Carbonate electrolytes are one of the most desirable electrolytes for high-energy lithium-sulfur batteries(LSBs)because of their successful implementation in commercial Li-ion batteries.The low-polysulfide-solubility ...Carbonate electrolytes are one of the most desirable electrolytes for high-energy lithium-sulfur batteries(LSBs)because of their successful implementation in commercial Li-ion batteries.The low-polysulfide-solubility feature of some carbonate solvents also makes them very promising for overcoming the shuttle effects of LSBs.However,regular sulfur electrodes experience undesired electrochemical mechanisms in carbonate electrolytes due to side reactions.In this study,we report a catalytic redox mechanism of sulfur in propylene carbonate(PC)electrolyte based on a compari-son study.The catalytic mechanism is characterized by the interactions between polysulfides and dual N/O functional groups on the host carbon,which largely prevents side reactions between pol-ysulfides and the carbonate electrolyte.Such a mechanism coupled with the low-polysulfide-solubility feature leads to stable cycling of LSBs in PC electrolyte.Favorable dual N/O functional groups are identified via a density functional theory study.This work provides an alternative route for enabling LSBs in carbonate electrolytes.展开更多
To facilitate the electrochemical CO_(2) reduction(ECR)to fuels and valuable chemicals,the development of active,low cost,and selective catalysts is crucial.We report a novel ECR catalyst consisting of CuO nanoparticl...To facilitate the electrochemical CO_(2) reduction(ECR)to fuels and valuable chemicals,the development of active,low cost,and selective catalysts is crucial.We report a novel ECR catalyst consisting of CuO nanoparticles with sizes ranging from 1.4 to 3.3 nm anchored on Cu metal‐organic framework(Cu‐MOF)nanosheets obtained through a one‐step facile solvothermal method.The nanocomposites provide multiple sites for efficient ambient ECR,delivering an average C_(2)H_(4) faradaic efficiency(FE)of~50.0%at–1.1 V(referred to the reversible hydrogen electrode)in 0.1 mol/L aqueous KHCO_(3) using a two‐compartment cell,in stark contrast to a C_(2)H_(4) FE of 25.5%and 37.6%over individual CuO and Cu‐MOF respectively,also surpassing most newly reported Cu‐based materials under similar cathodic voltages.The C_(2)H_(4) FE remains at over 45.0%even after 10.0 h of successive polarization.Also,a~7.0 mA cm^(–2) C_(2)H_(4) partial geometric current density and 27.7%half‐cell C_(2)H_(4) power conversion efficiency are achieved.The good electrocatalytic performance can be attributed to the interface between CuO and Cu‐MOF,with accessible metallic moieties and the unique two‐dimensional structure of the Cu‐MOF enhancing the adsorption and activation of CO_(2) molecules.This finding offers a simple avenue to upgrading CO_(2) to value‐added hydrocarbons by rational design of MOF‐based composites.展开更多
The Chepaizi Exploration Area,Junggar Basin(NW China)holds substantial importance for seismic exploration endeavors,yet it poses notable challenges due to the intricate nature of its subsurface and near-surface condit...The Chepaizi Exploration Area,Junggar Basin(NW China)holds substantial importance for seismic exploration endeavors,yet it poses notable challenges due to the intricate nature of its subsurface and near-surface conditions.To address these challenges,we introduce a novel and comprehensive workflow tailored to evaluate and optimize seismic acquisition geometries while considering the impacts of near-surface viscosity.By integrating geological knowledge,historical seismic data,and subsurface modeling,we conduct simulations employing the visco-acoustic wave equation and reverse-time migration to produce detailed subsurface images.The quality of these images is quantitatively evaluated using a local similarity metric,a pivotal tool for evaluating the accuracy of seismic imaging.The culmination of this workflow results in an automated optimization strategy for acquisition geometries that enhances subsurface exploration.Our proposed methodology underscores the importance of incorporating near-surface viscosity effects in seismic imaging,offering a robust framework for improving the accuracy of subsurface imaging.Herein,we aim to contribute to the advancement of seismic imaging methodologies by providing valuable insights for achieving high-quality seismic exploration outcomes in regions characterized by complex subsurface and near-surface conditions.展开更多
Since the D-band center theory was proposed,it has been widely used in the fields of surface chemistry by almost all researchers,due to its easy understanding,convenient operation and relative accuracy.However,with th...Since the D-band center theory was proposed,it has been widely used in the fields of surface chemistry by almost all researchers,due to its easy understanding,convenient operation and relative accuracy.However,with the continuous development of material systems and modification strategies,researchers have gradually found that D-band center theory is usually effective for large metal particle systems,but for small metal particle systems or semiconductors,such as single atom systems,the opposite conclusion to the D-band center theory is often obtained.To solve the issue above,here we propose a bonding and anti-bonding orbitals stable electron intensity difference(BASED)theory for surface chemistry.The newly-proposed BASED theory can not only successfully explain the abnormal phenomena of D-band center theory,but also exhibits a higher accuracy for prediction of adsorption energy and bond length of intermediates on active sites.Importantly,a new phenomenon of the spin transition state in the adsorption process is observed based on the BASED theory,where the active center atom usually yields an unstable high spin transition state to enhance its adsorption capability in the adsorption process of intermediates when their distance is about 2.5Å.In short,the BASED theory can be considered as a general principle to understand catalytic mechanism of intermediates on surfaces.展开更多
The hydrogenation of CO_(2) into methanol has attracted much attention and In_(2)O_(3) is a promising catalyst.Introducing metal elements into In_(2)O_(3)(M/In_(2)O_(3))is one of the main strategies to improve its per...The hydrogenation of CO_(2) into methanol has attracted much attention and In_(2)O_(3) is a promising catalyst.Introducing metal elements into In_(2)O_(3)(M/In_(2)O_(3))is one of the main strategies to improve its performance.However,its mechanism and active sites remain unclear and need to be further elucidated.Here,the noble‐metal‐free In_(x)‐Co_(y) oxides catalysts were prepared.Much‐improved performance and obvious product selectivity shift were observed.The optimized catalyst(In_(1)‐Co_(4))(9.7 mmol g_(cat)^(–1) h^(–1))showed five times methanol yields than pure In_(2)O_(3)(2.2 mmol g_(cat)^(–1) h^(–1))(P=4.0 MPa,T=300°C,GHSV=24000 cm^(3)_(STP) g_(cat)^(–1) h^(–1),H_(2):CO_(2)=3).And the cobalt‐catalyzed CO_(2) methanation activity was suppressed,although cobalt was most of the metal element.To unravel this selectivity shift,detailed catalysts performance evaluation,together with several in‐situ and ex‐situ characterizations,were employed on cobalt and In‐Co for comparative study.The results indicated CO_(2) hydrogenation on cobalt and In‐Co catalyst both followed the formate pathway,and In‐Co reconstructed and generated a surface In_(2)O_(3)‐enriched core‐shell‐like structure under a reductive atmosphere.The enriched In_(2)O_(3) at the surface significantly enhanced CO_(2) adsorption capacity and well stabilized the intermediates of CO_(2) hydrogenation.CO_(2) and carbon‐containing intermediates adsorbed much stronger on In‐Co than cobalt led to a feasible surface C/H ratio,thus allowing the*CH_(3)O to desorb to produce CH_(3)OH instead of being over‐hydrogenated to CH_(4).展开更多
NOx can cause severe environmental problems such as acid rain and photochemical smog,endangering human health and the living environment.Among them,NO pollution accounts for about 95%.NO can exist stably in the air fo...NOx can cause severe environmental problems such as acid rain and photochemical smog,endangering human health and the living environment.Among them,NO pollution accounts for about 95%.NO can exist stably in the air for a long time when the concentration is lower than the ppm level.Therefore,the conversion of low concentration of NO has attracted more and more attention.However,traditional physical or chemical methods are difficult to deal with low concentration of NO,having high requirements on equipment and being not cost‐effective.Semiconductor photocatalytic technology can convert low concentration of NO into non‐toxic products and reduce its harm.This work briefly surveys the commonly used materials,modification methods,and mechanisms for semiconductor photocatalytic conversion of low concentration of NO.In addition,the challenges and prospects of ppb level of NO treatment are also discussed,aiming to promote the development of semiconductor photocatalytic conversion of NO.展开更多
The recyclable and stable ZnFe_(2)O_(4) small particle decorated one‐dimensional perylene diimide(PDI)S‐scheme heterojunction(1D PDI/ZnFe_(2)O_(4))is prepared by the hydrochloric acid‐mediated(HCl‐mediated)strateg...The recyclable and stable ZnFe_(2)O_(4) small particle decorated one‐dimensional perylene diimide(PDI)S‐scheme heterojunction(1D PDI/ZnFe_(2)O_(4))is prepared by the hydrochloric acid‐mediated(HCl‐mediated)strategy,interestingly,the morphology of the 1D PDI/ZnFe_(2)O_(4) can also be effectively regulated by HCl‐mediated process,the existence of HCl can regulate PDI into a uniform rod structure,while the co‐existence of HCl and PDI can limit ZnFe_(2)O_(4) to become the uniform small particles.More importantly,based on the 1D rod structure of PDI and the small size effect of ZnFe_(2)O_(4),carriers can migrate to the surface more easily,which can improve the photocatalytic activity.Meanwhile,due to the appropriate energy level structure,the S‐scheme heterojunction structure is formed between PDI and ZnFe_(2)O_(4),which eliminates meaningless photo‐generated charge carriers through recombination and introduces strong redox to further enhance the photodegradation effect,thereby,1D PDI/ZnFe_(2)O_(4) exhibits excellent photocatalytic ability,under the visible light irradiation,the degradation rate of tetracycline(TC)with 1D PDI/ZnFe_(2)O_(4)(66.67%)is 9.18 times that with PDI(7.26%)and 9.73 times that with ZnFe_(2)O_(4)(6.85%).This work proposes new ideas for the assembly of magnetic organic‐inorganic S‐scheme heterojunction photocatalysts.展开更多
This paper proposes a self-tuning iterative learning control method for the attitude control of a flexible solar power satellite,which is simplified as an Euler-Bernoulli beam moving in space.An orbit-attitude-structu...This paper proposes a self-tuning iterative learning control method for the attitude control of a flexible solar power satellite,which is simplified as an Euler-Bernoulli beam moving in space.An orbit-attitude-structure coupled dynamic model is established using absolute nodal coordinate formulation,and the attitude control is performed using two control moment gyros.In order to improve control accuracy of the classic proportional-derivative control method,a switched iterative learning control method is presented using the control moments of the previous periods as feedforward control moments.Although the iterative learning control is a model-free method,the parameters of the controller must be selected manually.This would be undesirable for complicated systems with multiple control parameters.Thus,a self-tuning method is proposed using fuzzy logic.The control frequency of the controller is adjusted according to the averaged control error in one control period.Simulation results show that the proposed controller increases the control accuracy greatly and reduces the influence of measurement noise.Moreover,the control frequency is automatically adjusted to a suitable value.展开更多
Spin engineering is recognized as a promising strategy that modulates the association between d‐orbital electrons and the oxygenated species,and enhances the catalytic kinetics.However,few efforts have been made to c...Spin engineering is recognized as a promising strategy that modulates the association between d‐orbital electrons and the oxygenated species,and enhances the catalytic kinetics.However,few efforts have been made to clarify whether spin engineering could make a considerable enhancement for electrocatalytic water oxidation.Herein,we report the spin engineering of a nanocage‐structured(Co,Ni)Se_(2)/C@FeOOH,that showed significant oxygen evolution reaction(OER)activity.Magnetization measurement presented that the(Co,Ni)Se_(2)/C@FeOOH sample possesses higher polarization spin number(μb=6.966μB/f.u.)compared with that of the(Co,Ni)Se_(2)/C sample(μb=6.398μB/f.u.),for which the enlarged spin polarization number favors the adsorption and desorption energy of the intermediate oxygenated species,as confirmed by surface valance band spectra.Consequently,the(Co,Ni)Se_(2)/C@FeOOH affords remarkable OER product with a low overpotential of 241 mV at a current of 10 mA cm^(-2) and small Tafel slope of 44 mV dec^(-1) in 1.0 mol/L KOH alkaline solution,significantly surpassing the parent(Co,Ni)Se_(2)/C catalyst.This work will trigger a solid step for the design of highly‐efficient OER electrocatalysts.展开更多
The ethanol oxidation reaction is a significant anodic reaction for direct alcohol fuel cells.The most commonly used catalysts for this reaction are Pt‐based materials;however,Pt‐based electrocatalysts cause carbon ...The ethanol oxidation reaction is a significant anodic reaction for direct alcohol fuel cells.The most commonly used catalysts for this reaction are Pt‐based materials;however,Pt‐based electrocatalysts cause carbon monoxide poisoning with intermediates before the complete transformation of alcohol to CO_(2).Herein,we present hierarchical AgAu bimetallic nanoarchitectures for ethanol electrooxidation,which were fabricated via a partial galvanic reduction reaction between Ag and HAuCl_(4).The ethanol electrooxidation performance of the optimal AgAu nanohybrid was increased to 1834 mA mg^(‒1),which is almost 10 times higher than that of the pristine Au catalyst(190 mA mg^(‒1))in alkaline solutions.This was achieved by introducing Ag into the Au catalyst and controlling the time of the replacement reaction.The heterostructure also presents a higher current density than that of commercial Pt/C(1574 mA mg^(‒1)).Density functional theory calculations revealed that the enhanced activity and stability may stem from unavoidable defects on the surface of the integrated AgAu nanoarchitectures.Ethanol oxidation reactions over these defects are more energetically favorable,which facilitates the oxidative removal of carbonaceous poison and boosts the combination with radicals on adjacent Au active sites.展开更多
To improve the comfortability and safety of aircraft,the demand of rectangular submerged inlets(RSIs)with low resistance is proposed to increase the inlet flow rate of ram air. A theoretical model is built to numerica...To improve the comfortability and safety of aircraft,the demand of rectangular submerged inlets(RSIs)with low resistance is proposed to increase the inlet flow rate of ram air. A theoretical model is built to numerically analyze the effects of geometric parameters on the inlet mass flow rate of RSIs. The geometric parameters in question here encompass the aspect ratio of 2—4,the ramp angle of 6°—7°,the characteristic parameter of the throat of 0.20 —0.30,the ramp length of 939—1 337 mm,and the cone angle of 0° —3°. Simulation results demonstrate that the mass flow rate(MFR)is positively correlated with the aspect ratio,ramp angle,ramp length,and cone angle,and negatively correlated with characteristic parameter of the throat. Within the range of the geometric parameters considered,the RSI with the aspect ratio of 3,the ramp angle of 6°,the characteristic parameter of the throat of 0.20,the ramp length of 1 337 mm,and the cone angle of 3° obtains the largest MFR value of about 2.251 kg/s.展开更多
The high linearity low-noise filter is an indispensable key circuit in the communication system.Based on the structure of current-reuse source-degradation operational transconductance amplifier(OTA),a 5 GHz current-mo...The high linearity low-noise filter is an indispensable key circuit in the communication system.Based on the structure of current-reuse source-degradation operational transconductance amplifier(OTA),a 5 GHz current-mode low-noise Gm-C filter suitable for high-speed communication systems is proposed.Thanks to the proposed current mode structure and the OTA’s high-power efficiency and high linearity,the filter obtains good noise and high linearity performance with very low power consumption.The filter is designed in standard 65 nm CMOS technology and occupies a core area of 0.06 mm^(2).The simulation results show that the operating bandwidth is 5 GHz,the IIP3 is35 d Bm,and the power consumption is only 3.2 m W.展开更多
The problem of correcting simultaneously mass and stiffness matrices of finite element model of undamped structural systems using vibration tests is considered in this paper.The desired matrix properties,including sat...The problem of correcting simultaneously mass and stiffness matrices of finite element model of undamped structural systems using vibration tests is considered in this paper.The desired matrix properties,including satisfaction of the characteristic equation,symmetry,positive semidefiniteness and sparsity,are imposed as side constraints to form the optimal matrix pencil approximation problem.Using partial Lagrangian multipliers,we transform the nonlinearly constrained optimization problem into an equivalent matrix linear variational inequality,develop a proximal point-like method for solving the matrix linear variational inequality,and analyze its global convergence.Numerical results are included to illustrate the performance and application of the proposed method.展开更多
文摘Carbonate electrolytes are one of the most desirable electrolytes for high-energy lithium-sulfur batteries(LSBs)because of their successful implementation in commercial Li-ion batteries.The low-polysulfide-solubility feature of some carbonate solvents also makes them very promising for overcoming the shuttle effects of LSBs.However,regular sulfur electrodes experience undesired electrochemical mechanisms in carbonate electrolytes due to side reactions.In this study,we report a catalytic redox mechanism of sulfur in propylene carbonate(PC)electrolyte based on a compari-son study.The catalytic mechanism is characterized by the interactions between polysulfides and dual N/O functional groups on the host carbon,which largely prevents side reactions between pol-ysulfides and the carbonate electrolyte.Such a mechanism coupled with the low-polysulfide-solubility feature leads to stable cycling of LSBs in PC electrolyte.Favorable dual N/O functional groups are identified via a density functional theory study.This work provides an alternative route for enabling LSBs in carbonate electrolytes.
文摘To facilitate the electrochemical CO_(2) reduction(ECR)to fuels and valuable chemicals,the development of active,low cost,and selective catalysts is crucial.We report a novel ECR catalyst consisting of CuO nanoparticles with sizes ranging from 1.4 to 3.3 nm anchored on Cu metal‐organic framework(Cu‐MOF)nanosheets obtained through a one‐step facile solvothermal method.The nanocomposites provide multiple sites for efficient ambient ECR,delivering an average C_(2)H_(4) faradaic efficiency(FE)of~50.0%at–1.1 V(referred to the reversible hydrogen electrode)in 0.1 mol/L aqueous KHCO_(3) using a two‐compartment cell,in stark contrast to a C_(2)H_(4) FE of 25.5%and 37.6%over individual CuO and Cu‐MOF respectively,also surpassing most newly reported Cu‐based materials under similar cathodic voltages.The C_(2)H_(4) FE remains at over 45.0%even after 10.0 h of successive polarization.Also,a~7.0 mA cm^(–2) C_(2)H_(4) partial geometric current density and 27.7%half‐cell C_(2)H_(4) power conversion efficiency are achieved.The good electrocatalytic performance can be attributed to the interface between CuO and Cu‐MOF,with accessible metallic moieties and the unique two‐dimensional structure of the Cu‐MOF enhancing the adsorption and activation of CO_(2) molecules.This finding offers a simple avenue to upgrading CO_(2) to value‐added hydrocarbons by rational design of MOF‐based composites.
基金supported by the Research on Vibroseis Ultra-wideband Excitation Technology in Re-exploration Area of Quasi Western Margin(Project No.:SG22-44K)。
文摘The Chepaizi Exploration Area,Junggar Basin(NW China)holds substantial importance for seismic exploration endeavors,yet it poses notable challenges due to the intricate nature of its subsurface and near-surface conditions.To address these challenges,we introduce a novel and comprehensive workflow tailored to evaluate and optimize seismic acquisition geometries while considering the impacts of near-surface viscosity.By integrating geological knowledge,historical seismic data,and subsurface modeling,we conduct simulations employing the visco-acoustic wave equation and reverse-time migration to produce detailed subsurface images.The quality of these images is quantitatively evaluated using a local similarity metric,a pivotal tool for evaluating the accuracy of seismic imaging.The culmination of this workflow results in an automated optimization strategy for acquisition geometries that enhances subsurface exploration.Our proposed methodology underscores the importance of incorporating near-surface viscosity effects in seismic imaging,offering a robust framework for improving the accuracy of subsurface imaging.Herein,we aim to contribute to the advancement of seismic imaging methodologies by providing valuable insights for achieving high-quality seismic exploration outcomes in regions characterized by complex subsurface and near-surface conditions.
文摘Since the D-band center theory was proposed,it has been widely used in the fields of surface chemistry by almost all researchers,due to its easy understanding,convenient operation and relative accuracy.However,with the continuous development of material systems and modification strategies,researchers have gradually found that D-band center theory is usually effective for large metal particle systems,but for small metal particle systems or semiconductors,such as single atom systems,the opposite conclusion to the D-band center theory is often obtained.To solve the issue above,here we propose a bonding and anti-bonding orbitals stable electron intensity difference(BASED)theory for surface chemistry.The newly-proposed BASED theory can not only successfully explain the abnormal phenomena of D-band center theory,but also exhibits a higher accuracy for prediction of adsorption energy and bond length of intermediates on active sites.Importantly,a new phenomenon of the spin transition state in the adsorption process is observed based on the BASED theory,where the active center atom usually yields an unstable high spin transition state to enhance its adsorption capability in the adsorption process of intermediates when their distance is about 2.5Å.In short,the BASED theory can be considered as a general principle to understand catalytic mechanism of intermediates on surfaces.
文摘The hydrogenation of CO_(2) into methanol has attracted much attention and In_(2)O_(3) is a promising catalyst.Introducing metal elements into In_(2)O_(3)(M/In_(2)O_(3))is one of the main strategies to improve its performance.However,its mechanism and active sites remain unclear and need to be further elucidated.Here,the noble‐metal‐free In_(x)‐Co_(y) oxides catalysts were prepared.Much‐improved performance and obvious product selectivity shift were observed.The optimized catalyst(In_(1)‐Co_(4))(9.7 mmol g_(cat)^(–1) h^(–1))showed five times methanol yields than pure In_(2)O_(3)(2.2 mmol g_(cat)^(–1) h^(–1))(P=4.0 MPa,T=300°C,GHSV=24000 cm^(3)_(STP) g_(cat)^(–1) h^(–1),H_(2):CO_(2)=3).And the cobalt‐catalyzed CO_(2) methanation activity was suppressed,although cobalt was most of the metal element.To unravel this selectivity shift,detailed catalysts performance evaluation,together with several in‐situ and ex‐situ characterizations,were employed on cobalt and In‐Co for comparative study.The results indicated CO_(2) hydrogenation on cobalt and In‐Co catalyst both followed the formate pathway,and In‐Co reconstructed and generated a surface In_(2)O_(3)‐enriched core‐shell‐like structure under a reductive atmosphere.The enriched In_(2)O_(3) at the surface significantly enhanced CO_(2) adsorption capacity and well stabilized the intermediates of CO_(2) hydrogenation.CO_(2) and carbon‐containing intermediates adsorbed much stronger on In‐Co than cobalt led to a feasible surface C/H ratio,thus allowing the*CH_(3)O to desorb to produce CH_(3)OH instead of being over‐hydrogenated to CH_(4).
文摘NOx can cause severe environmental problems such as acid rain and photochemical smog,endangering human health and the living environment.Among them,NO pollution accounts for about 95%.NO can exist stably in the air for a long time when the concentration is lower than the ppm level.Therefore,the conversion of low concentration of NO has attracted more and more attention.However,traditional physical or chemical methods are difficult to deal with low concentration of NO,having high requirements on equipment and being not cost‐effective.Semiconductor photocatalytic technology can convert low concentration of NO into non‐toxic products and reduce its harm.This work briefly surveys the commonly used materials,modification methods,and mechanisms for semiconductor photocatalytic conversion of low concentration of NO.In addition,the challenges and prospects of ppb level of NO treatment are also discussed,aiming to promote the development of semiconductor photocatalytic conversion of NO.
文摘The recyclable and stable ZnFe_(2)O_(4) small particle decorated one‐dimensional perylene diimide(PDI)S‐scheme heterojunction(1D PDI/ZnFe_(2)O_(4))is prepared by the hydrochloric acid‐mediated(HCl‐mediated)strategy,interestingly,the morphology of the 1D PDI/ZnFe_(2)O_(4) can also be effectively regulated by HCl‐mediated process,the existence of HCl can regulate PDI into a uniform rod structure,while the co‐existence of HCl and PDI can limit ZnFe_(2)O_(4) to become the uniform small particles.More importantly,based on the 1D rod structure of PDI and the small size effect of ZnFe_(2)O_(4),carriers can migrate to the surface more easily,which can improve the photocatalytic activity.Meanwhile,due to the appropriate energy level structure,the S‐scheme heterojunction structure is formed between PDI and ZnFe_(2)O_(4),which eliminates meaningless photo‐generated charge carriers through recombination and introduces strong redox to further enhance the photodegradation effect,thereby,1D PDI/ZnFe_(2)O_(4) exhibits excellent photocatalytic ability,under the visible light irradiation,the degradation rate of tetracycline(TC)with 1D PDI/ZnFe_(2)O_(4)(66.67%)is 9.18 times that with PDI(7.26%)and 9.73 times that with ZnFe_(2)O_(4)(6.85%).This work proposes new ideas for the assembly of magnetic organic‐inorganic S‐scheme heterojunction photocatalysts.
基金supported by the Guangdong Basic and Applied Basic Research Foundation(No.2019A1515110730)the Young Elite Scientists Sponsorship Program by China Association for Science and Technology(No.2021QNRC001)the Fundamental Research Funds for the Central Universities of Sun Yat-sen University(No.22qntd0703)。
文摘This paper proposes a self-tuning iterative learning control method for the attitude control of a flexible solar power satellite,which is simplified as an Euler-Bernoulli beam moving in space.An orbit-attitude-structure coupled dynamic model is established using absolute nodal coordinate formulation,and the attitude control is performed using two control moment gyros.In order to improve control accuracy of the classic proportional-derivative control method,a switched iterative learning control method is presented using the control moments of the previous periods as feedforward control moments.Although the iterative learning control is a model-free method,the parameters of the controller must be selected manually.This would be undesirable for complicated systems with multiple control parameters.Thus,a self-tuning method is proposed using fuzzy logic.The control frequency of the controller is adjusted according to the averaged control error in one control period.Simulation results show that the proposed controller increases the control accuracy greatly and reduces the influence of measurement noise.Moreover,the control frequency is automatically adjusted to a suitable value.
文摘Spin engineering is recognized as a promising strategy that modulates the association between d‐orbital electrons and the oxygenated species,and enhances the catalytic kinetics.However,few efforts have been made to clarify whether spin engineering could make a considerable enhancement for electrocatalytic water oxidation.Herein,we report the spin engineering of a nanocage‐structured(Co,Ni)Se_(2)/C@FeOOH,that showed significant oxygen evolution reaction(OER)activity.Magnetization measurement presented that the(Co,Ni)Se_(2)/C@FeOOH sample possesses higher polarization spin number(μb=6.966μB/f.u.)compared with that of the(Co,Ni)Se_(2)/C sample(μb=6.398μB/f.u.),for which the enlarged spin polarization number favors the adsorption and desorption energy of the intermediate oxygenated species,as confirmed by surface valance band spectra.Consequently,the(Co,Ni)Se_(2)/C@FeOOH affords remarkable OER product with a low overpotential of 241 mV at a current of 10 mA cm^(-2) and small Tafel slope of 44 mV dec^(-1) in 1.0 mol/L KOH alkaline solution,significantly surpassing the parent(Co,Ni)Se_(2)/C catalyst.This work will trigger a solid step for the design of highly‐efficient OER electrocatalysts.
文摘The ethanol oxidation reaction is a significant anodic reaction for direct alcohol fuel cells.The most commonly used catalysts for this reaction are Pt‐based materials;however,Pt‐based electrocatalysts cause carbon monoxide poisoning with intermediates before the complete transformation of alcohol to CO_(2).Herein,we present hierarchical AgAu bimetallic nanoarchitectures for ethanol electrooxidation,which were fabricated via a partial galvanic reduction reaction between Ag and HAuCl_(4).The ethanol electrooxidation performance of the optimal AgAu nanohybrid was increased to 1834 mA mg^(‒1),which is almost 10 times higher than that of the pristine Au catalyst(190 mA mg^(‒1))in alkaline solutions.This was achieved by introducing Ag into the Au catalyst and controlling the time of the replacement reaction.The heterostructure also presents a higher current density than that of commercial Pt/C(1574 mA mg^(‒1)).Density functional theory calculations revealed that the enhanced activity and stability may stem from unavoidable defects on the surface of the integrated AgAu nanoarchitectures.Ethanol oxidation reactions over these defects are more energetically favorable,which facilitates the oxidative removal of carbonaceous poison and boosts the combination with radicals on adjacent Au active sites.
基金supported by the Open Project of Key Laboratory of Aircraft Environment Control and Life Support,MIIT(No.KLAECLS-E-202001)。
文摘To improve the comfortability and safety of aircraft,the demand of rectangular submerged inlets(RSIs)with low resistance is proposed to increase the inlet flow rate of ram air. A theoretical model is built to numerically analyze the effects of geometric parameters on the inlet mass flow rate of RSIs. The geometric parameters in question here encompass the aspect ratio of 2—4,the ramp angle of 6°—7°,the characteristic parameter of the throat of 0.20 —0.30,the ramp length of 939—1 337 mm,and the cone angle of 0° —3°. Simulation results demonstrate that the mass flow rate(MFR)is positively correlated with the aspect ratio,ramp angle,ramp length,and cone angle,and negatively correlated with characteristic parameter of the throat. Within the range of the geometric parameters considered,the RSI with the aspect ratio of 3,the ramp angle of 6°,the characteristic parameter of the throat of 0.20,the ramp length of 1 337 mm,and the cone angle of 3° obtains the largest MFR value of about 2.251 kg/s.
基金supported in part by the National Key R&D Program of China(No.2018YFE0205900)in part by the Natural Science Foundation of Jiangsu Province of China(No.BK20180368)。
文摘The high linearity low-noise filter is an indispensable key circuit in the communication system.Based on the structure of current-reuse source-degradation operational transconductance amplifier(OTA),a 5 GHz current-mode low-noise Gm-C filter suitable for high-speed communication systems is proposed.Thanks to the proposed current mode structure and the OTA’s high-power efficiency and high linearity,the filter obtains good noise and high linearity performance with very low power consumption.The filter is designed in standard 65 nm CMOS technology and occupies a core area of 0.06 mm^(2).The simulation results show that the operating bandwidth is 5 GHz,the IIP3 is35 d Bm,and the power consumption is only 3.2 m W.
基金The work was supported by the National Natural Science Foundation of China(No.11571171)。
文摘The problem of correcting simultaneously mass and stiffness matrices of finite element model of undamped structural systems using vibration tests is considered in this paper.The desired matrix properties,including satisfaction of the characteristic equation,symmetry,positive semidefiniteness and sparsity,are imposed as side constraints to form the optimal matrix pencil approximation problem.Using partial Lagrangian multipliers,we transform the nonlinearly constrained optimization problem into an equivalent matrix linear variational inequality,develop a proximal point-like method for solving the matrix linear variational inequality,and analyze its global convergence.Numerical results are included to illustrate the performance and application of the proposed method.
