Photocatalysis is considered to be a clean, green and efficient method to purify water. In this report, we first developed a highly efficient ultrafine TiO2 nanorods/g-C3N4 nanosheets （TiO2 NR/CN NS） composites via ...Photocatalysis is considered to be a clean, green and efficient method to purify water. In this report, we first developed a highly efficient ultrafine TiO2 nanorods/g-C3N4 nanosheets （TiO2 NR/CN NS） composites via a simple hydrothermal method. Tiny TiO2 nanorods （diameter： ～1.5 nm and length： ～8.3 nm） were first loaded in situ on the CN NS by adding graphitic carbon nitride （g-C3N4） to the reaction solution. The TiO2 NR/CN NS composites present high charge separation efficiency and broader light absorbance than P25 TiO2. Furthermore, we illustrate that the TiO2 NR/CN NS catalyst possesses high performance for the photocatalytic degradation of the common and stubborn pollutants in water, such as the rhodamine B （RhB） dye and phenol. Under visible light （λ 〉 420 nm） irradiation, the apparent rate of the TiO2 NR/CN NR is 172 and 41 times higher than that of the P25 TiO2 and TiO2 NR, respectively. Additionally, we speculated that the heterojunction formed between TiO2 NR and CN NS, which is the basis for the experiments we have designed and the corresponding results. We demonstrated that reactive oxidative species such as superoxide anion radical and holes play critical roles in the degradation, and the hydroxyl radical contributes nothing to the degradation.展开更多
In this paper,a comparative study on the photocatalytic degradation of the Rhodamine B(Rh B)dye as a model compound using N–Fe codoped Ti O2 nanorods under UV and visible-light(λ≥420 nm)irradiations has been perfor...In this paper,a comparative study on the photocatalytic degradation of the Rhodamine B(Rh B)dye as a model compound using N–Fe codoped Ti O2 nanorods under UV and visible-light(λ≥420 nm)irradiations has been performed.Ti O2 photocatalysts were fabricated as aligned nanorod arrays by liquid-phase deposition process,annealed at different temperatures from 400 to 800℃.The effects of annealing temperature on the phase structure,crystallinity,BET surface area,and resulting photocatalytic activity of N–Fe codoped Ti O2 nanorods were also investigated.The degradation studies confirmed that the nanorods annealed at 600℃composed of both anatase(79%)and rutile phases(21%)and offered the highest activity and stability among the series of nanorods,as it degraded 94.8%and 87.2%Rh B in 120 min irradiation under UV and visible-light,respectively.Above 600℃,the photocatalytic performance of nanorods decreased owning to a phase change,decreased surface area and bandgap,and growth of Ti O2 crystallites induced by the annealing temperature.It is hoped that this work could provide precious information on the design of 1 D catalyst materials with more superior photodegradation properties especially under visible-light for the further industrial applications.展开更多
Despite one-dimensional （1D） semiconductor nanostructure arrays attracting increasing attention due to their many advantages, highly ordered TiO2 nanorod arrays （TiO2 NR） are rarely grown in situ on Ti substrates....Despite one-dimensional （1D） semiconductor nanostructure arrays attracting increasing attention due to their many advantages, highly ordered TiO2 nanorod arrays （TiO2 NR） are rarely grown in situ on Ti substrates. Herein, a feasible method to fabricate TiO2 NRs on Ti substrates by using a through-mask anodization process is reported. Self-ordered anodic aluminum oxide （AAO） overlaid on Ti substrate was used as a nanotemplate to induce the growth of TiO2 NRs. The NR length and diameter could be controlled by adjusting anodization parameters such as electrochemical anodization voltage, anodization time and temperature, and electrolyte composition. Furthermore, according to the proposed NR formation mechanism, the anodized Ti ions migrate and deposit in the AAO nanochannels to form Ti（OH）4 or amorphous TiO2 NRs under electric field, owing to the confinement effect of the template. Photoelectrochemical tests indicated that, after hydrogenation, the TiO2 NRs presented higher photocurrent density under simulated sunlight and visible light illuminations, suggesting their potential use in photoelectrochemical water splitting, photocatalysis, solar cells, and sensors.展开更多
Treatment of implant-associated infection is becoming more challenging,especially when bacterial biofilms form on the surface of the implants.Developing multi-mechanism antibacterial methods to combat bacterial biofil...Treatment of implant-associated infection is becoming more challenging,especially when bacterial biofilms form on the surface of the implants.Developing multi-mechanism antibacterial methods to combat bacterial biofilm infections by the synergistic effects are superior to those based on single modality due to avoiding the adverse effects arising from the latter.In this work,TiO2 nanorod arrays in combination with irradiation with 808 nearinfrared(NIR)light are proven to eradicate single specie biofilms by combining photothermal therapy,photodynamic therapy,and physical killing of bacteria.The TiO2 nanorod arrays possess efficient photothermal conversion ability and produce a small amount of reactive oxygen species(ROS).Physiologically,the combined actions of hyperthermia,ROS,and puncturing by nanorods give rise to excellent antibacterial properties on titanium requiring irradiation for only 15 min as demonstrated by our experiments conducted in vitro and in vivo.More importantly,bone biofilm infection is successfully treated efficiently by the synergistic antibacterial effects and at the same time,the TiO2 nanorod arrays improve the new bone formation around implants.In this protocol,besides the biocompatible TiO2 nanorod arrays,an extra photosensitizer is not needed and no other ions would be released.Our findings reveal a rapid bacteria-killing method based on the multiple synergetic antibacterial modalities with high biosafety that can be implemented in vivo and obviate the need for a second operation.The concept and antibacterial system described here have large clinical potential in orthopedic and dental applications.展开更多
Rutile TiO_2 nanorod(TiNR) arrays were fabricated on a boron-doped diamond(BDD) substrate by a simple hydrothermal synthesis method. A fluorine-doped tin oxide(FTO) electrode grown with TiNR arrays was also prepared u...Rutile TiO_2 nanorod(TiNR) arrays were fabricated on a boron-doped diamond(BDD) substrate by a simple hydrothermal synthesis method. A fluorine-doped tin oxide(FTO) electrode grown with TiNR arrays was also prepared using the same technology for comparison. Field-emission scanning electron microscopy results show that oriented TiNR arrays can grow vertically on the surface of BDD and FTO electrodes. TiNR arrays grown on both electrodes had the same length(3 μm). In comparison with the TiNR/FTO electrode, the TiNR/BDD electrode demonstrated a higher photoelectrocatalytic activity for the degradation of water and organic compounds, which is mostly attributed to the formation of a p-n heterojunction between the TiNR arrays and BDD at high potential, apart from the density of TiNR. A linear relationship between the photoelectrocatalytic current and the organic concentration can be observed on both electrodes. However, the linear range between net photoelectrocatalytic current values and organic compound concentrations for the TiNR/BDD electrode are much greater than those for the TiNR/FTO electrode, which makes the TiNR/BDD electrode a versatile material for the photocatalytic degradation and sensing of organic compounds.展开更多
In this work, TiO2 nanorods with uniform diameter of about 100 nm and a length of several micrometers were successfully prepared by the sol-gel template method. Also the influence of molar ratios of precursor on the m...In this work, TiO2 nanorods with uniform diameter of about 100 nm and a length of several micrometers were successfully prepared by the sol-gel template method. Also the influence of molar ratios of precursor on the morphology and structure of TiO2 nanorods has been investigated. The prepared samples were characterized by Fourier transform infrared spectroscopy （FTIR）, X-ray diffraction （XRD） and scanning electron microscopy （SEM）. The XRD results indicated that the TiO2 nanorods were crystallized in the anatase and rutile phases, after annealing to 400-700℃ up to 2 h.展开更多
CdSe/CdS semiconductor quantum dots co-sensitized TiO2 nanorod array was fabricated on the transparent conductive fluorine-doped tin oxide （FTO） substrate using the hydrothermal and successive ionic layer adsorption...CdSe/CdS semiconductor quantum dots co-sensitized TiO2 nanorod array was fabricated on the transparent conductive fluorine-doped tin oxide （FTO） substrate using the hydrothermal and successive ionic layer adsorption and reaction （SILAR） process. The structural and morphological properties of the samples were characterized by X-ray diffraction （XRD）, field-emission scanning electron microscopy （FESEM）, and transmission electron microscopy （TEM）. The results indicate that CdSe/CdS QDs are uniformly coated on the surface of the TiO2 nanorods. The shift of light absorption edge was monitored by taking UV-visible absorption spectra. Compared with the absorption spectra of the TiO2 nanorod array, deposition of CdSe/CdS QDs shifts the absorption edge to the higher wavelength. The enhanced light absorption in the visible-light region of CdSe/CdS/TiO2 nanorod array indicates that CdSe/CdS layers can act as co-sensitizers in quantum dots sensitized solar cells （QDSSCs）. By optimizing the CdSe layer deposition cycles, a photocurrent of 5.78 mA/cm2, an open circuit photovoltage of 0.469 V and a conversion efficiency of 1.34 % were obtained under an illumination of 100 mw/cm2.展开更多
YiO2 nanorods have been prepared on ITO substrates by dc reactive magnetron sputtering technique. The hydroxyl groups have been introduced on the nanorods surface. The structure and the optical properties of these nan...YiO2 nanorods have been prepared on ITO substrates by dc reactive magnetron sputtering technique. The hydroxyl groups have been introduced on the nanorods surface. The structure and the optical properties of these nanorods have been studied. The dye-sensitized solar cells （DSSCs） have been assembled using these TiO2 nanorods as photoelectrode. And the effect of the hydroxyl groups on the properties of the photoelectric conversion of the DSSCs has been studied.展开更多
The rutile TiO2 nanorod arrays with 240 nm in length, 30 nm in diameter, and 420 btm 2 in areal density were prepared by the hydrothermal method to replace the typical 200-300 nm thick mesoporous TiO2 thin films in pe...The rutile TiO2 nanorod arrays with 240 nm in length, 30 nm in diameter, and 420 btm 2 in areal density were prepared by the hydrothermal method to replace the typical 200-300 nm thick mesoporous TiO2 thin films in perovskite solar cells. The CH3NH3PbI3 xBrx capping layers with different thicknesses were obtained on the TiO2 nanorod arrays using different concentration PbI2.DMSO complex precursor solutions in DMF and the photovoltaic performances of the corresponding solar cells were compared. The perovskite solar cells based on 240 nm long TiO2 nanorod arrays and 420 nm thick CH3NH3PbI3 xBrx capping layers showed the best photoelectric conversion efficiency （PCE） of 15.56% and the average PCE of 14.93 ± 0.63% at the relative humidity of 50%-54% under the illumination of simulated AM 1.5 sunlight （100 mW.cm-2）.展开更多
基金supported by the Beijing Municipal High Level Innovative Team Building Program(IDHT20180504)the National Natural Science Foundation of China(21671011)+4 种基金Beijing High Talent ProgramBeijing Natural Science Foundation(KZ201710005002)the Large-scale Instrument and Equipment Platform of Beijing University of TechnologyChina Postdoctoral Science FoundationBeijing Postdoctoral Research Foundation
文摘Photocatalysis is considered to be a clean, green and efficient method to purify water. In this report, we first developed a highly efficient ultrafine TiO2 nanorods/g-C3N4 nanosheets （TiO2 NR/CN NS） composites via a simple hydrothermal method. Tiny TiO2 nanorods （diameter： ～1.5 nm and length： ～8.3 nm） were first loaded in situ on the CN NS by adding graphitic carbon nitride （g-C3N4） to the reaction solution. The TiO2 NR/CN NS composites present high charge separation efficiency and broader light absorbance than P25 TiO2. Furthermore, we illustrate that the TiO2 NR/CN NS catalyst possesses high performance for the photocatalytic degradation of the common and stubborn pollutants in water, such as the rhodamine B （RhB） dye and phenol. Under visible light （λ 〉 420 nm） irradiation, the apparent rate of the TiO2 NR/CN NR is 172 and 41 times higher than that of the P25 TiO2 and TiO2 NR, respectively. Additionally, we speculated that the heterojunction formed between TiO2 NR and CN NS, which is the basis for the experiments we have designed and the corresponding results. We demonstrated that reactive oxidative species such as superoxide anion radical and holes play critical roles in the degradation, and the hydroxyl radical contributes nothing to the degradation.
文摘In this paper,a comparative study on the photocatalytic degradation of the Rhodamine B(Rh B)dye as a model compound using N–Fe codoped Ti O2 nanorods under UV and visible-light(λ≥420 nm)irradiations has been performed.Ti O2 photocatalysts were fabricated as aligned nanorod arrays by liquid-phase deposition process,annealed at different temperatures from 400 to 800℃.The effects of annealing temperature on the phase structure,crystallinity,BET surface area,and resulting photocatalytic activity of N–Fe codoped Ti O2 nanorods were also investigated.The degradation studies confirmed that the nanorods annealed at 600℃composed of both anatase(79%)and rutile phases(21%)and offered the highest activity and stability among the series of nanorods,as it degraded 94.8%and 87.2%Rh B in 120 min irradiation under UV and visible-light,respectively.Above 600℃,the photocatalytic performance of nanorods decreased owning to a phase change,decreased surface area and bandgap,and growth of Ti O2 crystallites induced by the annealing temperature.It is hoped that this work could provide precious information on the design of 1 D catalyst materials with more superior photodegradation properties especially under visible-light for the further industrial applications.
基金Thanks for the financial support of the National Natural Science Foundation of China （Nos. 21303227, 21573259, and 51403220）, Qingdao science and tech- nology plan application foundation research project（No. 14-2-4-60-JCH） and the ＂Hundred Talents Pro- gram＂ of Chinese Academy of Sciences （D. A. W.）.
文摘Despite one-dimensional （1D） semiconductor nanostructure arrays attracting increasing attention due to their many advantages, highly ordered TiO2 nanorod arrays （TiO2 NR） are rarely grown in situ on Ti substrates. Herein, a feasible method to fabricate TiO2 NRs on Ti substrates by using a through-mask anodization process is reported. Self-ordered anodic aluminum oxide （AAO） overlaid on Ti substrate was used as a nanotemplate to induce the growth of TiO2 NRs. The NR length and diameter could be controlled by adjusting anodization parameters such as electrochemical anodization voltage, anodization time and temperature, and electrolyte composition. Furthermore, according to the proposed NR formation mechanism, the anodized Ti ions migrate and deposit in the AAO nanochannels to form Ti（OH）4 or amorphous TiO2 NRs under electric field, owing to the confinement effect of the template. Photoelectrochemical tests indicated that, after hydrogenation, the TiO2 NRs presented higher photocurrent density under simulated sunlight and visible light illuminations, suggesting their potential use in photoelectrochemical water splitting, photocatalysis, solar cells, and sensors.
基金the National Natural Science Foundation of China(31700834 and 11632013)Major Projects in Research and Development of Shanxi(Projects of International Cooperation,201803D421090)+2 种基金Fund for Shanxi“1331 Project”Key Innovative Research Team(PY201809)Hong Kong Research Grants Council(RGC)General Research Funds(GRF)(CityU 11205617)Guangdong-Hong Kong Technology Cooperation Funding Scheme(TCFS)GHP/085/18SZ(CityU 9440230).
文摘Treatment of implant-associated infection is becoming more challenging,especially when bacterial biofilms form on the surface of the implants.Developing multi-mechanism antibacterial methods to combat bacterial biofilm infections by the synergistic effects are superior to those based on single modality due to avoiding the adverse effects arising from the latter.In this work,TiO2 nanorod arrays in combination with irradiation with 808 nearinfrared(NIR)light are proven to eradicate single specie biofilms by combining photothermal therapy,photodynamic therapy,and physical killing of bacteria.The TiO2 nanorod arrays possess efficient photothermal conversion ability and produce a small amount of reactive oxygen species(ROS).Physiologically,the combined actions of hyperthermia,ROS,and puncturing by nanorods give rise to excellent antibacterial properties on titanium requiring irradiation for only 15 min as demonstrated by our experiments conducted in vitro and in vivo.More importantly,bone biofilm infection is successfully treated efficiently by the synergistic antibacterial effects and at the same time,the TiO2 nanorod arrays improve the new bone formation around implants.In this protocol,besides the biocompatible TiO2 nanorod arrays,an extra photosensitizer is not needed and no other ions would be released.Our findings reveal a rapid bacteria-killing method based on the multiple synergetic antibacterial modalities with high biosafety that can be implemented in vivo and obviate the need for a second operation.The concept and antibacterial system described here have large clinical potential in orthopedic and dental applications.
基金supported by the National Natural Science Foundation of China(21677018)the Importation and Development of High-Caliber Talents Project of Beijing Municipal Institutions(CIT&TCD201304098)
文摘Rutile TiO_2 nanorod(TiNR) arrays were fabricated on a boron-doped diamond(BDD) substrate by a simple hydrothermal synthesis method. A fluorine-doped tin oxide(FTO) electrode grown with TiNR arrays was also prepared using the same technology for comparison. Field-emission scanning electron microscopy results show that oriented TiNR arrays can grow vertically on the surface of BDD and FTO electrodes. TiNR arrays grown on both electrodes had the same length(3 μm). In comparison with the TiNR/FTO electrode, the TiNR/BDD electrode demonstrated a higher photoelectrocatalytic activity for the degradation of water and organic compounds, which is mostly attributed to the formation of a p-n heterojunction between the TiNR arrays and BDD at high potential, apart from the density of TiNR. A linear relationship between the photoelectrocatalytic current and the organic concentration can be observed on both electrodes. However, the linear range between net photoelectrocatalytic current values and organic compound concentrations for the TiNR/BDD electrode are much greater than those for the TiNR/FTO electrode, which makes the TiNR/BDD electrode a versatile material for the photocatalytic degradation and sensing of organic compounds.
文摘In this work, TiO2 nanorods with uniform diameter of about 100 nm and a length of several micrometers were successfully prepared by the sol-gel template method. Also the influence of molar ratios of precursor on the morphology and structure of TiO2 nanorods has been investigated. The prepared samples were characterized by Fourier transform infrared spectroscopy （FTIR）, X-ray diffraction （XRD） and scanning electron microscopy （SEM）. The XRD results indicated that the TiO2 nanorods were crystallized in the anatase and rutile phases, after annealing to 400-700℃ up to 2 h.
基金National Natural Science Foundation of China(No.11174071)the International Cooperation Project of Wuhan City and Hubei Province(Nos.201070934339 and 2010BFA010)
文摘CdSe/CdS semiconductor quantum dots co-sensitized TiO2 nanorod array was fabricated on the transparent conductive fluorine-doped tin oxide （FTO） substrate using the hydrothermal and successive ionic layer adsorption and reaction （SILAR） process. The structural and morphological properties of the samples were characterized by X-ray diffraction （XRD）, field-emission scanning electron microscopy （FESEM）, and transmission electron microscopy （TEM）. The results indicate that CdSe/CdS QDs are uniformly coated on the surface of the TiO2 nanorods. The shift of light absorption edge was monitored by taking UV-visible absorption spectra. Compared with the absorption spectra of the TiO2 nanorod array, deposition of CdSe/CdS QDs shifts the absorption edge to the higher wavelength. The enhanced light absorption in the visible-light region of CdSe/CdS/TiO2 nanorod array indicates that CdSe/CdS layers can act as co-sensitizers in quantum dots sensitized solar cells （QDSSCs）. By optimizing the CdSe layer deposition cycles, a photocurrent of 5.78 mA/cm2, an open circuit photovoltage of 0.469 V and a conversion efficiency of 1.34 % were obtained under an illumination of 100 mw/cm2.
文摘YiO2 nanorods have been prepared on ITO substrates by dc reactive magnetron sputtering technique. The hydroxyl groups have been introduced on the nanorods surface. The structure and the optical properties of these nanorods have been studied. The dye-sensitized solar cells （DSSCs） have been assembled using these TiO2 nanorods as photoelectrode. And the effect of the hydroxyl groups on the properties of the photoelectric conversion of the DSSCs has been studied.
基金Project supported by the National Natural Science Foundation of China(Grant Nos.51472071 and 51272061)Talent Project of Hefei University of Technology,China(Grant Nos.75010-037004 and 75010-037003)
文摘The rutile TiO2 nanorod arrays with 240 nm in length, 30 nm in diameter, and 420 btm 2 in areal density were prepared by the hydrothermal method to replace the typical 200-300 nm thick mesoporous TiO2 thin films in perovskite solar cells. The CH3NH3PbI3 xBrx capping layers with different thicknesses were obtained on the TiO2 nanorod arrays using different concentration PbI2.DMSO complex precursor solutions in DMF and the photovoltaic performances of the corresponding solar cells were compared. The perovskite solar cells based on 240 nm long TiO2 nanorod arrays and 420 nm thick CH3NH3PbI3 xBrx capping layers showed the best photoelectric conversion efficiency （PCE） of 15.56% and the average PCE of 14.93 ± 0.63% at the relative humidity of 50%-54% under the illumination of simulated AM 1.5 sunlight （100 mW.cm-2）.
