The photochromic performances of the resulting materials obtained via comb...WO2 and TiO2 colMds were synthesized by the hydrolysis technique and part of the TiO2 colloid was treated by means of the hydrothermal method. The photochromic performances of the resulting materials obtained via combining the WO3 colloid with the treated TiO2 colloid and the non-treated TiO2 colloid, respectively, are very different. The TiO2 colloid without hydrothermal treatment can effectively improve the photochromic performance of the WO3colloid. The TiO2 nanoparticles were investigated in detail by XRD, TEM, surface photovohage spectra(SPS) and field-induced surface photovoltage spectrometry(FISPS). The photochromism mechanism of WO3 colloid is discussed.展开更多
In this work, we developed a templated self-assembly approach to fabricate self-supporting Au/TiO2 binary nanoparticles-nanotubes (NPNTs) for the first time. The stable Au/TiO2 nanoparticles colloids were pre-synthe...In this work, we developed a templated self-assembly approach to fabricate self-supporting Au/TiO2 binary nanoparticles-nanotubes (NPNTs) for the first time. The stable Au/TiO2 nanoparticles colloids were pre-synthesized and then deposited onto an AAO template, following by a mild calcination process. Au/TiO2 binary NPNTs can be achieved after removing the AAO template by NaOH solution. In addition, Au/TiO2 NPNTs with different thicknesses and size distributions could be achieved by tailoring the process parameters, such as the molar ratio of AuNPs to TiO2NPs, deposition modes and calcinations conditions. Therefore, these findings made controllable formation of Au/TiO2 NPNTs attractive for promising fabrication methodologies of metal/metal oxides NPNTs.展开更多
TiO2 nanotubes were prepared under normal pressure at a temperature of 120 ℃. Ag, Au, Pt nanoparticles supported on TiO2 nanotubes were prepared by m icrowave assisted heating polyol process. TEM images showed that m...TiO2 nanotubes were prepared under normal pressure at a temperature of 120 ℃. Ag, Au, Pt nanoparticles supported on TiO2 nanotubes were prepared by m icrowave assisted heating polyol process. TEM images showed that microwave prepa red Ag, Au, Pt nanoparticles supported on TiO2 nanotubes were small and well dis persed on the surface of the TiO2 nanotubes. UV-Vis absorption spectra showed th at the absorbance of Ag/TiO2 nanotubes and Au/TiO2 nanotubes in the visible ligh t range increased greatly compared to the single titania nanotubes.展开更多
Due to increasingly serious environmental problems,many researchers are investigating green cleanenergy to solve the world’s energy supply issues.So the strategy that Au nanoparticles(Au NPs)and bismuth sulfide(Bi2S3...Due to increasingly serious environmental problems,many researchers are investigating green cleanenergy to solve the world’s energy supply issues.So the strategy that Au nanoparticles(Au NPs)and bismuth sulfide(Bi2S3)NPs are used to evenly decorate TiO2 nanotube arrays(TiO2 NTAs)was carried out.Composite materials demonstrated enhanced solar light absorption ability and excellent photoelectrochemical performance.This was attributed to the presence of Bi2S3 NPs with a narrow band gap and the decoration with noble metallic Au NPs which resulted in local surface plasmon resonance(LSPR)effects.The Au/Bi2S3@TiO2 NTAs composites exhibit improved photocatalytic activity for the degradation of methylene blue(MB)under irradiation of UV and visible light.Moreover,the Au/Bi2S3@TiO2 NTAs exhibits high fluorescence emission at 822 nm.Due to the better binding affinity between Bi2S3,TiO2 and Fe3+ions,the synthesized nanocomposites exhibit high selectivity to Fe3+ions.The number of binding sites for Au/Bi2S3@TiO2 NTAs was estimated to be 1.41 according to the double logarithmic regression method.The calculated value of"K"was 1862 M-1.Fluorescence emission intensity decreases with increasing concentration(30μM–5000μM).The detection limit of the synthesized sensor is 0.221μM.展开更多
Cold plasma generated by dielectric barrier discharge (DBD) at atmospheric pressure was adopted for preparation of commercial TiO2 Degussa P25 supported Au catalysts (Au/P25- P) with the assistance of the depositi...Cold plasma generated by dielectric barrier discharge (DBD) at atmospheric pressure was adopted for preparation of commercial TiO2 Degussa P25 supported Au catalysts (Au/P25- P) with the assistance of the deposition-precipitation procedure. The influences of the plasma reduction time and calcination on the performance of the Au/P25-P catalysts were investigated. CO oxidation was performed to investigate the catalytic activity of the Au/P25 catalysts. The results show that DBD cold plasma for the fabrication of Au/P25-P catalysts is a fast process, and Au/P25-P (4 min) exhibited the highest CO oxidation activity due to the complete reduction of Au compounds and less consumption of oxygen vacancies. In order to form more oxygen vacancies active species, Au/P25-P was calcined to obtain Au/P25-PC catalysts. Interestingly, Au/P25- PC exhibited the highest activity for CO oxidation among the Au/P25 samples. The results of transmission electron microscopy (TEM) indicated that the smaller size and high distribution of Au nanoparticles are the mean reasons for a high performance of Au/P25-PC. Atmospheric- pressure DBD cold plasma was proved to be of great efficiency in preparing high performance supported Au catalysts.展开更多
Anatase TiO2 nanocrystals and sub-microcrystals with truncated octahedral bipyramidal morphologies were prepared by direct calcination of TiOF2 precursors. The as-prepared TiO2 samples were thoroughly characterized by...Anatase TiO2 nanocrystals and sub-microcrystals with truncated octahedral bipyramidal morphologies were prepared by direct calcination of TiOF2 precursors. The as-prepared TiO2 samples were thoroughly characterized by X-ray diffraction, Raman spectroscopy, field-emission scanning electron microscopy, N2 adsorption-desorption isotherms, X-ray photoelectron spectroscopy, and UV-visible diffuse spectroscopy. It was found that the crystallinity, grain size, and {001}/{101} ratio of the samples can be increased by raising the calcination temperature from 500 to 800℃. The higher crystallinity and {001}/{101} facet ratio resulted in an increase in both aqueous and gas-phase photocatalytic activities, by inhibiting the recombination and separation of electrons and holes. After selecting two TiO2 samples with high crystallinity and {001}/{101} ratio, Au nanoparticles were decorated on their surfaces, and the photocatalytic activity of the resulting samples under visible light illumination was studied. It was found that the visible light-induced photocatalytic activity increased by 2.6 and 4.8 times, respectively, upon Au decoration of the samples prepared by calcination of TiOF2 at 700 and 800℃.展开更多
Highly ordered TiO2 nanotube array (TNA) films are fabricated by using an anodic oxidation method. Au nanoparticles (NPs) films are decorated onto the top of TNA films with the aid of ion-sputtering and thermal an...Highly ordered TiO2 nanotube array (TNA) films are fabricated by using an anodic oxidation method. Au nanoparticles (NPs) films are decorated onto the top of TNA films with the aid of ion-sputtering and thermal annealing. An enhanced photocatalytic activity under ultraviolet C (UVC, 266 nm) light irradiation is obtained compared with that of the pristine TNA, which is shown by the steady-state photoluminescence (PL) spectra. Furthermore, a distinct blue shift in the nanosecond time-resolved transient photoluminescence (NTRT-PL) spectra is observed. Such a phenomenon could be well explained by considering the competition between the surface photocatalytic process and the recombination of the photo-generated carriers. The enhanced UV photocatalytic activities of the Au-TNA composite are evaluated through photo-degradation of methyl orange (MO) in an aqueous solution with ultraviolet-visible absorption spectrometry. Our current work may provide a simple strategy to synthesize defect-related composite photocatalytic devices.展开更多
摘要WO2 and TiO2 colMds were synthesized by the hydrolysis technique and part of the TiO2 colloid was treated by means of the hydrothermal method. The photochromic performances of the resulting materials obtained via combining the WO3 colloid with the treated TiO2 colloid and the non-treated TiO2 colloid, respectively, are very different. The TiO2 colloid without hydrothermal treatment can effectively improve the photochromic performance of the WO3colloid. The TiO2 nanoparticles were investigated in detail by XRD, TEM, surface photovohage spectra(SPS) and field-induced surface photovoltage spectrometry(FISPS). The photochromism mechanism of WO3 colloid is discussed.
基金supports provided by National Natural Science Foundation of China(No. 51104194)Doctoral Fund of Ministry of Education of China(No. 20110191120014)+1 种基金No.43 Scientific Research Foundation for the Returned Overseas Chinese ScholarsState Education Ministry and Fundamental Research Funds for the Central Universities(Nos. CDJZR13130035,CDJZR12248801 and CDJZR12135501.Chongqing University,China)
摘要In this work, we developed a templated self-assembly approach to fabricate self-supporting Au/TiO2 binary nanoparticles-nanotubes (NPNTs) for the first time. The stable Au/TiO2 nanoparticles colloids were pre-synthesized and then deposited onto an AAO template, following by a mild calcination process. Au/TiO2 binary NPNTs can be achieved after removing the AAO template by NaOH solution. In addition, Au/TiO2 NPNTs with different thicknesses and size distributions could be achieved by tailoring the process parameters, such as the molar ratio of AuNPs to TiO2NPs, deposition modes and calcinations conditions. Therefore, these findings made controllable formation of Au/TiO2 NPNTs attractive for promising fabrication methodologies of metal/metal oxides NPNTs.
摘要TiO2 nanotubes were prepared under normal pressure at a temperature of 120 ℃. Ag, Au, Pt nanoparticles supported on TiO2 nanotubes were prepared by m icrowave assisted heating polyol process. TEM images showed that microwave prepa red Ag, Au, Pt nanoparticles supported on TiO2 nanotubes were small and well dis persed on the surface of the TiO2 nanotubes. UV-Vis absorption spectra showed th at the absorbance of Ag/TiO2 nanotubes and Au/TiO2 nanotubes in the visible ligh t range increased greatly compared to the single titania nanotubes.
基金supported by the National Natural Science Foundation of China(Nos.51972063 and 21501127)the 111 Project(No.D17005)the Priority Academic Program Development of Jiangsu Higher Education Institutions(PAPD).
摘要Due to increasingly serious environmental problems,many researchers are investigating green cleanenergy to solve the world’s energy supply issues.So the strategy that Au nanoparticles(Au NPs)and bismuth sulfide(Bi2S3)NPs are used to evenly decorate TiO2 nanotube arrays(TiO2 NTAs)was carried out.Composite materials demonstrated enhanced solar light absorption ability and excellent photoelectrochemical performance.This was attributed to the presence of Bi2S3 NPs with a narrow band gap and the decoration with noble metallic Au NPs which resulted in local surface plasmon resonance(LSPR)effects.The Au/Bi2S3@TiO2 NTAs composites exhibit improved photocatalytic activity for the degradation of methylene blue(MB)under irradiation of UV and visible light.Moreover,the Au/Bi2S3@TiO2 NTAs exhibits high fluorescence emission at 822 nm.Due to the better binding affinity between Bi2S3,TiO2 and Fe3+ions,the synthesized nanocomposites exhibit high selectivity to Fe3+ions.The number of binding sites for Au/Bi2S3@TiO2 NTAs was estimated to be 1.41 according to the double logarithmic regression method.The calculated value of"K"was 1862 M-1.Fluorescence emission intensity decreases with increasing concentration(30μM–5000μM).The detection limit of the synthesized sensor is 0.221μM.
基金supported by National Natural Science Foundation of China(Nos.11505019,21173028)the Science and Technology Research Project of Liaoning Provincial Education Department(No.L2013464)+1 种基金the Scientific Research Foundation for the Doctor of Liaoning Province(No.20131004)the Dalian Jinzhou New District Science and Technology Plan Project(No.KJCX-ZTPY-2014-0001)
摘要Cold plasma generated by dielectric barrier discharge (DBD) at atmospheric pressure was adopted for preparation of commercial TiO2 Degussa P25 supported Au catalysts (Au/P25- P) with the assistance of the deposition-precipitation procedure. The influences of the plasma reduction time and calcination on the performance of the Au/P25-P catalysts were investigated. CO oxidation was performed to investigate the catalytic activity of the Au/P25 catalysts. The results show that DBD cold plasma for the fabrication of Au/P25-P catalysts is a fast process, and Au/P25-P (4 min) exhibited the highest CO oxidation activity due to the complete reduction of Au compounds and less consumption of oxygen vacancies. In order to form more oxygen vacancies active species, Au/P25-P was calcined to obtain Au/P25-PC catalysts. Interestingly, Au/P25- PC exhibited the highest activity for CO oxidation among the Au/P25 samples. The results of transmission electron microscopy (TEM) indicated that the smaller size and high distribution of Au nanoparticles are the mean reasons for a high performance of Au/P25-PC. Atmospheric- pressure DBD cold plasma was proved to be of great efficiency in preparing high performance supported Au catalysts.
基金supported by the National Natural Science Foundation of China(51772230,51461135004)the Hubei Foreign Science and Technology Cooperation Project(2017AHB059)the Japan Society for the Promotion of Science(JSPS)for an Invitational Fellowship for Foreign Researchers(L16531)~~
摘要Anatase TiO2 nanocrystals and sub-microcrystals with truncated octahedral bipyramidal morphologies were prepared by direct calcination of TiOF2 precursors. The as-prepared TiO2 samples were thoroughly characterized by X-ray diffraction, Raman spectroscopy, field-emission scanning electron microscopy, N2 adsorption-desorption isotherms, X-ray photoelectron spectroscopy, and UV-visible diffuse spectroscopy. It was found that the crystallinity, grain size, and {001}/{101} ratio of the samples can be increased by raising the calcination temperature from 500 to 800℃. The higher crystallinity and {001}/{101} facet ratio resulted in an increase in both aqueous and gas-phase photocatalytic activities, by inhibiting the recombination and separation of electrons and holes. After selecting two TiO2 samples with high crystallinity and {001}/{101} ratio, Au nanoparticles were decorated on their surfaces, and the photocatalytic activity of the resulting samples under visible light illumination was studied. It was found that the visible light-induced photocatalytic activity increased by 2.6 and 4.8 times, respectively, upon Au decoration of the samples prepared by calcination of TiOF2 at 700 and 800℃.
基金supported by the National Natural Science Foundation of China(Grant No.11274082)the Shandong Excellent Young Scientist Research Award Fund Project,China(Grant No.BS2011CL002)
摘要Highly ordered TiO2 nanotube array (TNA) films are fabricated by using an anodic oxidation method. Au nanoparticles (NPs) films are decorated onto the top of TNA films with the aid of ion-sputtering and thermal annealing. An enhanced photocatalytic activity under ultraviolet C (UVC, 266 nm) light irradiation is obtained compared with that of the pristine TNA, which is shown by the steady-state photoluminescence (PL) spectra. Furthermore, a distinct blue shift in the nanosecond time-resolved transient photoluminescence (NTRT-PL) spectra is observed. Such a phenomenon could be well explained by considering the competition between the surface photocatalytic process and the recombination of the photo-generated carriers. The enhanced UV photocatalytic activities of the Au-TNA composite are evaluated through photo-degradation of methyl orange (MO) in an aqueous solution with ultraviolet-visible absorption spectrometry. Our current work may provide a simple strategy to synthesize defect-related composite photocatalytic devices.