In the future power-electronics-dominated power systems,grid-forming(GFM)converters have been regarded as important devices to actively establish frequency and voltage,so as to provide essential grid support.However,d...In the future power-electronics-dominated power systems,grid-forming(GFM)converters have been regarded as important devices to actively establish frequency and voltage,so as to provide essential grid support.However,due to their voltage source behavior and emulated swing dynamics,GFM converters may encounter low-frequency oscillations(LFOs)when connected to strong grids,which belongs to the self-stability problem of GFM converters.Moreover,GFM converters will also interact with grid-following(GFL)converters and thus impact the mid-frequency oscillations(MFOs)induced by phase-locked loops(PLLs).It has been preliminarily shown in the literature that GFM converters can help stabilize the PLL-induced MFOs,but currently,there is a lack of systematic design methods to coordinate the self-stability and stabilizing ability of GFM converters.This paper addresses this gap by revisiting the impedance model of a typical GFM converter and briefly analyze the oscillations caused by converters.Based on our analysis,we propose a frequency-partitioned synthesis design framework to enable dynamic virtual impedance(DVI)in GFM converters,aiming to enhance their self-stability and stabilizing ability simultaneously.Particularly,a self-stabilizing module is designed to ensure robust device-level damping,with control parameters auto-tuned using H∞methods.In parallel,a stabilizing module is introduced to stabilize GFL converters and enhance the system-level stability,which utilizes a perceive-and-optimize tuning strategy.Simulation results validate the effectiveness of the proposed synthesis DVI framework.展开更多
Understanding the factors triggering slope failure is essential to ensure the safety of buildings and transportation infrastructure on slopes. Specifically,the failure of stabilizing piles due to groundwater migration...Understanding the factors triggering slope failure is essential to ensure the safety of buildings and transportation infrastructure on slopes. Specifically,the failure of stabilizing piles due to groundwater migration and freeze–thaw(FT) cycles is a significant factor causing slope failure. This study aims to investigate the transmedia seepage characteristics at slope–concrete stabilizing pile interface systems by using silty clay and concrete with varying microstructure characteristics under FT cycles. To this end, a self-developed indoor test device for transmedia water migration, combined with a macro-meso-micro multiscale testing approach, was used to analyze the laws and mechanisms of transmedia seepage at the interface systems. The effect of the medium's microstructure characteristics on the transmedia seepage behavior at the interface systems under FT cycles was also assessed. Results indicated that the transmedia water migration exhibited particularity due to the migration of soil particles and the low permeability characteristics of concrete. The water content in the media increased significantly within the range of 1/3–2/3 of the height from the interface for soil and within 5 mm from the interface for concrete.FT cycles promoted the increase and penetration of cracks within the medium, enhancing the permeability of the slope-concrete stabilizing pile interface systems.With the increase in FT cycles, the porosity inside the medium first decreased and then increased, and the porosity reached the minimum after 25 FT cycles and the maximum after 75 FT cycles, and the water content of the medium after water migration was positively correlated with the porosity. FT cycles also significantly influenced the temporal variation characteristics of soil moisture and the migration path of water in concrete. The study results could serve as a reference for related research on slope stability assessment.展开更多
Aqueous sodium-ion batteries(ASIBs) offer significant advantages for energy storage on a large scale,attributed to their economical cost,secure operatio n,and eco-friend ly natu re.Among the leading cathode materials ...Aqueous sodium-ion batteries(ASIBs) offer significant advantages for energy storage on a large scale,attributed to their economical cost,secure operatio n,and eco-friend ly natu re.Among the leading cathode materials for ASIBs,Na_(3)V_(2)(PO_(4))_(3)(NVP) exhibits excellent structural stability and a high Na+diffusion coefficient,making it a promising option.However,the high solubility of vanadium-based materials in aqueous electrolytes engenders suboptimal cycling stability for Na_(3)V_(2)(PO_(4))_(3),constraining its application in ASIBs.Herein,the Cr-substituted Na_(3)V_(1.3)Cr_(0.7)(PO_(4))3@C(NV_(1.3)Cr_(0.7)P) cathode material was synthesized via a simple sol-gel method.It is found that Cr substitution reduces the cell parameters of NV_(1.3)Cr_(0.7)P,effectively reinforcing the crystal structure.Furthermore,NV_(1.3)Cr_(0.7)P alters the Na^(+)insertion/extraction mechanism,transforming the typical two-phase reaction between Na_(1)V_(2)(PO_(4))_(3)and Na_(3)V_(2)(PO_(4))3into continuous solid-solution reactions with stable intermediates.The Cr substitution diminishes the sodium-ion diffusion energy barrier in NV_(1.3)Cr_(0.7)P,leading to smoother Na+insertion and extraction processes.Consequently,NV_(1.3)Cr_(0.7)P exhibits impressive cycling stability,retaining 74.8% of its capacity after 5,000 cycles at a current density of 5 A g^(-1),along with an outstanding rate performance of 79,2% at 10 A g^(-1).This work elucidates the stable Na^(+)insertion/extraction processes in Cr-substituted NV_(1.3)Cr_(0.7)P,offering insights into the application of vanadium-based materials in aqueous sodium-ion batteries.展开更多
Selective electrocatalytic semi-hydrogenation(ECSH)of alkynes in water using Cu catalysts is highly relevant for the production of value-added chemicals.However,achieving high olefin selectivity still poses extreme ch...Selective electrocatalytic semi-hydrogenation(ECSH)of alkynes in water using Cu catalysts is highly relevant for the production of value-added chemicals.However,achieving high olefin selectivity still poses extreme challenges due to the susceptibility of the copper cathode in a reduction environment.Herein,a small molecule modulation electrodeposition strategy is introduced that regulates the structure of Cubased materials through modification with citric acid(CA)ligands,aiming for highly active and selective ECSH.The as-prepared EDCu-CA electrode achieves more than 97%alkyne conversion and 99%olefin selectivity.In-situ Raman and Auger electron spectroscopy(AES)data provide evidence that active Cu^(+)sites can stably exist in the EDCu-CA during the catalytic process.Density functional theory(DFT)calculations indicate that the modulation by CA contributes to maintaining Cu in a positive valence state,and Cu^(+)can inhibit the over-hydrogenation of olefins.Moreover,by utilizing a large-area electrode for longterm electrolysis,g-level conversion and a 92%separation yield of olefin can be achieved,demonstrating a viable application prospect.This study offers a promising route for designing Cu-based catalysts for the highly selective electrocata lytic conversion of organic substrates to value-added chemicals in water.展开更多
ln order to improve the level of investment promotion and redouble effortsto enhance services,on February l9th,the 2025 Action Plan for StabilizingForeign lnvestment was released,proposing 20 measures in four aspects....ln order to improve the level of investment promotion and redouble effortsto enhance services,on February l9th,the 2025 Action Plan for StabilizingForeign lnvestment was released,proposing 20 measures in four aspects.Cur-rently,with increasing uncertainties in the external environment,China facesmultple difficulties and challenges in attracting foreign investment.展开更多
Augmenting the working voltage is an effective way to maximize the energy density of Ni-rich layered Li[Ni_(0.8)Co_(0.1)Mn_(0.1)]O_(2)(NCM)to approach its theoretical capacity.However,NCM suffers from structural degra...Augmenting the working voltage is an effective way to maximize the energy density of Ni-rich layered Li[Ni_(0.8)Co_(0.1)Mn_(0.1)]O_(2)(NCM)to approach its theoretical capacity.However,NCM suffers from structural degradation in deep delithiation state,which is often accompanied by severe surface lattice oxygen loss and transition metal dissolution,leading to restricted cycle life.Herein,a facile and effective surfacestrengthening strategy is proposed,in which Mn(OH)_(2)nanoshells are uniformly grown on the NCM surface as a Li~+capturer and then converted to thin spinel Li_(4)Mn_(5)O_(12)layers during subsequent hightemperature sintering.The resultant Li_(4)Mn_(5)O_(12)layers can enhance cathode-electrolyte interface electrochemical stability with inhibited electrolyte corrosion and accelerated Li~+kinetics.The theoretical calculations confirms that the Mn-O bonds formed at the interfaces can effectively decrease the oxygen activity,thereby further inhibiting the lattice oxygen release and structural degradation caused by the irreversible phase transition.Consequently,the Li_(4)Mn_(5)O_(12)-coated NCM displays high capacity retention of 80.3%and 94.9%at 1 C and 5 C compared to the pristine NCM(52.5%and 10.1%)after 200 cycles and can operate stably at 2.7-4.6 V and 60℃.The spinel Li_(4)Mn_(5)O_(12)-coating demonstrates an effective route to enhance the structural/electrochemical stability of NCM for next-generation advanced lithium-ion batteries.展开更多
P2-type layered oxides are highly promising cathode candidates for sodium-ion batteries(SIBs)owing to their substantial theoretical capacity.Nevertheless,structural degradation caused by transition metal dissolution a...P2-type layered oxides are highly promising cathode candidates for sodium-ion batteries(SIBs)owing to their substantial theoretical capacity.Nevertheless,structural degradation caused by transition metal dissolution and irreversible phase transitions at high voltage severely compromises cycling stability.To address this limitation,we propose a Li/Ti co-doping strategy to design a Na_(0.67)Li_(0.06)Ni_(0.27)Mn_(0.5)7Ti_(0.1)O_(2)(NLMT) cathode for SIBs.In-situ X-ray diffraction(XRD) confirms that this deliberate strategy eliminates the adverse phase transition at high voltage and sustains the unitary P2phase throughout cycling.In addition,strengthened transition metal-oxygen(TM-O) bonding via electronic modulation suppresses transition metal dissolution and reinforces the layered oxide framework,contributing to exceptional electrochemical performance.Consequently,the NLMT cathode exhibits an outstanding capacity of 92.8 mA h g^(-1) within 2.5-4.3 V at 5 C(865 mA g^(-1)),with 87 % capacity retention over 200 cycles.Configured into a full cell,which achieves a competitive capacity of 107.7 mA h g^(-1) at0.1 C and retains 86.4 % capacity over 100 cycles at 0.5 C.This study validates co-doping as a potent strategy for significantly improving the long-term cyclability of layered oxide cathodes in SIBs.展开更多
Neutral oxygen evolution reaction(OER)is a crucial half-reaction for electrocatalytic chemical production under mild condition,but with limited development due to low activity and poor stability.Herein,a tungsten-dope...Neutral oxygen evolution reaction(OER)is a crucial half-reaction for electrocatalytic chemical production under mild condition,but with limited development due to low activity and poor stability.Herein,a tungsten-doped cobalt molybdate(WDCMO)catalyst was synthesized for efficient and durable OER under neutral electrolyte.It is demonstrated that catalyst reconstruction is suppressed by W doping,which stabilizes the Co-O-Mo point-to-point connection in CoMoO_(4) architecture and stimulates to a lower valence state of active sites over the surface phase.Thereby,the surface structure maintains to avoid compound dissolution caused by over-oxidation during OER.Meanwhile,the WDCMO catalyst promotes charge transfer and optimizes*OH intermediate adsorption,which improves reaction kinetics and intrinsic activity.Consequently,the WDCMO electrode exhibits an overpotential of 302 mV at 10 mA cm^(-2) in neutral electrolyte with an improvement of 182 mV compared with CoMoO4 electrode.Furthermore,W doping significantly improves the electrode stability from 50 h to more than 320 h,with a suppressive potential attenuation from 2.82 to 0.29 mV h^(-1).This work will shed new light on designing rational electrocatalysts for neutral OER.展开更多
Vitamin C,a potent antioxidant with broad therapeutic applications,is limited by rapid degradation under environmental stressors,which compromises its stability and bioactivity.This study addresses these limitations b...Vitamin C,a potent antioxidant with broad therapeutic applications,is limited by rapid degradation under environmental stressors,which compromises its stability and bioactivity.This study addresses these limitations by formulating a double nano-emulsion(W/O/W)system incorporating macadamia oil and tea tree oil,using homogenization and phase inversion temperature(PIT)techniques.Comprehensive physicochemical charac-terization,including droplet size,polydispersity index(PDI),zeta potential,turbidity,Fourier transform infrared spectroscopy(FTIR),and SEM,was conducted alongside stability assessments under varying pH,temperature,and storage conditions.The optimized nano-emulsions exhibited nanoscale droplet sizes(10-40 nm),low PDI values(indicating high uniformity),and robust stability.Interestingly,the formulation with 2%W/O loading,with a particle size of 11.57 nm and a PDI of 0.04,demonstrated an antioxidant capacity of 4622.62μg ascorbic acid equivalents(AA)/g,which was significantly higher(p<0.05)compared to both natural oils(macadamia oil:20.91μg AA/g,tea tree oil:16.86μg AA/g)and a 10%Vitamin C aqueous solution(592.94μg AA/g).FTIR analysis confirmed the molecular integrity of Vitamin C and its successful encapsulation with macadamia and tea tree oils,while SEM images revealed uniformly spherical and well-dispersed droplets.Moreover,the formulation retained its structural integrity and antioxidant functionality under diverse pH and thermal conditions.These findings underscore the potential of double nano-emulsion systems to overcome the stability challenges of Vitamin C,offering a promising approach to enhance its bioavailability and therapeutic performance in phar-maceutical and cosmetic applications.展开更多
The uncontrollable dendrite growth of lithium anode and active material dissolution of transition metal oxides cathodes severely hinder the development of lithium metal batteries.An effective strategy to address these...The uncontrollable dendrite growth of lithium anode and active material dissolution of transition metal oxides cathodes severely hinder the development of lithium metal batteries.An effective strategy to address these issues is optimizing the separator to regulate ion transport and trap the lost active component.Herein,a crosslinked gelatin nonwoven(CGN)separator is elaborately fabricated through electrospinning and in-situ vapor phase crosslinking process to manipulate the dual electrode interface.Benefitting from the characteristic composition of gelatin,and porous structure of electrospun nonwoven,the CGN separator exhibits excellent interface wettability and low interface resistance,featuring a high Li^(+)transference number of 0.70 and high ionic conductivity of 3.75 m S/cm.As expected,the symmetrical Li/Li cells present stable cycling behavior for 1900 h at 0.5 mA/cm^(2)with low overpotential of 20 mV.The optimized LiMn_(2)O_(4)/Li cells deliver high reversible capacity of 103 m Ah/g as well as high capacityretention ratio of 83.7%after 100 cycles at 0.3 C,which can be effectively attributed to the strong interaction between CGN separator and Mn ions to prevent the loss of active Mn component.This study indicates the application potential of protein-based electrospun membrane for high-performance lithium metal batteries.展开更多
The microstructures of as-extruded and stabilizing heat-treated Zn-10Al-2Cu-0.02Ti alloys were observed by scanning electron microscopy,transmission electron microscopy,electron probe microanalysis and X-ray diffracti...The microstructures of as-extruded and stabilizing heat-treated Zn-10Al-2Cu-0.02Ti alloys were observed by scanning electron microscopy,transmission electron microscopy,electron probe microanalysis and X-ray diffraction analysis techniques.The change in structure after heat treatment and its effects on room temperature creep behavior were investigated by creep experiments at constant stress and slow strain rate tensile tests.The results show that after stabilizing heat treatment（（350℃,30 min,water-cooling）＋（100℃,12 h,air-cooling））,the amount of α＋η lamellar structure decreases,while the amount of cellular and granular structure increases.The heat-treated Zn-10Al-2Cu-0.02Ti alloy exhibits better creep resistance than the as-extruded alloy,and the rate of steady state creep decreases by 96.9% after stabilizing heat treatment.展开更多
基金supported by National Natural Science Foundation of China(U24B6008,U22B6008)State Grid Zhejiang Electric Power Co.,Ltd.Science,and Technology Project(B311DS240015).
文摘In the future power-electronics-dominated power systems,grid-forming(GFM)converters have been regarded as important devices to actively establish frequency and voltage,so as to provide essential grid support.However,due to their voltage source behavior and emulated swing dynamics,GFM converters may encounter low-frequency oscillations(LFOs)when connected to strong grids,which belongs to the self-stability problem of GFM converters.Moreover,GFM converters will also interact with grid-following(GFL)converters and thus impact the mid-frequency oscillations(MFOs)induced by phase-locked loops(PLLs).It has been preliminarily shown in the literature that GFM converters can help stabilize the PLL-induced MFOs,but currently,there is a lack of systematic design methods to coordinate the self-stability and stabilizing ability of GFM converters.This paper addresses this gap by revisiting the impedance model of a typical GFM converter and briefly analyze the oscillations caused by converters.Based on our analysis,we propose a frequency-partitioned synthesis design framework to enable dynamic virtual impedance(DVI)in GFM converters,aiming to enhance their self-stability and stabilizing ability simultaneously.Particularly,a self-stabilizing module is designed to ensure robust device-level damping,with control parameters auto-tuned using H∞methods.In parallel,a stabilizing module is introduced to stabilize GFL converters and enhance the system-level stability,which utilizes a perceive-and-optimize tuning strategy.Simulation results validate the effectiveness of the proposed synthesis DVI framework.
基金financially supported by Jilin Provincial Natural Science Foundation (No.20220101164JC)。
文摘Understanding the factors triggering slope failure is essential to ensure the safety of buildings and transportation infrastructure on slopes. Specifically,the failure of stabilizing piles due to groundwater migration and freeze–thaw(FT) cycles is a significant factor causing slope failure. This study aims to investigate the transmedia seepage characteristics at slope–concrete stabilizing pile interface systems by using silty clay and concrete with varying microstructure characteristics under FT cycles. To this end, a self-developed indoor test device for transmedia water migration, combined with a macro-meso-micro multiscale testing approach, was used to analyze the laws and mechanisms of transmedia seepage at the interface systems. The effect of the medium's microstructure characteristics on the transmedia seepage behavior at the interface systems under FT cycles was also assessed. Results indicated that the transmedia water migration exhibited particularity due to the migration of soil particles and the low permeability characteristics of concrete. The water content in the media increased significantly within the range of 1/3–2/3 of the height from the interface for soil and within 5 mm from the interface for concrete.FT cycles promoted the increase and penetration of cracks within the medium, enhancing the permeability of the slope-concrete stabilizing pile interface systems.With the increase in FT cycles, the porosity inside the medium first decreased and then increased, and the porosity reached the minimum after 25 FT cycles and the maximum after 75 FT cycles, and the water content of the medium after water migration was positively correlated with the porosity. FT cycles also significantly influenced the temporal variation characteristics of soil moisture and the migration path of water in concrete. The study results could serve as a reference for related research on slope stability assessment.
基金financially supported by the Scientific and Technological Plan Project of Guizhou Province ([2024]054)Additional support came from the Industry and Education Combination Innovation Platform of Intelligent Manufacturing and Graduate Joint Training Base at Guizhou University (2020-520000-83-01324061)the Guizhou Engineering Research Center for Smart Services (2203-520102-04-04-298868)。
文摘Aqueous sodium-ion batteries(ASIBs) offer significant advantages for energy storage on a large scale,attributed to their economical cost,secure operatio n,and eco-friend ly natu re.Among the leading cathode materials for ASIBs,Na_(3)V_(2)(PO_(4))_(3)(NVP) exhibits excellent structural stability and a high Na+diffusion coefficient,making it a promising option.However,the high solubility of vanadium-based materials in aqueous electrolytes engenders suboptimal cycling stability for Na_(3)V_(2)(PO_(4))_(3),constraining its application in ASIBs.Herein,the Cr-substituted Na_(3)V_(1.3)Cr_(0.7)(PO_(4))3@C(NV_(1.3)Cr_(0.7)P) cathode material was synthesized via a simple sol-gel method.It is found that Cr substitution reduces the cell parameters of NV_(1.3)Cr_(0.7)P,effectively reinforcing the crystal structure.Furthermore,NV_(1.3)Cr_(0.7)P alters the Na^(+)insertion/extraction mechanism,transforming the typical two-phase reaction between Na_(1)V_(2)(PO_(4))_(3)and Na_(3)V_(2)(PO_(4))3into continuous solid-solution reactions with stable intermediates.The Cr substitution diminishes the sodium-ion diffusion energy barrier in NV_(1.3)Cr_(0.7)P,leading to smoother Na+insertion and extraction processes.Consequently,NV_(1.3)Cr_(0.7)P exhibits impressive cycling stability,retaining 74.8% of its capacity after 5,000 cycles at a current density of 5 A g^(-1),along with an outstanding rate performance of 79,2% at 10 A g^(-1).This work elucidates the stable Na^(+)insertion/extraction processes in Cr-substituted NV_(1.3)Cr_(0.7)P,offering insights into the application of vanadium-based materials in aqueous sodium-ion batteries.
基金financially supported by the National Natural Science Foundation of China(NSFC)(22179056,22172018)the Liaoning Revitalization Talents Program(XLYC2002097,1807210)+2 种基金the Key Projects of Liaoning Provincial Education Department(JYTZD2023001)the Fundamental Research Funds for the Central Universities(DUT23LAB611)Yingkou Talents Program。
文摘Selective electrocatalytic semi-hydrogenation(ECSH)of alkynes in water using Cu catalysts is highly relevant for the production of value-added chemicals.However,achieving high olefin selectivity still poses extreme challenges due to the susceptibility of the copper cathode in a reduction environment.Herein,a small molecule modulation electrodeposition strategy is introduced that regulates the structure of Cubased materials through modification with citric acid(CA)ligands,aiming for highly active and selective ECSH.The as-prepared EDCu-CA electrode achieves more than 97%alkyne conversion and 99%olefin selectivity.In-situ Raman and Auger electron spectroscopy(AES)data provide evidence that active Cu^(+)sites can stably exist in the EDCu-CA during the catalytic process.Density functional theory(DFT)calculations indicate that the modulation by CA contributes to maintaining Cu in a positive valence state,and Cu^(+)can inhibit the over-hydrogenation of olefins.Moreover,by utilizing a large-area electrode for longterm electrolysis,g-level conversion and a 92%separation yield of olefin can be achieved,demonstrating a viable application prospect.This study offers a promising route for designing Cu-based catalysts for the highly selective electrocata lytic conversion of organic substrates to value-added chemicals in water.
文摘ln order to improve the level of investment promotion and redouble effortsto enhance services,on February l9th,the 2025 Action Plan for StabilizingForeign lnvestment was released,proposing 20 measures in four aspects.Cur-rently,with increasing uncertainties in the external environment,China facesmultple difficulties and challenges in attracting foreign investment.
基金financial support from the Key Research and Development Project in Shaanxi Province(2023-YBGY-446)the Shanxi-Zheda Institute of Advanced Materials and Chemical Engineering(No.2022SX-TD003)+1 种基金the Natural Science Basic Research Program of Shaanxi(No.2024JC-YBQN-0108)the Key Laboratory of Interface Science and Engineering in Advanced Materials,Ministry of Education(KLISEAM202202)。
文摘Augmenting the working voltage is an effective way to maximize the energy density of Ni-rich layered Li[Ni_(0.8)Co_(0.1)Mn_(0.1)]O_(2)(NCM)to approach its theoretical capacity.However,NCM suffers from structural degradation in deep delithiation state,which is often accompanied by severe surface lattice oxygen loss and transition metal dissolution,leading to restricted cycle life.Herein,a facile and effective surfacestrengthening strategy is proposed,in which Mn(OH)_(2)nanoshells are uniformly grown on the NCM surface as a Li~+capturer and then converted to thin spinel Li_(4)Mn_(5)O_(12)layers during subsequent hightemperature sintering.The resultant Li_(4)Mn_(5)O_(12)layers can enhance cathode-electrolyte interface electrochemical stability with inhibited electrolyte corrosion and accelerated Li~+kinetics.The theoretical calculations confirms that the Mn-O bonds formed at the interfaces can effectively decrease the oxygen activity,thereby further inhibiting the lattice oxygen release and structural degradation caused by the irreversible phase transition.Consequently,the Li_(4)Mn_(5)O_(12)-coated NCM displays high capacity retention of 80.3%and 94.9%at 1 C and 5 C compared to the pristine NCM(52.5%and 10.1%)after 200 cycles and can operate stably at 2.7-4.6 V and 60℃.The spinel Li_(4)Mn_(5)O_(12)-coating demonstrates an effective route to enhance the structural/electrochemical stability of NCM for next-generation advanced lithium-ion batteries.
基金supported by the National Science Foundation of China (Grant No.22179094)the Science and Technology Program of Cangzhou (Grant No.222103001)the research funding of Cangzhou Institute of Tiangong University (Grant No.TGCYY-Z0202)。
文摘P2-type layered oxides are highly promising cathode candidates for sodium-ion batteries(SIBs)owing to their substantial theoretical capacity.Nevertheless,structural degradation caused by transition metal dissolution and irreversible phase transitions at high voltage severely compromises cycling stability.To address this limitation,we propose a Li/Ti co-doping strategy to design a Na_(0.67)Li_(0.06)Ni_(0.27)Mn_(0.5)7Ti_(0.1)O_(2)(NLMT) cathode for SIBs.In-situ X-ray diffraction(XRD) confirms that this deliberate strategy eliminates the adverse phase transition at high voltage and sustains the unitary P2phase throughout cycling.In addition,strengthened transition metal-oxygen(TM-O) bonding via electronic modulation suppresses transition metal dissolution and reinforces the layered oxide framework,contributing to exceptional electrochemical performance.Consequently,the NLMT cathode exhibits an outstanding capacity of 92.8 mA h g^(-1) within 2.5-4.3 V at 5 C(865 mA g^(-1)),with 87 % capacity retention over 200 cycles.Configured into a full cell,which achieves a competitive capacity of 107.7 mA h g^(-1) at0.1 C and retains 86.4 % capacity over 100 cycles at 0.5 C.This study validates co-doping as a potent strategy for significantly improving the long-term cyclability of layered oxide cathodes in SIBs.
文摘Neutral oxygen evolution reaction(OER)is a crucial half-reaction for electrocatalytic chemical production under mild condition,but with limited development due to low activity and poor stability.Herein,a tungsten-doped cobalt molybdate(WDCMO)catalyst was synthesized for efficient and durable OER under neutral electrolyte.It is demonstrated that catalyst reconstruction is suppressed by W doping,which stabilizes the Co-O-Mo point-to-point connection in CoMoO_(4) architecture and stimulates to a lower valence state of active sites over the surface phase.Thereby,the surface structure maintains to avoid compound dissolution caused by over-oxidation during OER.Meanwhile,the WDCMO catalyst promotes charge transfer and optimizes*OH intermediate adsorption,which improves reaction kinetics and intrinsic activity.Consequently,the WDCMO electrode exhibits an overpotential of 302 mV at 10 mA cm^(-2) in neutral electrolyte with an improvement of 182 mV compared with CoMoO4 electrode.Furthermore,W doping significantly improves the electrode stability from 50 h to more than 320 h,with a suppressive potential attenuation from 2.82 to 0.29 mV h^(-1).This work will shed new light on designing rational electrocatalysts for neutral OER.
基金Ho Chi Minh City University of Technology(HCMUT),VNU-HCM for supporting this study.
文摘Vitamin C,a potent antioxidant with broad therapeutic applications,is limited by rapid degradation under environmental stressors,which compromises its stability and bioactivity.This study addresses these limitations by formulating a double nano-emulsion(W/O/W)system incorporating macadamia oil and tea tree oil,using homogenization and phase inversion temperature(PIT)techniques.Comprehensive physicochemical charac-terization,including droplet size,polydispersity index(PDI),zeta potential,turbidity,Fourier transform infrared spectroscopy(FTIR),and SEM,was conducted alongside stability assessments under varying pH,temperature,and storage conditions.The optimized nano-emulsions exhibited nanoscale droplet sizes(10-40 nm),low PDI values(indicating high uniformity),and robust stability.Interestingly,the formulation with 2%W/O loading,with a particle size of 11.57 nm and a PDI of 0.04,demonstrated an antioxidant capacity of 4622.62μg ascorbic acid equivalents(AA)/g,which was significantly higher(p<0.05)compared to both natural oils(macadamia oil:20.91μg AA/g,tea tree oil:16.86μg AA/g)and a 10%Vitamin C aqueous solution(592.94μg AA/g).FTIR analysis confirmed the molecular integrity of Vitamin C and its successful encapsulation with macadamia and tea tree oils,while SEM images revealed uniformly spherical and well-dispersed droplets.Moreover,the formulation retained its structural integrity and antioxidant functionality under diverse pH and thermal conditions.These findings underscore the potential of double nano-emulsion systems to overcome the stability challenges of Vitamin C,offering a promising approach to enhance its bioavailability and therapeutic performance in phar-maceutical and cosmetic applications.
基金supported by National Natural Science Foundation of China(No.22309029)Guangdong Basic and Applied Basic Research Foundation(No.2024A1515140011)+1 种基金Dongguan Social Development Technology Foundation(No.20231800907933)Collaborative Innovation Center of Marine Science and Technology of Hainan University(No.XTCX2022HYC14)。
文摘The uncontrollable dendrite growth of lithium anode and active material dissolution of transition metal oxides cathodes severely hinder the development of lithium metal batteries.An effective strategy to address these issues is optimizing the separator to regulate ion transport and trap the lost active component.Herein,a crosslinked gelatin nonwoven(CGN)separator is elaborately fabricated through electrospinning and in-situ vapor phase crosslinking process to manipulate the dual electrode interface.Benefitting from the characteristic composition of gelatin,and porous structure of electrospun nonwoven,the CGN separator exhibits excellent interface wettability and low interface resistance,featuring a high Li^(+)transference number of 0.70 and high ionic conductivity of 3.75 m S/cm.As expected,the symmetrical Li/Li cells present stable cycling behavior for 1900 h at 0.5 mA/cm^(2)with low overpotential of 20 mV.The optimized LiMn_(2)O_(4)/Li cells deliver high reversible capacity of 103 m Ah/g as well as high capacityretention ratio of 83.7%after 100 cycles at 0.3 C,which can be effectively attributed to the strong interaction between CGN separator and Mn ions to prevent the loss of active Mn component.This study indicates the application potential of protein-based electrospun membrane for high-performance lithium metal batteries.
基金Project(2009BAE71B00) supported by the National Key Technology R&D Program during the Eleventh Five-Year Plan Period
文摘The microstructures of as-extruded and stabilizing heat-treated Zn-10Al-2Cu-0.02Ti alloys were observed by scanning electron microscopy,transmission electron microscopy,electron probe microanalysis and X-ray diffraction analysis techniques.The change in structure after heat treatment and its effects on room temperature creep behavior were investigated by creep experiments at constant stress and slow strain rate tensile tests.The results show that after stabilizing heat treatment（（350℃,30 min,water-cooling）＋（100℃,12 h,air-cooling））,the amount of α＋η lamellar structure decreases,while the amount of cellular and granular structure increases.The heat-treated Zn-10Al-2Cu-0.02Ti alloy exhibits better creep resistance than the as-extruded alloy,and the rate of steady state creep decreases by 96.9% after stabilizing heat treatment.
