The ability to control the electrode interfaces in an electrochemical energy storage system is essential for achieving the desired electrochemical performance.However,achieving this ability requires an in-depth unders...The ability to control the electrode interfaces in an electrochemical energy storage system is essential for achieving the desired electrochemical performance.However,achieving this ability requires an in-depth understanding of the detailed interfacial nanostructures of the electrode under electrochemical operating conditions.In-situ transmission electron microscopy(TEM)is one of the most powerful techniques for revealing electrochemical energy storage mechanisms with high spatiotemporal resolution and high sensitivity in complex electrochemical environments.These attributes play a unique role in understanding how ion transport inside electrode nanomaterials and across interfaces under the dynamic conditions within working batteries.This review aims to gain an in-depth insight into the latest developments of in-situ TEM imaging techniques for probing the interfacial nanostructures of electrochemical energy storage systems,including atomic-scale structural imaging,strain field imaging,electron holography,and integrated differential phase contrast imaging.Significant examples will be described to highlight the fundamental understanding of atomic-scale and nanoscale mechanisms from employing state-of-the-art imaging techniques to visualize structural evolution,ionic valence state changes,and strain mapping,ion transport dynamics.The review concludes by providing a perspective discussion of future directions of the development and application of in-situ TEM techniques in the field of electrochemical energy storage systems.展开更多
High-performance aqueous zinc(Zn)-ion batteries(AZIBs)have emerged as one of the greatest favorable candidates for next-generation energy storage systems because of their low cost,sustainability,high safety,and eco-fr...High-performance aqueous zinc(Zn)-ion batteries(AZIBs)have emerged as one of the greatest favorable candidates for next-generation energy storage systems because of their low cost,sustainability,high safety,and eco-friendliness.In this report,we prepared magnesium vanadate(MgVO)-based nanostructures by a facile single-step solvothermal method with varying experimental reaction times(1,3,and 6 h)and investigated the effect of the reaction time on the morphology and layered structure for MgVO-based compounds.The newly prepared MgVO-1 h,MgVO-3 h and MgVO-6 h samples were used as cathode materials for AZIBs.Compared to the MgVO-1 h and MgVO-6 h cathodes,the MgVO-3 h cathode showed a higher specific capacity of 492.74 mA h g^(-1) at 1 A g^(-1) over 500 cycles and excellent rate behavior(291.58 mA h g^(-1) at 3.75 A g^(-1))with high cycling stability(116%)over 2000 cycles at 5 A g^(-1).Moreover,the MgVO-3 h electrode exhibited good electrochemical performance owing to its fast Zn-ion diffusion kinetics.Additionally,various ex-situ analyses confirmed that the MgVO-3 h cathode displayed excellent insertion/extraction of Zn^(2+)ions during charge and discharge processes.This study offers an efficient method for the synthesis of nanostructured MgVO-based cathode materials for high-performance AZIBs.展开更多
The effects of gradient nanostructures induced by supersonic fine particle bombardment(SFPB)on the surface integrity,microstructural evolution,and mechanical properties of a Ni-W-Co-Ta medium-heavy alloy(MHA)were syst...The effects of gradient nanostructures induced by supersonic fine particle bombardment(SFPB)on the surface integrity,microstructural evolution,and mechanical properties of a Ni-W-Co-Ta medium-heavy alloy(MHA)were systematically investigated.The results show that gradient nanostructures are formed on the surface of Ni-W-Co-Ta MHA after SFPB treatment.At a gas pressure of 1.0 MPa and an impact time of 60 s,the ultimate tensile strength and yield strength of the alloy reached the maximum values of 1236 MPa and 758 MPa,respectively,which are 22.5%and 38.8%higher than those of the solid solution treated alloy,and the elongation(46.3%)is close to that of the solid solution treated alloy,achieving the optimal strength–ductility synergy.However,microcracks appear on the surface with excessive gas pressure and impact time,generating the relaxed residual stress and decreased strength.With the increase of the impact time and gas pressure,the depth of the deformation layer and the surface microhardness gradually increase,reaching the maximum values(29μm and HV 451)at 1.0 MPa and 120 s.The surface grain size is refined to a minimum of 11.67 nm.Notably,SFPB treatment has no obvious effect on elongation,and the fracture mode changes from the ductile fracture before treatment to ductile–brittle mixed fracture after treatment.展开更多
Understanding the dynamic assembly process of DNA nanostructures is important for developing novel strategy to design and construct functional devices.In this work,temperature-controlled dynamic light scattering(DLS)s...Understanding the dynamic assembly process of DNA nanostructures is important for developing novel strategy to design and construct functional devices.In this work,temperature-controlled dynamic light scattering(DLS)strategy has been applied to study the global assembly process of DNA origami and DNA bricks.Through the temperature dependent size and intensity profiles,the self-assembly process of various DNA nanostructures with different morphologies have been well-studied and the temperature transition ranges could be observed.Taking advantage of the DLS information,rapid preparation of the DNA origami and the brick assembly has been realized through a constant temperature annealing.Our results demonstrate that the DLS-based strategy provides a convenient and robust tool to study the dynamic process of forming hieratical DNA structures,which will benefit understanding the mechanism of self-assembly of DNA nanostructures.展开更多
Crystallineγ-Ga_(2)O_(3)@rGO core-shell nanostructures are synthesized in gram scale,which are accomplished by a facile sonochemical strategy under ambient condition.They are composed of uniformγ-Ga_(2)O_(3)nanosphe...Crystallineγ-Ga_(2)O_(3)@rGO core-shell nanostructures are synthesized in gram scale,which are accomplished by a facile sonochemical strategy under ambient condition.They are composed of uniformγ-Ga_(2)O_(3)nanospheres encapsulated by reduced graphene oxide(rGO)nanolayers,and their formation is mainly attributed to the existed opposite zeta potential between the Ga_(2)O_(3)and rGO.The as-constructed lithium-ion batteries(LIBs)based on as-fabricatedγ-Ga_(2)O_(3)@rGO nanostructures deliver an initial discharge capacity of 1000 mAh g^(-1)at 100 mA g^(-1)and reversible capacity of 600 mAh g^(-1)under 500 mA g^(-1)after 1000 cycles,respectively,which are remarkably higher than those of pristineγ-Ga_(2)O_(3)with a much reduced lifetime of 100 cycles and much lower capacity.Ex situ XRD and XPS analyses demonstrate that the reversible LIBs storage is dominant by a conversion reaction and alloying mechanism,where the discharged product of liquid metal Ga exhibits self-healing ability,thus preventing the destroy of electrodes.Additionally,the rGO shell could act robustly as conductive network of the electrode for significantly improved conductivity,endowing the efficient Li storage behaviors.This work might provide some insight on mass production of advanced electrode materials under mild condition for energy storage and conversion applications.展开更多
This paper describes mass-based energy phase-space projection of microwave-assisted synthesis of transition metals (zinc oxide, palladium, silver, platinum, and gold) nanostructures. The projection uses process energy...This paper describes mass-based energy phase-space projection of microwave-assisted synthesis of transition metals (zinc oxide, palladium, silver, platinum, and gold) nanostructures. The projection uses process energy budget (measured in kJ) on the horizontal axes and process density (measured in kJg−1) on the vertical axes. These two axes allow both mass usage efficiency (Environmental-Factor) and energy efficiency to be evaluated for a range of microwave applicator and metal synthesis. The metrics are allied to the: second, sixth and eleventh principle of the twelve principle of Green Chemistry. This analytical approach to microwave synthesis (widely considered as a useful Green Chemistry energy source) allows a quantified dynamic environmental quotient to be given to renewable plant-based biomass associated with the reduction of the metal precursors. Thus allowing a degree of quantification of claimed “eco-friendly” and “sustainable” synthesis with regard to waste production and energy usage.展开更多
This research focuses on the electric behavior of a mixed ferrielectric sulflower-like nanostructure.The structure includes a core with spin S_(i)^(Z)-1 atoms and a shell with spin σ_(j)^(Z)-5/2 atoms.The Blume–Cape...This research focuses on the electric behavior of a mixed ferrielectric sulflower-like nanostructure.The structure includes a core with spin S_(i)^(Z)-1 atoms and a shell with spin σ_(j)^(Z)-5/2 atoms.The Blume–Capel model and the Monte Carlo technique(MCt)with the Metropolis algorithm are employed.Diagrams are established for absolute zero,investigating stable spin configurations correlated with various physical parameters.The MCt method explores phase transition behavior and electric hysteresis cycles under different physical parameters.展开更多
MOF-based core-shell structures with high surface area, abundant active sites, and broad absorption bands are viable alternatives to traditional single-component photocatalysts. In this report, we describe the design ...MOF-based core-shell structures with high surface area, abundant active sites, and broad absorption bands are viable alternatives to traditional single-component photocatalysts. In this report, we describe the design and construction of delicate Ag nanowires@NH_(2)-UiO-66 with a core-shell structure for use as photocatalysts in imine synthesis under light. The optimized composites exhibited 80% imine production, which was higher than both MOF and Ag NWs. The significant improvement in photocatalytic activity under light may be attributed to the plasmonic effect of silver nanowires and their core-shell structure, which promotes the separation of electron-hole pairs. Moreover, the photocatalytic activity of the core-shell nanostructure may provide valuable insight into the design and construction of MOF-based composite photocatalysts for oxidative coupling of amines.展开更多
Triangular Au-Ag framework nanostructures （TFN） were synthesized via a multi-step galvanic replacement reaction （MGRR） of single-crystalline triangular silver nanoplates in a chlorauric acid （HAuCl4） solution at...Triangular Au-Ag framework nanostructures （TFN） were synthesized via a multi-step galvanic replacement reaction （MGRR） of single-crystalline triangular silver nanoplates in a chlorauric acid （HAuCl4） solution at room temperature. The morphological, compositional, and crystal structural changes involved with reaction steps were analyzed by using transmission electron microscopy（TEM）, energy-dispersive X-ray spectrometry （EDX）, and X-ray diffraction. TEM combined with EDX and selected area electron diffraction confirmed the replacement of Ag with Au. The in-plane dipolar surface plasmon resonance （SPR） absorption band of the Ag nanoplates locating initially at around 700 nm gradually redshifted to 1 100 nm via a multi-stage replacement manner after 7 stages. The adding amount of HAuCl4 per stage influenced the average redshift value per stage, thus enabled a fine tuning of the in-plane dipolar band. A proposed formation mechanism of the original Ag nanoplates developing pores while growing Au nanoparticles covering this underlying structure at more reaction steps was confirmed by exploiting surface-enhanced Raman scattering （SERS）.展开更多
Chirality is ubiquitous in natural world.Although with similar physical and chemical properties,chiral enantiomers could play different roles in biochemical processes.Discrimination of chiral enantiomers is extremely ...Chirality is ubiquitous in natural world.Although with similar physical and chemical properties,chiral enantiomers could play different roles in biochemical processes.Discrimination of chiral enantiomers is extremely important in biochemical,analytical chemistry,and pharmaceutical industries.Conventional chiroptical spectroscopic methods are disadvantageous at a limited detection sensitivity because of the weak signals of natural chiral molecules.Recently,superchiral fields were proposed to effectively enhance the interaction between light and molecules,allowing for ultrasensitive chiral detection.Intensive theoretical and experimental works have been devoted to generation of superchiral fields based on artificial nanostructures and their application in ultrasensitive chiral sensing.In this review,we present a survey on these works.We begin with the introduction of chiral properties of electromagnetic fields.Then,the optical chirality enhancement and ultrasensitive chiral detection based on chiral and achiral nanostructures are discussed respectively.Finally,we give a short summary and a perspective for the future ultrasensitive chiral sensing.展开更多
Micron sized hexagon- and flower-like nanostructures of lead oxide（α-PbO2） have been synthesized by very simple and cost effective route of anodic oxidation of lead sheet. These structures were easily obtained by t...Micron sized hexagon- and flower-like nanostructures of lead oxide（α-PbO2） have been synthesized by very simple and cost effective route of anodic oxidation of lead sheet. These structures were easily obtained by the simple variation of applied voltage from 2-6 V between the electrodes. Lead sheet was used as an anode and platinum sheet served as a cathode. Anodic oxidation at 2 V resulted in the variable edge sized（1-2 μm） hexagon-like structures in the electrolyte. When the applied potential was increased to 4 V a structure of distorted hexagons consisting of some flower-like structures were obtained. Further increment of potential up to 6 V resulted in flower like structures of α-PbO2 having six petals. The diameter of the flower-like structures was 200-500 nm and the size of a petal was 100-200 nm.展开更多
ZnO-CeO2 nanostructures were synthesized by simple and effcient low temperature method. The structure and morphology of the ZnO-CeO2 nanostructures were characterized by X-ray powder diffraction （XRD） and field emis...ZnO-CeO2 nanostructures were synthesized by simple and effcient low temperature method. The structure and morphology of the ZnO-CeO2 nanostructures were characterized by X-ray powder diffraction （XRD） and field emission scanning electron microscopy （FESEM）, which revealed elongated shaped CeO2 nanoparticles with diameters of 40–90 nm distributed on the surface of elongated ZnO nanostructures with diameters of 50–200 nm （edge–centre）. Further the structure of the synthesized ZnO-CeO2 nanostructure was supported by Raman spectra and Fourier transform infrared spectroscopy （FTIR）. UV-vis absorption spectrum was used to confirm the optical properties of the CeO2 doped ZnO nanostructures. Photo-catalytic activity of CeO2 doped ZnO nanostructure was evaluated by degradation of acridine orange and methylene blue which degraded 84.55% and 48.65% in 170 min, respectively. ZnO-CeO2 nanostructures also showed good sensitivity （0.8331 μA·cm-2·（mol/l）-1） in short response time （10 s） by applying to chemical sensing using ethanol as a target compound by I-V technique. These degradation and chemical sensing properties of ZnO-CeO2 nanostructures are of great importance for the application of ZnO-CeO2 system as a photo-catalyst and chemical sensor.展开更多
The burgeoning global economy during the past decades gives rise to the continuous increase in fossil fuels consumption and rapid growth of CO_(2) emission,which demands an urgent exploration into green and sustainabl...The burgeoning global economy during the past decades gives rise to the continuous increase in fossil fuels consumption and rapid growth of CO_(2) emission,which demands an urgent exploration into green and sustainable devices for energy storage and power management.Supercapacitors based on activated carbon electrodes are promising systems for highly efficient energy harvesting and power supply,but their promotion is hindered by the moderate energy density compared with batteries.Therefore,scalable conversion of CO_(2) into novel carbon nanostructures offers a powerful alternative to tackle both issues:mitigating the greenhouse effect caused by redundant atmospheric CO_(2) and providing carbon materials with enhanced electrochemical performances.In this tutorial review,the techniques,opportunities and barriers in the design and fabrication of advanced carbon materials using CO_(2) as feedstock as well as their impact on the energy-storage performances of supercapacitors are critically examined.In particular,the chemical aspects of various Cv2 conversion reactions are highlighted to establish a detailed understanding for the science and technology involved in the microstructural evolution,surface engineering and porosity control of CO_(2)-converted carbon nanostructures.Finally,the prospects and challenges associated with the industrialization of CO_(2) conversion and their practical application in supercapacitors are also discussed.展开更多
Metal organic frameworks(MOFs) represent a class of porous material which is formed by strong bonds between metal ions and organic linkers. By careful selection of constituents, MOFs can exhibit very high surface area...Metal organic frameworks(MOFs) represent a class of porous material which is formed by strong bonds between metal ions and organic linkers. By careful selection of constituents, MOFs can exhibit very high surface area, large pore volume, and excellent chemical stability.Research on synthesis, structures and properties of various MOFs has shown that they are promising materials for many applications, such as energy storage, gas storage, heterogeneous catalysis and sensing. Apart from direct use, MOFs have also been used as support substrates for nanomaterials or as sacrificial templates/precursors for preparation of various functional nanostructures. In this review, we aim to present the most recent development of MOFs as precursors for the preparation of various nanostructures and their potential applications in energy-related devices and processes. Specifically, this present survey intends to push the boundaries and covers the literatures from the year 2013 to early 2017,on supercapacitors, lithium ion batteries, electrocatalysts, photocatalyst, gas sensing, water treatment, solar cells, and carbon dioxide capture.Finally, an outlook in terms of future challenges and potential prospects towards industrial applications are also discussed.展开更多
Chirality,the property that an object cannot coincide with its mirror image arising from lack of mirror symmetry,is ubiquitous in nature at various length scales.The physical and chemical properties are strongly relat...Chirality,the property that an object cannot coincide with its mirror image arising from lack of mirror symmetry,is ubiquitous in nature at various length scales.The physical and chemical properties are strongly related to the nature of chiral complexes,playing a significant role in various fields such as photonics,biochemistry,medicine and catalysis.In particular,the recent flexible design of chiral metal nanostructures offers one platform for deeply understanding the origin of chirality and one roadmap for the precise construction of chiral nanomaterials directed by the applications.Herein,we summarize the different geometries and classical synthetic approaches to chiral noble metal nanomaterials.Moreover,chiroptical properties and potential applications of chiral metal nanostructures are discussed as well.Finally,the opportunities and challenges toward the synthesis and application of chiral metal nanostructures are proposed.展开更多
Photoelectrochemical(PEC) water splitting using solar energy has attracted great attention for generation of renewable hydrogen with less carbon footprint, while there are enormous challenges that still remain for imp...Photoelectrochemical(PEC) water splitting using solar energy has attracted great attention for generation of renewable hydrogen with less carbon footprint, while there are enormous challenges that still remain for improving solar energy water splitting efficiency, due to limited light harvesting, energy loss associated to fast recombination of photogenerated charge carriers, as well as electrode degradation. This overview focuses on the recent development about catalyst nanomaterials and nanostructures in different PEC water splitting systems. As photoanode, Au nanoparticle-decorated TiO_2 nanowire electrodes exhibited enhanced photoactivity in both the UV and the visible regions due to surface plasmon resonance of Au and showed the largest photocurrent generation of up to 710 nm. Pt/Cd S/CGSe electrodes were developed as photocathode. With the role of p–n heterojunction, the photoelectrode showed high stability and evolved hydrogen continuously for more than 10 days. Further, in the Z-scheme system(Bi_2S_3/TNA as photoanode and Pt/Si PVC as photocathode at the same time), a self-bias(open-circuit voltage Voc= 0.766 V) was formed between two photoelectrodes, which could facilitate photogenerated charge transfers and enhance the photoelectrochemical performance, and which might provide new hints for PEC water splitting. Meanwhile, the existing problems and prospective solutions have also been reviewed.展开更多
Versatile liquid manipulating surfaces combining patternable and controllable wettability have recently motivated considerable attention owing to their significant advantages in droplet-solid impacting behaviors,micro...Versatile liquid manipulating surfaces combining patternable and controllable wettability have recently motivated considerable attention owing to their significant advantages in droplet-solid impacting behaviors,microdroplet self-removal,and liquid–liquid interface reaction applications.However,developing a facile and efficient method to fabricate these versatile surfaces remains an enormous challenge.In this paper,a strategy for the fabrication of liquid manipulating surfaces with patternable and controllable wettability on Polyimide(PI)film based on femtosecond laser thermal accumulation engineering is proposed.Because of its controllable micro-/nanostructures and chemical composition through adjusting the local thermal accumulation,the wettability of PI film can be tuned from superhydrophilicity(~3.6°)to superhydrophobicity(~151.6°).Furthermore,three diverse surfaces with patternable and heterogeneous wettability were constructed and various applications were successfully realized,including water transport,droplet arrays,and liquid wells.This work may provide a facile strategy for achieving patternable and controllable wettability efficiently and developing multifunctional liquid steering surfaces.展开更多
We demonstrate a novel preparative strategy for the well-controlled MnCo_2O_(4.5)@MnO_2 hierarchical nanostructures.Bothδ-MnO_2 nanosheets andα-MnO_2 nanorods can uniformly decorate the surface of MnCo_2O_(4.5)nanow...We demonstrate a novel preparative strategy for the well-controlled MnCo_2O_(4.5)@MnO_2 hierarchical nanostructures.Bothδ-MnO_2 nanosheets andα-MnO_2 nanorods can uniformly decorate the surface of MnCo_2O_(4.5)nanowires to form core-shell heterostructures.Detailed electrochemical characterization reveals that MnCo_2O_(4.5)@δ-MnO_2 pattern exhibits not only high specific capacitance of 357.5 F g^(-1)at a scan rate of 0.5 A g^(-1),but also good cycle stability(97%capacitance retention after 1000 cycles at a scan rate of 5 A g^(-1)),which make it have a promising application as a supercapacitor electrode material.展开更多
The effect of synthesized nanostructures,including graphene oxide,chemically reduced graphene oxide with sodium dodecyl sulfate(SDS),chemically reduced graphene oxide with polyvinylpyrrolidone,and multi-walled carbon ...The effect of synthesized nanostructures,including graphene oxide,chemically reduced graphene oxide with sodium dodecyl sulfate(SDS),chemically reduced graphene oxide with polyvinylpyrrolidone,and multi-walled carbon nanotubes,on the kinetics of methane hydrate formation was investigated in this work.The experiments were carried out at a pressure of 4.5 MPa and a temperature of 0 ℃ in a batch reactor.By adding nanostructures,the induction time decreases,and the shortest induction time appeares at certain concentrations of reduced graphene oxide with SDS and graphene oxide,that is,at a concentration of 360 ppm for reduced graphene oxide with SDS and 180 ppm for graphene oxide,with a 98% decrease in induction time compared to that in pure water.Moreover,utilization of carbon nanostructures increases the amount and the rate of methane consumed during the hydrate formation process.Utilization of multi-walled carbon nanotubes with a concentration of 90 ppm showes the highest amount of methane consumption.The amount of methane consumption increases by 173% in comparison with that in pure water.The addition of carbon nanostructures does not change the storage capacity of methane hydrate in the hydrate formation process,while the percentage of water conversion to hydrate in the presence of carbon nanotubes increases considerably,the greatest value of which occurres at a 90 ppm concentration of carbon nanotubes,that is,a 253% increase in the presence of carbon nanotubes compared to that of pure water.展开更多
This article reviews recent advances in the utilization of various water based synthesis routes towards the shape-controlled synthesis of silver nanoparticles and microstructures in a diverse range of shapes and sizes...This article reviews recent advances in the utilization of various water based synthesis routes towards the shape-controlled synthesis of silver nanoparticles and microstructures in a diverse range of shapes and sizes from several nanometers to micrometers. A variety of very simple one-pot methods, at times employing com- mercial microwave ovens, inexpensive low power ultrasound cleaners, or two-electrode electro-chemistry, can be surprisingly effective in the controlled synthesis of a wide range of nanostructured products, if only parameters are carefully chosen. Many approaches which are adopted include synthesis of Ag nanostructures with various shapes in solution, doping of Ag nanoparticles on unmodified silica and on/inside carbon spheres, kinetically controlled growth of Ag micro-particles with novel nanostructures on flat substrates, and galvanic replace- ment towards bimetallic Ag-Au dendrites and carbon composites. Characterizations of shape, composition and microstructure are carried out via scanning and transmission electron microscopy, various spectroscopy methods, N2 absorption measurements and suchlike. The involved growth mechanisms are investigated in order to discover new means towards better control. Size, location and shape control, including micro- and nanostructure features, allows tuning the products properties towards desired applications. We focus on the optical properties and catalytic activities, but also the stability of compounds can be an issue of interest.展开更多
基金supported by the National Key Research Program of China under Grant No.2024YFA1408000the National Natural Science Foundation of China(52231007,12327804,T2321003,22088101)+1 种基金in part by the National Key Research Program of China under Grant 2021YFA1200600the support from the U.S.National Science Foundation(CHE 2102482)。
文摘The ability to control the electrode interfaces in an electrochemical energy storage system is essential for achieving the desired electrochemical performance.However,achieving this ability requires an in-depth understanding of the detailed interfacial nanostructures of the electrode under electrochemical operating conditions.In-situ transmission electron microscopy(TEM)is one of the most powerful techniques for revealing electrochemical energy storage mechanisms with high spatiotemporal resolution and high sensitivity in complex electrochemical environments.These attributes play a unique role in understanding how ion transport inside electrode nanomaterials and across interfaces under the dynamic conditions within working batteries.This review aims to gain an in-depth insight into the latest developments of in-situ TEM imaging techniques for probing the interfacial nanostructures of electrochemical energy storage systems,including atomic-scale structural imaging,strain field imaging,electron holography,and integrated differential phase contrast imaging.Significant examples will be described to highlight the fundamental understanding of atomic-scale and nanoscale mechanisms from employing state-of-the-art imaging techniques to visualize structural evolution,ionic valence state changes,and strain mapping,ion transport dynamics.The review concludes by providing a perspective discussion of future directions of the development and application of in-situ TEM techniques in the field of electrochemical energy storage systems.
基金supported by the National Research Foundation of Korea(NRF)grant funded by the Korean government(MSIP)(No.2018R1A6A1A03025708).
文摘High-performance aqueous zinc(Zn)-ion batteries(AZIBs)have emerged as one of the greatest favorable candidates for next-generation energy storage systems because of their low cost,sustainability,high safety,and eco-friendliness.In this report,we prepared magnesium vanadate(MgVO)-based nanostructures by a facile single-step solvothermal method with varying experimental reaction times(1,3,and 6 h)and investigated the effect of the reaction time on the morphology and layered structure for MgVO-based compounds.The newly prepared MgVO-1 h,MgVO-3 h and MgVO-6 h samples were used as cathode materials for AZIBs.Compared to the MgVO-1 h and MgVO-6 h cathodes,the MgVO-3 h cathode showed a higher specific capacity of 492.74 mA h g^(-1) at 1 A g^(-1) over 500 cycles and excellent rate behavior(291.58 mA h g^(-1) at 3.75 A g^(-1))with high cycling stability(116%)over 2000 cycles at 5 A g^(-1).Moreover,the MgVO-3 h electrode exhibited good electrochemical performance owing to its fast Zn-ion diffusion kinetics.Additionally,various ex-situ analyses confirmed that the MgVO-3 h cathode displayed excellent insertion/extraction of Zn^(2+)ions during charge and discharge processes.This study offers an efficient method for the synthesis of nanostructured MgVO-based cathode materials for high-performance AZIBs.
基金supported by the National key Research and Development Program of China(No.2022YFB3705200)the National Natural Science Foundation of China(Nos.U1804146,51905153,52111530068)+1 种基金the Science and Technology Innovation Team Project of Henan University of Science and Technology,China(No.2015XTD006)the Major Science and Technology Project of Henan Province,China(No.221100230200)。
文摘The effects of gradient nanostructures induced by supersonic fine particle bombardment(SFPB)on the surface integrity,microstructural evolution,and mechanical properties of a Ni-W-Co-Ta medium-heavy alloy(MHA)were systematically investigated.The results show that gradient nanostructures are formed on the surface of Ni-W-Co-Ta MHA after SFPB treatment.At a gas pressure of 1.0 MPa and an impact time of 60 s,the ultimate tensile strength and yield strength of the alloy reached the maximum values of 1236 MPa and 758 MPa,respectively,which are 22.5%and 38.8%higher than those of the solid solution treated alloy,and the elongation(46.3%)is close to that of the solid solution treated alloy,achieving the optimal strength–ductility synergy.However,microcracks appear on the surface with excessive gas pressure and impact time,generating the relaxed residual stress and decreased strength.With the increase of the impact time and gas pressure,the depth of the deformation layer and the surface microhardness gradually increase,reaching the maximum values(29μm and HV 451)at 1.0 MPa and 120 s.The surface grain size is refined to a minimum of 11.67 nm.Notably,SFPB treatment has no obvious effect on elongation,and the fracture mode changes from the ductile fracture before treatment to ductile–brittle mixed fracture after treatment.
基金supported by the National Natural Science Foundation of China(No.21971248)。
文摘Understanding the dynamic assembly process of DNA nanostructures is important for developing novel strategy to design and construct functional devices.In this work,temperature-controlled dynamic light scattering(DLS)strategy has been applied to study the global assembly process of DNA origami and DNA bricks.Through the temperature dependent size and intensity profiles,the self-assembly process of various DNA nanostructures with different morphologies have been well-studied and the temperature transition ranges could be observed.Taking advantage of the DLS information,rapid preparation of the DNA origami and the brick assembly has been realized through a constant temperature annealing.Our results demonstrate that the DLS-based strategy provides a convenient and robust tool to study the dynamic process of forming hieratical DNA structures,which will benefit understanding the mechanism of self-assembly of DNA nanostructures.
基金supported by National Natural Science Foundation of China(NSFC,Grant No.51972178)Natural Science Foundation of Ningbo(2022J139)Ningbo Yongjiang Talent Introduction Programme(2022A-227-G)
文摘Crystallineγ-Ga_(2)O_(3)@rGO core-shell nanostructures are synthesized in gram scale,which are accomplished by a facile sonochemical strategy under ambient condition.They are composed of uniformγ-Ga_(2)O_(3)nanospheres encapsulated by reduced graphene oxide(rGO)nanolayers,and their formation is mainly attributed to the existed opposite zeta potential between the Ga_(2)O_(3)and rGO.The as-constructed lithium-ion batteries(LIBs)based on as-fabricatedγ-Ga_(2)O_(3)@rGO nanostructures deliver an initial discharge capacity of 1000 mAh g^(-1)at 100 mA g^(-1)and reversible capacity of 600 mAh g^(-1)under 500 mA g^(-1)after 1000 cycles,respectively,which are remarkably higher than those of pristineγ-Ga_(2)O_(3)with a much reduced lifetime of 100 cycles and much lower capacity.Ex situ XRD and XPS analyses demonstrate that the reversible LIBs storage is dominant by a conversion reaction and alloying mechanism,where the discharged product of liquid metal Ga exhibits self-healing ability,thus preventing the destroy of electrodes.Additionally,the rGO shell could act robustly as conductive network of the electrode for significantly improved conductivity,endowing the efficient Li storage behaviors.This work might provide some insight on mass production of advanced electrode materials under mild condition for energy storage and conversion applications.
文摘This paper describes mass-based energy phase-space projection of microwave-assisted synthesis of transition metals (zinc oxide, palladium, silver, platinum, and gold) nanostructures. The projection uses process energy budget (measured in kJ) on the horizontal axes and process density (measured in kJg−1) on the vertical axes. These two axes allow both mass usage efficiency (Environmental-Factor) and energy efficiency to be evaluated for a range of microwave applicator and metal synthesis. The metrics are allied to the: second, sixth and eleventh principle of the twelve principle of Green Chemistry. This analytical approach to microwave synthesis (widely considered as a useful Green Chemistry energy source) allows a quantified dynamic environmental quotient to be given to renewable plant-based biomass associated with the reduction of the metal precursors. Thus allowing a degree of quantification of claimed “eco-friendly” and “sustainable” synthesis with regard to waste production and energy usage.
基金supported by the Basic Science Research Program through the National Research Foundation of Korea (NRF) funded by the Ministry of Education (2020R1I1A3052258)funded by Researcher Supporting Project number (RSP2024R117), King Saud University, Riyadh, Saudi Arabia
文摘This research focuses on the electric behavior of a mixed ferrielectric sulflower-like nanostructure.The structure includes a core with spin S_(i)^(Z)-1 atoms and a shell with spin σ_(j)^(Z)-5/2 atoms.The Blume–Capel model and the Monte Carlo technique(MCt)with the Metropolis algorithm are employed.Diagrams are established for absolute zero,investigating stable spin configurations correlated with various physical parameters.The MCt method explores phase transition behavior and electric hysteresis cycles under different physical parameters.
基金the Fujian Science Technology Innovation Laboratory for Optoelectronic Information of China (Nos.2021ZR105 and 2021ZZ103)financial support from the National Natural Science Foundation of China (Nos.22071246 and22033008)。
文摘MOF-based core-shell structures with high surface area, abundant active sites, and broad absorption bands are viable alternatives to traditional single-component photocatalysts. In this report, we describe the design and construction of delicate Ag nanowires@NH_(2)-UiO-66 with a core-shell structure for use as photocatalysts in imine synthesis under light. The optimized composites exhibited 80% imine production, which was higher than both MOF and Ag NWs. The significant improvement in photocatalytic activity under light may be attributed to the plasmonic effect of silver nanowires and their core-shell structure, which promotes the separation of electron-hole pairs. Moreover, the photocatalytic activity of the core-shell nanostructure may provide valuable insight into the design and construction of MOF-based composite photocatalysts for oxidative coupling of amines.
基金Project(10804101)supported by the National Natural Science Foundation of ChinaProject(2007CB815102)supported by the National Basic Research Program of ChinaProject(2007B08007)supported by the Science and Technology Development Foundation of Chinese Academy of Engineering Physics,China
文摘Triangular Au-Ag framework nanostructures （TFN） were synthesized via a multi-step galvanic replacement reaction （MGRR） of single-crystalline triangular silver nanoplates in a chlorauric acid （HAuCl4） solution at room temperature. The morphological, compositional, and crystal structural changes involved with reaction steps were analyzed by using transmission electron microscopy（TEM）, energy-dispersive X-ray spectrometry （EDX）, and X-ray diffraction. TEM combined with EDX and selected area electron diffraction confirmed the replacement of Ag with Au. The in-plane dipolar surface plasmon resonance （SPR） absorption band of the Ag nanoplates locating initially at around 700 nm gradually redshifted to 1 100 nm via a multi-stage replacement manner after 7 stages. The adding amount of HAuCl4 per stage influenced the average redshift value per stage, thus enabled a fine tuning of the in-plane dipolar band. A proposed formation mechanism of the original Ag nanoplates developing pores while growing Au nanoparticles covering this underlying structure at more reaction steps was confirmed by exploiting surface-enhanced Raman scattering （SERS）.
基金Project supported by the National Natural Science Foundation of China(Grant Nos.91850205 and 11904021).
文摘Chirality is ubiquitous in natural world.Although with similar physical and chemical properties,chiral enantiomers could play different roles in biochemical processes.Discrimination of chiral enantiomers is extremely important in biochemical,analytical chemistry,and pharmaceutical industries.Conventional chiroptical spectroscopic methods are disadvantageous at a limited detection sensitivity because of the weak signals of natural chiral molecules.Recently,superchiral fields were proposed to effectively enhance the interaction between light and molecules,allowing for ultrasensitive chiral detection.Intensive theoretical and experimental works have been devoted to generation of superchiral fields based on artificial nanostructures and their application in ultrasensitive chiral sensing.In this review,we present a survey on these works.We begin with the introduction of chiral properties of electromagnetic fields.Then,the optical chirality enhancement and ultrasensitive chiral detection based on chiral and achiral nanostructures are discussed respectively.Finally,we give a short summary and a perspective for the future ultrasensitive chiral sensing.
基金financial support from USACH-Chile, Council of Scientific and Industrial Research (CSIR) and University Grant Commission (UGC) New Delhi, India
文摘Micron sized hexagon- and flower-like nanostructures of lead oxide（α-PbO2） have been synthesized by very simple and cost effective route of anodic oxidation of lead sheet. These structures were easily obtained by the simple variation of applied voltage from 2-6 V between the electrodes. Lead sheet was used as an anode and platinum sheet served as a cathode. Anodic oxidation at 2 V resulted in the variable edge sized（1-2 μm） hexagon-like structures in the electrolyte. When the applied potential was increased to 4 V a structure of distorted hexagons consisting of some flower-like structures were obtained. Further increment of potential up to 6 V resulted in flower like structures of α-PbO2 having six petals. The diameter of the flower-like structures was 200-500 nm and the size of a petal was 100-200 nm.
基金the Deanship of Scientific Research, Najran University, Najran, Kingdom of Saudi Arabia for all financial support
文摘ZnO-CeO2 nanostructures were synthesized by simple and effcient low temperature method. The structure and morphology of the ZnO-CeO2 nanostructures were characterized by X-ray powder diffraction （XRD） and field emission scanning electron microscopy （FESEM）, which revealed elongated shaped CeO2 nanoparticles with diameters of 40–90 nm distributed on the surface of elongated ZnO nanostructures with diameters of 50–200 nm （edge–centre）. Further the structure of the synthesized ZnO-CeO2 nanostructure was supported by Raman spectra and Fourier transform infrared spectroscopy （FTIR）. UV-vis absorption spectrum was used to confirm the optical properties of the CeO2 doped ZnO nanostructures. Photo-catalytic activity of CeO2 doped ZnO nanostructure was evaluated by degradation of acridine orange and methylene blue which degraded 84.55% and 48.65% in 170 min, respectively. ZnO-CeO2 nanostructures also showed good sensitivity （0.8331 μA·cm-2·（mol/l）-1） in short response time （10 s） by applying to chemical sensing using ethanol as a target compound by I-V technique. These degradation and chemical sensing properties of ZnO-CeO2 nanostructures are of great importance for the application of ZnO-CeO2 system as a photo-catalyst and chemical sensor.
基金financially supported by the National Natural Science Foundation of China(No.51907193 and No.51677182)the Dalian National Laboratory(DNL)for Clean Energy Cooperation Fund,CAS(No.DNL201915 and No.DNL201912)+2 种基金the Beijing Municipal Science and Technology Commission(No.Z181100000118006)the Key Research Program of Frontier Sciences,CAS(No.ZDBS-LY-JSC047)the Youth Innovation Promotion Association,CAS(No.2020000022)。
文摘The burgeoning global economy during the past decades gives rise to the continuous increase in fossil fuels consumption and rapid growth of CO_(2) emission,which demands an urgent exploration into green and sustainable devices for energy storage and power management.Supercapacitors based on activated carbon electrodes are promising systems for highly efficient energy harvesting and power supply,but their promotion is hindered by the moderate energy density compared with batteries.Therefore,scalable conversion of CO_(2) into novel carbon nanostructures offers a powerful alternative to tackle both issues:mitigating the greenhouse effect caused by redundant atmospheric CO_(2) and providing carbon materials with enhanced electrochemical performances.In this tutorial review,the techniques,opportunities and barriers in the design and fabrication of advanced carbon materials using CO_(2) as feedstock as well as their impact on the energy-storage performances of supercapacitors are critically examined.In particular,the chemical aspects of various Cv2 conversion reactions are highlighted to establish a detailed understanding for the science and technology involved in the microstructural evolution,surface engineering and porosity control of CO_(2)-converted carbon nanostructures.Finally,the prospects and challenges associated with the industrialization of CO_(2) conversion and their practical application in supercapacitors are also discussed.
基金financial support from Ningbo Municipal Government (Innovation Team 2012882011,3315 Plan,2014A35001-1)the EPSRC (EP/J000582/1,GR/R68078)
文摘Metal organic frameworks(MOFs) represent a class of porous material which is formed by strong bonds between metal ions and organic linkers. By careful selection of constituents, MOFs can exhibit very high surface area, large pore volume, and excellent chemical stability.Research on synthesis, structures and properties of various MOFs has shown that they are promising materials for many applications, such as energy storage, gas storage, heterogeneous catalysis and sensing. Apart from direct use, MOFs have also been used as support substrates for nanomaterials or as sacrificial templates/precursors for preparation of various functional nanostructures. In this review, we aim to present the most recent development of MOFs as precursors for the preparation of various nanostructures and their potential applications in energy-related devices and processes. Specifically, this present survey intends to push the boundaries and covers the literatures from the year 2013 to early 2017,on supercapacitors, lithium ion batteries, electrocatalysts, photocatalyst, gas sensing, water treatment, solar cells, and carbon dioxide capture.Finally, an outlook in terms of future challenges and potential prospects towards industrial applications are also discussed.
基金financially supported by the National Natural Science Foundation of China(Nos.22071172,21902148,12205165,50835002 and 51105102)。
文摘Chirality,the property that an object cannot coincide with its mirror image arising from lack of mirror symmetry,is ubiquitous in nature at various length scales.The physical and chemical properties are strongly related to the nature of chiral complexes,playing a significant role in various fields such as photonics,biochemistry,medicine and catalysis.In particular,the recent flexible design of chiral metal nanostructures offers one platform for deeply understanding the origin of chirality and one roadmap for the precise construction of chiral nanomaterials directed by the applications.Herein,we summarize the different geometries and classical synthetic approaches to chiral noble metal nanomaterials.Moreover,chiroptical properties and potential applications of chiral metal nanostructures are discussed as well.Finally,the opportunities and challenges toward the synthesis and application of chiral metal nanostructures are proposed.
基金supported by the EU-China EcoFuel project(FP7,246772)from the European Commission
文摘Photoelectrochemical(PEC) water splitting using solar energy has attracted great attention for generation of renewable hydrogen with less carbon footprint, while there are enormous challenges that still remain for improving solar energy water splitting efficiency, due to limited light harvesting, energy loss associated to fast recombination of photogenerated charge carriers, as well as electrode degradation. This overview focuses on the recent development about catalyst nanomaterials and nanostructures in different PEC water splitting systems. As photoanode, Au nanoparticle-decorated TiO_2 nanowire electrodes exhibited enhanced photoactivity in both the UV and the visible regions due to surface plasmon resonance of Au and showed the largest photocurrent generation of up to 710 nm. Pt/Cd S/CGSe electrodes were developed as photocathode. With the role of p–n heterojunction, the photoelectrode showed high stability and evolved hydrogen continuously for more than 10 days. Further, in the Z-scheme system(Bi_2S_3/TNA as photoanode and Pt/Si PVC as photocathode at the same time), a self-bias(open-circuit voltage Voc= 0.766 V) was formed between two photoelectrodes, which could facilitate photogenerated charge transfers and enhance the photoelectrochemical performance, and which might provide new hints for PEC water splitting. Meanwhile, the existing problems and prospective solutions have also been reviewed.
基金This research is supported by National Natural Science Foundation of China(Nos.52075557,51805553)Natural Science Foundation of Hunan Province(No.2021JJ20067)+1 种基金The Science and Technology Innovation Program of Hunan Province(No.2021RC3011)Open access funding provided by Shanghai Jiao Tong University
文摘Versatile liquid manipulating surfaces combining patternable and controllable wettability have recently motivated considerable attention owing to their significant advantages in droplet-solid impacting behaviors,microdroplet self-removal,and liquid–liquid interface reaction applications.However,developing a facile and efficient method to fabricate these versatile surfaces remains an enormous challenge.In this paper,a strategy for the fabrication of liquid manipulating surfaces with patternable and controllable wettability on Polyimide(PI)film based on femtosecond laser thermal accumulation engineering is proposed.Because of its controllable micro-/nanostructures and chemical composition through adjusting the local thermal accumulation,the wettability of PI film can be tuned from superhydrophilicity(~3.6°)to superhydrophobicity(~151.6°).Furthermore,three diverse surfaces with patternable and heterogeneous wettability were constructed and various applications were successfully realized,including water transport,droplet arrays,and liquid wells.This work may provide a facile strategy for achieving patternable and controllable wettability efficiently and developing multifunctional liquid steering surfaces.
基金financial supports provided by National Natural Science Foundation of China(Grant no.51104194 and 51104121)International S&T Cooperation Projects of Chongqing(CSTC 2013 gjhz90001)+1 种基金National Key laboratory of Fundamental Science of Micro/Nano-device and System Technology(2013MS06,Chongqing University)State Education Ministry and Fundamental Research Funds for the Central Universities(Project no.CDJZR14135501 and CDJZR13130036,Chongqing University,PR China)
文摘We demonstrate a novel preparative strategy for the well-controlled MnCo_2O_(4.5)@MnO_2 hierarchical nanostructures.Bothδ-MnO_2 nanosheets andα-MnO_2 nanorods can uniformly decorate the surface of MnCo_2O_(4.5)nanowires to form core-shell heterostructures.Detailed electrochemical characterization reveals that MnCo_2O_(4.5)@δ-MnO_2 pattern exhibits not only high specific capacitance of 357.5 F g^(-1)at a scan rate of 0.5 A g^(-1),but also good cycle stability(97%capacitance retention after 1000 cycles at a scan rate of 5 A g^(-1)),which make it have a promising application as a supercapacitor electrode material.
文摘The effect of synthesized nanostructures,including graphene oxide,chemically reduced graphene oxide with sodium dodecyl sulfate(SDS),chemically reduced graphene oxide with polyvinylpyrrolidone,and multi-walled carbon nanotubes,on the kinetics of methane hydrate formation was investigated in this work.The experiments were carried out at a pressure of 4.5 MPa and a temperature of 0 ℃ in a batch reactor.By adding nanostructures,the induction time decreases,and the shortest induction time appeares at certain concentrations of reduced graphene oxide with SDS and graphene oxide,that is,at a concentration of 360 ppm for reduced graphene oxide with SDS and 180 ppm for graphene oxide,with a 98% decrease in induction time compared to that in pure water.Moreover,utilization of carbon nanostructures increases the amount and the rate of methane consumed during the hydrate formation process.Utilization of multi-walled carbon nanotubes with a concentration of 90 ppm showes the highest amount of methane consumption.The amount of methane consumption increases by 173% in comparison with that in pure water.The addition of carbon nanostructures does not change the storage capacity of methane hydrate in the hydrate formation process,while the percentage of water conversion to hydrate in the presence of carbon nanotubes increases considerably,the greatest value of which occurres at a 90 ppm concentration of carbon nanotubes,that is,a 253% increase in the presence of carbon nanotubes compared to that of pure water.
基金supported by the National Basic Research Program of China (No.2010CB631004)the National Natural Science Foundation of China (No.50831004)Doctoral Fund of Ministry of Education of China (No.20090091120034)
文摘This article reviews recent advances in the utilization of various water based synthesis routes towards the shape-controlled synthesis of silver nanoparticles and microstructures in a diverse range of shapes and sizes from several nanometers to micrometers. A variety of very simple one-pot methods, at times employing com- mercial microwave ovens, inexpensive low power ultrasound cleaners, or two-electrode electro-chemistry, can be surprisingly effective in the controlled synthesis of a wide range of nanostructured products, if only parameters are carefully chosen. Many approaches which are adopted include synthesis of Ag nanostructures with various shapes in solution, doping of Ag nanoparticles on unmodified silica and on/inside carbon spheres, kinetically controlled growth of Ag micro-particles with novel nanostructures on flat substrates, and galvanic replace- ment towards bimetallic Ag-Au dendrites and carbon composites. Characterizations of shape, composition and microstructure are carried out via scanning and transmission electron microscopy, various spectroscopy methods, N2 absorption measurements and suchlike. The involved growth mechanisms are investigated in order to discover new means towards better control. Size, location and shape control, including micro- and nanostructure features, allows tuning the products properties towards desired applications. We focus on the optical properties and catalytic activities, but also the stability of compounds can be an issue of interest.
