As battery technology evolves and demand for efficient energy storage solutions,aqueous zinc ion batteries(AZIBs)have garnered significant attention due to their safety and environmental benefits.However,the stability...As battery technology evolves and demand for efficient energy storage solutions,aqueous zinc ion batteries(AZIBs)have garnered significant attention due to their safety and environmental benefits.However,the stability of cathode materials under high-voltage conditions remains a critical challenge in improving its energy density.This review systematically explores the failure mechanisms of high-voltage cathode materials in AZIBs,including hydrogen evolution reaction,phase transformation and dissolution phenomena.To address these challenges,we propose a range of advanced strategies aimed at improving the stability of cathode materials.These strategies include surface coating and doping techniques designed to fortify the surface properties and structure integrity of the cathode materials under high-voltage conditions.Additionally,we emphasize the importance of designing antioxidant electrolytes,with a focus on understanding and optimizing electrolyte decomposition mechanisms.The review also highlights the significance of modifying conductive agents and employing innovative separators to further enhance the stability of AZIBs.By integrating these cutting-edge approaches,this review anticipates substantial advancements in the stability of high-voltage cathode materials,paving the way for the broader application and development of AZIBs in energy storage.展开更多
Despite relevant advances,the pharmaceutical industry continues to strive with the limited adaptability,moisture management,and discomfort caused by existing wound dressings.Adding to these challenges are the bioavail...Despite relevant advances,the pharmaceutical industry continues to strive with the limited adaptability,moisture management,and discomfort caused by existing wound dressings.Adding to these challenges are the bioavailability and pharmacokinetics of common(bio)therapeutics,overall leading to unmet clinical demands,safety concerns,and poor patient compliance.Ionogels,a versatile class of materials comprising ionic liquids(ILs)confined in an organic or inorganic solid network,have been proposed to overcome these drawbacks.They have demonstrated the ability to enhance the antimicrobial and mechanical properties of the resulting materials while allowing remarkable improvements in drug solubility and their delivery to targeted sites.Nowadays,safety investigations and clinical trials are still required to fully leverage the potential of ionogels for human applications.However,the recent FDA approval of the New Drug Application MRX-5LBT®,a transdermal drug delivery system,opens promising perspectives toward the clinical translation of ionogels.This review focuses on recent advances achieved in the design of ionogels for pharmaceutical applications,viz.in topical formulations to promote wound healing with antimicrobial activity,and as platforms to improve drug pharmacokinetics(solubility and bioavailability),and their delivery at targeted specific sites with controlled release behaviour.展开更多
The bulge test is a widely utilized method for assessing the mechanical properties of thin films,including metals,polymers,and semiconductors.However,as film thickness diminishes to nanometer scales,boundary condition...The bulge test is a widely utilized method for assessing the mechanical properties of thin films,including metals,polymers,and semiconductors.However,as film thickness diminishes to nanometer scales,boundary conditions dominated by weak van der Waals forces significantly impact mechanical responses.Instead of sample fracture,interfacial shear deformation and delamination become the primary deformation modes,thereby challenging the applicability of conventional bulge models.To accommodate the interfacial effect,a modified mechanical model based on the bulge test has been proposed.This review summarizes recent advancements in the bulge test to highlight the potential challenges and opportunities for future research.展开更多
Additive manufacturing(AM)offers the unique capability of directly creating three-dimensional complicated ceramic components with high process flexibility and outstanding geometry controllability.However,current ceram...Additive manufacturing(AM)offers the unique capability of directly creating three-dimensional complicated ceramic components with high process flexibility and outstanding geometry controllability.However,current ceramic AM technology is mainly limited to the creation of a single material,which falls short of meeting the multiple functional requirements under increasingly harsh service circumstances.Ceramic multi-material additive manufacturing(MMAM)technology has great potential for integrally producing multi-dimensional multi-functional components,allowing for point-by-point precision manufacturing of programmable performance/functions.However,there is a huge gap between the capabilities of the existing ceramic MMAM technology and the requirements for industrial application.In this review,we discuss and summarize the research status of ceramic MMAM technology from the perspectives of feedstock selection,printing process,post-processing,component performance,and application.Throughout the discussion,the challenges associated with ceramic MMAM such as heterogeneous material coupled printing,heterogeneous interfacial bonding,and co-sintering densification have been put forward.This review aims to bridge the gap between AM technologies and the requirements for multifunctional ceramic components by analyzing the existing limitations in ceramic MMAM and pointing out future needs.展开更多
Single-atom catalysts(SACs)have demonstrated exceptional performance in electrocatalytic water splitting,owing to their maximized atomic utilization efficiency and superior reaction kinetics.The incorporation of SACs ...Single-atom catalysts(SACs)have demonstrated exceptional performance in electrocatalytic water splitting,owing to their maximized atomic utilization efficiency and superior reaction kinetics.The incorporation of SACs typically depends on robust metal-support interactions,which stabilize the single atoms on the support through various unsaturated chemical sites or spatial confinement.A critical challenge lies in precisely modulating the electronic structure and coordination environment of metal atoms.However,current research primarily focuses on single-atom metals,often neglecting the significant role of support materials in SACs.Two-dimensional(2D)atomically thin materials(ATMs)possess unique physicochemical properties and tunable reaction environments,which can modulate catalytic performance via metal-support interactions,positioning them as promising platforms for SAC loading.This paper reviews the recent advancements and the current status of SACs supported on 2D ATMs(SACs@ATMs).The structural design theory and synthesis strategies of SACs@ATMs are systematically discussed.The significance of advanced characterization techniques in elucidating the coordination environment and metal-support interactions is highlighted.Additionally,the reaction mechanisms and applications of SACs in electrocatalytic water splitting are summarized.Finally,the future challenges and opportunities for SACs@ATMs are outlined.This paper aims to provide insights and guidance for the rational design of SACs@ATMs with high-performance electrocatalytic water splitting capabilities.展开更多
Among various architectures of polymers,end-group-free rings have attracted growing interests due to their distinct physicochemical performances over the linear counterparts which are exemplified by reduced hydrodynam...Among various architectures of polymers,end-group-free rings have attracted growing interests due to their distinct physicochemical performances over the linear counterparts which are exemplified by reduced hydrodynamic size and slower degradation.It is key to develop facile methods to large-scale synthesis of polymer rings with tunable compositions and microstructures.Recent progresses in large-scale synthesis of polymer rings against single-chain dynamic nanoparticles,and the example applications in synchronous enhancing toughness and strength of polymer nanocomposites are summarized.Once there is the breakthrough in rational design and effective large-scale synthesis of polymer rings and their functional derivatives,a family of cyclic functional hybrids would be available,thus providing a new paradigm in developing polymer science and engineering.展开更多
The 6-isoquinolinyl system was incorporated into mechanically interlocked molecules(MIMs)syntheses for comparative analysis of its assembly behavior with 4-pyridyl-based coordination ligands,where a coordination-drive...The 6-isoquinolinyl system was incorporated into mechanically interlocked molecules(MIMs)syntheses for comparative analysis of its assembly behavior with 4-pyridyl-based coordination ligands,where a coordination-driven self-assembly strategy by half-sandwich Cp^(*)Rh units was employed to construct diverse molecular links.The pyridyl ligand,adorned with thiophene moieties,assembles into[2]catenanes(2_(1)^(2)links),whereas the isoquinolinyl ligand produces molecular Borromean links(6_(2)^(3)links).Intriguingly,when utilizing extended bithiophene segments,the pyridyl ligand forms Borromean rings(6_(2)^(3)links),while isoquinolinyl counterparts produced a rare low-symmetry cyclic[3]catenane(6_(3)^(3)topology).The results were confirmed through single-crystal X-ray diffraction analysis,nuclear magnetic resonance(NMR)spectroscopy,and electrospray ionization time-of-flight mass spectrometry(ESI-TOF/MS)experiments.Synergistic π-π stacking,C-H···π interactions,and solvophobic effects governed the complex self-assembly system,with independent gradient model(IGM)analyses and solventaccessible surface area(SASA)calculations providing atomistic insights into the pathway selectivity of distinct topological links.展开更多
The detection and characterization of non-metallic inclusions are essential for clean steel production.Recently,imaging analysis combined with high-dimensional data processing of metallic materials using artificial in...The detection and characterization of non-metallic inclusions are essential for clean steel production.Recently,imaging analysis combined with high-dimensional data processing of metallic materials using artificial intelligence(AI)-based machine learning(ML)has developed rapidly.This technique has achieved impressive results in the field of inclusion classification in process metallurgy.The present study surveys the ML modeling of inclusion prediction in advanced steels,including the detection,classification,and feature prediction of inclusions in different steel grades.Studies on clean steel with different features based on data and image analysis via ML are summarized.Regarding the data analysis,the inclusion prediction methodology based on ML establishes a connection between the experimental parameters and inclusion characteristics and analyzes the importance of the experimental parameters.Regarding the image analysis,the focus is placed on the classification of different types of inclusions via deep learning,in comparison with data analysis.Finally,further development of inclusion analyses using ML-based methods is recommended.This work paves the way for the application of AIbased methodologies for ultraclean-steel studies from a sustainable metallurgy perspective.展开更多
In comparison with their 2D and 3D counterparts,1D covalent organic frameworks(COFs)have rarely been investigated due to the synthetic challenge arising from the strict necessary matching in the molecular symmetry bet...In comparison with their 2D and 3D counterparts,1D covalent organic frameworks(COFs)have rarely been investigated due to the synthetic challenge arising from the strict necessary matching in the molecular symmetry between corresponding building blocks and linking units in addition to the unmanageable packing of 1D organic chains once formed.Herein,two novel imide-linked 1D COFs with phthalocyanine building blocks,namely NiPc-CZDM-COF and NiPc-CZDL-COF,were fabricated from the hydrothermal synthesis reaction of 2,3,9,10,16,17,23,24-octacarboxyphthalocyaninato nickel(II)(NiPc(COOH)_(8))with 9H-carbazole-3,6-diamine(CZDM)and 4,4′-(9H-carbazole-3,6-diyl)dianiline(CZDL),respectively.Two COFs have high crystallinity on the basis of powder X-ray diffraction analysis and high-resolution transmission electron microscopy.Due to their high ratio of exposed active centers on the edge sites of porous ribbons,both NiPc-CZDM-COF and NiPc-CZDL-COF electrodes display high utilization efficiency of NiPc electroactive sites of 8.0%and 7.5% according to the electrochemical measurement,resulting in their excellent capacity toward electrocatalytic nitrate reduction with the nitrate-to-NH3 Faradaic efficiency of nearly 100%.In particular,NiPc-CZDM-COF electrode exhibits superior electrocatalytic performance with high NH3 partial current density of−246 mA/cm^(2),ammonia yield rate of 19.5 mg cm^(−2) h^(−1),and turnover frequency of 5.8 s^(−1) at−1.2 V in an H-type cell associated with its higher conductivity.This work reveals the good potential of 1D porous crystalline materials in electrocatalysis.展开更多
Organic photovoltaics(OPVs)have achieved remarkable progress,with laboratory-scale single-junction devices now demonstrating power conversion efficiencies(PCEs)exceeding 20%.However,these efficiencies are highly depen...Organic photovoltaics(OPVs)have achieved remarkable progress,with laboratory-scale single-junction devices now demonstrating power conversion efficiencies(PCEs)exceeding 20%.However,these efficiencies are highly dependent on the thickness of the photoactive layer,which is typically around 100 nm.This sensitivity poses a challenge for industrial-scale fabrication.Achieving high PCEs in thick-film OPVs is therefore essential.This review systematically examines recent advancements in thick-film OPVs,focusing on the fundamental mechanisms that lead to efficiency loss and strategies to enhance performance.We provide a comprehensive analysis spanning the complete photovoltaic process chain:from initial exciton generation and diffusion dynamics,through dissociation mechanisms,to subsequent charge-carrier transport,balance optimization,and final collection efficiency.Particular emphasis is placed on cutting-edge solutions in molecular engineering and device architecture optimization.By synthesizing these interdisciplinary approaches and investigating the potential contributions in stability,cost,and machine learning aspects,this work establishes comprehensive guidelines for designing high-performance OPVs devices with minimal thickness dependence,ultimately aiming to bridge the gap between laboratory achievements and industrial manufacturing requirements.展开更多
Correction to:Nano-Micro Letters(2026)18:10.https://doi.org/10.1007/s40820-025-01852-8 Following publication of the original article[1],the authors reported that the last author’s name was inadvertently misspelled.Th...Correction to:Nano-Micro Letters(2026)18:10.https://doi.org/10.1007/s40820-025-01852-8 Following publication of the original article[1],the authors reported that the last author’s name was inadvertently misspelled.The published version showed“Hongzhen Chen”,whereas the correct spelling should be“Hongzheng Chen”.The correct author name has been provided in this Correction,and the original article[1]has been corrected.展开更多
Poly(ester amide)s(PEAs)represent promising biomaterials because of their well-balanced mechanical properties,biodegradability,and biocompatibility.However,practical applications of PEAs are still limited by challenge...Poly(ester amide)s(PEAs)represent promising biomaterials because of their well-balanced mechanical properties,biodegradability,and biocompatibility.However,practical applications of PEAs are still limited by challenges in functional versatility and environmental adaptability.Here,we present the first synthesis of periodic selenium-incorporated PEAs(Se-PEAs)via a rapid,catalyst-free selenol-yne click polymerization process.By harnessing the versatility of selenium,we achieved precise modulation of material properties.The resulting Se-PEAs demonstrated tunable mechanical behavior,spanning rigid plastics to elastomers,alongside exceptional thermal stability and high optical clarity.Programmable degradation profiles ensure long-term stability in physiological environments while facilitating rapid oxidative degradation at the end of the lifecycle.Surface selenoniumization further conferred robust antibacterial efficacy without compromising mechanical integrity.This multifunctionality positions Se-PEAs as transformative materials for biomedical implants,sustainable packaging,and high-refractiveindex optics.Our work advanced functional polymer design and underscored the potential of selenium chemistry in addressing global challenges in terms of plastic waste and ecological sustainability.展开更多
Ruthenium-based materials(Ru and RuO_(2))are promising electrocatalysts toward electrochemical water splitting(EWS)though there are still issues with them that needs to be resolved such as relatively strong adsorption...Ruthenium-based materials(Ru and RuO_(2))are promising electrocatalysts toward electrochemical water splitting(EWS)though there are still issues with them that needs to be resolved such as relatively strong adsorption strength of intermediates over Ru and oxidative dissolution of RuO_(2).In this article,an overview of the recent progress and challenges with Ru-based electrocatalysts for EWS is provided.Firstly,fundamentals of EWS are summarized from the aspects of reaction mechanisms and activity descriptors.Next,the typical methods of fabricating Ru-based catalysts are demonstrated mainly including hydrothermal/solvothermal syntheses,organic ligand-assisted syntheses,pyrolysis,acid etching,cation exchange methods and molten salt-assisted syntheses.We then focus on illustrating the enhancing strategies toward creating advanced Ru-based electrocatalysts by demonstrating the typical examples,which include alloying,doping,structure design,interface engineering,single-atom catalyst design,high-entropy alloy design,phase engineering and defecting engineering.In this section,the structureproperty correlation is elucidated aiming to the design of more efficient Ru-based electrocatalysts for EWS.Finally,we conclude the review by addressing the challenges and prospects of electrochemical water splitting and the development of Rubased catalysts.展开更多
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
INTRODUCTIONIn 1976, Alan MacDiarmid, Hideki Shirakawa and I, together with a talented group of graduate students andpost-doctoral researchers discovered conducting polymers and the ability to dope these polymers over...INTRODUCTIONIn 1976, Alan MacDiarmid, Hideki Shirakawa and I, together with a talented group of graduate students andpost-doctoral researchers discovered conducting polymers and the ability to dope these polymers over the fullrange from insulator to metal. This was particularly exciting because it created a new field of research on theboundary between chemistry and condensed matter physics, and because it created a number of opportunities:展开更多
Ⅲ-nitride light-emitting diodes(LEDs)are now used almost everywhere,due to their energy-saving capability.In the near future,the vast majority of lighting sources will undoubtedly be based on LEDs.What future technol...Ⅲ-nitride light-emitting diodes(LEDs)are now used almost everywhere,due to their energy-saving capability.In the near future,the vast majority of lighting sources will undoubtedly be based on LEDs.What future technologies and applications can we expect from Ⅲ-nitride-based and particularly gallium nitride(Ga N)-based,materials and devices?展开更多
The continuous increase of global atmospheric CO_(2) concentrations brutally damages our environment. A series of methods have been developed to convert CO_(2) to valuable fuels and value-added chemicals to maintain t...The continuous increase of global atmospheric CO_(2) concentrations brutally damages our environment. A series of methods have been developed to convert CO_(2) to valuable fuels and value-added chemicals to maintain the equilibrium of carbon cycles. The electrochemical CO_(2) reduction reaction(CO_(2)RR) is one of the promising methods to produce fuels and chemicals, and it could offer sustainable paths to decrease carbon intensity and support renewable energy. Thus, significant research efforts and highly efficient catalysts are essential for converting CO_(2) into other valuable chemicals and fuels. Transition metal-based single atoms catalysts(TM-SACs) have recently received much attention and offer outstanding electrochemical applications with high activity and selectivity opportunities. By taking advantage of both heterogeneous and homogeneous catalysts, TM-SACs are the new rising star for electrochemical conversion of CO_(2) to the value-added product with high selectivity. In recent years, enormous research effort has been made to synthesize different TM-SACs with different M–Nxsites and study the electrochemical conversion of CO_(2) to CO. This review has discussed the development and characterization of different TMSACs with various catalytic sites, fundamental understanding of the electrochemical process in CO_(2) RR,intrinsic catalytic activity, and molecular strategics of SACs responsible for CO_(2)RR. Furthermore, we extensively review previous studies on 1 st-row transition metals TM-SACs(Ni, Co, Fe, Cu, Zn, Sn) and dual-atom catalysts(DACs) utilized for electrochemical CO_(2) conversions and highlight the opportunities and challenges.展开更多
Powder metallurgical Cu-Ti alloys with different titanium additions produced by hot pressing were characterized by optical microscopy, scanning electron microscopy, X-ray diffraction analysis, and hardness, wear and b...Powder metallurgical Cu-Ti alloys with different titanium additions produced by hot pressing were characterized by optical microscopy, scanning electron microscopy, X-ray diffraction analysis, and hardness, wear and bending tests. The addition of titanium to copper caused the formation of different intermetallic layers around titanium particles. The titanium content of the intermetallics decreased from the center of the particle to the copper matrix. The hardness, wear resistance, and bending strength of the materials increased with increasing Ti content, whereas strain in the bending test decreased. Worn surface analyses showed that different wear mechanisms were active during the wear test of specimens with different chemical compositions. Changes in the properties of the materials with titanium addition were explained by the high hardness of different Cu-Ti intermetallic phases.展开更多
An Al2O3-TiB2 nanocomposite was successfully synthesized by ball milling of Al, TiO2 and two B source materials of B2O3 （system （1）） and H3BO3 （system （2））. Phase identification of the milled samples was exami...An Al2O3-TiB2 nanocomposite was successfully synthesized by ball milling of Al, TiO2 and two B source materials of B2O3 （system （1）） and H3BO3 （system （2））. Phase identification of the milled samples was examined by Xray diffraction. The morphology and microstructure of the milled powders were monitored by scanning electron microscopy and transmission electron microscopy. It was found that the formation of this composite was completed after 15 and 30 h of milling time in systems （1） and （2）, respectively. More milling energy was required for the formation of this composite in system （2） due to the lubricant properties of HaBO3 and also its decomposition to HBO2 and B2O3 during milling. On the basis of X-ray diffraction patterns and thermodynamic calculations, this composite was formed by highly exothermic mechanically induced self-sustaining reactions （MSR） in both systems. The MSR mode took place around 9 h and 25 h of milling in systems （1） and （2）, respectively. At the end of milling （15 h for system （1） and 30 h for system （2）） the grain size of about 35-50 nm was obtained in both systems.展开更多
基金supported by the Exchange Program of Highend Foreign Experts of Ministry of Science and Technology of People’s Republic of China(No.G2023041003L)the Natural Science Foundation of Shaanxi Provincial Department of Education(No.23JK0367)+1 种基金the Scientific Research Startup Program for Introduced Talents of Shaanxi University of Technology(Nos.SLGRCQD2208,SLGRCQD2306,SLGRCQD2133)Contaminated Soil Remediation and Resource Utilization Innovation Team at Shaanxi University of Technology。
文摘As battery technology evolves and demand for efficient energy storage solutions,aqueous zinc ion batteries(AZIBs)have garnered significant attention due to their safety and environmental benefits.However,the stability of cathode materials under high-voltage conditions remains a critical challenge in improving its energy density.This review systematically explores the failure mechanisms of high-voltage cathode materials in AZIBs,including hydrogen evolution reaction,phase transformation and dissolution phenomena.To address these challenges,we propose a range of advanced strategies aimed at improving the stability of cathode materials.These strategies include surface coating and doping techniques designed to fortify the surface properties and structure integrity of the cathode materials under high-voltage conditions.Additionally,we emphasize the importance of designing antioxidant electrolytes,with a focus on understanding and optimizing electrolyte decomposition mechanisms.The review also highlights the significance of modifying conductive agents and employing innovative separators to further enhance the stability of AZIBs.By integrating these cutting-edge approaches,this review anticipates substantial advancements in the stability of high-voltage cathode materials,paving the way for the broader application and development of AZIBs in energy storage.
基金the scope of the project CICECO Aveiro Institute of Materials,UIDB/50011/2020(DOI 10.54499/UIDB/50011/2020),UIDP/50011/2020(DOI 10.54499/UIDP/50011/2020)&LA/P/0006/2020(DOI 10.54499/LA/P/0006/2020),financed by national funds through the FCT/MCTES(PIDDAC)the scope of the projects mVACCIL(EXPL/BII-BTI/0731/2021,DOI 10.54499/EXPL/BII-BTI/0731/2021)and PureDNA(2022.03394.PTDC,DOI 10.54499/2022.03394.PTDC),financially supported by national funds(OE),through FCT/MCTES+1 种基金FCT,respectively,for the research contract CEEC-IND/02599/2020(DOI 10.54499/2020.02599.CEECIND/CP1589/CT0023)under the Scientific Stimulus-Individual Callthe PhD grant 2020/05090/BD(DOI:10.54499/2020.05090.BD).
文摘Despite relevant advances,the pharmaceutical industry continues to strive with the limited adaptability,moisture management,and discomfort caused by existing wound dressings.Adding to these challenges are the bioavailability and pharmacokinetics of common(bio)therapeutics,overall leading to unmet clinical demands,safety concerns,and poor patient compliance.Ionogels,a versatile class of materials comprising ionic liquids(ILs)confined in an organic or inorganic solid network,have been proposed to overcome these drawbacks.They have demonstrated the ability to enhance the antimicrobial and mechanical properties of the resulting materials while allowing remarkable improvements in drug solubility and their delivery to targeted sites.Nowadays,safety investigations and clinical trials are still required to fully leverage the potential of ionogels for human applications.However,the recent FDA approval of the New Drug Application MRX-5LBT®,a transdermal drug delivery system,opens promising perspectives toward the clinical translation of ionogels.This review focuses on recent advances achieved in the design of ionogels for pharmaceutical applications,viz.in topical formulations to promote wound healing with antimicrobial activity,and as platforms to improve drug pharmacokinetics(solubility and bioavailability),and their delivery at targeted specific sites with controlled release behaviour.
基金supported by the National Natural Science Foundation of China(Grant Nos.22072031,12372107,11832010,and 11890682)the Strategic Priority Research Program of Chinese Academy of Sciences(Grant No.XDB36000000).
文摘The bulge test is a widely utilized method for assessing the mechanical properties of thin films,including metals,polymers,and semiconductors.However,as film thickness diminishes to nanometer scales,boundary conditions dominated by weak van der Waals forces significantly impact mechanical responses.Instead of sample fracture,interfacial shear deformation and delamination become the primary deformation modes,thereby challenging the applicability of conventional bulge models.To accommodate the interfacial effect,a modified mechanical model based on the bulge test has been proposed.This review summarizes recent advancements in the bulge test to highlight the potential challenges and opportunities for future research.
基金supported by Grants from the National Natural Science Foundation of China(Nos.52205363,52235008 and U2037203)Fundamental Research Funds for the Central Universities(Nos.2019kfyRCPY044 and 2021GCRC002)+1 种基金Program for HUST Academic Frontier Youth Team(No.2018QYTD04)the Program for Innovative Research Team of the Ministry of Education(No.IRT1244)。
文摘Additive manufacturing(AM)offers the unique capability of directly creating three-dimensional complicated ceramic components with high process flexibility and outstanding geometry controllability.However,current ceramic AM technology is mainly limited to the creation of a single material,which falls short of meeting the multiple functional requirements under increasingly harsh service circumstances.Ceramic multi-material additive manufacturing(MMAM)technology has great potential for integrally producing multi-dimensional multi-functional components,allowing for point-by-point precision manufacturing of programmable performance/functions.However,there is a huge gap between the capabilities of the existing ceramic MMAM technology and the requirements for industrial application.In this review,we discuss and summarize the research status of ceramic MMAM technology from the perspectives of feedstock selection,printing process,post-processing,component performance,and application.Throughout the discussion,the challenges associated with ceramic MMAM such as heterogeneous material coupled printing,heterogeneous interfacial bonding,and co-sintering densification have been put forward.This review aims to bridge the gap between AM technologies and the requirements for multifunctional ceramic components by analyzing the existing limitations in ceramic MMAM and pointing out future needs.
基金financially supported by the National Oversea Postdoctoral Talent Attraction Programthe Pilot Group Program of the Research Fund for International Senior Scientists(52350710795)the Youth Fund of the National Natural Science Foundation of China(52402288).
文摘Single-atom catalysts(SACs)have demonstrated exceptional performance in electrocatalytic water splitting,owing to their maximized atomic utilization efficiency and superior reaction kinetics.The incorporation of SACs typically depends on robust metal-support interactions,which stabilize the single atoms on the support through various unsaturated chemical sites or spatial confinement.A critical challenge lies in precisely modulating the electronic structure and coordination environment of metal atoms.However,current research primarily focuses on single-atom metals,often neglecting the significant role of support materials in SACs.Two-dimensional(2D)atomically thin materials(ATMs)possess unique physicochemical properties and tunable reaction environments,which can modulate catalytic performance via metal-support interactions,positioning them as promising platforms for SAC loading.This paper reviews the recent advancements and the current status of SACs supported on 2D ATMs(SACs@ATMs).The structural design theory and synthesis strategies of SACs@ATMs are systematically discussed.The significance of advanced characterization techniques in elucidating the coordination environment and metal-support interactions is highlighted.Additionally,the reaction mechanisms and applications of SACs in electrocatalytic water splitting are summarized.Finally,the future challenges and opportunities for SACs@ATMs are outlined.This paper aims to provide insights and guidance for the rational design of SACs@ATMs with high-performance electrocatalytic water splitting capabilities.
基金The Spanish authors acknowledge financial support from the PCI2023-143355 European research projectfunded by the European Union-Agencia Estatal de Investigación,and is entitled“Mastering electrode surface to achieve ultra-high reversible capacity”(MASTER)+4 种基金the Regional government of“Junta de Andalucía”(group FQM288)excellence project no.0001020as well as Instituto Químico para la Energía y el Medioambiente(IQUEMA),UCO-SCAI,and UMA-SCAI for their technical supportfunding institutions for their financial support:Debora Ferreira dos Santos and Mauricio Bomio are grateful for the financial support from the National Council for Scientific and Technological Development(CNPq)-Finance Code 200196/2024-3 and 403335/2023-0,respectivelyCoordination for the Improvement of Higher Education Personnel(CAPES)-Brazil with Finance Code 001.
基金Supported by the National Natural Science Foundation of China(Nos.52293472,22473096 and 22471164)。
文摘Among various architectures of polymers,end-group-free rings have attracted growing interests due to their distinct physicochemical performances over the linear counterparts which are exemplified by reduced hydrodynamic size and slower degradation.It is key to develop facile methods to large-scale synthesis of polymer rings with tunable compositions and microstructures.Recent progresses in large-scale synthesis of polymer rings against single-chain dynamic nanoparticles,and the example applications in synchronous enhancing toughness and strength of polymer nanocomposites are summarized.Once there is the breakthrough in rational design and effective large-scale synthesis of polymer rings and their functional derivatives,a family of cyclic functional hybrids would be available,thus providing a new paradigm in developing polymer science and engineering.
基金supported by the Department of Chemistry,Fudan Universitythe National Natural Science Foundation of China(22031003,21720102004)the Shanghai Science Technology Committee(19DZ2270100)。
文摘The 6-isoquinolinyl system was incorporated into mechanically interlocked molecules(MIMs)syntheses for comparative analysis of its assembly behavior with 4-pyridyl-based coordination ligands,where a coordination-driven self-assembly strategy by half-sandwich Cp^(*)Rh units was employed to construct diverse molecular links.The pyridyl ligand,adorned with thiophene moieties,assembles into[2]catenanes(2_(1)^(2)links),whereas the isoquinolinyl ligand produces molecular Borromean links(6_(2)^(3)links).Intriguingly,when utilizing extended bithiophene segments,the pyridyl ligand forms Borromean rings(6_(2)^(3)links),while isoquinolinyl counterparts produced a rare low-symmetry cyclic[3]catenane(6_(3)^(3)topology).The results were confirmed through single-crystal X-ray diffraction analysis,nuclear magnetic resonance(NMR)spectroscopy,and electrospray ionization time-of-flight mass spectrometry(ESI-TOF/MS)experiments.Synergistic π-π stacking,C-H···π interactions,and solvophobic effects governed the complex self-assembly system,with independent gradient model(IGM)analyses and solventaccessible surface area(SASA)calculations providing atomistic insights into the pathway selectivity of distinct topological links.
基金support from the National Key Research and Development Program of China(No.2024YFB3713705)is acknowledgedWangzhong Mu would like to acknowledge the Strategic Mobility,Sweden(SSF,No.SM22-0039)+1 种基金the Swedish Foundation for International Cooperation in Research and Higher Education(STINT,No.IB2022-9228)the Jernkontoret(Sweden)for supporting this clean steel research.Gonghao Lian would like to acknowledge China Scholarship Council(CSC,No.202306080032).
文摘The detection and characterization of non-metallic inclusions are essential for clean steel production.Recently,imaging analysis combined with high-dimensional data processing of metallic materials using artificial intelligence(AI)-based machine learning(ML)has developed rapidly.This technique has achieved impressive results in the field of inclusion classification in process metallurgy.The present study surveys the ML modeling of inclusion prediction in advanced steels,including the detection,classification,and feature prediction of inclusions in different steel grades.Studies on clean steel with different features based on data and image analysis via ML are summarized.Regarding the data analysis,the inclusion prediction methodology based on ML establishes a connection between the experimental parameters and inclusion characteristics and analyzes the importance of the experimental parameters.Regarding the image analysis,the focus is placed on the classification of different types of inclusions via deep learning,in comparison with data analysis.Finally,further development of inclusion analyses using ML-based methods is recommended.This work paves the way for the application of AIbased methodologies for ultraclean-steel studies from a sustainable metallurgy perspective.
基金supported by the Natural Science Foundation(NSF)of China(Nos.22205015,22175020,and 22235001)the National Postdoctoral Program for Innovative Talents(No.BX20220032)+2 种基金the China Postdoctoral Science Foundation Funded Project(No.2022BG013)the Fundamental Research Funds for the Central Universities(Nos.00007709,00007770,and FRFBR-23-02B)University of Science and Technology Beijing is gratefully acknowledged.
文摘In comparison with their 2D and 3D counterparts,1D covalent organic frameworks(COFs)have rarely been investigated due to the synthetic challenge arising from the strict necessary matching in the molecular symmetry between corresponding building blocks and linking units in addition to the unmanageable packing of 1D organic chains once formed.Herein,two novel imide-linked 1D COFs with phthalocyanine building blocks,namely NiPc-CZDM-COF and NiPc-CZDL-COF,were fabricated from the hydrothermal synthesis reaction of 2,3,9,10,16,17,23,24-octacarboxyphthalocyaninato nickel(II)(NiPc(COOH)_(8))with 9H-carbazole-3,6-diamine(CZDM)and 4,4′-(9H-carbazole-3,6-diyl)dianiline(CZDL),respectively.Two COFs have high crystallinity on the basis of powder X-ray diffraction analysis and high-resolution transmission electron microscopy.Due to their high ratio of exposed active centers on the edge sites of porous ribbons,both NiPc-CZDM-COF and NiPc-CZDL-COF electrodes display high utilization efficiency of NiPc electroactive sites of 8.0%and 7.5% according to the electrochemical measurement,resulting in their excellent capacity toward electrocatalytic nitrate reduction with the nitrate-to-NH3 Faradaic efficiency of nearly 100%.In particular,NiPc-CZDM-COF electrode exhibits superior electrocatalytic performance with high NH3 partial current density of−246 mA/cm^(2),ammonia yield rate of 19.5 mg cm^(−2) h^(−1),and turnover frequency of 5.8 s^(−1) at−1.2 V in an H-type cell associated with its higher conductivity.This work reveals the good potential of 1D porous crystalline materials in electrocatalysis.
基金supported by Natural Science Foundation of Zhejiang Province(Nos.LQ23E030002,LZ23B040001)the National Natural Science Foundation of China(Nos.52303226,21971049)L.Zhan acknowledges the research start-up fund from Hangzhou Normal University(4095C50222204002).
文摘Organic photovoltaics(OPVs)have achieved remarkable progress,with laboratory-scale single-junction devices now demonstrating power conversion efficiencies(PCEs)exceeding 20%.However,these efficiencies are highly dependent on the thickness of the photoactive layer,which is typically around 100 nm.This sensitivity poses a challenge for industrial-scale fabrication.Achieving high PCEs in thick-film OPVs is therefore essential.This review systematically examines recent advancements in thick-film OPVs,focusing on the fundamental mechanisms that lead to efficiency loss and strategies to enhance performance.We provide a comprehensive analysis spanning the complete photovoltaic process chain:from initial exciton generation and diffusion dynamics,through dissociation mechanisms,to subsequent charge-carrier transport,balance optimization,and final collection efficiency.Particular emphasis is placed on cutting-edge solutions in molecular engineering and device architecture optimization.By synthesizing these interdisciplinary approaches and investigating the potential contributions in stability,cost,and machine learning aspects,this work establishes comprehensive guidelines for designing high-performance OPVs devices with minimal thickness dependence,ultimately aiming to bridge the gap between laboratory achievements and industrial manufacturing requirements.
文摘Correction to:Nano-Micro Letters(2026)18:10.https://doi.org/10.1007/s40820-025-01852-8 Following publication of the original article[1],the authors reported that the last author’s name was inadvertently misspelled.The published version showed“Hongzhen Chen”,whereas the correct spelling should be“Hongzheng Chen”.The correct author name has been provided in this Correction,and the original article[1]has been corrected.
基金supported by the National Natural Science Foundation of China(21971177)the Natural Science Foundation of the Jiangsu Higher Education Institution of China(22KJA150004)+3 种基金the Suzhou Science and Technology Bureau(SZM2021008)the Priority Academic Program Development(PAPD)of Jiangsu Higher Education Institutionsthe Jiangsu Key Laboratory of Advanced Functional Polymers Design and Application,Soochow University,Suzhou Medical and Industrial Cooperation Innovation Project(SZM2022011)the Suzhou Key Laboratory of Macromolecular Design and Precision Synthesis and the Program of Innovative Research Team of Soochow University。
文摘Poly(ester amide)s(PEAs)represent promising biomaterials because of their well-balanced mechanical properties,biodegradability,and biocompatibility.However,practical applications of PEAs are still limited by challenges in functional versatility and environmental adaptability.Here,we present the first synthesis of periodic selenium-incorporated PEAs(Se-PEAs)via a rapid,catalyst-free selenol-yne click polymerization process.By harnessing the versatility of selenium,we achieved precise modulation of material properties.The resulting Se-PEAs demonstrated tunable mechanical behavior,spanning rigid plastics to elastomers,alongside exceptional thermal stability and high optical clarity.Programmable degradation profiles ensure long-term stability in physiological environments while facilitating rapid oxidative degradation at the end of the lifecycle.Surface selenoniumization further conferred robust antibacterial efficacy without compromising mechanical integrity.This multifunctionality positions Se-PEAs as transformative materials for biomedical implants,sustainable packaging,and high-refractiveindex optics.Our work advanced functional polymer design and underscored the potential of selenium chemistry in addressing global challenges in terms of plastic waste and ecological sustainability.
基金supported by the National Natural Science Foundation of China(U2106216,51971121,52002228,22025108,U21A20327,and 22121001)the National Key R&D Program of China(2022YFA1504500 and 2024YFA1509500)+7 种基金the Major-Special Science and Technology Project in Shandong Province(2023ZLGX05)the Natural Science Foundation of Shandong Province for Major Basic Research Project(ZR2022ZD12)the Qingdao Marine Science and Technology Innovation Project(22-3-3-hygg-27-hy)the Fundamental Research Fund for Central University(202141027)the Key R&D Plan of Shandong Province(2022JMRH0202)the Taishan Scholar of Climbing Plan(tspd20230603)the Taishan Scholar of Youth Plan(tsqn202211072)the Natural Science Foundation of Shandong Province(ZR2024MB065)。
文摘Ruthenium-based materials(Ru and RuO_(2))are promising electrocatalysts toward electrochemical water splitting(EWS)though there are still issues with them that needs to be resolved such as relatively strong adsorption strength of intermediates over Ru and oxidative dissolution of RuO_(2).In this article,an overview of the recent progress and challenges with Ru-based electrocatalysts for EWS is provided.Firstly,fundamentals of EWS are summarized from the aspects of reaction mechanisms and activity descriptors.Next,the typical methods of fabricating Ru-based catalysts are demonstrated mainly including hydrothermal/solvothermal syntheses,organic ligand-assisted syntheses,pyrolysis,acid etching,cation exchange methods and molten salt-assisted syntheses.We then focus on illustrating the enhancing strategies toward creating advanced Ru-based electrocatalysts by demonstrating the typical examples,which include alloying,doping,structure design,interface engineering,single-atom catalyst design,high-entropy alloy design,phase engineering and defecting engineering.In this section,the structureproperty correlation is elucidated aiming to the design of more efficient Ru-based electrocatalysts for EWS.Finally,we conclude the review by addressing the challenges and prospects of electrochemical water splitting and the development of Rubased catalysts.
基金supported by the National Nature Science Foundation of China(62504130)National Key Research and Development Program of China(2018YFB0704100)+1 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).
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The copyright of this paper is owned by the Nobel Foundation.
文摘INTRODUCTIONIn 1976, Alan MacDiarmid, Hideki Shirakawa and I, together with a talented group of graduate students andpost-doctoral researchers discovered conducting polymers and the ability to dope these polymers over the fullrange from insulator to metal. This was particularly exciting because it created a new field of research on theboundary between chemistry and condensed matter physics, and because it created a number of opportunities:
文摘Ⅲ-nitride light-emitting diodes(LEDs)are now used almost everywhere,due to their energy-saving capability.In the near future,the vast majority of lighting sources will undoubtedly be based on LEDs.What future technologies and applications can we expect from Ⅲ-nitride-based and particularly gallium nitride(Ga N)-based,materials and devices?
基金BRNS,Mumbai,India(No-2013/37P/67/BRNS),MNRE,New Delhi,India(No-102/87/2011-NT),and CSIR,New Delhi,India{YSP-02(P-81-113),OLP-95}for the financial supportUGC,New Delhi,for a fellowship。
文摘The continuous increase of global atmospheric CO_(2) concentrations brutally damages our environment. A series of methods have been developed to convert CO_(2) to valuable fuels and value-added chemicals to maintain the equilibrium of carbon cycles. The electrochemical CO_(2) reduction reaction(CO_(2)RR) is one of the promising methods to produce fuels and chemicals, and it could offer sustainable paths to decrease carbon intensity and support renewable energy. Thus, significant research efforts and highly efficient catalysts are essential for converting CO_(2) into other valuable chemicals and fuels. Transition metal-based single atoms catalysts(TM-SACs) have recently received much attention and offer outstanding electrochemical applications with high activity and selectivity opportunities. By taking advantage of both heterogeneous and homogeneous catalysts, TM-SACs are the new rising star for electrochemical conversion of CO_(2) to the value-added product with high selectivity. In recent years, enormous research effort has been made to synthesize different TM-SACs with different M–Nxsites and study the electrochemical conversion of CO_(2) to CO. This review has discussed the development and characterization of different TMSACs with various catalytic sites, fundamental understanding of the electrochemical process in CO_(2) RR,intrinsic catalytic activity, and molecular strategics of SACs responsible for CO_(2)RR. Furthermore, we extensively review previous studies on 1 st-row transition metals TM-SACs(Ni, Co, Fe, Cu, Zn, Sn) and dual-atom catalysts(DACs) utilized for electrochemical CO_(2) conversions and highlight the opportunities and challenges.
文摘Powder metallurgical Cu-Ti alloys with different titanium additions produced by hot pressing were characterized by optical microscopy, scanning electron microscopy, X-ray diffraction analysis, and hardness, wear and bending tests. The addition of titanium to copper caused the formation of different intermetallic layers around titanium particles. The titanium content of the intermetallics decreased from the center of the particle to the copper matrix. The hardness, wear resistance, and bending strength of the materials increased with increasing Ti content, whereas strain in the bending test decreased. Worn surface analyses showed that different wear mechanisms were active during the wear test of specimens with different chemical compositions. Changes in the properties of the materials with titanium addition were explained by the high hardness of different Cu-Ti intermetallic phases.
文摘An Al2O3-TiB2 nanocomposite was successfully synthesized by ball milling of Al, TiO2 and two B source materials of B2O3 （system （1）） and H3BO3 （system （2））. Phase identification of the milled samples was examined by Xray diffraction. The morphology and microstructure of the milled powders were monitored by scanning electron microscopy and transmission electron microscopy. It was found that the formation of this composite was completed after 15 and 30 h of milling time in systems （1） and （2）, respectively. More milling energy was required for the formation of this composite in system （2） due to the lubricant properties of HaBO3 and also its decomposition to HBO2 and B2O3 during milling. On the basis of X-ray diffraction patterns and thermodynamic calculations, this composite was formed by highly exothermic mechanically induced self-sustaining reactions （MSR） in both systems. The MSR mode took place around 9 h and 25 h of milling in systems （1） and （2）, respectively. At the end of milling （15 h for system （1） and 30 h for system （2）） the grain size of about 35-50 nm was obtained in both systems.
