Gallium oxide(Ga_2O_3) thin films were deposited on a-Al2O3(1120) substrates by pulsed laser deposition(PLD) with different oxygen pressures at 650?C. By reducing the oxygen pressure, mixed-phase Ga_2O_3 films with α...Gallium oxide(Ga_2O_3) thin films were deposited on a-Al2O3(1120) substrates by pulsed laser deposition(PLD) with different oxygen pressures at 650?C. By reducing the oxygen pressure, mixed-phase Ga_2O_3 films with α and β phases can be obtained, and on the basis of this, mixed-phase Ga_2O_3 thin film solar-blind photodetectors(SBPDs) were prepared.Comparing the responsivities of the mixed-phase Ga_2O_3 SBPDs and the single β-Ga_2O_3 SBPDs at a bias voltage of 25 V,it is found that the former has a maximum responsivity of approximately 12 A/W, which is approximately two orders of magnitude larger than that of the latter. This result shows that the mixed-phase structure of Ga_2O_3 thin films can be used to prepare high-responsivity SBPDs. Moreover, the cause of this phenomenon was investigated, which will provide a feasible way to improve the responsivity of Ga_2O_3 thin film SBPDs.展开更多
Mixed-phase TiO_2 photocatalysts with small particle size of anatase and rutile(~5 nm) have been successfully synthesized using hydrothermal method. The effects of curing temperature and curing time before the hydroth...Mixed-phase TiO_2 photocatalysts with small particle size of anatase and rutile(~5 nm) have been successfully synthesized using hydrothermal method. The effects of curing temperature and curing time before the hydrothermal treatment on the crystalline phase, the phase composition, and the particle size of TiO_2 were investigated by the X-ray diffraction spectroscopy(XRD) and the transmission electron microscopy(TEM), respectively. It was found that the anatase and rutile phase contents in the TiO_2 particles were successfully controlled by simply adjusting the curing temperature and the curing time. More importantly, the particle size of both anatase and rutile is small in the mixed-phase TiO_2 particles. The photocatalytic activity of TiO_2 was evaluated by the degradation of Rhodamine B(Rh B) in aqueous solution. The Ti O2 with phase junction formed by anatase and rutile exhibited higher separation rate between the photo-induced electrons and holes, which was confirmed by the surface photovoltage(SPV) spectra, and at the same time exhibited the higher photocatalytic degradation on Rh B than pure anatase-phase TiO_2. Moreover, it was found that TiO_2 with 83% of anatase and 17% of rutile showed a highest photocatalytic activity among the mixed-phase TiO_2 samples.展开更多
Much attention has been paid to the pollutant dimethylarsenic acid(DMA),because of its high toxicity even at very low doses.Although TiO2 photocatalytic oxidation(PCO)is one of the few effective methods for treating D...Much attention has been paid to the pollutant dimethylarsenic acid(DMA),because of its high toxicity even at very low doses.Although TiO2 photocatalytic oxidation(PCO)is one of the few effective methods for treating DMA-containing water,the efficient decomposition of DMA and simultaneous removal of toxic arsenic species remains a significant but challenging task.Here,defective mesoporous TiO2 with mixed-phase structure was synthesized and used as both photocatalyst and adsorbent for DMA removal.Due to the reduced band-gap and enhanced separation of photogenerated charge carriers,the oxygen-deficient TiO2 nanostructures exhibited 4.2 times higher PCO efficiency than commercial TiO2(P25).More importantly,the high surface area of the mesoporous TiO2 provided sufficient active sites for in-situ adsorption and reaction,resulting in the efficient removal of as-formed As(V).Combining the experimental and characterization results,the different roles of reactive species during PCO reactions were clarified.In the presence of hole(h+)as the dominant oxidation species,DMA was demethylated and transformed into MMA.Thereafter,MMA was subsequently reduced to As(Ⅲ)by photo-generated electrons.Superoxide radicals(O2·-)played a significant role in oxidizing As(Ⅲ)into As(Ⅴ),which was finally adsorptively removed by the mesoporous TiO2.展开更多
Na_(2)Ti_(3)O_(7)and Na_(2)Ti_(6)O_(13)are two typical titanate-based sodium-storage materials,featuring the high theoretical capacity and favorable structure stability,respectively.Regulating the ratio of them in the...Na_(2)Ti_(3)O_(7)and Na_(2)Ti_(6)O_(13)are two typical titanate-based sodium-storage materials,featuring the high theoretical capacity and favorable structure stability,respectively.Regulating the ratio of them in the composite material is the key to strengthen its electrochemical characteristics.Herein,based on the high specific surface area and abundant surface functional groups of carbon dots(CDs),sodium titanate precursors containing CDs were in situ prepared by one-step hydrothermal method.After the thermal conversion of the precursors,a composite material(NNTO/C)of Na_(2)Ti_(3)O_(7)and Na_(2)Ti_(6)O_(13)was obtained,containing conductive carbon derived from CDs.The introduc⁃tion of conductive carbon not only adjusts the composition ratio of the mixed phases,but also provides a small charge transfer impedance(Rct,7.48Ω)and a big specific surface area(100.8 m^(2)/g).As a result,NNTO/C composites exhibit better sodium storage behavior while playing the synergistic interaction of mixed phases.When employed as the anode,after 200 cycles at 0.05 A/g,NNTO/C still maintains a specific capacity of 143.8 mA‧h/g.After 400 cycles at 1.00 A/g,the specific capacity remains as high as 108 mA‧h/g.This study suggests an innovative thinking for designing two-phase structures of electrode materials and the greater use of CDs in electrochemical energy storage.展开更多
Synergistic interplays involving multiple active centers originating from TiO2 nanotube layers(TNT)and ruthenium(Ru)species comprising of both single atoms(SAs)and nanoparticles(NPs)augment the alkaline hydrogen evolu...Synergistic interplays involving multiple active centers originating from TiO2 nanotube layers(TNT)and ruthenium(Ru)species comprising of both single atoms(SAs)and nanoparticles(NPs)augment the alkaline hydrogen evolution reaction(HER)by enhancing Volmer kinetics from rapid water dissociation and improving Tafel kinetics from efficient H*desorption.Atomic layer deposition of Ru with 50 process cycles results in a mixture of Ru SAs and 2.8-0.4 nm NPs present on TNT layers,and it emerges with the highest HER activity among all the electrodes synthesized.A detailed study of the Ti and Ru species using different high-resolution techniques confirmed the presence of Ti^(3+)states and the coexistence of Ru SAs and NPs.With insights from literature,the role of Ti^(3+),appropriate work functions of TNT layers and Ru,and the synergistic effect of Ru SAs and Ru NPs in improving the performance of alkaline HER were elaborated and justified.The aforementioned characteristics led to a remarkable performance by having 9mV onset potentials and 33 mV dec^(-1) of Tafel slopes and a higher turnover frequency of 1.72 H2 s^(-1) at 30 mV.Besides,a notable stability from 28 h staircase chronopotentiometric measurements for TNT@Ru surpasses TNT@Pt in comparison.展开更多
We prepared TiO 2(anatase) and Sn doped TiO 2 nanoparticlate film by Plasma enhanced Chemical Vapor Deposition(PECVD) method. XRD and XPS experiments showed that Sn was doped into the lattice of TiO 2 with a ratio of ...We prepared TiO 2(anatase) and Sn doped TiO 2 nanoparticlate film by Plasma enhanced Chemical Vapor Deposition(PECVD) method. XRD and XPS experiments showed that Sn was doped into the lattice of TiO 2 with a ratio of n (Sn)∶ n (Ti)=1∶10 . Sn doping largely enhanced the photocatalytic activity of TiO 2 film for phenol degradation. The enhancement in photoactivity by doping was discussed, based on the characterization with AFM, FTIR and EFISPS. Sn doping produced localized level of Sn 4+ in the band gap of TiO 2, about 0.4 eV below the conduction band, which could capture photogenerated electrons and reduce O 2 adsorbed on the surface of TiO 2 film, thus accelerated the photocatalytic reaction.展开更多
The transition metal ion doped TiO 2 nanoparticles were prepared with hydrothermal method, and the effects of doping different metal ions on the ability of TiO 2 in photocatalyzing degradation of rhodamine B(RB) were ...The transition metal ion doped TiO 2 nanoparticles were prepared with hydrothermal method, and the effects of doping different metal ions on the ability of TiO 2 in photocatalyzing degradation of rhodamine B(RB) were studied. The results showed that the doping of Fe 3+ , Co 2+ , Ni 2+ and Cr 3+ in TiO 2 nanoparticles made the photocatalytic efficiency of the TiO 2 particles reduce and the higher the initial content of Fe 3+ , the lower the ability of TiO 2 in photocatalyzing the degradation of RB. But the doping of Zn 2+ and Cd 2+ , especially Zn 2+ , made the photocatalytic efficiency of the TiO 2 particles enhance, showing a great increase of the rate constant( k ) and the initial reaction rate( r ini ).展开更多
基金Project supported by the National Natural Science Foundation of China(Grant Nos.51872187,51302174,11774241,and 61704111)the National Key Research and Development Program of China(Grant No.2017YFB0400304)+3 种基金the Natural Science Foundation of Guangdong Province,China(Grant Nos.2016A030313060 and 2017A030310524)the Project of Department of Education of Guangdong Province,China(Grant No.2014KTSCX110)the Fundamental Research Project of Shenzhen,China(Grant No.JCYJ20180206162132006)the Science and Technology Foundation of Shenzhen,China(Grant No.JCYJ2015-2018)
文摘Gallium oxide(Ga_2O_3) thin films were deposited on a-Al2O3(1120) substrates by pulsed laser deposition(PLD) with different oxygen pressures at 650?C. By reducing the oxygen pressure, mixed-phase Ga_2O_3 films with α and β phases can be obtained, and on the basis of this, mixed-phase Ga_2O_3 thin film solar-blind photodetectors(SBPDs) were prepared.Comparing the responsivities of the mixed-phase Ga_2O_3 SBPDs and the single β-Ga_2O_3 SBPDs at a bias voltage of 25 V,it is found that the former has a maximum responsivity of approximately 12 A/W, which is approximately two orders of magnitude larger than that of the latter. This result shows that the mixed-phase structure of Ga_2O_3 thin films can be used to prepare high-responsivity SBPDs. Moreover, the cause of this phenomenon was investigated, which will provide a feasible way to improve the responsivity of Ga_2O_3 thin film SBPDs.
基金supported by the National Natural Science Foundation of China (21573101)the Liaoning Provincial Natural Science Foundation (2014020107)+5 种基金the Program for Liaoning Excellent Talents in University (LJQ2014041)the Support Plan for Distinguished Professors of Liaoning Province ([2015]153)the Liaoning BaiQianWan Talents Program ([2017]96)the fund of the State Key Laboratory of Catalysis in DICP (N-15-10)the Talent Scientific Research Fund of LSHU (2016XJJ-012)the University Innovation Talent Support Plan of Liaoning Province (LR2017011)
文摘Mixed-phase TiO_2 photocatalysts with small particle size of anatase and rutile(~5 nm) have been successfully synthesized using hydrothermal method. The effects of curing temperature and curing time before the hydrothermal treatment on the crystalline phase, the phase composition, and the particle size of TiO_2 were investigated by the X-ray diffraction spectroscopy(XRD) and the transmission electron microscopy(TEM), respectively. It was found that the anatase and rutile phase contents in the TiO_2 particles were successfully controlled by simply adjusting the curing temperature and the curing time. More importantly, the particle size of both anatase and rutile is small in the mixed-phase TiO_2 particles. The photocatalytic activity of TiO_2 was evaluated by the degradation of Rhodamine B(Rh B) in aqueous solution. The Ti O2 with phase junction formed by anatase and rutile exhibited higher separation rate between the photo-induced electrons and holes, which was confirmed by the surface photovoltage(SPV) spectra, and at the same time exhibited the higher photocatalytic degradation on Rh B than pure anatase-phase TiO_2. Moreover, it was found that TiO_2 with 83% of anatase and 17% of rutile showed a highest photocatalytic activity among the mixed-phase TiO_2 samples.
基金supported by the National Natural Science Foundation of China(Nos.51678556 and 51578531)the National Key Research&Development Program of China(No.2016YFC0400806)
文摘Much attention has been paid to the pollutant dimethylarsenic acid(DMA),because of its high toxicity even at very low doses.Although TiO2 photocatalytic oxidation(PCO)is one of the few effective methods for treating DMA-containing water,the efficient decomposition of DMA and simultaneous removal of toxic arsenic species remains a significant but challenging task.Here,defective mesoporous TiO2 with mixed-phase structure was synthesized and used as both photocatalyst and adsorbent for DMA removal.Due to the reduced band-gap and enhanced separation of photogenerated charge carriers,the oxygen-deficient TiO2 nanostructures exhibited 4.2 times higher PCO efficiency than commercial TiO2(P25).More importantly,the high surface area of the mesoporous TiO2 provided sufficient active sites for in-situ adsorption and reaction,resulting in the efficient removal of as-formed As(V).Combining the experimental and characterization results,the different roles of reactive species during PCO reactions were clarified.In the presence of hole(h+)as the dominant oxidation species,DMA was demethylated and transformed into MMA.Thereafter,MMA was subsequently reduced to As(Ⅲ)by photo-generated electrons.Superoxide radicals(O2·-)played a significant role in oxidizing As(Ⅲ)into As(Ⅴ),which was finally adsorptively removed by the mesoporous TiO2.
文摘Na_(2)Ti_(3)O_(7)and Na_(2)Ti_(6)O_(13)are two typical titanate-based sodium-storage materials,featuring the high theoretical capacity and favorable structure stability,respectively.Regulating the ratio of them in the composite material is the key to strengthen its electrochemical characteristics.Herein,based on the high specific surface area and abundant surface functional groups of carbon dots(CDs),sodium titanate precursors containing CDs were in situ prepared by one-step hydrothermal method.After the thermal conversion of the precursors,a composite material(NNTO/C)of Na_(2)Ti_(3)O_(7)and Na_(2)Ti_(6)O_(13)was obtained,containing conductive carbon derived from CDs.The introduc⁃tion of conductive carbon not only adjusts the composition ratio of the mixed phases,but also provides a small charge transfer impedance(Rct,7.48Ω)and a big specific surface area(100.8 m^(2)/g).As a result,NNTO/C composites exhibit better sodium storage behavior while playing the synergistic interaction of mixed phases.When employed as the anode,after 200 cycles at 0.05 A/g,NNTO/C still maintains a specific capacity of 143.8 mA‧h/g.After 400 cycles at 1.00 A/g,the specific capacity remains as high as 108 mA‧h/g.This study suggests an innovative thinking for designing two-phase structures of electrode materials and the greater use of CDs in electrochemical energy storage.
基金support from the European Union Horizon 2020 program(project HERMES,nr.952184)the Ministry of Education,Youth and Sports of the Czech Republic for supporting CEMNAT(LM2023037)+1 种基金Czech-NanoLab(LM2023051)infrastructures for providing ALD,SEM,EDX,XPS,TEM,and XRDCzech Science Foundation(project 23-08019X,EXPRO).
文摘Synergistic interplays involving multiple active centers originating from TiO2 nanotube layers(TNT)and ruthenium(Ru)species comprising of both single atoms(SAs)and nanoparticles(NPs)augment the alkaline hydrogen evolution reaction(HER)by enhancing Volmer kinetics from rapid water dissociation and improving Tafel kinetics from efficient H*desorption.Atomic layer deposition of Ru with 50 process cycles results in a mixture of Ru SAs and 2.8-0.4 nm NPs present on TNT layers,and it emerges with the highest HER activity among all the electrodes synthesized.A detailed study of the Ti and Ru species using different high-resolution techniques confirmed the presence of Ti^(3+)states and the coexistence of Ru SAs and NPs.With insights from literature,the role of Ti^(3+),appropriate work functions of TNT layers and Ru,and the synergistic effect of Ru SAs and Ru NPs in improving the performance of alkaline HER were elaborated and justified.The aforementioned characteristics led to a remarkable performance by having 9mV onset potentials and 33 mV dec^(-1) of Tafel slopes and a higher turnover frequency of 1.72 H2 s^(-1) at 30 mV.Besides,a notable stability from 28 h staircase chronopotentiometric measurements for TNT@Ru surpasses TNT@Pt in comparison.
文摘We prepared TiO 2(anatase) and Sn doped TiO 2 nanoparticlate film by Plasma enhanced Chemical Vapor Deposition(PECVD) method. XRD and XPS experiments showed that Sn was doped into the lattice of TiO 2 with a ratio of n (Sn)∶ n (Ti)=1∶10 . Sn doping largely enhanced the photocatalytic activity of TiO 2 film for phenol degradation. The enhancement in photoactivity by doping was discussed, based on the characterization with AFM, FTIR and EFISPS. Sn doping produced localized level of Sn 4+ in the band gap of TiO 2, about 0.4 eV below the conduction band, which could capture photogenerated electrons and reduce O 2 adsorbed on the surface of TiO 2 film, thus accelerated the photocatalytic reaction.
文摘The transition metal ion doped TiO 2 nanoparticles were prepared with hydrothermal method, and the effects of doping different metal ions on the ability of TiO 2 in photocatalyzing degradation of rhodamine B(RB) were studied. The results showed that the doping of Fe 3+ , Co 2+ , Ni 2+ and Cr 3+ in TiO 2 nanoparticles made the photocatalytic efficiency of the TiO 2 particles reduce and the higher the initial content of Fe 3+ , the lower the ability of TiO 2 in photocatalyzing the degradation of RB. But the doping of Zn 2+ and Cd 2+ , especially Zn 2+ , made the photocatalytic efficiency of the TiO 2 particles enhance, showing a great increase of the rate constant( k ) and the initial reaction rate( r ini ).
