Ca3CO4O9 （CCO） and Ca2.95K0.05Co4O9 （CKCO） powders have been prepared by the polyacrylamide gel method. CKCO shows increased capacity and better cycling stability compared with CCO. After cycled for 50 cycles at 0...Ca3CO4O9 （CCO） and Ca2.95K0.05Co4O9 （CKCO） powders have been prepared by the polyacrylamide gel method. CKCO shows increased capacity and better cycling stability compared with CCO. After cycled for 50 cycles at 0.5 C, CKCO retains a capacity of 223 mAh.g-1, almost twice than CCO. The electrochemical impedance spectroscopy （EIS） tests shows the CKCO sample has a lower initial charge transfer resistance （Rot） and undergoes smaller Rot change during cycling than the CCO sample, indicating improved electrochemical performance by K-doping.展开更多
Visible-light-driven photocatalysis is a promising technology for the treatment of dye wastewater.In this work,a novel photocatalyst of K-doped g-C_(3)N_(4) loaded on magnetic attapulgite(ATP)(Kω-g-C_(3)N_(4)@ATP-Fe_...Visible-light-driven photocatalysis is a promising technology for the treatment of dye wastewater.In this work,a novel photocatalyst of K-doped g-C_(3)N_(4) loaded on magnetic attapulgite(ATP)(Kω-g-C_(3)N_(4)@ATP-Fe_(3)O_(4))with excellent visible light photocatalytic properties and stability were successfully prepared and characterized.The removal efficiency of Kω-g-C_(3)N_(4)@ATP-Fe_(3)O_(4) for malachite green(MG)was studied,and the degradation mechanism was analyzed and proposed.It was found that the K_(5)-g-C_(3)N_(4)@ATP-Fe_(3)O_(4) photocatalyst possessed excellent degradation efficiency of over 98.0%for the MG dye wastewater under optimal conditions.Moreover,the K_(5)-g-C_(3)N_(4)@ATP-Fe_(3)O_(4) materials possessed good recyclability with a removal rate over 82%after 4 cycles.Under visible light condition,the K_(5)-g-C_(3)N_(4)@ATP-Fe_(3)O_(4) photocatalyst produce radicals of·OH and O_(2)^(-)to degrade the MG dyes,which was supported by electron paramagnetic resonance(EPR)and radical trapping experiments.In addition,the LC-MS analysis interpreted the degradation pathways and intermediates of MG in the solution.The findings in this work indicate that the prepared photocatalytic material has excellent degradation efficiency for MG and can be applied in dye wastewater treatment.展开更多
In this study,K_(x)-Mn-Ce catalysts prepared by sol-gel method were investigated for toluene oxidation.Compared with Mn-Ce,the catalytic performance of K_(x)-Mn-Ce was further improved.X-ray diffraction(XRD),high reso...In this study,K_(x)-Mn-Ce catalysts prepared by sol-gel method were investigated for toluene oxidation.Compared with Mn-Ce,the catalytic performance of K_(x)-Mn-Ce was further improved.X-ray diffraction(XRD),high resolution transmission electron microscopy(HRTEM)and Raman analyses demonstrate that K ions enter the lattice of CeO_(2) and disperse uniformly.The results of X-ray photoelectron spectroscopy(XPS),H_(2)-temperature programmed reduction(H_(2)-TPR).and O_(2)-temperature programmed desorption(O_(2)-TPD)analyses indicate that there is a strong interaction between K,Mn and Ce;the charge co mpensation effect would be induced when K ions enter the lattice of CeO_(2),which leads to more oxygen vacancies due to the generation of more Ce^(3+).Toluene-TPD shows that K-doping enhances the activation ability of toluene.Among all catalysts,K0.1-Mn-Ce shows the highest concentration of Mn^(4+),Ce^(3+),Osur,and redox ability,resulting in higher low-temperature catalytic activity.Additionally,the results of stability and water resistance also prove that K0.1-Mn-Ce catalyst possesses excellent stability and water resistance.展开更多
Photocatalytic selective synthesis of lactic acid(LA)from biomass sugars with a single heterogeneous catalyst is promising but challenging due to the multiple reaction steps involved.Herein,a K-doped C-rich red polyme...Photocatalytic selective synthesis of lactic acid(LA)from biomass sugars with a single heterogeneous catalyst is promising but challenging due to the multiple reaction steps involved.Herein,a K-doped C-rich red polymerized carbon nitride(RPCN)photocatalyst with uniform K/C dual sites was constructed by a molten salt template method,which was highly efficient for cascade isomerization dehydration of glucose to LA with>90%selectivity under visible light and gentle conditions.Control experiments and theoretical calculations expounded that the introduced K/C dual sites could improve the light capture ability and photogenerated charge separation efficiency,while the K species provided sufficient Lewis acid sites(adsorption sites)for the isomerization of glucose to fructose.Meanwhile,the introduced C sites that substitute N atoms could promote electrons to be captured by adsorbed oxygen for selective generation of superoxide radicals,which was highly efficient for the scission of the C3-C4 bond in fructose,exclusively furnishing LA.Importantly,the RPCN photocatalyst was also suitable for the photocatalytic upgrading of various biomass saccharides into LA with high yields of 81.3%-95.3%and could be recycled for five consecutive cycles.The tailored construction of dual sites by localization of space charge lightens an avenue for multi-step conversion of biomass with pronounced selectivity.展开更多
Ba0.6Sr0.4TiO3 thin films doped with K were deposited on Pt/Ti/SiO2/Si substrates by the chemical solution deposition method. The structure, surface morphology and the dielectric and tunable properties of Bao.6Sro.4Ti...Ba0.6Sr0.4TiO3 thin films doped with K were deposited on Pt/Ti/SiO2/Si substrates by the chemical solution deposition method. The structure, surface morphology and the dielectric and tunable properties of Bao.6Sro.4TiO3 thin films have been studied in detail. The K content in Ba0.6Sro.4TiO3 thin films has a strong influence on the material＇s properties including surface morphology and the dielectric and tunable properties. It was found that the Curie temperature of K-doped Bao.6Sr0.4TiO3 films shifts to a higher value compared with that of undoped Ba0.6Sr0.4TiO3 thin films, which leads to a dielectric enhancement of K-doped Ba0.6Sr0.4TiO3 films at room temperature. At the optimized content of 0.02 mol, the dielectric loss tangent is reduced significantly from 0.057 to 0.020. Meanwhile, the tunability is enhanced obviously from 26% to 48% at the measured frequency of 1 MHz and the maximum value of the figure of merit is 23.8. This suggests that such films have potential applications for tunable devices.展开更多
The specific capacities and power performances of conventional cathode materials are still needed to improve in order to meet the demand for electrical vehicles.Li-rich layered oxide delivers a high specific capacity,...The specific capacities and power performances of conventional cathode materials are still needed to improve in order to meet the demand for electrical vehicles.Li-rich layered oxide delivers a high specific capacity,but poor rate performances.Chemical doping is an effective way to address this challenge due to the expanded crystal lattice.Unlike a single ion substitution in the literature,here Li-rich layered oxides were doped by Sn and K to achieve the favorite rate performance,where Sn and K were assumed to replace transition metal ion and Li ion,respectively.Results indicate the co-doped samples result in an increasing capacity retention by more than 40%from 107.9(contrast sample)to 151.5 mAh g^(-1)(co-doped sample)at 10 C-rate.Electrochemical impedance spectroscopy(EIS)and calculated diffusion coefficient of Li^(+) also confirmed the favorite rate performances for co-doped sample.Combining results of Rietveld structure refinement,we proposed that the reason for rate performances comes from the enlarged crystal lattices,which provides a smooth diffusion tunnel for Lithium ions during the charge/discharge processes.The as-adopted method provides a possibility to achieve the improved rate performances by co-doping big-size ions at the different crystal sites.展开更多
A comparison study has been conducted on the strategies for synthesizing nanocrystalline Li2ZrO3 and K- doped Li2ZrO3 absorbents for CO2 capture at high temperatures, including solid-state and liquid-phase meth- ods, ...A comparison study has been conducted on the strategies for synthesizing nanocrystalline Li2ZrO3 and K- doped Li2ZrO3 absorbents for CO2 capture at high temperatures, including solid-state and liquid-phase meth- ods, citrate route, and starch-assisted sol-gel method combined with freeze-drying technique. The absorption properties, including uptake rate and absorption capacity, of synthesized absorbents were investigated by thermo- gravimetric analysis （TGA） at different CO2 partial pressures. The nanosized Li2ZrO3 crystals synthesized by the citrate route exhibit a faster uptake and a higher, nearly stoichiometric absorption capacity than those synthesized by the solid-state and liquid-phase methods. The doping of K into Li2ZrO3 can significantly improve the uptake rate of CO2, especially at low CO2 partial pressures. For the synthesis of K-doped Li2ZrO3, the citrate route has poor reproducibility and scalability, whereas the starch-assisted sol-gel method combined with freeze-drying technique is reproducible and easily scaled up, and the thus synthesized absorbents possess excellent CO2 capture properties.展开更多
文摘Ca3CO4O9 （CCO） and Ca2.95K0.05Co4O9 （CKCO） powders have been prepared by the polyacrylamide gel method. CKCO shows increased capacity and better cycling stability compared with CCO. After cycled for 50 cycles at 0.5 C, CKCO retains a capacity of 223 mAh.g-1, almost twice than CCO. The electrochemical impedance spectroscopy （EIS） tests shows the CKCO sample has a lower initial charge transfer resistance （Rot） and undergoes smaller Rot change during cycling than the CCO sample, indicating improved electrochemical performance by K-doping.
基金funded by the National Natural Science Foundation of China(22078138)the“Thousand Talents Plan”of Jiangxi Province(Jxsq2018101018)key projects of the Natural Science Foundation of Jiangxi Province(20202ACBL203009).
文摘Visible-light-driven photocatalysis is a promising technology for the treatment of dye wastewater.In this work,a novel photocatalyst of K-doped g-C_(3)N_(4) loaded on magnetic attapulgite(ATP)(Kω-g-C_(3)N_(4)@ATP-Fe_(3)O_(4))with excellent visible light photocatalytic properties and stability were successfully prepared and characterized.The removal efficiency of Kω-g-C_(3)N_(4)@ATP-Fe_(3)O_(4) for malachite green(MG)was studied,and the degradation mechanism was analyzed and proposed.It was found that the K_(5)-g-C_(3)N_(4)@ATP-Fe_(3)O_(4) photocatalyst possessed excellent degradation efficiency of over 98.0%for the MG dye wastewater under optimal conditions.Moreover,the K_(5)-g-C_(3)N_(4)@ATP-Fe_(3)O_(4) materials possessed good recyclability with a removal rate over 82%after 4 cycles.Under visible light condition,the K_(5)-g-C_(3)N_(4)@ATP-Fe_(3)O_(4) photocatalyst produce radicals of·OH and O_(2)^(-)to degrade the MG dyes,which was supported by electron paramagnetic resonance(EPR)and radical trapping experiments.In addition,the LC-MS analysis interpreted the degradation pathways and intermediates of MG in the solution.The findings in this work indicate that the prepared photocatalytic material has excellent degradation efficiency for MG and can be applied in dye wastewater treatment.
基金Project supported by the Fundamental Research Funds for the Cornell University(30919011220)the Key Project of Jiangsu Province Programs for Research and Development(BE2019115)+1 种基金Top-notch Academic Programs Project of Jiangsu Higher Education InstitutionsChina-Finland Industrial R&D Program(BZ2018015)。
文摘In this study,K_(x)-Mn-Ce catalysts prepared by sol-gel method were investigated for toluene oxidation.Compared with Mn-Ce,the catalytic performance of K_(x)-Mn-Ce was further improved.X-ray diffraction(XRD),high resolution transmission electron microscopy(HRTEM)and Raman analyses demonstrate that K ions enter the lattice of CeO_(2) and disperse uniformly.The results of X-ray photoelectron spectroscopy(XPS),H_(2)-temperature programmed reduction(H_(2)-TPR).and O_(2)-temperature programmed desorption(O_(2)-TPD)analyses indicate that there is a strong interaction between K,Mn and Ce;the charge co mpensation effect would be induced when K ions enter the lattice of CeO_(2),which leads to more oxygen vacancies due to the generation of more Ce^(3+).Toluene-TPD shows that K-doping enhances the activation ability of toluene.Among all catalysts,K0.1-Mn-Ce shows the highest concentration of Mn^(4+),Ce^(3+),Osur,and redox ability,resulting in higher low-temperature catalytic activity.Additionally,the results of stability and water resistance also prove that K0.1-Mn-Ce catalyst possesses excellent stability and water resistance.
基金supported by the National Natural Science Foundation of China(Nos.22368014 and 22478087)Guizhou Provincial S&T Project(Nos.GCC[2023]011 and ZK[2022]011).
文摘Photocatalytic selective synthesis of lactic acid(LA)from biomass sugars with a single heterogeneous catalyst is promising but challenging due to the multiple reaction steps involved.Herein,a K-doped C-rich red polymerized carbon nitride(RPCN)photocatalyst with uniform K/C dual sites was constructed by a molten salt template method,which was highly efficient for cascade isomerization dehydration of glucose to LA with>90%selectivity under visible light and gentle conditions.Control experiments and theoretical calculations expounded that the introduced K/C dual sites could improve the light capture ability and photogenerated charge separation efficiency,while the K species provided sufficient Lewis acid sites(adsorption sites)for the isomerization of glucose to fructose.Meanwhile,the introduced C sites that substitute N atoms could promote electrons to be captured by adsorbed oxygen for selective generation of superoxide radicals,which was highly efficient for the scission of the C3-C4 bond in fructose,exclusively furnishing LA.Importantly,the RPCN photocatalyst was also suitable for the photocatalytic upgrading of various biomass saccharides into LA with high yields of 81.3%-95.3%and could be recycled for five consecutive cycles.The tailored construction of dual sites by localization of space charge lightens an avenue for multi-step conversion of biomass with pronounced selectivity.
基金Project supported by the National Natural Science Foundation of China （Grant Nos. 10874051 and 50802096） and the Innovation Project for Young Talents of Hefei Institutes of Physical Science, Chinese Academy of Sciences （Grant No. O84N391123）.
文摘Ba0.6Sr0.4TiO3 thin films doped with K were deposited on Pt/Ti/SiO2/Si substrates by the chemical solution deposition method. The structure, surface morphology and the dielectric and tunable properties of Bao.6Sro.4TiO3 thin films have been studied in detail. The K content in Ba0.6Sro.4TiO3 thin films has a strong influence on the material＇s properties including surface morphology and the dielectric and tunable properties. It was found that the Curie temperature of K-doped Bao.6Sr0.4TiO3 films shifts to a higher value compared with that of undoped Ba0.6Sr0.4TiO3 thin films, which leads to a dielectric enhancement of K-doped Ba0.6Sr0.4TiO3 films at room temperature. At the optimized content of 0.02 mol, the dielectric loss tangent is reduced significantly from 0.057 to 0.020. Meanwhile, the tunability is enhanced obviously from 26% to 48% at the measured frequency of 1 MHz and the maximum value of the figure of merit is 23.8. This suggests that such films have potential applications for tunable devices.
基金This work was financially supported by the National Natural Science Foundation of China under Grant No.51772296,51672071,51802085the Foundation for State Key Laboratory of Biochemical Engineering,and“111”Project(D17007).
文摘The specific capacities and power performances of conventional cathode materials are still needed to improve in order to meet the demand for electrical vehicles.Li-rich layered oxide delivers a high specific capacity,but poor rate performances.Chemical doping is an effective way to address this challenge due to the expanded crystal lattice.Unlike a single ion substitution in the literature,here Li-rich layered oxides were doped by Sn and K to achieve the favorite rate performance,where Sn and K were assumed to replace transition metal ion and Li ion,respectively.Results indicate the co-doped samples result in an increasing capacity retention by more than 40%from 107.9(contrast sample)to 151.5 mAh g^(-1)(co-doped sample)at 10 C-rate.Electrochemical impedance spectroscopy(EIS)and calculated diffusion coefficient of Li^(+) also confirmed the favorite rate performances for co-doped sample.Combining results of Rietveld structure refinement,we proposed that the reason for rate performances comes from the enlarged crystal lattices,which provides a smooth diffusion tunnel for Lithium ions during the charge/discharge processes.The as-adopted method provides a possibility to achieve the improved rate performances by co-doping big-size ions at the different crystal sites.
基金The financial supports from the National Basic Research Program of China （2009CB626607）, the National Natural Science Foundation of China （21036006）, the Program for Changjiang Scholars and Innovative Research Team in Chinese Universities （IRT0980）, and the Program for Zhejiang Leading Team of Science and Technology Innovation （2011 R09020-05） are gratefully acknowledged.
文摘A comparison study has been conducted on the strategies for synthesizing nanocrystalline Li2ZrO3 and K- doped Li2ZrO3 absorbents for CO2 capture at high temperatures, including solid-state and liquid-phase meth- ods, citrate route, and starch-assisted sol-gel method combined with freeze-drying technique. The absorption properties, including uptake rate and absorption capacity, of synthesized absorbents were investigated by thermo- gravimetric analysis （TGA） at different CO2 partial pressures. The nanosized Li2ZrO3 crystals synthesized by the citrate route exhibit a faster uptake and a higher, nearly stoichiometric absorption capacity than those synthesized by the solid-state and liquid-phase methods. The doping of K into Li2ZrO3 can significantly improve the uptake rate of CO2, especially at low CO2 partial pressures. For the synthesis of K-doped Li2ZrO3, the citrate route has poor reproducibility and scalability, whereas the starch-assisted sol-gel method combined with freeze-drying technique is reproducible and easily scaled up, and the thus synthesized absorbents possess excellent CO2 capture properties.
