Tilted metasurface nanostructures,with excellent physical properties and enormous application potential,pose an urgent need for manufacturing methods.Here,electric-field-driven generative-nanoimprinting technique is p...Tilted metasurface nanostructures,with excellent physical properties and enormous application potential,pose an urgent need for manufacturing methods.Here,electric-field-driven generative-nanoimprinting technique is proposed.The electric field applied between the template and the substrate drives the contact,tilting,filling,and holding processes.By accurately controlling the introduced included angle between the flexible template and the substrate,tilted nanostructures with a controllable angle are imprinted onto the substrate,although they are vertical on the template.By flexibly adjusting the electric field intensity and the included angle,large-area uniform-tilted,gradient-tilted,and high-angle-tilted nanostructures are fabricated.In contrast to traditional replication,the morphology of the nanoimprinting structure is extended to customized control.This work provides a cost-effective,efficient,and versatile technology for the fabrication of various large-area tilted metasurface structures.As an illustration,a tilted nanograting with a high coupling efficiency is fabricated and integrated into augmented reality displays,demonstrating superior imaging quality.展开更多
Peroxymonosulfate(PMS)-based advanced oxidation processes(AOPs)are an effective way to remove emerging contaminants(ECs)from water.The catalytic process involving PMS is hindered by the suboptimal electron trans-fer e...Peroxymonosulfate(PMS)-based advanced oxidation processes(AOPs)are an effective way to remove emerging contaminants(ECs)from water.The catalytic process involving PMS is hindered by the suboptimal electron trans-fer efficiency of current catalysts,the further application of AOPs technology is limited.Here,it is proposed that the interfacial electric field can be controlled by bor(B)-doped FeNC catalysts,which shows significant advantages in the efficient generation,release and participation of reactive oxygen species(ROS)in the reaction.The super exchange interaction between Fe sites and N and B sites is realized through the directional transfer of electrons in the interfacial electric field,which ensures the high efficiency and stability of the PMS catalytic process.B doping increases the d orbitals distribution at Fermi level,which facilitates enhanced electron transition activity,thereby promoting the effective generation of (1)^O_(2).At the same time,orbital hybridization causes the center of the d band to move to a lower energy level,which not only contributes to the desorption process of (1)^O_(2),but also accelerates its release.In addition,B-doping also improved the adsorption capacity of organic pollutants and shortened the migration distance of ROS,thereby significantly improving the degradation efficiency of ECs.The B-doping strategy outlined offers a novel approach to the development of FeNC catalysts,it lays a theoretical foundation and offers technical insights for the integration of PMS/AOPs technology in the ECs management.展开更多
Development of robust electrocatalyst for oxygen reduction reaction(ORR)in a seawater electrolyte is the key to realize seawater electrolyte-based zinc-air batteries(SZABs).Herein,constructing a local electric field c...Development of robust electrocatalyst for oxygen reduction reaction(ORR)in a seawater electrolyte is the key to realize seawater electrolyte-based zinc-air batteries(SZABs).Herein,constructing a local electric field coupled with chloride ions(Cl-)fixation strategy in dual single-atom catalysts(DSACs)was proposed,and the resultant catalyst delivered considerable ORR performance in a seawater electrolyte,with a high half-wave potential(E_(1/2))of 0.868 V and a good maximum power density(Pmax)of 182 mW·cm^(−2)in the assembled SZABs,much higher than those of the Pt/C catalyst(E_(1/2):0.846 V;Pmax:150 mW·cm^(−2)).The in-situ characterization and theoretical calculations revealed that the Fe sites have a higher Cl^(−)adsorption affinity than the Co sites,and preferentially adsorbs Cl^(−)in a seawater electrolyte during the ORR process,and thus constructs a low-concentration Cl^(−)local microenvironment through the common-ion exclusion effect,which prevents Cl^(−)adsorption and corrosion in the Co active centers,achieving impressive catalytic stability.In addition,the directional charge movement between Fe and Co atomic pairs establishes a local electric field,optimizing the adsorption energy of Co sites for oxygen-containing intermediates,and further improving the ORR activity.展开更多
In photocatalysis field,S-scheme heterojunctions show unique advantages and prospects.However,the carrier shielding effect of heterojunctions limits the separation and migration of interfacial charges.In this study,a ...In photocatalysis field,S-scheme heterojunctions show unique advantages and prospects.However,the carrier shielding effect of heterojunctions limits the separation and migration of interfacial charges.In this study,a strategy of“dynamic cascade electric fields to deplete unilaterally accumulated charges”was innovatively proposed to overcome this drawback.By modulating g-C_(3)N_(4)(CN)and Bi_(2)WO_(6)(BWO)using the polarized electric field(PEF)of spontaneously polarized ceramic(SPC),a BWO/SPC-CN composite with cascade internal electric field(IEF)and PEF was successfully constructed for efficient piezophotocatalytic degradation of recalcitrant pollutants.BWO/SPC-CN contributed to 96.8% degradation of carbamazepine,significantly surpassing BWO/CN(70.5%).BWO/SPC-CN performed excellent capacity of harvesting piezoelectric energy due to its unique three-dimensional porous nano-network structure.The PEF of SPC modulated the electronic band structure and thus strengthened the IEF of BWO/SPC-CN,providing a persistent driving force for interfacial charge migration.Moreover,SPC with a strong PEF unilaterally consumed the charges accumulated on CN under periodic piezoelectricity,weakening the shielding electric field to inhibit the recombination of electron-hole pairs.As a consequence,the dynamic cascade PEF-IEF ultimately broke the carrier shielding effect in heterojunction photocatalysis and enhanced interfacial electron transfer.This work provides reliable methods to enhance the interfacial charge transfer in heterojunction and new insights into piezo-photocatalytic mechanism.展开更多
The slow-proton-fast-electron process severely limits the catalytic efficiency of oxygen evolution reaction.A method is proposed to accelerate proton transfer by building up local electric fields.Modifying acetic,etha...The slow-proton-fast-electron process severely limits the catalytic efficiency of oxygen evolution reaction.A method is proposed to accelerate proton transfer by building up local electric fields.Modifying acetic,ethanedioic and propanetricarboxylic(C_(6)H_(8)O_(6))ligands on BiVO_(4)surface results in a potential difference between BiVO_(4)and ligands that generates a local electric field which serves as a driving force for proton transfer.Among the ligands,carrying the strongest electron-withdrawing ability,the modification of C_(6)H_(8)O_(6) forms the strongest local electric field and leads to the fastest proton transfer and the smallest thermodynamic overpotential.C_(6)H_(8)O_(6)-BiVO_(4)exhibits 3.5 times photocurrent density as high as that of pure BiVO_(4),which is 3.50 mA cm^(-2)at 1.23 VRHE.The onset potential of C_(6)H_(8)O_(6)-BiVO_(4)shifts negatively from 0.70 to 0.38 VRHE.The mechanism for OER transitions from thermodynamically high energy proton-coupled electron transfer to thermodynamically low energy electron transfer as proton transfer is accelerated.展开更多
Simultaneously inducing dual built-in electric fields(EFs)both within a single component and at the heterojunction interface creates a dual-driving force that is crucial for promoting spatial charge separation.This is...Simultaneously inducing dual built-in electric fields(EFs)both within a single component and at the heterojunction interface creates a dual-driving force that is crucial for promoting spatial charge separation.This is particularly significant in challenging coupled systems,such as CO_(2)photoreduction integrated with selective oxidation of toluene to benzaldehyde.However,developing such a system is quite challenging and often requires a precise design and engineering.Herein,we demonstrate a unique Ni-CdS@Ni(OH)_(2)heterojunction synthesized via an in-situ self-assembly method.Comprehensive mechanistic and theoretical investigations reveal that the NiCdS@Ni(OH)_(2)heterojunction induces dual electric fields(EFs):an intrinsic polarized electric-field within the CdS lattice from Ni doping and an interfacial electric-field from the growth of ultrathin nanosheets of Ni(OH)_(2)on NiCdS nanorods,enabling efficient spatial charge separation and enhanced redox potential.As proof of concept,the Ni-CdS@Ni(OH)_(2)heterojunction simultaneously exhibits outstanding bifunctional photocatalytic performance,producing CO at a rate of 427μmol g^(-1)h^(-1)and selectively oxidizing toluene to benzaldehyde at a rate of 1476μmol g^(-1)h^(-1)with a selectivity exceeding 85%.This work offers a promising strategy to optimize the utilization of photogenerated carriers in heterojunction photocatalysts,advancing synergistic photocatalytic redox systems.展开更多
Anodic bonding between silicon and glass with dou bl e electric fields is presented.By this means,the damage caused by the electric f ield to the movable part during bonding can be avoided and the experiment result s ...Anodic bonding between silicon and glass with dou bl e electric fields is presented.By this means,the damage caused by the electric f ield to the movable part during bonding can be avoided and the experiment result s show that.展开更多
The difficulty in fabricating a multifaceted composite heterojunction system based on Cd_(x) Zn_(1-x) S limits the enhancement of photocatalytic performance.In the present scrutiny,novel ZnO/Cd_(x) Zn_(1-x) S/CdS com-...The difficulty in fabricating a multifaceted composite heterojunction system based on Cd_(x) Zn_(1-x) S limits the enhancement of photocatalytic performance.In the present scrutiny,novel ZnO/Cd_(x) Zn_(1-x) S/CdS com-posite heterojunctions are successfully prepared by the alkaline dissolution etching method.The internal electric field at the interface of I-type and Z-scheme heterojunction improved the effective charge sepa-ration.The ZC 8 sample exhibits excellent photocatalytic performance and the H2 production efficiency is 15.67 mmol g^(−1) h^(−1) with good stability up to 82.9%in 24-hour cycles.The performance of CH_(4) and CO capacity in the CO_(2) RR process is 3.47μmol g^(−1) h^(−1) and 23.5μmol g^(−1) h^(−1),respectively.The photogener-ated accelerated charge transport is then examined in detail by in situ X-ray photoelectron spectroscopy(ISXPS)and density functional theory(DFT)calculations.This work presents a new idea for the synthe-sis of Cd_(x) Zn_(1-x) S solid-solution-based materials and provides a solid reference for the detailed mechanism regarding the electric field at the heterojunction interface.展开更多
We investigate the energy bands,magnetism,and superconductivity of bilayer octagraphene with A-A stackingunder a perpendicular electric field.A tight-binding model is used to analyze the band structure of the system.T...We investigate the energy bands,magnetism,and superconductivity of bilayer octagraphene with A-A stackingunder a perpendicular electric field.A tight-binding model is used to analyze the band structure of the system.The doubling of the unit cell results in each band of the single layer splitting into two.We find that applyinga perpendicular electric field increases the band splitting.As the electric field strength increases,the nestingof the Fermi surface(FS)weakens,eventually disrupting the antiferromagnetic order,and bilayer octagrapheneexhibits superconductivity.Spin fluctuations can induce unconventional superconductivity with s±-wave pairing.Applying a perpendicular electric field to bilayer octagraphene parent weakens the nesting of the FS,ultimatelykilling the spin-density-wave(SDW)ordered state and transitioning it into the superconducting state,whichworks as a doping effect.We use the random-phase approximation approach to obtain the pairing eigenvaluesand pairing symmetries of the perpendicular electric field-tuned bilayer octagraphene in the weak coupling limit.By tuning the strength of the perpendicular electric field,the critical interaction strength for SDW order can bemodified,which in turn may promote the emergence of unconventional superconductivity.展开更多
Einstein aimed to find a unified theoretical model to explain various interactions in nature,and the relationship between gravitational and electric fields was particularly important.For the first time,this paper prov...Einstein aimed to find a unified theoretical model to explain various interactions in nature,and the relationship between gravitational and electric fields was particularly important.For the first time,this paper provides the internal relationship equations of the electric and magnetic fields.Further,the relationship between the magnetic and gravity fields is analyzed,and the relationship equations of the electric,magnetic,and gravity fields are established.On this basis,a general formula for calculating the radius of charged particles is derived.Simultaneously,we also discussed and made predictions on black holes,providing convenience for future research and experimental detection.展开更多
Developing an efficient photocatalyst is the key to realize the practical application of photocatalysis.The S-scheme heterojunction has great potential in photocatalysis due to its unique charge-carrier migration path...Developing an efficient photocatalyst is the key to realize the practical application of photocatalysis.The S-scheme heterojunction has great potential in photocatalysis due to its unique charge-carrier migration pathway,effective light absorption and high redox capacity.However,further enhancing the built-in electric field of the S-scheme,accelerating carrier separation,and achieving higher photocatalytic performance remain unresolved challenges.Herein,based on the continuously adjustable band structure of continuous solid-solution,a novel 0D/2D all solid-solution S-scheme heterojunction with adjustable internal electric field was designed and fabricated by employing a solid-solution of ZnxCd_(1–x)S and Bi_(2)MoyW_(1–y)O_(6)respectively as reduction and oxidation semiconductors.The synergistic optimization of effective light absorption,fast photogenerated carrier separation,and high redox potential leads can be tuned to promote photocatalytic activity.Under visible light,the S-scheme system constructed by Zn_(0.4)Cd_(0.6)S quantum dot(QDs)and Bi_(2)Mo_(0.2)W_(0.8)O_(6)monolayer exhibits a high rate for photocatalytic degradation C_(2)H_(4)(150.6×10^(–3)min^(–1)),which is 16.5 times higher than that of pure Zn_(0.4)Cd_(0.6)S(9.1×10^(–3)min^(–1))and 53.8 times higher than pure Bi_(2)Mo_(0.2)W_(0.8)O_(6)(2.8×10^(–3)min^(–1)).Due to the unique charge-carrier migration pathway,photo-corrosion of Zn_(x)Cd_(1–x)S is further inhibited simultaneously.In-situ irradiation X-ray photoelectron spectroscopy,photoluminescence spectroscopy,time-resolved photoluminescence,transient absorption spectroscopy and electron paramagnetic resonance provide compelling evidence for interfacial charge transfer via S-scheme pathways,while in-situ diffuse reflectance infrared Fourier transform spectroscopy identifies the reaction pathway for C_(2)H_(4)degradation.This novel S-scheme photocatalysts demonstrates excellent performance and potential for the practical application of the fruits and vegetables preservation at room temperatures.展开更多
Efficient selective adsorption and separation using porous frameworks are critical in many industrial processes,where adsorption energy and dynamic diffusion rate are predominant factors governing selectivity.They are...Efficient selective adsorption and separation using porous frameworks are critical in many industrial processes,where adsorption energy and dynamic diffusion rate are predominant factors governing selectivity.They are highly susceptible to framework charge,which plays a significant role in selective adsorption.Currently,ionic porous frameworks can be divided into two types.One of them is composed of a charged backbone and counter ions.The framework with zwitterionic channels is another type.It is composed of regular and alternating arrangements of cationic and anionic building units.Herein,we report a hydrogen-bonded ionic framework(HIF)of{(CN_(3)H_(6))_(2)[Ti(μ_(2)-O)(SO_(4))_(2)]}_nwith 1D channel exhibits unique adsorption selectivity for Ar against N_(2)and CO_(2).Density functional theory(DFT)results suggest that CO_(2)cannot be adsorbed by HIF at the experimental temperature due to a positive adsorption free energy.In addition,due to a relatively large diffusion barrier at 77 K,N_(2)molecules hardly diffuse in HIF channels,while Ar has a negligible diffusion barrier.The unique net positively-charged space in the channel is the key to the unusual phenomena,based on DFT simulations and structural analysis.The findings in this work proposes the new adsorption mechanism and provides unique perspective for special separation applications,such as isotope and noble gasses separations.展开更多
A fatal issue of Zn-based electrochemical energy storage is uneven Zn^(2+)deposition on the Zn metal anode.Unfortunately,the modulation for the inherent electric field,the origin of driving force for ion diffusion,has...A fatal issue of Zn-based electrochemical energy storage is uneven Zn^(2+)deposition on the Zn metal anode.Unfortunately,the modulation for the inherent electric field,the origin of driving force for ion diffusion,has been given insufficient importance.Herein,the redistribution of the surrounding electric field is demonstrated to depend on the permittivity of the surface medium for the first time,where highpermittivity particles can simultaneously enhance vertical components and reduce horizontal components of the electric field through polarization.Consequently,a bacterial cellulose-based separator is proposed by incorporating a high-permittivity surface medium.Cellulose serves as a robust substrate with a rather low thickness to enable homogeneous dispersion of high-permittivity particles on the surface,which can regulate the localized electric field to guide even Zn deposition by inhibiting twodimensional(2D)Zn^(2+)diffusion and suppressing side reactions by repulsing anion migration toward the Zn anode.The separator achieves significantly enhanced Zn anode stability of 2880 h at 1 mA cm^(-2)and a cumulative capacity of 3.5 Ah cm^(-2)at 10 mA cm^(-2).It also enables a long-term lifespan of 50,000 cycles in Zn||AC capacitor and 1000 cycles at a limited negative/positive(N/P)ratio of 3:1.This work provides a new view to stabilize Zn anode by electric field modulation.展开更多
The quest for sustainable energy solutions has intensified the need for efficient water electrolysis techniques,pivotal for hydrogen production.However,developing effective bifunctional electrocatalysts capable of dri...The quest for sustainable energy solutions has intensified the need for efficient water electrolysis techniques,pivotal for hydrogen production.However,developing effective bifunctional electrocatalysts capable of driving the hydrogen evolution reaction(HER)and oxygen evolution reaction(OER)remains a formidable challenge.Addressing this,we introduce a novel built-in electric field(BEF)strategy to synthesize NiCoP–Co nanoarrays directly on Ti_(3)C_(2)T_(x) MXene substrates(NiCoP–Co/MXene).This approach leverages a significant work function difference(ΔΦ),propelling these nanoarrays as adept bifunctional electrocatalysts for comprehensive water splitting.MXene,in this process,plays a dual role.It acts as a conductive support,enhancing the catalyst’s overall conductivity,and facilitates an effective charge transport pathway,ensuring efficient charge transfer.Our study reveals that the BEF induces an electric field at the interface,prompting charge transfer from Co to NiCoP.This transfer modulates asymmetric charge distributions,which intricately control intermediates’adsorption and desorption dynamics.Such regulation is crucial for enhancing the reaction kinetics of both HER and OER.Furthermore,under oxidative conditions,the NiCoP–Co/MXene catalyst undergoes a structural metamorphosis into Ni(Co)oxides/hydroxides/MXene,increasing OER performance.This research demonstrates the BEF’s role in fine-tuning interfacial charge redistribution and underscores its potential in crafting more sophisticated electrocatalytic designs.The insights gained here could pave the way for the next generation of electrocatalysis,with far-reaching implications for energy conversion and storage technologies.展开更多
The rational configuration of built-in electric field(IEF)in heterogeneous materials can significantly optimize the band structure to accelerate the separation of photogenerated charge carriers.However,the strength mo...The rational configuration of built-in electric field(IEF)in heterogeneous materials can significantly optimize the band structure to accelerate the separation of photogenerated charge carriers.However,the strength modulation of IEF formed by various materials has an uncertain enhancing effect on the separation of photogenerated carriers.Herein,a mesoporous MIL-125(Ti)@BiOCl S-scheme heterojunction with controllable IEF is prepared by green photoreduction reaction to investigate the relationship between IEF,microstructure,and photocatalytic activity.Moreover,the corresponding results demonstrate the MIL-125(Ti)@BiOCl effectively regulates the IEF strength through controlling the concentration of ligand defects,thereby optimizing the band structure and improving the efficiency of photogenerated charge separation.The optimized IEF significantly enhances the photocatalytic degradation performance of mesoporous MIL-125(Ti)-3@BiOCl towards tetracycline,with a k value of 0.07 min^(–1),which are approximately 5.5 and 4.7 times greater than that of BiOCl(0.0127 min^(–1))and MIL-125(Ti)-3(0.015 min^(–1)).These findings provide a new pathway for regulating IEF within MOF-based heterojunctions,and offer new insights into the intrinsic correlations between defect structure,IEF,and photocatalytic activity.展开更多
Ferroelectric materials find extensive applications in brake systems due to their capability to convert electrical energy into mechanical energy.Recent research has focused on lead-free materials for their environment...Ferroelectric materials find extensive applications in brake systems due to their capability to convert electrical energy into mechanical energy.Recent research has focused on lead-free materials for their environmentally friendly characteristics.However,they exhibit several challenges such as significant negative strain,limited strain values,and large driving field.In this work,novel preparation techniques(electrospinning)were utilized for BaTiO_(3)to introduce oxygen vacancies and barium defects,facilitating the creation of oriented defect dipoles coupled with an intrinsic electric field(Ei)after poling and aging.Due to the existence of Ei,two minimum points in the strain hysteresis loop were shifted to the same quadrant in the Strain-Electric field space.Thus,when applying an electric field along the Ei direction,negative strain is eliminated.Additionally,the actual electric field is the sum of the applied electric field and Ei,thereby reducing the required driving field of the piezoelectric.The stretching of defect dipoles under the electric field further amplified the total strain.Through the proposed mechanisms,this work achieved a substantial unipolar electrostrain of 1.04%under a relatively low electric field(30 kV/cm)in BaTiO_(3).This work successfully addressed the challenges of high-driving electric fields,limited strain values,and negative strain,providing a comprehensive approach for improving field-induced strain performance through point defect engineering in ferroelectric materials.展开更多
Atmospheric particle adsorption on insulator surfaces,coupled with humid environments,significantly affects contamination flashover,necessitating a clear understanding of the electric field distribution on insulator s...Atmospheric particle adsorption on insulator surfaces,coupled with humid environments,significantly affects contamination flashover,necessitating a clear understanding of the electric field distribution on insulator surfaces with adsorbed particles.This is crucial for accurately assessing insulator safety and informing critical decision-making.Although previous research has demonstrated that particle arrangement significantly influences the electric field distribution around transmission lines,an in-depth analysis of its effects on insulator surfaces remains lacking.To address this gap,this study establishes a composite insulator model to examine how three types of spherical contamination layers affect the electric field distribution on insulator surfaces under varying environmental conditions.The results reveal that in dry environments,the electric field strength at the apex of single-particle contamination layers increases with the particle size and relative permittivity.For the double-particle contamination layers,the electric field intensity on the insulator surface decreases as the particle spacing increases,and larger particles are more likely to attract smaller charged particles.For triple-particle contamination layers arranged in a triangular pattern,the maximum surface field strength is nearly double that of the chain-arranged particles.Furthermore,within the chain-arranged triple-particle contamination layers,a large-small-large size arrangement has a more pronounced impact on the surface electric field than a small-large-small size arrangement.In humid environments,the surface electric field strength of insulators decreases with increasing contamination levels.These findings are of significant theoretical and practical importance for ensuring the safe operation of power systems.展开更多
This study aimed to evaluate the wake effect on the electric field detector(EFD) onboard the China Seismo-Electromagnetic Satellite(CSES-01). Through a series of experiments and analyses, we confirmed that the disturb...This study aimed to evaluate the wake effect on the electric field detector(EFD) onboard the China Seismo-Electromagnetic Satellite(CSES-01). Through a series of experiments and analyses, we confirmed that the disturbance phenomenon from probe B of the EFD is not caused by the boom layout. To validate and determine whether it is influenced by the wake effect, we conducted two experiments. In the first experiment, the entire satellite platform underwent a 90° counterclockwise yaw maneuver to allow probe B to avoid the plasma wake region. We then verified whether the disturbance was improved. In the second experiment, the satellite platform performed a 180° counterclockwise yaw maneuver, positioning probe B on the ram side of the satellite and completely avoiding all satellite wakes. The plasma wake effect of the satellite did not significantly influence the spherical probes of the EFD because the measurement accuracy stayed relatively stable under the two experiments, despite the observed abnormalities in the operating state of spherical probe B. This consistency in performance is important for electric field detection missions because the spatial electric field vector data obtained from these probes continue to effectively reflect information on spatial electromagnetic disturbances. These two experimental results showed that probe B consistently exhibited data jump phenomena under various maneuver states, whereas probes A, C, and D did not display such phenomena in any maneuver state.展开更多
The major challenge in photocatalytic water splitting lies in water oxidation reactions,which still suffer from poor charge separation.This study overcame inefficient charge separation by establishing a robust interfa...The major challenge in photocatalytic water splitting lies in water oxidation reactions,which still suffer from poor charge separation.This study overcame inefficient charge separation by establishing a robust interfacial electric field through the electrostatic-driven assembly of Co_(3)O_(4) nanoparticles with a perylene imide supramolecule(PDINH).The well-aligned band structures and intimate interfacial contact in the PDINH/Co_(3)O_(4) heterostructure create an enhanced interfacial electric field that is 4.1-and 53.2-fold stronger than those of individual PDINH and Co_(3)O_(4),thus promoting directional charge separation and transfer.Moreover,S-scheme charge transfer strongly preserves the oxidative holes in PDINH to drive efficient water oxidation reactions.Consequently,PDINH/Co_(3)O_(4) composite achieves a photocatalytic oxygen evolution rate of 29.26 mmol g^(–1) h^(–1) under visible light irradiation,8.2-fold improvement over pristine PDINH,with an apparent quantum yield of 6.66%at 420 nm.This study provides fundamental insights into interfacial electric field control for the development of high-performance organic photocatalysts for efficient water oxidation.展开更多
In this work,we aim to develop a novel post-treatment process combining cryogenic and pulsed electric field treatment to enhance WC-Co cemented carbides.The results show a 15.62%increase in hardness from 1831.38 to 21...In this work,we aim to develop a novel post-treatment process combining cryogenic and pulsed electric field treatment to enhance WC-Co cemented carbides.The results show a 15.62%increase in hardness from 1831.38 to 2117.38 HV30,a 9.60%rise in fracture toughness from 9.06 to 9.93 MPa·m^(1/2),while the friction coefficient decreases from 0.63 to 0.47.Through the residual stress evolution,WC orientation change and the martensitic transformation of Co,and the internal enhancement mechanism of cryogenic combined with pulsed electric field treatment are revealed.The electron wind generated by the pulsed electric field can efficiently reduce the residual stress induced by cryogenic process.The evolution of residual stress promotes the base slip of WC,increasing the degree of{0001}orientation.In addition,the degree of martensitic transformation of Co intensifies,with the hcp-Co/fcc-Co ratio rising from 0.41%to 17.86%.The enhanced WC{0001}orientation and increased hcp-Co content contribute to significant improvements in hardness and wear resistance.This work provides a novel efficient enhancement strategy for ceramics and alloys,with the potential to be a mainstream strengthening method in the future.展开更多
基金supported by National Natural Science Foundation of China(No.52025055 and 52275571)Basic Research Operation Fund of China(No.xzy012024024).
文摘Tilted metasurface nanostructures,with excellent physical properties and enormous application potential,pose an urgent need for manufacturing methods.Here,electric-field-driven generative-nanoimprinting technique is proposed.The electric field applied between the template and the substrate drives the contact,tilting,filling,and holding processes.By accurately controlling the introduced included angle between the flexible template and the substrate,tilted nanostructures with a controllable angle are imprinted onto the substrate,although they are vertical on the template.By flexibly adjusting the electric field intensity and the included angle,large-area uniform-tilted,gradient-tilted,and high-angle-tilted nanostructures are fabricated.In contrast to traditional replication,the morphology of the nanoimprinting structure is extended to customized control.This work provides a cost-effective,efficient,and versatile technology for the fabrication of various large-area tilted metasurface structures.As an illustration,a tilted nanograting with a high coupling efficiency is fabricated and integrated into augmented reality displays,demonstrating superior imaging quality.
基金supported by the National Natural Science Foundation of China(No.22278156)the Guangdong Special Support Program Project(No.2021JC060580)+1 种基金the Young Elite Scientists Sponsorship Program by CAST-Doctoral Student Special Plan,the China Scholarship Council Program(No.202406150148)the Natural Science Foundation of Guangdong Province(No.2023A1515011186).
文摘Peroxymonosulfate(PMS)-based advanced oxidation processes(AOPs)are an effective way to remove emerging contaminants(ECs)from water.The catalytic process involving PMS is hindered by the suboptimal electron trans-fer efficiency of current catalysts,the further application of AOPs technology is limited.Here,it is proposed that the interfacial electric field can be controlled by bor(B)-doped FeNC catalysts,which shows significant advantages in the efficient generation,release and participation of reactive oxygen species(ROS)in the reaction.The super exchange interaction between Fe sites and N and B sites is realized through the directional transfer of electrons in the interfacial electric field,which ensures the high efficiency and stability of the PMS catalytic process.B doping increases the d orbitals distribution at Fermi level,which facilitates enhanced electron transition activity,thereby promoting the effective generation of (1)^O_(2).At the same time,orbital hybridization causes the center of the d band to move to a lower energy level,which not only contributes to the desorption process of (1)^O_(2),but also accelerates its release.In addition,B-doping also improved the adsorption capacity of organic pollutants and shortened the migration distance of ROS,thereby significantly improving the degradation efficiency of ECs.The B-doping strategy outlined offers a novel approach to the development of FeNC catalysts,it lays a theoretical foundation and offers technical insights for the integration of PMS/AOPs technology in the ECs management.
基金supported by the National Natural Science Foundation of China(52164028,52274297)the Start-up Research Foundation of Hainan University(KYQD(ZR)20008,KYQD(ZR)21125,KYQD(ZR)23169))+1 种基金Collaborative Innovation Center of Marine Science and Technology of Hainan University(XTCX2022HYC14)Innovative Research Project for Postgraduate Students in Hainan Province(Qhyb2024-95).
文摘Development of robust electrocatalyst for oxygen reduction reaction(ORR)in a seawater electrolyte is the key to realize seawater electrolyte-based zinc-air batteries(SZABs).Herein,constructing a local electric field coupled with chloride ions(Cl-)fixation strategy in dual single-atom catalysts(DSACs)was proposed,and the resultant catalyst delivered considerable ORR performance in a seawater electrolyte,with a high half-wave potential(E_(1/2))of 0.868 V and a good maximum power density(Pmax)of 182 mW·cm^(−2)in the assembled SZABs,much higher than those of the Pt/C catalyst(E_(1/2):0.846 V;Pmax:150 mW·cm^(−2)).The in-situ characterization and theoretical calculations revealed that the Fe sites have a higher Cl^(−)adsorption affinity than the Co sites,and preferentially adsorbs Cl^(−)in a seawater electrolyte during the ORR process,and thus constructs a low-concentration Cl^(−)local microenvironment through the common-ion exclusion effect,which prevents Cl^(−)adsorption and corrosion in the Co active centers,achieving impressive catalytic stability.In addition,the directional charge movement between Fe and Co atomic pairs establishes a local electric field,optimizing the adsorption energy of Co sites for oxygen-containing intermediates,and further improving the ORR activity.
基金financially supported by the National Natural Science Foundation of China(No.22068007).
文摘In photocatalysis field,S-scheme heterojunctions show unique advantages and prospects.However,the carrier shielding effect of heterojunctions limits the separation and migration of interfacial charges.In this study,a strategy of“dynamic cascade electric fields to deplete unilaterally accumulated charges”was innovatively proposed to overcome this drawback.By modulating g-C_(3)N_(4)(CN)and Bi_(2)WO_(6)(BWO)using the polarized electric field(PEF)of spontaneously polarized ceramic(SPC),a BWO/SPC-CN composite with cascade internal electric field(IEF)and PEF was successfully constructed for efficient piezophotocatalytic degradation of recalcitrant pollutants.BWO/SPC-CN contributed to 96.8% degradation of carbamazepine,significantly surpassing BWO/CN(70.5%).BWO/SPC-CN performed excellent capacity of harvesting piezoelectric energy due to its unique three-dimensional porous nano-network structure.The PEF of SPC modulated the electronic band structure and thus strengthened the IEF of BWO/SPC-CN,providing a persistent driving force for interfacial charge migration.Moreover,SPC with a strong PEF unilaterally consumed the charges accumulated on CN under periodic piezoelectricity,weakening the shielding electric field to inhibit the recombination of electron-hole pairs.As a consequence,the dynamic cascade PEF-IEF ultimately broke the carrier shielding effect in heterojunction photocatalysis and enhanced interfacial electron transfer.This work provides reliable methods to enhance the interfacial charge transfer in heterojunction and new insights into piezo-photocatalytic mechanism.
文摘The slow-proton-fast-electron process severely limits the catalytic efficiency of oxygen evolution reaction.A method is proposed to accelerate proton transfer by building up local electric fields.Modifying acetic,ethanedioic and propanetricarboxylic(C_(6)H_(8)O_(6))ligands on BiVO_(4)surface results in a potential difference between BiVO_(4)and ligands that generates a local electric field which serves as a driving force for proton transfer.Among the ligands,carrying the strongest electron-withdrawing ability,the modification of C_(6)H_(8)O_(6) forms the strongest local electric field and leads to the fastest proton transfer and the smallest thermodynamic overpotential.C_(6)H_(8)O_(6)-BiVO_(4)exhibits 3.5 times photocurrent density as high as that of pure BiVO_(4),which is 3.50 mA cm^(-2)at 1.23 VRHE.The onset potential of C_(6)H_(8)O_(6)-BiVO_(4)shifts negatively from 0.70 to 0.38 VRHE.The mechanism for OER transitions from thermodynamically high energy proton-coupled electron transfer to thermodynamically low energy electron transfer as proton transfer is accelerated.
基金The authors sincerely appreciate funding from“Producing Hydrogen in Trentino-H2@TN”(PAT-Trento)through the research grant(SAP 40104237)Researchers Supporting Project number(RSP2025R399)King Saud University,Riyadh,Saudi Arabia.
文摘Simultaneously inducing dual built-in electric fields(EFs)both within a single component and at the heterojunction interface creates a dual-driving force that is crucial for promoting spatial charge separation.This is particularly significant in challenging coupled systems,such as CO_(2)photoreduction integrated with selective oxidation of toluene to benzaldehyde.However,developing such a system is quite challenging and often requires a precise design and engineering.Herein,we demonstrate a unique Ni-CdS@Ni(OH)_(2)heterojunction synthesized via an in-situ self-assembly method.Comprehensive mechanistic and theoretical investigations reveal that the NiCdS@Ni(OH)_(2)heterojunction induces dual electric fields(EFs):an intrinsic polarized electric-field within the CdS lattice from Ni doping and an interfacial electric-field from the growth of ultrathin nanosheets of Ni(OH)_(2)on NiCdS nanorods,enabling efficient spatial charge separation and enhanced redox potential.As proof of concept,the Ni-CdS@Ni(OH)_(2)heterojunction simultaneously exhibits outstanding bifunctional photocatalytic performance,producing CO at a rate of 427μmol g^(-1)h^(-1)and selectively oxidizing toluene to benzaldehyde at a rate of 1476μmol g^(-1)h^(-1)with a selectivity exceeding 85%.This work offers a promising strategy to optimize the utilization of photogenerated carriers in heterojunction photocatalysts,advancing synergistic photocatalytic redox systems.
文摘Anodic bonding between silicon and glass with dou bl e electric fields is presented.By this means,the damage caused by the electric f ield to the movable part during bonding can be avoided and the experiment result s show that.
基金financially supported by the National Key Re-search and Development Program of China[No.2022YFF1202500,2022YFF1202502]the National Natural Science Foundation of China[62071459]+1 种基金the Subject arrangement Foundation of Shen-zhen[No.JCYJ20180507182057026]the International Science and Technology Cooperation Project of Bingtuan[No.2022BC008]。
文摘The difficulty in fabricating a multifaceted composite heterojunction system based on Cd_(x) Zn_(1-x) S limits the enhancement of photocatalytic performance.In the present scrutiny,novel ZnO/Cd_(x) Zn_(1-x) S/CdS com-posite heterojunctions are successfully prepared by the alkaline dissolution etching method.The internal electric field at the interface of I-type and Z-scheme heterojunction improved the effective charge sepa-ration.The ZC 8 sample exhibits excellent photocatalytic performance and the H2 production efficiency is 15.67 mmol g^(−1) h^(−1) with good stability up to 82.9%in 24-hour cycles.The performance of CH_(4) and CO capacity in the CO_(2) RR process is 3.47μmol g^(−1) h^(−1) and 23.5μmol g^(−1) h^(−1),respectively.The photogener-ated accelerated charge transport is then examined in detail by in situ X-ray photoelectron spectroscopy(ISXPS)and density functional theory(DFT)calculations.This work presents a new idea for the synthe-sis of Cd_(x) Zn_(1-x) S solid-solution-based materials and provides a solid reference for the detailed mechanism regarding the electric field at the heterojunction interface.
基金supported by the National Key R&D Program of China(Grant No.2022YFA1402802)the National Natural Science Foundation of China(Grant Nos.12494591 and 92165204)+4 种基金the Leading Talent Program of Guangdong Special Projects(Grant No.201626003)the Guangdong Provincial Key Laboratory of Magnetoelectric Physics and Devices(Grant No.2022B1212010008)the Research Center for Magnetoelectric Physics of Guangdong Province(Grant No.2024B0303390001)the Guangdong Provincial Quantum Science Strategic Initiative(Grant No.GDZX2401010)supported by the National Natural Science Foundation of China(Grant Nos.12234016 and 12074031)。
文摘We investigate the energy bands,magnetism,and superconductivity of bilayer octagraphene with A-A stackingunder a perpendicular electric field.A tight-binding model is used to analyze the band structure of the system.The doubling of the unit cell results in each band of the single layer splitting into two.We find that applyinga perpendicular electric field increases the band splitting.As the electric field strength increases,the nestingof the Fermi surface(FS)weakens,eventually disrupting the antiferromagnetic order,and bilayer octagrapheneexhibits superconductivity.Spin fluctuations can induce unconventional superconductivity with s±-wave pairing.Applying a perpendicular electric field to bilayer octagraphene parent weakens the nesting of the FS,ultimatelykilling the spin-density-wave(SDW)ordered state and transitioning it into the superconducting state,whichworks as a doping effect.We use the random-phase approximation approach to obtain the pairing eigenvaluesand pairing symmetries of the perpendicular electric field-tuned bilayer octagraphene in the weak coupling limit.By tuning the strength of the perpendicular electric field,the critical interaction strength for SDW order can bemodified,which in turn may promote the emergence of unconventional superconductivity.
基金supported by the Hunan Provincial Natural Science Foundation(No.2016JJ3034).
文摘Einstein aimed to find a unified theoretical model to explain various interactions in nature,and the relationship between gravitational and electric fields was particularly important.For the first time,this paper provides the internal relationship equations of the electric and magnetic fields.Further,the relationship between the magnetic and gravity fields is analyzed,and the relationship equations of the electric,magnetic,and gravity fields are established.On this basis,a general formula for calculating the radius of charged particles is derived.Simultaneously,we also discussed and made predictions on black holes,providing convenience for future research and experimental detection.
文摘Developing an efficient photocatalyst is the key to realize the practical application of photocatalysis.The S-scheme heterojunction has great potential in photocatalysis due to its unique charge-carrier migration pathway,effective light absorption and high redox capacity.However,further enhancing the built-in electric field of the S-scheme,accelerating carrier separation,and achieving higher photocatalytic performance remain unresolved challenges.Herein,based on the continuously adjustable band structure of continuous solid-solution,a novel 0D/2D all solid-solution S-scheme heterojunction with adjustable internal electric field was designed and fabricated by employing a solid-solution of ZnxCd_(1–x)S and Bi_(2)MoyW_(1–y)O_(6)respectively as reduction and oxidation semiconductors.The synergistic optimization of effective light absorption,fast photogenerated carrier separation,and high redox potential leads can be tuned to promote photocatalytic activity.Under visible light,the S-scheme system constructed by Zn_(0.4)Cd_(0.6)S quantum dot(QDs)and Bi_(2)Mo_(0.2)W_(0.8)O_(6)monolayer exhibits a high rate for photocatalytic degradation C_(2)H_(4)(150.6×10^(–3)min^(–1)),which is 16.5 times higher than that of pure Zn_(0.4)Cd_(0.6)S(9.1×10^(–3)min^(–1))and 53.8 times higher than pure Bi_(2)Mo_(0.2)W_(0.8)O_(6)(2.8×10^(–3)min^(–1)).Due to the unique charge-carrier migration pathway,photo-corrosion of Zn_(x)Cd_(1–x)S is further inhibited simultaneously.In-situ irradiation X-ray photoelectron spectroscopy,photoluminescence spectroscopy,time-resolved photoluminescence,transient absorption spectroscopy and electron paramagnetic resonance provide compelling evidence for interfacial charge transfer via S-scheme pathways,while in-situ diffuse reflectance infrared Fourier transform spectroscopy identifies the reaction pathway for C_(2)H_(4)degradation.This novel S-scheme photocatalysts demonstrates excellent performance and potential for the practical application of the fruits and vegetables preservation at room temperatures.
基金support from the Chinese Academy of Sciences and University of Science and Technology of China,National Key Research and Development Program of China(No.2021YFA1500402)National Natural Science Foundation of China(Nos.21571167,51502282 and 22075266)Fundamental Research Funds for the Central Universities(Nos.WK2060190053 and WK2060190100)。
文摘Efficient selective adsorption and separation using porous frameworks are critical in many industrial processes,where adsorption energy and dynamic diffusion rate are predominant factors governing selectivity.They are highly susceptible to framework charge,which plays a significant role in selective adsorption.Currently,ionic porous frameworks can be divided into two types.One of them is composed of a charged backbone and counter ions.The framework with zwitterionic channels is another type.It is composed of regular and alternating arrangements of cationic and anionic building units.Herein,we report a hydrogen-bonded ionic framework(HIF)of{(CN_(3)H_(6))_(2)[Ti(μ_(2)-O)(SO_(4))_(2)]}_nwith 1D channel exhibits unique adsorption selectivity for Ar against N_(2)and CO_(2).Density functional theory(DFT)results suggest that CO_(2)cannot be adsorbed by HIF at the experimental temperature due to a positive adsorption free energy.In addition,due to a relatively large diffusion barrier at 77 K,N_(2)molecules hardly diffuse in HIF channels,while Ar has a negligible diffusion barrier.The unique net positively-charged space in the channel is the key to the unusual phenomena,based on DFT simulations and structural analysis.The findings in this work proposes the new adsorption mechanism and provides unique perspective for special separation applications,such as isotope and noble gasses separations.
基金financial support from the National Natural Science Foundation of China(NSFC No.52202253,ter for Microscopy and Analysis at the Nanjing University of Aero52372193,52472211,22293041)the Natural Science Foundation of Jiangsu Province(No.BK20220914)the Large Instrument and Equipment Sharing Fund of NUAA。
文摘A fatal issue of Zn-based electrochemical energy storage is uneven Zn^(2+)deposition on the Zn metal anode.Unfortunately,the modulation for the inherent electric field,the origin of driving force for ion diffusion,has been given insufficient importance.Herein,the redistribution of the surrounding electric field is demonstrated to depend on the permittivity of the surface medium for the first time,where highpermittivity particles can simultaneously enhance vertical components and reduce horizontal components of the electric field through polarization.Consequently,a bacterial cellulose-based separator is proposed by incorporating a high-permittivity surface medium.Cellulose serves as a robust substrate with a rather low thickness to enable homogeneous dispersion of high-permittivity particles on the surface,which can regulate the localized electric field to guide even Zn deposition by inhibiting twodimensional(2D)Zn^(2+)diffusion and suppressing side reactions by repulsing anion migration toward the Zn anode.The separator achieves significantly enhanced Zn anode stability of 2880 h at 1 mA cm^(-2)and a cumulative capacity of 3.5 Ah cm^(-2)at 10 mA cm^(-2).It also enables a long-term lifespan of 50,000 cycles in Zn||AC capacitor and 1000 cycles at a limited negative/positive(N/P)ratio of 3:1.This work provides a new view to stabilize Zn anode by electric field modulation.
基金supported by Guangdong Basic and Applied Basic Research Foundation(Nos.2021A1515010261 and 2023A1515140153)Guangdong Special Innovative Projects of General Universities(No.2022KTSCX136)+1 种基金the Major and Special Project in the Field of Intelligent Manufacturing of the Universities in Guangdong Province(No.2020ZDZX2067)the Innovative Team Project of the Universities in Guangdong Province(No.2023KCXTD035).
文摘The quest for sustainable energy solutions has intensified the need for efficient water electrolysis techniques,pivotal for hydrogen production.However,developing effective bifunctional electrocatalysts capable of driving the hydrogen evolution reaction(HER)and oxygen evolution reaction(OER)remains a formidable challenge.Addressing this,we introduce a novel built-in electric field(BEF)strategy to synthesize NiCoP–Co nanoarrays directly on Ti_(3)C_(2)T_(x) MXene substrates(NiCoP–Co/MXene).This approach leverages a significant work function difference(ΔΦ),propelling these nanoarrays as adept bifunctional electrocatalysts for comprehensive water splitting.MXene,in this process,plays a dual role.It acts as a conductive support,enhancing the catalyst’s overall conductivity,and facilitates an effective charge transport pathway,ensuring efficient charge transfer.Our study reveals that the BEF induces an electric field at the interface,prompting charge transfer from Co to NiCoP.This transfer modulates asymmetric charge distributions,which intricately control intermediates’adsorption and desorption dynamics.Such regulation is crucial for enhancing the reaction kinetics of both HER and OER.Furthermore,under oxidative conditions,the NiCoP–Co/MXene catalyst undergoes a structural metamorphosis into Ni(Co)oxides/hydroxides/MXene,increasing OER performance.This research demonstrates the BEF’s role in fine-tuning interfacial charge redistribution and underscores its potential in crafting more sophisticated electrocatalytic designs.The insights gained here could pave the way for the next generation of electrocatalysis,with far-reaching implications for energy conversion and storage technologies.
文摘The rational configuration of built-in electric field(IEF)in heterogeneous materials can significantly optimize the band structure to accelerate the separation of photogenerated charge carriers.However,the strength modulation of IEF formed by various materials has an uncertain enhancing effect on the separation of photogenerated carriers.Herein,a mesoporous MIL-125(Ti)@BiOCl S-scheme heterojunction with controllable IEF is prepared by green photoreduction reaction to investigate the relationship between IEF,microstructure,and photocatalytic activity.Moreover,the corresponding results demonstrate the MIL-125(Ti)@BiOCl effectively regulates the IEF strength through controlling the concentration of ligand defects,thereby optimizing the band structure and improving the efficiency of photogenerated charge separation.The optimized IEF significantly enhances the photocatalytic degradation performance of mesoporous MIL-125(Ti)-3@BiOCl towards tetracycline,with a k value of 0.07 min^(–1),which are approximately 5.5 and 4.7 times greater than that of BiOCl(0.0127 min^(–1))and MIL-125(Ti)-3(0.015 min^(–1)).These findings provide a new pathway for regulating IEF within MOF-based heterojunctions,and offer new insights into the intrinsic correlations between defect structure,IEF,and photocatalytic activity.
基金supported by the National Nature Science Foundation(Nos.52372125 and 52333009)the National Key Research and Development Project(Nos.2020YFC1521900 and 2020YFC1521904)+4 种基金the Shaanxi Provincial Science Foundation(No.2021GXLH-01-11)the Yulin Project(No.2022-19-11)the Fundamental Research Funds for the Central Universities(No.D5000230071)the 111 Program(No.B08040)of MOE of Chinasponsored by Innovation Foundation for Doctor Dissertation of Northwestern Polytechnical University(No.CX2024063).
文摘Ferroelectric materials find extensive applications in brake systems due to their capability to convert electrical energy into mechanical energy.Recent research has focused on lead-free materials for their environmentally friendly characteristics.However,they exhibit several challenges such as significant negative strain,limited strain values,and large driving field.In this work,novel preparation techniques(electrospinning)were utilized for BaTiO_(3)to introduce oxygen vacancies and barium defects,facilitating the creation of oriented defect dipoles coupled with an intrinsic electric field(Ei)after poling and aging.Due to the existence of Ei,two minimum points in the strain hysteresis loop were shifted to the same quadrant in the Strain-Electric field space.Thus,when applying an electric field along the Ei direction,negative strain is eliminated.Additionally,the actual electric field is the sum of the applied electric field and Ei,thereby reducing the required driving field of the piezoelectric.The stretching of defect dipoles under the electric field further amplified the total strain.Through the proposed mechanisms,this work achieved a substantial unipolar electrostrain of 1.04%under a relatively low electric field(30 kV/cm)in BaTiO_(3).This work successfully addressed the challenges of high-driving electric fields,limited strain values,and negative strain,providing a comprehensive approach for improving field-induced strain performance through point defect engineering in ferroelectric materials.
基金Project supported by the National Natural Science Foundation of China(Grant Nos.12064034 and 11562017)the Leading Talents Program of Science and Technology Innovation in Ningxia Hui Autonomous Region,China(Grant No.2020GKLRLX08)the Natural Science Foundation of Ningxia Hui Autonomous Region,China(Grant No.2024AAC05040)。
文摘Atmospheric particle adsorption on insulator surfaces,coupled with humid environments,significantly affects contamination flashover,necessitating a clear understanding of the electric field distribution on insulator surfaces with adsorbed particles.This is crucial for accurately assessing insulator safety and informing critical decision-making.Although previous research has demonstrated that particle arrangement significantly influences the electric field distribution around transmission lines,an in-depth analysis of its effects on insulator surfaces remains lacking.To address this gap,this study establishes a composite insulator model to examine how three types of spherical contamination layers affect the electric field distribution on insulator surfaces under varying environmental conditions.The results reveal that in dry environments,the electric field strength at the apex of single-particle contamination layers increases with the particle size and relative permittivity.For the double-particle contamination layers,the electric field intensity on the insulator surface decreases as the particle spacing increases,and larger particles are more likely to attract smaller charged particles.For triple-particle contamination layers arranged in a triangular pattern,the maximum surface field strength is nearly double that of the chain-arranged particles.Furthermore,within the chain-arranged triple-particle contamination layers,a large-small-large size arrangement has a more pronounced impact on the surface electric field than a small-large-small size arrangement.In humid environments,the surface electric field strength of insulators decreases with increasing contamination levels.These findings are of significant theoretical and practical importance for ensuring the safe operation of power systems.
基金a project funded by the China National Space Administration (CNSA) and China Earthquake Administration (CEA)supported by the National Key R&D Program of Intergovernmental Cooperation in Science and Technology (Grant No. 2023YFE0117300)+3 种基金the International Space Science Institute (ISSI in Bern, Switzerland, and ISSI-BJ in Beijing, China)supporting International Team 23-583 led by Dedalo Marchetti and Essam Ghamrythe Hebei Province Graduate Professional Degree Excellent Teaching Case (Library) Construction Project (Grant No. KCJPZ2023060)the Open Fund for the Key Laboratory of Seismic Disaster Instruments and Monitoring Technology in Hebei Province (Grant No. FZ224104)。
文摘This study aimed to evaluate the wake effect on the electric field detector(EFD) onboard the China Seismo-Electromagnetic Satellite(CSES-01). Through a series of experiments and analyses, we confirmed that the disturbance phenomenon from probe B of the EFD is not caused by the boom layout. To validate and determine whether it is influenced by the wake effect, we conducted two experiments. In the first experiment, the entire satellite platform underwent a 90° counterclockwise yaw maneuver to allow probe B to avoid the plasma wake region. We then verified whether the disturbance was improved. In the second experiment, the satellite platform performed a 180° counterclockwise yaw maneuver, positioning probe B on the ram side of the satellite and completely avoiding all satellite wakes. The plasma wake effect of the satellite did not significantly influence the spherical probes of the EFD because the measurement accuracy stayed relatively stable under the two experiments, despite the observed abnormalities in the operating state of spherical probe B. This consistency in performance is important for electric field detection missions because the spatial electric field vector data obtained from these probes continue to effectively reflect information on spatial electromagnetic disturbances. These two experimental results showed that probe B consistently exhibited data jump phenomena under various maneuver states, whereas probes A, C, and D did not display such phenomena in any maneuver state.
文摘The major challenge in photocatalytic water splitting lies in water oxidation reactions,which still suffer from poor charge separation.This study overcame inefficient charge separation by establishing a robust interfacial electric field through the electrostatic-driven assembly of Co_(3)O_(4) nanoparticles with a perylene imide supramolecule(PDINH).The well-aligned band structures and intimate interfacial contact in the PDINH/Co_(3)O_(4) heterostructure create an enhanced interfacial electric field that is 4.1-and 53.2-fold stronger than those of individual PDINH and Co_(3)O_(4),thus promoting directional charge separation and transfer.Moreover,S-scheme charge transfer strongly preserves the oxidative holes in PDINH to drive efficient water oxidation reactions.Consequently,PDINH/Co_(3)O_(4) composite achieves a photocatalytic oxygen evolution rate of 29.26 mmol g^(–1) h^(–1) under visible light irradiation,8.2-fold improvement over pristine PDINH,with an apparent quantum yield of 6.66%at 420 nm.This study provides fundamental insights into interfacial electric field control for the development of high-performance organic photocatalysts for efficient water oxidation.
基金supported by the National Natural Science Foundation of China(Nos.U21A20399 and 52274407)Liaoning Province Applied Basic Research Program(No.2022JH2/101300212).
文摘In this work,we aim to develop a novel post-treatment process combining cryogenic and pulsed electric field treatment to enhance WC-Co cemented carbides.The results show a 15.62%increase in hardness from 1831.38 to 2117.38 HV30,a 9.60%rise in fracture toughness from 9.06 to 9.93 MPa·m^(1/2),while the friction coefficient decreases from 0.63 to 0.47.Through the residual stress evolution,WC orientation change and the martensitic transformation of Co,and the internal enhancement mechanism of cryogenic combined with pulsed electric field treatment are revealed.The electron wind generated by the pulsed electric field can efficiently reduce the residual stress induced by cryogenic process.The evolution of residual stress promotes the base slip of WC,increasing the degree of{0001}orientation.In addition,the degree of martensitic transformation of Co intensifies,with the hcp-Co/fcc-Co ratio rising from 0.41%to 17.86%.The enhanced WC{0001}orientation and increased hcp-Co content contribute to significant improvements in hardness and wear resistance.This work provides a novel efficient enhancement strategy for ceramics and alloys,with the potential to be a mainstream strengthening method in the future.
