Two-step-processed(TSP)inverted p-i-n perovskite solar cells(PSCs)have demonstrated significant promise in tandem applications.However,the power conversion efficiency(PCE)of TSP p-i-n PSCs rarely exceeds 24%.Here,we d...Two-step-processed(TSP)inverted p-i-n perovskite solar cells(PSCs)have demonstrated significant promise in tandem applications.However,the power conversion efficiency(PCE)of TSP p-i-n PSCs rarely exceeds 24%.Here,we demonstrate that TSP perovskite films exhibit a vertically gradient distribution of residual PbI_(2)clusters,which form Schottky heterojunctions with the perovskite,leading to substantial interfacial energy-level mismatches within NiO_(x)-based TSP p-i-n PSCs.These limitations were effectively addressed via a vertical interfacial engineering enabled by dual-interface modification incorporating tin trifluoromethanesulfonate(Sn(OTF)_(2))and 4-Fluorophenylethylamine chloride(F-PEA)at the NiO_(x)/perovskite and perovskite/C60 interfaces,respectively.The functional Sn(OTF)_(2)not only enhances the conductivity of NiO_(x)films but also suppresses ion migration,while inducing the formation of a Pb-Sn mixed perovskite interlayer that precisely regulates the energy level at the NiO_(x)/perovskite interface.Complementally,F-PEA post-treatment effectively converts surface residual PbI_(2)clusters into a 2D perovskite capping layer,which simultaneously passivates surface defects and enhances energy-level alignment at the perovskite/C60 interface.Consequently,the optimized NiO_(x)-based TSP p-i-n PSCs achieve a notable PCE of 25.6%with superior operational stability.This study elucidates the underlying mechanisms limiting the efficiency of TSP p-i-n PSCs,while establishing design principles for these devices targeting 26%efficiency.展开更多
Steel slag(SS)accumulates unavoidably due to its complex and unstable composition,high production volumes,and limited value-added resource utilization.Single or multiple interface modifiers were proposed to enhance th...Steel slag(SS)accumulates unavoidably due to its complex and unstable composition,high production volumes,and limited value-added resource utilization.Single or multiple interface modifiers were proposed to enhance the properties of SS through high-speed dispersion,transforming its inherent hydrophilic and oleophobic characteristics into hydrophily and lipophilicity.The modification effects were innovatively assessed by observing the color changes of modified steel slag solutions following the dissolution-settlement equilibrium constant.This approach avoided human-induced errors and improved estimated accuracy in conformance with conventional methods such as oil absorption value,activation index,sedimentation volume,and lipophilicity.The hydrolysis of 3-aminopropyltriethoxysilane(KH)generated–Si(OH)_(3)structure to form hydrogen or covalent bonds with active substances(OH groups)from SS.Concurrently,SS underwent encapsulation via Si–O–Si structure resulting from the dehydration of–Si(OH)_(3).The stearic acid coupling agent(SA),aluminate coupling agent(AC),and titanate coupling agent(TN)underwent chemical reactions with Ca(OH)_(2),Al(OH)_(3),and CaCO_(3)in SS.The acidic SA primarily created stable chemical bonds and acted as a supplement due to its package,reducing surface activity and hydrophilicity while enhancing lipophilicity.Specifically,the optimal modification effect was obtained at 3 wt.%SA.Consequently,3 wt.%SA was established as the benchmark for multiple modifiers and the most effective combination was 3 wt.%SA and 3 wt.%AC.Compared with a single interface modifier,SA corroded the SS surface to provide numerous active sites for further modification by KH,AC,or TN,resulting in a more densely packed structure.In addition,more organic groups on SS prevent the proximity of other particles from agglomerating to achieve dispersion and a synergistic modification,laying a theoretical foundation of SS in a new pathway for organic composite materials.展开更多
Biomass-derived carbon materials are favored for their abundance and sustainability,and ease of preparation and modification.By surface activation and modification they can have a good electrical conductivity,excellen...Biomass-derived carbon materials are favored for their abundance and sustainability,and ease of preparation and modification.By surface activation and modification they can have a good electrical conductivity,excellent catalytic activity,a remarkable adsorption capacity,and different interfacial physicochemical functionalities.Surface-modified biochars have found wide applications in energy storage,environmental remediation,and catalysis.However,achieving precise and controllable modification of their active sites remains a challenge.Recent advances and future prospects for controlling their surface morphology,defect engineering,and surface coating strategies,with particular attention to their means of fabrication,are reviewed.展开更多
Benzoic acid containing fluorine atom at ortho-,meta-,and para-position are employed as self-assembled monolayers to modify the buried interface in perovskite solar cells(PSCs).It is demonstrated that the position of ...Benzoic acid containing fluorine atom at ortho-,meta-,and para-position are employed as self-assembled monolayers to modify the buried interface in perovskite solar cells(PSCs).It is demonstrated that the position of fluorine atom influences the passivation effect and para-fluorinated one provided the most substantial performance enhancement mainly originating from ameliorated contact and energy band alignment between NiOx and perovskite,improved perovskite quality and defect healing.Resultantly,PSC with a power conversion efficiency of 24%can be achieved.Meanwhile,which can maintain 96.8%of the initial PCE after a 1000 h storage,presenting enhanced durability.This work highlights the critical role of molecular functionality and conformation in the buried interface modification of PSCs,providing valuable insights for future developments.展开更多
In the realm of large-scale power system energy storage,sodium-based batteries represent a cost-effective post-lithium energy storage technology,making inorganic solid-state sodium batteries(ISSSB)a critical branch of...In the realm of large-scale power system energy storage,sodium-based batteries represent a cost-effective post-lithium energy storage technology,making inorganic solid-state sodium batteries(ISSSB)a critical branch of this development.Inorganic solid-state electrolytes(ISSEs)are the core components of sodium batteries;however,they face significant challenges such as insufficient ionic conductivity,interfacial instability,and dendrite growth,all of which severely hinder practical application.This review critically assesses experimental protocols and theoretical frameworks related to mainstream ISSEs and systematizes optimization strategies aimed at overcoming these challenges.Leveraging integrated insights from both experimental and computational studies,the review first categorizes and summarizes the primary types of ISSEs,namely oxide-,sulfide-,and halide-based electrolytes.It then details interfacial optimization strategies focused on addressing three core interfacial issues:ion transport barriers resulting from mechanical incompatibility,side reactions stemming from electrochemical mismatch,and dendrite formation.Finally,the review advocates prioritizing in-depth research that integrates experimental and theoretical approaches to establish a closed-loop methodology encompassing predictive design,multiscale investigation,mechanistic exploration,and high-throughput automated experimentation,with feedback-driven refinement.This work serves as a comprehensive reference and systematic roadmap for future research on solid-state electrolytes(SSEs).展开更多
As one of the most promising new energy sources,hydrogen energy is expected to usher in a full-fledged“hydrogen economy”in the 21st century.Compared with traditional high-pressure gaseous and cryogenic liquid hydrog...As one of the most promising new energy sources,hydrogen energy is expected to usher in a full-fledged“hydrogen economy”in the 21st century.Compared with traditional high-pressure gaseous and cryogenic liquid hydrogen storage methods,solid-state chemical hydrogen storage shows significant advantages in safety,high efficiency,and cost-effectiveness.Magnesium-based lightweight hydrogen storage materials have attracted widespread attention due to their high gravimetric hydrogen storage density(7.6%)and favorable reversibility.However,their sluggish reaction kinetics and stringent operating conditions(with H2 release temperatures exceeding 350°C and H2 absorption pressures above 4 MPa)pose major challenges for practical applications.Domestic and international researchers have conducted in-depth studies to address these issues,achieving substantial progress in the modification of magnesium-based hydrogen storage alloys.This paper systematically elaborates on major modification techniques such as alloying,nanostructuring,and catalytic material doping,providing a comprehensive analysis of the strengths and limitations of each approach.Furthermore,it offers prospects for the future development of magnesium-based hydrogen storage materials by integrating current theoretical and experimental research findings.展开更多
All-solid-state batteries(ASSBs)assembled with sulfide solid electrolytes(SSEs)and nickel(Ni)-rich oxide cathode materials are expected to achieve high energy density and safety,representing potential candidates for t...All-solid-state batteries(ASSBs)assembled with sulfide solid electrolytes(SSEs)and nickel(Ni)-rich oxide cathode materials are expected to achieve high energy density and safety,representing potential candidates for the next-generation energy storage systems.However,interfacial issues between SSEs and Nirich oxide cathode materials,attributed to space charge layer,interfacial side reactions,and mechanical contact failure,significantly restrict the performances of ASSBs.The interface degradation is closely related to the components of the composite cathode and the process of electrode fabrication.Focusing on the influencing factors of interface compatibility between SSEs and Ni-rich oxide cathode,this article systematically discusses how cathode active materials(CAMs),electrolytes,conductive additives,binders,and electrode fabrication impact the interface compatibility.In addition,the strategies for the compatibility modification are reviewed.Furthermore,the challenges and prospects of intensive research on the degradation and modification of the SSE/Ni-rich cathode material interface are discussed.This review is intended to inspire the development of high-energy-density and high-safety all-solid-state batteries.展开更多
Silicon carbide(SiC)is a highly valued material for power semiconductor devices due to its wide bandgap,high thermal conductivity,and high breakdown electric field.However,its high hardness,brittleness,and chemical st...Silicon carbide(SiC)is a highly valued material for power semiconductor devices due to its wide bandgap,high thermal conductivity,and high breakdown electric field.However,its high hardness,brittleness,and chemical stability present substantial challenges for efficient and high-quality processing.This study investigated the effects of picosecond laser surface scanning on 4H-SiC to enhance the material removal performance.The research focused on surface morphology,phase transitions,subsurface/interface characteristics,and material removal mechanisms under varying laser parameters.The results demonstrate that the laser thermal effect decomposes 4H-SiC into amorphous silicon(a-Si),disordered carbon,and graphite,forming a resolidified layer containing Si-O and Si-C-O oxides.Crystalline silicon(c-Si)is produced under high fluences or extensive irradiations.The variation in the resolidified layer thickness with changing laser parameters is revealed.A detailed laser-induced subsurface damage model is developed,encompassing a resolidified layer that includes the above decomposition and oxidation products,and a deformed layer formed primarily under laser-induced stress.The presence of the resolidified layer and the deformed layer leads to a decreased elastic recovery rate and an increased scratching depth,exceeding 2.5 times that of the unmodified condition.Enhanced material removal performance is mainly driven by the resolidified layer at low fluence and by the deformed layer at high fluence.When aligning the total of the ablation depth and the resolidified layer thickness with the subsurface damage depth in the original material,excellent polishing performance is achieved.These findings provide critical insights for understanding the phase evolution,subsurface damage mechanisms,and material removal behavior of 4H-SiC,offering valuable guidance for optimizing the laser surface modification parameters to achieve high-efficiency processing.展开更多
The interfacial structure and its regulation play a crucial role in determining the overall performance of advanced functional composites.Weak interfacial interactions between carbon fibers and the matrix present a cr...The interfacial structure and its regulation play a crucial role in determining the overall performance of advanced functional composites.Weak interfacial interactions between carbon fibers and the matrix present a critical challenge limiting the general performance and functional applications of carbon fiberreinforced composites.In this paper,a novel strategy for bioinspired root-soil interfacial structure was presented to enhance the mechanical properties of polymer bonded explosives.A multiscale nanowire heterostructure was constructed through the in-situ growth of morphologically controllable zinc oxide nanowires on the carbon fiber surface via a facile hydrothermal method,with polydopamine as the interfacial reinforcement layer.This structure emulated the function of the"root",and combined with a network-distributed polymer binder representing the"soil",formed a robust root-soil interlocking interfacial structure within the polymer bonded explosives.Due to the multiscale interfacial reinforcement structure,the tensile strength of the polymer bonded explosives was visibly increased by 41%,the strain at the break by 110%,and the creep resistance by 51%with only 0.4 wt%filler adopted.The thermal stress resistance was improved by 57%owing to the synergistic enhancement of thermal conductivity and mechanical properties.This study provides new perspectives and insights for designing and constructing high-performance polymer bonded explosives and other functional composites.展开更多
Rotary friction welding is a highly effective solid-state technique for joining dissimilar materials,which offers the potential for significant weight reduction without compromising strength.Traditionally,during rotar...Rotary friction welding is a highly effective solid-state technique for joining dissimilar materials,which offers the potential for significant weight reduction without compromising strength.Traditionally,during rotary friction welding,the severely deformed material,or flash,is expelled from the interface and machined away to achieve the desired joint geometry.However,this work introduces a novel approach:trapping the flash within the joint to improve joint properties.The study investigates two different interface geometry combinationsdflat-flat and flat-taper interfaces.Previous research shows that Ni interlayer between steel and titanium can enhance the joint strength.This study builds on the existing knowledge(effect of Ni interlayer)by examining the influence of interface geometry to further improve the dissimilar joint performance.The experimental results,including tensile testing and microstructural characterization,highlight the superior performance of the flat-taper interface.The modified geometry minimizes flash loss,providing a cavity that retains both the flash and the Ni interlayer within the joint.This retention promotes dynamic recrystallization,resulting in refined grain structures near the interface.Moreover,the trapped Ni interlayer effectively prevents the formation of brittle Fe-Ti intermetallic compounds at the dissimilar material interface.The findings reveal that the flat-taper interface improved joint strength by an impressive 105%compared to the flat-flat interface.This innovative geometry modification demonstrates the potential to enhance mechanical properties of dissimilar joints through better flash and interlayer management.展开更多
Photoelectrochemical(PEC)water splitting is an effective approach to directly convert solar energy into clean hydrogen fuel.As a visible-light-responsive p-type semiconductor,CuBi_(2)O_(4)possesses a suitable bandgap ...Photoelectrochemical(PEC)water splitting is an effective approach to directly convert solar energy into clean hydrogen fuel.As a visible-light-responsive p-type semiconductor,CuBi_(2)O_(4)possesses a suitable bandgap and good stability.However,its performance is inhibited by high interfacial resistance and severe charge carrier recombination.In this study,a CuO interlayer was introduced between fluorine-doped tin oxide(FTO)and CuBi_(2)O_(4)to construct CuO/CuBi_(2)O_(4)photocathodes,aiming to improve interfacial charge transfer.The results showed that CuO/CuBi_(2)O_(4)-200 exhibited a photocurrent density of−1.71 mA/cm^(2)at 0 V vs.RHE,which was more than 3.5 times higher than that of bare CuBi_(2)O_(4).The incident photon-to-current efficiency(IPCE)at 365 nm was enhanced to~13%and the maximum applied bias photon-to-current efficiency(ABPE)reached 0.17%.Water splitting experiments revealed a hydrogen yield of 2.05μmol/cm^(2),significantly surpassing that of the unmodified photoelectrode.The enhanced PEC performance indicated that the CuO layer established a favorable band alignment,promoted hole transport toward the FTO substrate and effectively suppressed interfacial carrier recombination.This work demonstrated a simple and efficient interfacial engineering strategy,offering new insights and guidance for the design and development of high-performance semiconductor-based PEC photoelectrodes.展开更多
With the growing global energy demand and the pressing need for a clean energy transition,supercapacitors(SCs)have demonstrated significant application potential in electric vehicles,wearable electronics,and renewable...With the growing global energy demand and the pressing need for a clean energy transition,supercapacitors(SCs)have demonstrated significant application potential in electric vehicles,wearable electronics,and renewable energy storage systems owing to their rapid charge-discharge capability,exceptional power density,and prolonged cycle life.The improvement of their overall performance fundamentally depends on the synergistic design of electrode materials and electrolyte systems,as well as the precise regulation of the electrode-electrolyte interface.This review focuses on the key components of supercapacitors,systematically reviewing the design strategies of high-performance electrode materials,outlining recent advances in novel electrolyte systems,and comprehensively discussing the critical roles of interfacial reinforcement and optimization in enhancing device energy density,power performance,and cycling stability.Furthermore,interfacial engineering strategies and innovations in device architecture are proposed to address interfacial degradation in flexible SCs under mechanical stress.Finally,key future research directions are highlighted,including the development of high-voltage and wide-temperature-range electrolyte systems and the integrated advancement of multiscale in situ characterization techniques and theoretical modeling.This review aims to provide theoretical guidance and innovative strategies for material design,contributing toward the realization of next-generation supercapacitors with enhanced energy density and reliability.展开更多
In view of the frequent deterioration of molten steel quality during the tundish filling process,the slag-steel-air interface behavior in a tundish,including liquid level fluctuation,slag eyes,slag entrapment and air ...In view of the frequent deterioration of molten steel quality during the tundish filling process,the slag-steel-air interface behavior in a tundish,including liquid level fluctuation,slag eyes,slag entrapment and air suction during the steady-state casting and filling process,was comparatively studied through physical modeling and mathematical simulation methods.During the filling process,the liquid surface forms a large-size slag eye under the impact of molten steel from a ladle shroud,which simultaneously results in a violent fluctuation of liquid level.Concurrently,the liquid flow entrains the air phase and the cover slag into the tundish impact zone,resulting in slag entrapment and air suction.At filling flow rates of 1.5Q,2.0Q,and 2.5Q(Q is the flow rate under steady-state casting),the amount of slag entrapped is 8.39×10^(-5),9.65×10^(-5),and 12.7×10^(-5)m^(3),respectively,while the volume of air aspirated is 0.84×10^(-4),1.47×10^(-4),and 2.01×10^(-4)m^(3),indicating that slag entrapment and air suction intensify with an increase in tundish filling flow rate.Flow field characterization identifies eddy currents in the impact zone as the primary driver of the above phenomena.Proper filling process parameters were proposed to improve the steel quality during the tundish filling.展开更多
Invasive as well as non-invasive neurotechnologies conceptualized to interface the central and peripheral nervous system have been probed for the past decades,which refer to electroencephalography,electrocorticography...Invasive as well as non-invasive neurotechnologies conceptualized to interface the central and peripheral nervous system have been probed for the past decades,which refer to electroencephalography,electrocorticography and microelectrode arrays.The challenges of these mentioned approaches are characterized by the bandwidth of the spatiotemporal resolution,which in turn is essential for large-area neuron recordings(Abiri et al.,2019).展开更多
Post-translational modifications(PTMs)regulate the occurrence and development of cancer,and lactylation modification is a new form of PTMs.Recent studies have found that lactic acid modification can regulate the immun...Post-translational modifications(PTMs)regulate the occurrence and development of cancer,and lactylation modification is a new form of PTMs.Recent studies have found that lactic acid modification can regulate the immune tolerance of cancer cells.The classical theory holds that prostate apoptosis response-4(PAR-4)is a tumor suppressor protein.However,our recent research has found that PAR-4 has a biological function of promoting cancer in hepatocellular carcinoma(HCC),and our analysis shows that PAR-4 can be modified of lactic acid.These research evidences suggest that PAR-4 lactylation modification may drive immune tolerance in HCC.Therefore,inhibiting PAR-4 lactylation modification is very likely to increase the sensitivity of HCC to immunotherapy.展开更多
The network structure of M_(2)B in Fe-B-C alloy readily leads to the failure of material.In this work,by adding K2_SO4,the morphology of the M_(2)B was successfully regulated through a synergistic treatment combining ...The network structure of M_(2)B in Fe-B-C alloy readily leads to the failure of material.In this work,by adding K2_SO4,the morphology of the M_(2)B was successfully regulated through a synergistic treatment combining active element modification and heterogeneous nucleation modification.The results show that after the addition of K_(2)SO_(4),a new phaseα-MnS forms in the alloy,and the active element K enriches at the M_(2)B/matrix interface.This inhibits the growth of the network M_(2)B and promotes its transformation from a continuous network structure to an isolated blocky structure.As the K_(2)SO_(4) addition increases from 0wt.%to 4.46wt.%,the shape factor value of M_(2)B increases from 0.067 to 0.353,with an increase of 426%.The impact toughness of the alloy increases from 5.9 J·cm^(-2)to 14.2 J·cm^(-2),and the fracture mode transitions from cleavage fracture to ductile-cleavage mixed fracture.Three-body abrasion tests indicate that with increasing K_(2)SO_(4) addition,the wear weight loss of the alloy gradually decreases.The alloy with 4.46wt.%K_(2)SO_(4) addition exhibits the least wear damage and the best wear resistance.This work provides an effective approach for regulating the microstructure and improving the wear resistance of wear-resistant Fe-B-C alloys.展开更多
Photodetectors can convert light energy into electrical signals,so are widely used in photovoltaics,photon counting,monitoring,and imaging.Photodetectors are easy to prepare high-resolution photochips because of their...Photodetectors can convert light energy into electrical signals,so are widely used in photovoltaics,photon counting,monitoring,and imaging.Photodetectors are easy to prepare high-resolution photochips because of their small size unit integration.However,these photodetector units often exhibit poor photoelectric performance due to material defects and inadequate structures,which greatly limit the functions of devices.Designing modification strategies and micro-/nanostructures can compensate for defects,adjust the bandgap,and develop novel quantum structures,which consequently optimize photovoltaic units and revolutionize optoelectronic devices.Here,this paper aims to comprehensively elaborate on the surface/interface engineering scheme of micro-/nano-photodetectors.It starts from the fundamentals of photodetectors,such as principles,types,and parameters,and describes the influence of material selection,manufacturing techniques,and post-processing.Then,we analyse in detail the great influence of surface/interface engineering on the performance of photovoltaic devices,including surface/interface modification and micro-/nanostructural design.Finally,the applications and prospects of optoelectronic devices in various fields such as miniaturization of electronic devices,robotics,and human–computer interaction are shown.展开更多
Preferential magnesium(Mg)electrodeposition on separators is a ubiquitous yet poorly understood phenomenon in rechargeable Mg-metal batteries,posing a fundamental challenge to their development.In this work,the synerg...Preferential magnesium(Mg)electrodeposition on separators is a ubiquitous yet poorly understood phenomenon in rechargeable Mg-metal batteries,posing a fundamental challenge to their development.In this work,the synergy effects of interface-accelerating desolvation and spatial confinement have been demonstrated as the essential causation of this counterintuitive experimental phenomenon.At the molecular level,the imide ring(-CO-NR-CO-,in which R represents the phenyl)groups in an artificially introduced polyimide(PI)interlayer facilitate the strong electrostatic affinity towards Mg^(2+),which accelerates the desolvation process for Mg^(2+)solvation structures at the inner Helmholtz plane.At the nucleation scale,the wedge-like concave geometry formed at the PI/current collector interface provides energetically favorable sites for Mg nucleation.This unique architecture reduces the critical nucleus size,thereby significantly lowering nucleation energy barriers.As a result,the satisfactory Coulombic efficiency for Mg plating/stripping(98.22%)and cycle lifespan(1200 cycles,above 100 days)have been achieved,outperforming most of the previous results.This work pioneers a molecular-level understanding of separator-directed Mg deposition and resolves a long-standing confusion in Mg-metal batteries.展开更多
The implementation of multifunctional application scenarios for mobile terminal devices has increased the energy density requirements of batteries.Increasing the charging voltage can rapidly increase the specific capa...The implementation of multifunctional application scenarios for mobile terminal devices has increased the energy density requirements of batteries.Increasing the charging voltage can rapidly increase the specific capacity of layered transition metal oxides;however,it also exacerbates the release of lattice oxygen and the contraction of the unit cell.Ternary materials are designed in a secondary particle state to meet the requirements of power battery applications.Therefore,to create ternary materials that can operate under ultrahigh voltages,attention should be given to both surface modification and particle integrity maintenance.By utilizing elemental selenium(Se)with a low melting point,easy sublimation,and multiple variable valence states,deep grain boundary modification was implemented inside the particles.The performance of the cathode material was evaluated through pouch cells,and the improvement mechanism was explored through molecular dynamics simulation calculations.Under the protection of a three-dimensional Se-rich modified layer,LiNi_(1/3)Co_(1/3)Mn_(1/3)O_(2)achieved stable operation at ultrahigh voltages(4.6 V vs.Li/Li^(+));a sacrificial protection mechanism based on the chronic decomposition of the Se-rich layer was proposed to explain the efficacy of Se modification in stabilizing ternary materials.This deep grain boundary modification based on elemental Se provides a new solution for the ultrahigh-voltage operation of transition metal oxides and provides a scientific basis and technical support for solving the interface contact problem of all-solid-state batteries.展开更多
基金financially supported by the National Nature Science Foundation of China (62504130)National Key Research and Development Program of China (2018YFB0704100)+3 种基金the Key university laboratory of highly efficient utilization of solar energy and sustainable development of Guangdong (Y01256331)the Technology Development Project of Henan Province (252102240047)the Pico Center at SUSTech CRF which receives support from the Presidential FundDevelopment and Reform Commission of Shenzhen Municipality
文摘Two-step-processed(TSP)inverted p-i-n perovskite solar cells(PSCs)have demonstrated significant promise in tandem applications.However,the power conversion efficiency(PCE)of TSP p-i-n PSCs rarely exceeds 24%.Here,we demonstrate that TSP perovskite films exhibit a vertically gradient distribution of residual PbI_(2)clusters,which form Schottky heterojunctions with the perovskite,leading to substantial interfacial energy-level mismatches within NiO_(x)-based TSP p-i-n PSCs.These limitations were effectively addressed via a vertical interfacial engineering enabled by dual-interface modification incorporating tin trifluoromethanesulfonate(Sn(OTF)_(2))and 4-Fluorophenylethylamine chloride(F-PEA)at the NiO_(x)/perovskite and perovskite/C60 interfaces,respectively.The functional Sn(OTF)_(2)not only enhances the conductivity of NiO_(x)films but also suppresses ion migration,while inducing the formation of a Pb-Sn mixed perovskite interlayer that precisely regulates the energy level at the NiO_(x)/perovskite interface.Complementally,F-PEA post-treatment effectively converts surface residual PbI_(2)clusters into a 2D perovskite capping layer,which simultaneously passivates surface defects and enhances energy-level alignment at the perovskite/C60 interface.Consequently,the optimized NiO_(x)-based TSP p-i-n PSCs achieve a notable PCE of 25.6%with superior operational stability.This study elucidates the underlying mechanisms limiting the efficiency of TSP p-i-n PSCs,while establishing design principles for these devices targeting 26%efficiency.
基金supported by the National Natural Science Foundation of China(U23A20605)Anhui Graduate Innovation and Entrepreneurship Practice Project(2022cxcysj090)+2 种基金China Baowu Low Carbon Metallurgy Innovation Foundation(BWLCF202202)the University Synergy Innovation Program of Anhui Province(GXXT-2020-072)the Outstanding Youth Fund of Anhui Province(2208085J19).
文摘Steel slag(SS)accumulates unavoidably due to its complex and unstable composition,high production volumes,and limited value-added resource utilization.Single or multiple interface modifiers were proposed to enhance the properties of SS through high-speed dispersion,transforming its inherent hydrophilic and oleophobic characteristics into hydrophily and lipophilicity.The modification effects were innovatively assessed by observing the color changes of modified steel slag solutions following the dissolution-settlement equilibrium constant.This approach avoided human-induced errors and improved estimated accuracy in conformance with conventional methods such as oil absorption value,activation index,sedimentation volume,and lipophilicity.The hydrolysis of 3-aminopropyltriethoxysilane(KH)generated–Si(OH)_(3)structure to form hydrogen or covalent bonds with active substances(OH groups)from SS.Concurrently,SS underwent encapsulation via Si–O–Si structure resulting from the dehydration of–Si(OH)_(3).The stearic acid coupling agent(SA),aluminate coupling agent(AC),and titanate coupling agent(TN)underwent chemical reactions with Ca(OH)_(2),Al(OH)_(3),and CaCO_(3)in SS.The acidic SA primarily created stable chemical bonds and acted as a supplement due to its package,reducing surface activity and hydrophilicity while enhancing lipophilicity.Specifically,the optimal modification effect was obtained at 3 wt.%SA.Consequently,3 wt.%SA was established as the benchmark for multiple modifiers and the most effective combination was 3 wt.%SA and 3 wt.%AC.Compared with a single interface modifier,SA corroded the SS surface to provide numerous active sites for further modification by KH,AC,or TN,resulting in a more densely packed structure.In addition,more organic groups on SS prevent the proximity of other particles from agglomerating to achieve dispersion and a synergistic modification,laying a theoretical foundation of SS in a new pathway for organic composite materials.
文摘Biomass-derived carbon materials are favored for their abundance and sustainability,and ease of preparation and modification.By surface activation and modification they can have a good electrical conductivity,excellent catalytic activity,a remarkable adsorption capacity,and different interfacial physicochemical functionalities.Surface-modified biochars have found wide applications in energy storage,environmental remediation,and catalysis.However,achieving precise and controllable modification of their active sites remains a challenge.Recent advances and future prospects for controlling their surface morphology,defect engineering,and surface coating strategies,with particular attention to their means of fabrication,are reviewed.
基金the Key project of Nature Science Foundation of Tianjin(22JCZDJC00120)the 111 Project(B16027)for financial support.
文摘Benzoic acid containing fluorine atom at ortho-,meta-,and para-position are employed as self-assembled monolayers to modify the buried interface in perovskite solar cells(PSCs).It is demonstrated that the position of fluorine atom influences the passivation effect and para-fluorinated one provided the most substantial performance enhancement mainly originating from ameliorated contact and energy band alignment between NiOx and perovskite,improved perovskite quality and defect healing.Resultantly,PSC with a power conversion efficiency of 24%can be achieved.Meanwhile,which can maintain 96.8%of the initial PCE after a 1000 h storage,presenting enhanced durability.This work highlights the critical role of molecular functionality and conformation in the buried interface modification of PSCs,providing valuable insights for future developments.
基金the National Natural Science Foundation of China (52076076, 52006065)Fundamental Research Funds for Central Universities (2025JC003)Beijing Municipal Natural Science Foundation (3242022)
文摘In the realm of large-scale power system energy storage,sodium-based batteries represent a cost-effective post-lithium energy storage technology,making inorganic solid-state sodium batteries(ISSSB)a critical branch of this development.Inorganic solid-state electrolytes(ISSEs)are the core components of sodium batteries;however,they face significant challenges such as insufficient ionic conductivity,interfacial instability,and dendrite growth,all of which severely hinder practical application.This review critically assesses experimental protocols and theoretical frameworks related to mainstream ISSEs and systematizes optimization strategies aimed at overcoming these challenges.Leveraging integrated insights from both experimental and computational studies,the review first categorizes and summarizes the primary types of ISSEs,namely oxide-,sulfide-,and halide-based electrolytes.It then details interfacial optimization strategies focused on addressing three core interfacial issues:ion transport barriers resulting from mechanical incompatibility,side reactions stemming from electrochemical mismatch,and dendrite formation.Finally,the review advocates prioritizing in-depth research that integrates experimental and theoretical approaches to establish a closed-loop methodology encompassing predictive design,multiscale investigation,mechanistic exploration,and high-throughput automated experimentation,with feedback-driven refinement.This work serves as a comprehensive reference and systematic roadmap for future research on solid-state electrolytes(SSEs).
基金Supported by Design and Performance Study of High-flux Metal Hydride Reactor Based on the Bionic Optimization(2078262)the‘Four-Chain’Integration Project at the Qinchuangyuan Chief Platform(S2025-YF-ZDXM)。
文摘As one of the most promising new energy sources,hydrogen energy is expected to usher in a full-fledged“hydrogen economy”in the 21st century.Compared with traditional high-pressure gaseous and cryogenic liquid hydrogen storage methods,solid-state chemical hydrogen storage shows significant advantages in safety,high efficiency,and cost-effectiveness.Magnesium-based lightweight hydrogen storage materials have attracted widespread attention due to their high gravimetric hydrogen storage density(7.6%)and favorable reversibility.However,their sluggish reaction kinetics and stringent operating conditions(with H2 release temperatures exceeding 350°C and H2 absorption pressures above 4 MPa)pose major challenges for practical applications.Domestic and international researchers have conducted in-depth studies to address these issues,achieving substantial progress in the modification of magnesium-based hydrogen storage alloys.This paper systematically elaborates on major modification techniques such as alloying,nanostructuring,and catalytic material doping,providing a comprehensive analysis of the strengths and limitations of each approach.Furthermore,it offers prospects for the future development of magnesium-based hydrogen storage materials by integrating current theoretical and experimental research findings.
基金financially supported by the National Natural Science Foundation of China(52072036,52272187)the China Petroleum&Chemical Corporation(SINOPEC)project(223128).
文摘All-solid-state batteries(ASSBs)assembled with sulfide solid electrolytes(SSEs)and nickel(Ni)-rich oxide cathode materials are expected to achieve high energy density and safety,representing potential candidates for the next-generation energy storage systems.However,interfacial issues between SSEs and Nirich oxide cathode materials,attributed to space charge layer,interfacial side reactions,and mechanical contact failure,significantly restrict the performances of ASSBs.The interface degradation is closely related to the components of the composite cathode and the process of electrode fabrication.Focusing on the influencing factors of interface compatibility between SSEs and Ni-rich oxide cathode,this article systematically discusses how cathode active materials(CAMs),electrolytes,conductive additives,binders,and electrode fabrication impact the interface compatibility.In addition,the strategies for the compatibility modification are reviewed.Furthermore,the challenges and prospects of intensive research on the degradation and modification of the SSE/Ni-rich cathode material interface are discussed.This review is intended to inspire the development of high-energy-density and high-safety all-solid-state batteries.
基金supported by the research studentship of The Hong Kong Polytechnic University(Project code:RMAN)the Research and Innovation Office of The Hong Kong Polytechnic University(Project codes:1-W308 and 1-BECE)+2 种基金the Research Grants Council of the Government of the Hong Kong Special Administrative Region(HKSAR),China(No.15205423)funding support from the Innovation and Technology Commission(ITC)of HKSAR,China(MHP/151/22)funding support from the State Key Laboratory of Ultra-precision Machining Technology(Project code:BBX5).
文摘Silicon carbide(SiC)is a highly valued material for power semiconductor devices due to its wide bandgap,high thermal conductivity,and high breakdown electric field.However,its high hardness,brittleness,and chemical stability present substantial challenges for efficient and high-quality processing.This study investigated the effects of picosecond laser surface scanning on 4H-SiC to enhance the material removal performance.The research focused on surface morphology,phase transitions,subsurface/interface characteristics,and material removal mechanisms under varying laser parameters.The results demonstrate that the laser thermal effect decomposes 4H-SiC into amorphous silicon(a-Si),disordered carbon,and graphite,forming a resolidified layer containing Si-O and Si-C-O oxides.Crystalline silicon(c-Si)is produced under high fluences or extensive irradiations.The variation in the resolidified layer thickness with changing laser parameters is revealed.A detailed laser-induced subsurface damage model is developed,encompassing a resolidified layer that includes the above decomposition and oxidation products,and a deformed layer formed primarily under laser-induced stress.The presence of the resolidified layer and the deformed layer leads to a decreased elastic recovery rate and an increased scratching depth,exceeding 2.5 times that of the unmodified condition.Enhanced material removal performance is mainly driven by the resolidified layer at low fluence and by the deformed layer at high fluence.When aligning the total of the ablation depth and the resolidified layer thickness with the subsurface damage depth in the original material,excellent polishing performance is achieved.These findings provide critical insights for understanding the phase evolution,subsurface damage mechanisms,and material removal behavior of 4H-SiC,offering valuable guidance for optimizing the laser surface modification parameters to achieve high-efficiency processing.
基金supported by the Presidential Foundation of CAEP(No.YZJJZQ2022006)the National Natural Science Foundation of China(Nos.22275173 and 22475179).
文摘The interfacial structure and its regulation play a crucial role in determining the overall performance of advanced functional composites.Weak interfacial interactions between carbon fibers and the matrix present a critical challenge limiting the general performance and functional applications of carbon fiberreinforced composites.In this paper,a novel strategy for bioinspired root-soil interfacial structure was presented to enhance the mechanical properties of polymer bonded explosives.A multiscale nanowire heterostructure was constructed through the in-situ growth of morphologically controllable zinc oxide nanowires on the carbon fiber surface via a facile hydrothermal method,with polydopamine as the interfacial reinforcement layer.This structure emulated the function of the"root",and combined with a network-distributed polymer binder representing the"soil",formed a robust root-soil interlocking interfacial structure within the polymer bonded explosives.Due to the multiscale interfacial reinforcement structure,the tensile strength of the polymer bonded explosives was visibly increased by 41%,the strain at the break by 110%,and the creep resistance by 51%with only 0.4 wt%filler adopted.The thermal stress resistance was improved by 57%owing to the synergistic enhancement of thermal conductivity and mechanical properties.This study provides new perspectives and insights for designing and constructing high-performance polymer bonded explosives and other functional composites.
文摘Rotary friction welding is a highly effective solid-state technique for joining dissimilar materials,which offers the potential for significant weight reduction without compromising strength.Traditionally,during rotary friction welding,the severely deformed material,or flash,is expelled from the interface and machined away to achieve the desired joint geometry.However,this work introduces a novel approach:trapping the flash within the joint to improve joint properties.The study investigates two different interface geometry combinationsdflat-flat and flat-taper interfaces.Previous research shows that Ni interlayer between steel and titanium can enhance the joint strength.This study builds on the existing knowledge(effect of Ni interlayer)by examining the influence of interface geometry to further improve the dissimilar joint performance.The experimental results,including tensile testing and microstructural characterization,highlight the superior performance of the flat-taper interface.The modified geometry minimizes flash loss,providing a cavity that retains both the flash and the Ni interlayer within the joint.This retention promotes dynamic recrystallization,resulting in refined grain structures near the interface.Moreover,the trapped Ni interlayer effectively prevents the formation of brittle Fe-Ti intermetallic compounds at the dissimilar material interface.The findings reveal that the flat-taper interface improved joint strength by an impressive 105%compared to the flat-flat interface.This innovative geometry modification demonstrates the potential to enhance mechanical properties of dissimilar joints through better flash and interlayer management.
基金Supported by Educational Department(JYTMS20230310)Natural Science Foundation of Liaoning Province(2024-MS-215)。
文摘Photoelectrochemical(PEC)water splitting is an effective approach to directly convert solar energy into clean hydrogen fuel.As a visible-light-responsive p-type semiconductor,CuBi_(2)O_(4)possesses a suitable bandgap and good stability.However,its performance is inhibited by high interfacial resistance and severe charge carrier recombination.In this study,a CuO interlayer was introduced between fluorine-doped tin oxide(FTO)and CuBi_(2)O_(4)to construct CuO/CuBi_(2)O_(4)photocathodes,aiming to improve interfacial charge transfer.The results showed that CuO/CuBi_(2)O_(4)-200 exhibited a photocurrent density of−1.71 mA/cm^(2)at 0 V vs.RHE,which was more than 3.5 times higher than that of bare CuBi_(2)O_(4).The incident photon-to-current efficiency(IPCE)at 365 nm was enhanced to~13%and the maximum applied bias photon-to-current efficiency(ABPE)reached 0.17%.Water splitting experiments revealed a hydrogen yield of 2.05μmol/cm^(2),significantly surpassing that of the unmodified photoelectrode.The enhanced PEC performance indicated that the CuO layer established a favorable band alignment,promoted hole transport toward the FTO substrate and effectively suppressed interfacial carrier recombination.This work demonstrated a simple and efficient interfacial engineering strategy,offering new insights and guidance for the design and development of high-performance semiconductor-based PEC photoelectrodes.
基金supported by the National Natural Science Foundation of China(Nos.52072208 and 52261160384)supported by the Postdoctoral Fellowship Program(Grade B)of China Postdoctoral Science Foundation under Grant Number GZB20250057China Postdoctoral Science Foundation(2025M770223).
文摘With the growing global energy demand and the pressing need for a clean energy transition,supercapacitors(SCs)have demonstrated significant application potential in electric vehicles,wearable electronics,and renewable energy storage systems owing to their rapid charge-discharge capability,exceptional power density,and prolonged cycle life.The improvement of their overall performance fundamentally depends on the synergistic design of electrode materials and electrolyte systems,as well as the precise regulation of the electrode-electrolyte interface.This review focuses on the key components of supercapacitors,systematically reviewing the design strategies of high-performance electrode materials,outlining recent advances in novel electrolyte systems,and comprehensively discussing the critical roles of interfacial reinforcement and optimization in enhancing device energy density,power performance,and cycling stability.Furthermore,interfacial engineering strategies and innovations in device architecture are proposed to address interfacial degradation in flexible SCs under mechanical stress.Finally,key future research directions are highlighted,including the development of high-voltage and wide-temperature-range electrolyte systems and the integrated advancement of multiscale in situ characterization techniques and theoretical modeling.This review aims to provide theoretical guidance and innovative strategies for material design,contributing toward the realization of next-generation supercapacitors with enhanced energy density and reliability.
基金support from National Natural Science Foundation of China(Grant No.51874033)to Prof.Hai-Yan Tang.
文摘In view of the frequent deterioration of molten steel quality during the tundish filling process,the slag-steel-air interface behavior in a tundish,including liquid level fluctuation,slag eyes,slag entrapment and air suction during the steady-state casting and filling process,was comparatively studied through physical modeling and mathematical simulation methods.During the filling process,the liquid surface forms a large-size slag eye under the impact of molten steel from a ladle shroud,which simultaneously results in a violent fluctuation of liquid level.Concurrently,the liquid flow entrains the air phase and the cover slag into the tundish impact zone,resulting in slag entrapment and air suction.At filling flow rates of 1.5Q,2.0Q,and 2.5Q(Q is the flow rate under steady-state casting),the amount of slag entrapped is 8.39×10^(-5),9.65×10^(-5),and 12.7×10^(-5)m^(3),respectively,while the volume of air aspirated is 0.84×10^(-4),1.47×10^(-4),and 2.01×10^(-4)m^(3),indicating that slag entrapment and air suction intensify with an increase in tundish filling flow rate.Flow field characterization identifies eddy currents in the impact zone as the primary driver of the above phenomena.Proper filling process parameters were proposed to improve the steel quality during the tundish filling.
文摘Invasive as well as non-invasive neurotechnologies conceptualized to interface the central and peripheral nervous system have been probed for the past decades,which refer to electroencephalography,electrocorticography and microelectrode arrays.The challenges of these mentioned approaches are characterized by the bandwidth of the spatiotemporal resolution,which in turn is essential for large-area neuron recordings(Abiri et al.,2019).
基金supported by the National Natural Science Foundation of China(Nos.82573045,82460602,82560459)the Hainan Provincial Graduate Student Innovative Research Project(No.Qhys2024-440).
文摘Post-translational modifications(PTMs)regulate the occurrence and development of cancer,and lactylation modification is a new form of PTMs.Recent studies have found that lactic acid modification can regulate the immune tolerance of cancer cells.The classical theory holds that prostate apoptosis response-4(PAR-4)is a tumor suppressor protein.However,our recent research has found that PAR-4 has a biological function of promoting cancer in hepatocellular carcinoma(HCC),and our analysis shows that PAR-4 can be modified of lactic acid.These research evidences suggest that PAR-4 lactylation modification may drive immune tolerance in HCC.Therefore,inhibiting PAR-4 lactylation modification is very likely to increase the sensitivity of HCC to immunotherapy.
基金financially supported by the Natural Science Foundation of Guizhou Province(Grant No.:Qiankehe Foundation-ZK[2024]General 522)the Doctoral Research Start-up Fund of Guiyang University(Grant No.:GYUKY-[2025])+1 种基金the Young Talents Cultivation Program Project of Guangdong Association for Science and Technology(Grant No.:SKXRC2025059)the Fundamental Research Funds for the Central Universities(Grant No.:21625404)。
文摘The network structure of M_(2)B in Fe-B-C alloy readily leads to the failure of material.In this work,by adding K2_SO4,the morphology of the M_(2)B was successfully regulated through a synergistic treatment combining active element modification and heterogeneous nucleation modification.The results show that after the addition of K_(2)SO_(4),a new phaseα-MnS forms in the alloy,and the active element K enriches at the M_(2)B/matrix interface.This inhibits the growth of the network M_(2)B and promotes its transformation from a continuous network structure to an isolated blocky structure.As the K_(2)SO_(4) addition increases from 0wt.%to 4.46wt.%,the shape factor value of M_(2)B increases from 0.067 to 0.353,with an increase of 426%.The impact toughness of the alloy increases from 5.9 J·cm^(-2)to 14.2 J·cm^(-2),and the fracture mode transitions from cleavage fracture to ductile-cleavage mixed fracture.Three-body abrasion tests indicate that with increasing K_(2)SO_(4) addition,the wear weight loss of the alloy gradually decreases.The alloy with 4.46wt.%K_(2)SO_(4) addition exhibits the least wear damage and the best wear resistance.This work provides an effective approach for regulating the microstructure and improving the wear resistance of wear-resistant Fe-B-C alloys.
文摘Photodetectors can convert light energy into electrical signals,so are widely used in photovoltaics,photon counting,monitoring,and imaging.Photodetectors are easy to prepare high-resolution photochips because of their small size unit integration.However,these photodetector units often exhibit poor photoelectric performance due to material defects and inadequate structures,which greatly limit the functions of devices.Designing modification strategies and micro-/nanostructures can compensate for defects,adjust the bandgap,and develop novel quantum structures,which consequently optimize photovoltaic units and revolutionize optoelectronic devices.Here,this paper aims to comprehensively elaborate on the surface/interface engineering scheme of micro-/nano-photodetectors.It starts from the fundamentals of photodetectors,such as principles,types,and parameters,and describes the influence of material selection,manufacturing techniques,and post-processing.Then,we analyse in detail the great influence of surface/interface engineering on the performance of photovoltaic devices,including surface/interface modification and micro-/nanostructural design.Finally,the applications and prospects of optoelectronic devices in various fields such as miniaturization of electronic devices,robotics,and human–computer interaction are shown.
基金supported by the National Natural Science Foundation of China(22279068,52374306)the Taishan Scholars of Shandong Province(tsqn202408202)the Qingdao New Energy Shandong Laboratory Open Project(QNESL OP202312)。
文摘Preferential magnesium(Mg)electrodeposition on separators is a ubiquitous yet poorly understood phenomenon in rechargeable Mg-metal batteries,posing a fundamental challenge to their development.In this work,the synergy effects of interface-accelerating desolvation and spatial confinement have been demonstrated as the essential causation of this counterintuitive experimental phenomenon.At the molecular level,the imide ring(-CO-NR-CO-,in which R represents the phenyl)groups in an artificially introduced polyimide(PI)interlayer facilitate the strong electrostatic affinity towards Mg^(2+),which accelerates the desolvation process for Mg^(2+)solvation structures at the inner Helmholtz plane.At the nucleation scale,the wedge-like concave geometry formed at the PI/current collector interface provides energetically favorable sites for Mg nucleation.This unique architecture reduces the critical nucleus size,thereby significantly lowering nucleation energy barriers.As a result,the satisfactory Coulombic efficiency for Mg plating/stripping(98.22%)and cycle lifespan(1200 cycles,above 100 days)have been achieved,outperforming most of the previous results.This work pioneers a molecular-level understanding of separator-directed Mg deposition and resolves a long-standing confusion in Mg-metal batteries.
基金supported by the National Natural Science Foundation of China (52302259)the China Postdoctoral Science Foundation (CPSF) under Grant Number 2023M741479+4 种基金the Postdoctoral Fellowship Program of CPSF under Grant Number GZB20240280the Jiangxi Provincial Natural Science Foundation (20224ACB218006)the financial support from High-level Talent Research Special Funds of Jiangxi University of Science and Technology (Grant No. 205200100670)the Jiangxi Provincial Key Laboratory of Power Energy Storage Batteries and Materials (2024SSY10011)the Major Scientific and Technological Research R&D Special Project of Jiangxi Province(20244AFI92002)
文摘The implementation of multifunctional application scenarios for mobile terminal devices has increased the energy density requirements of batteries.Increasing the charging voltage can rapidly increase the specific capacity of layered transition metal oxides;however,it also exacerbates the release of lattice oxygen and the contraction of the unit cell.Ternary materials are designed in a secondary particle state to meet the requirements of power battery applications.Therefore,to create ternary materials that can operate under ultrahigh voltages,attention should be given to both surface modification and particle integrity maintenance.By utilizing elemental selenium(Se)with a low melting point,easy sublimation,and multiple variable valence states,deep grain boundary modification was implemented inside the particles.The performance of the cathode material was evaluated through pouch cells,and the improvement mechanism was explored through molecular dynamics simulation calculations.Under the protection of a three-dimensional Se-rich modified layer,LiNi_(1/3)Co_(1/3)Mn_(1/3)O_(2)achieved stable operation at ultrahigh voltages(4.6 V vs.Li/Li^(+));a sacrificial protection mechanism based on the chronic decomposition of the Se-rich layer was proposed to explain the efficacy of Se modification in stabilizing ternary materials.This deep grain boundary modification based on elemental Se provides a new solution for the ultrahigh-voltage operation of transition metal oxides and provides a scientific basis and technical support for solving the interface contact problem of all-solid-state batteries.
