The fabrication of a new type of one-dimensional Au-Ag porous nanotube（NPT） structure was presented based on a facile combination of nanocrystal growth and surface modification.Ag nanowires with various diameters we...The fabrication of a new type of one-dimensional Au-Ag porous nanotube（NPT） structure was presented based on a facile combination of nanocrystal growth and surface modification.Ag nanowires with various diameters were firstly served as the chemical plating templates via a polyol-process.Then,one-dimensional（1D） Au-Ag porous nanostructures with tailored structural features could be prepared by controlling the individual steps involved in this process,such as nanowire growth,surface modification,thermal diffusion,and dealloying.Structural characterizations reveal these Au-Ag porous nanotubes,non-porous nanotubes and porous nanowires possess novel nano-architectures with multimodal open porosity and excellent structural continuity and integrity,which make them particularly desirable as novel 1D nanocarriers for biomedical,drug delivery and sensing applications.展开更多
One-dimensional （1D） nanomaterials and nanostructures have received much attention due to their potential interest for understanding fundamental physical concepts and for applications in constructing nanoscale elect...One-dimensional （1D） nanomaterials and nanostructures have received much attention due to their potential interest for understanding fundamental physical concepts and for applications in constructing nanoscale electric and optoelectronic devices. Zinc sulfide （ZnS） is an important semiconductor compound of Ⅱ-Ⅵ group, and the synthesis of 1D ZnS nanomaterials and nanostructures has been of growing interest owing to their promising application in nanoscale optoelectronic devices. This paper reviews the recent progress on 1D ZnS nanomaterials and nanostructures, including nanowires, nanowire arrays, nanorods, nanobelts or nanoribbons, nanocables, and hierarchical nanostructures etc. This article begins with a survey of various methods that have been developed for generating 1D nanomaterials and nanostructures, and then mainly focuses on structures, synthesis, characterization, formation mechanisms and optical property tuning, and luminescence mechanisms of 1D ZnS nanomaterials and nanostructures. Finally, this review concludes with personal views towards future research on 1D ZnS nanomaterials and nanostructures.展开更多
The synthesis of one-dimensional （1D） semiconductor nanostructures has been studied intensively for a wide range of materials due to their unique structural and physical properties and promising potential for future...The synthesis of one-dimensional （1D） semiconductor nanostructures has been studied intensively for a wide range of materials due to their unique structural and physical properties and promising potential for future technological applications. Among various strategies for synthesizing 1D semiconductor nanostructures, solution-phase synthetic routes are advantageous in terms of cost, throughput, modulation of composition, and the potential for large-scale and environmentally benign production. This article gives a concise review on the recent developments in the solution-phase synthesis of ID semiconductor nanostructures of different compositions, sizes, shapes, and architectures. We first introduce several typical solution-phase synthetic routes based on controlled precipitation from homogeneous solutions, including hydrothermal/solvothermal process, solution-liquid-solid （SLS） process, high-temperature organic-solution process, and low-temperature aqueous-solution process. Subsequently, we discuss two solution-phase synthetic strategies involving solid tem- plates or substrates, such as the chemical transformation of 1D sacrificial templates and the oriented growth of 1D nanostructure arrays on solid substrates. Finally, prospects of the solution-phase approaches to 1D semiconductor nanostructures will be briefly discussed.展开更多
Aluminum nitride （AIN） nanowires, serrated nanoribbons, and nanoribbons were selectively obtained through a simple chloride assisted chemical vapor deposition process. The morphologies of the products could be contr...Aluminum nitride （AIN） nanowires, serrated nanoribbons, and nanoribbons were selectively obtained through a simple chloride assisted chemical vapor deposition process. The morphologies of the products could be controlled by adjusting the deposition position and the flux of the reactant gas. The morphologies and structures of the AIN products were investigated in detail. The formation mechanism of the as-prepared different morphologies of AIN one-dimensional （ID） nanostructures was discussed on the basis of the experimental results.展开更多
We designed and constructed a new family of 608 dendritic dipyridyl donors, from which two novel triangular metallodendrimers were successfully prepared via coordination-driven self-assembly.Inspired by the existence ...We designed and constructed a new family of 608 dendritic dipyridyl donors, from which two novel triangular metallodendrimers were successfully prepared via coordination-driven self-assembly.Inspired by the existence of multiple intermolecular interactions（e.g., p–p stacking and CH–p interactions） imposed by the DMIP-functionalized poly（benzyl ether） dendrons, their hierarchical selfassembly behaviors were studied in various mixed solvents by using scanning electron microscopy（SEM）. Interestingly, it was found that the morphologies of the obtained metallodendrimers were highly depended on the dendron generation. For example, the first-generation metallodendrimer was able to hierarchically self-assemble into the spherical nanostructures in various mixed solvents. However, the nanofibers were observed for the second-generation metallodendrimer under the similar conditions.Furthermore, the driven force for the formation of such ordered nanostructures was investigated by using1 H NMR and fluorescence spectroscopy.展开更多
Searching for one-dimensional(1D)nanostructure with ferromagnetic(FM)half-metallicity is of significance for the development of miniature spintronic devices.Here,based on the first-principles calculations,we propose t...Searching for one-dimensional(1D)nanostructure with ferromagnetic(FM)half-metallicity is of significance for the development of miniature spintronic devices.Here,based on the first-principles calculations,we propose that the 1D CrN nanostructure is a FM half-metal,which can generate the fully spin-polarized current.The ab initio molecular dynamic simulation and the phonon spectrum calculation demonstrate that the 1D CrN nanostructure is thermodynamically stable.The partially occupied Cr-d orbitals endow the nanostructure with FM half-metallicity,in which the half-metallic gap(?s)reaches up to 1.58 eV.The ferromagnetism in the nanostructure is attributed to the superexchange interaction between the magnetic Cr atoms,and a sizable magnetocrystalline anisotropy energy(MAE)is obtained.Moreover,the transverse stretching of nanostructure can effectively modulate?s and MAE,accompanied by the preservation of half-metallicity.A nanocable is designed by encapsulating the CrN nanostructure with a BN nanotube,and the intriguing magnetic and electronic properties of the nanostructure are retained.These novel characteristics render the 1D CrN nanostructure as a compelling candidate for exploiting high-performance spintronic devices.展开更多
In recent years,one-dimensional(1D)nanomaterials have raised researcher's interest because of their unique structur-al characteristic to generate and confine the optical signal and their promising prospects in pho...In recent years,one-dimensional(1D)nanomaterials have raised researcher's interest because of their unique structur-al characteristic to generate and confine the optical signal and their promising prospects in photonic applications.In this re-view,we summarized the recent research advances on the spectroscopy and carrier dynamics of 1D nanostructures.First,the condensation and propagation of exciton-polaritons in nanowires(NWs)are introduced.Second,we discussed the properties of 1D photonic crystal(PC)and applications in photonic-plasmonic structures.Third,the observation of topological edge states in 1D topological structures is introduced.Finally,the perspective on the potential opportunities and remaining chal-lenges of 1D nanomaterials is proposed.展开更多
Grain coalescence has been applied in many areas of nanofabrication technology, including modification of thinfilm properties, nanowelding, and self-assembly of nanostructures. However, very few systematic studies of ...Grain coalescence has been applied in many areas of nanofabrication technology, including modification of thinfilm properties, nanowelding, and self-assembly of nanostructures. However, very few systematic studies of selfassembly using the grain coalescence, especially for threedimensional(3D) nanostructures, exist at present. Here, we investigate the mechanism of plasma triggered grain coalescence to achieve the precise control of nanoscale phase and morphology of the grain coalescence induced by exothermic energy. Exothermic energy is generated through etching a silicon substrate via application of plasma. By tuning the plasma power and the flow rates of reactive gases, different etching rates and profiles can be achieved, resulting in various morphologies of grain coalescence. Balancing the isotropic/anisotropic substrate etching profile and the etching rate makes it possible to simultaneously release 2D nanostructures from the substrate and induce enough surface tension force,generated by grain coalescence, to form 3D nanostructures.Diverse morphologies of 3D nanostructures have been obtained by the grain coalescence, and a strategy to achieve self-assembly, resulting in desired 3D nanostructures, has been proposed and demonstrated.展开更多
An asymmetrical perylene diimide 3, N-（4-methoxyphenyl）-N＇-（4-nitrophenyl）-perylene-3,4,9,10-tetracarboxylic diimide, was synthesized, and its self-assembly and dissociation behaviors in chloroform was studied in...An asymmetrical perylene diimide 3, N-（4-methoxyphenyl）-N＇-（4-nitrophenyl）-perylene-3,4,9,10-tetracarboxylic diimide, was synthesized, and its self-assembly and dissociation behaviors in chloroform was studied in detail by UV-vis and fluorescence spectroscopies. The resulting unique helical nanostructures from 3 were proposed to be self-assembled via the cooperative actions of π-π stacking, steric hindrance and electrophile-nucleophile type pairing.展开更多
The self-assembling behavior of random copolymers of sodium 2-(acrylamido)-2-methylpropanesulfonate (AMPS)and hydrophobic comonomers possessing dodecyl groups linked by various spacer bonds was discussed with a focus ...The self-assembling behavior of random copolymers of sodium 2-(acrylamido)-2-methylpropanesulfonate (AMPS)and hydrophobic comonomers possessing dodecyl groups linked by various spacer bonds was discussed with a focus on theeffect of the spacer. The characterization of association behavior of such polymers in water using quasielastic light scattering,capillary electrophoresis, NMR relaxation, various fluorescence, and viscoelastic methods was described. These copolymersform a variety of self-assembled nanostructures depending on the type of the spacer. Random copolymers of AMPS and N-dodecylmethacrylamide show a strong preference for intrapolymer self-association even in concentrated aqueous solutionsforming single-macromolecular self-assemblies (unimolecular micelles). In contrast, random copolymers of AMPS anddodecyl methacrylate are prone to undergo interpolymer associations yielding multipolymer micelles. In random copolymersof AMPS and a methacrylate substituted a nonionic surfactant (HO(CH_2CH_2O)_(25)C_(12)H_(25)) (C_(12)E_(25)), dodecyl groups are muchless restricted by the polymer backbone because they are linked via a long, flexible hydrophilic spacer. Thus, the polymer-bound C_(12)E_(25) surfactant moieties form micelles similar to those formed by discrete surfactants, but they are bridged bypolymer chains forming a network structure.展开更多
Iron（Ⅲ）-doped nanostructure TiO2-coated SiO2 （TiO2/SiO2） particles were prepared using the layer-by-layer assembly technique and their photocatalytic property was studied. TiO2 colloids were synthesized employing...Iron（Ⅲ）-doped nanostructure TiO2-coated SiO2 （TiO2/SiO2） particles were prepared using the layer-by-layer assembly technique and their photocatalytic property was studied. TiO2 colloids were synthesized employing the sol-gel method with TiChas a precursor. The samples were characterized by Fourier transform infrared spectroscopy （FTIR）, SEM, EDS, XPS, and XRD. The experimental results show that TiO2 nanopowders on the surface of SiO2 particles are well distributed, the amount of TiO2 is increased with the adding of coating layers, the pure anatase-TiO2 coating layers are synthesized at 500℃, and the photocatalytic activity of Fe^3＋-doped TiO2/SiO2 is higher than that of undoped TiO2/SiO2.展开更多
The peony-like CuO micro/nanostructures were fabricated by a facile hydrothermal approach. The peony- like CuO micro/nanostructures about 3 -5μm in diameter were assembled by CuO nanoplates. These CuO nanoplates, as ...The peony-like CuO micro/nanostructures were fabricated by a facile hydrothermal approach. The peony- like CuO micro/nanostructures about 3 -5μm in diameter were assembled by CuO nanoplates. These CuO nanoplates, as the building block, were self-assembled into multilayer structures under the action of ethidene diamine, and then grew into uniform peony-like CuO architecture. The novel peony-like CuO micro/nanostructures exhibit a high cycling stability and improved rate capability. The peony-like CuO microJnanostructures electrodes show a high reversible capacity of 456 mAhJg after 200 cycles, much higher than that of the commercial CuO nanocrystals at a current 0.1 C. The excellent electrochemical performance of peony-like CuO micro/nanostructures might be ascribed to the unique assembly structure, which not only provide large electrode/electrolyte contact area to accelerate the lithiation reaction, but also the interval between the multilayer structures of CuO nanoplates electrode could provide enough interior space to accommodate the volume change during Li insertion and de-insertion process,展开更多
One-dimensional(1D) GaN nanomaterials exhibiting various morphologies and atomic structures were prepared via ammoniation of either Ga_2O_3 nanoribbons, Ga_2O_3 nanorods or Ga nanowires filled into carbon nanotubes(CN...One-dimensional(1D) GaN nanomaterials exhibiting various morphologies and atomic structures were prepared via ammoniation of either Ga_2O_3 nanoribbons, Ga_2O_3 nanorods or Ga nanowires filled into carbon nanotubes(CNTs). The 1D GaN nanomaterials transformed from Ga_2O_3 nanoribbons consisted of numerous GaN nanoplatelets having the close-packed plane, i.e.(0002)2H or(111)3C parallel to the axes of starting nanoribbons. The 1D GaN nanomaterials converted from Ga_2O_3 nanorods were polycrystalline rods covered with GaN nanoparticles along the axes. The 1D GaN nanomaterials prepared from Ga nanowires filled into CNTs displayed two dominant morphologies:(i) single crystalline Ga N nanocolumns coated by CNTs, and(ii) pure single crystalline Ga N nanowires. The cross-sectional shape of Ga N nanowires were analyzed through the transmission electron microscopy(TEM) images. Formation mechanism of all-mentioned 1D GaN nanomaterials is then thoroughly discussed.展开更多
Structural DNA nanotechnology, an emerging technique that utilizes the nucleic acid molecule as generic polymer to programmably assemble well-defined and nano-sized architectures, holds great promise for new material ...Structural DNA nanotechnology, an emerging technique that utilizes the nucleic acid molecule as generic polymer to programmably assemble well-defined and nano-sized architectures, holds great promise for new material synthesis and constructing functional nanodevices for different purposes. In the past three decades, rapid development of this technique has enabled the syntheses of hundreds and thousands of DNA nanostructures with various morphologies at different scales and dimensions. Among them, discrete three-dimensional （3D） DNA nanostructures not only represent the most advances in new material design, but also can serve as an excellent platform for many important applications. With precise spatial addressability and capability of arbitrary control over size, shape, and function, these nanostructures have drawn particular interests to scientists in different research fields. In this review article, we will briefly summarize the development regarding the synthesis of discrete DNA 3D nanostructures with various size, shape, geometry, and topology, including our previous work and recent progress by other groups. In detail, three methods majorly used to synthesize the DNA 3D objects will be introduced accordingly. Additionally, the principle, design rule, as well as pros and cons of each method will be highlighted. As functions of these discrete 3D nanostructures have drawn great interests to researchers, we will further discuss their cutting-edge applications in different areas, ranging from novel material synthesis, new device fabrication, and biomedical applications, etc. Lastly, challenges and outlook of these promising nanostructures will be given based on our point of view.展开更多
A facile approach for constructing diverse architectures of unmodified C60 was developed via simple evaporation of pure C60 solution in CS2 under various poor solvent atmospheres. Diverse architectures such as belts, ...A facile approach for constructing diverse architectures of unmodified C60 was developed via simple evaporation of pure C60 solution in CS2 under various poor solvent atmospheres. Diverse architectures such as belts, sheets, and starfishes were successfully constructed under different experimental conditions. C60 belts obtained under EtOH atmosphere were confirmed to be a face-centered cubic （fcc） structure. The solvent atmospheres not only slowed clown the evaporation speed, but also could reorganize the self-assembly of C60 by partially re-dissolving the initially formed architectures. This concept represents a novel method for preparation of nanostructures of C60 and could also be applied for controlling of the self-assembly of other functional organic molecules.展开更多
Under appropriate physicochemical conditions, short peptide fragments and their synthetic mimics have been shown to form elongated cross-fl nanostructures through self-assembly. The self-assembly process and the resul...Under appropriate physicochemical conditions, short peptide fragments and their synthetic mimics have been shown to form elongated cross-fl nanostructures through self-assembly. The self-assembly process and the resultant peptide nanos- tructures are not only related to neurodegenerative diseases but also provide inspiration for the development of novel bionanomaterials. Both experimental and theoretical studies on peptide self-assembly have shown that the self-assembly process spans multiple time and length scales and is hierarchical, β-sheet self-assembly consists of three sub-processes from the microscopic to the mesoscopic level： β-sheet locking, lateral stacking, and morphological transformation. De- tailed atomistic simulation studies have provided insight into the early stages of peptide nanostructure formation and the interplay between different non-covalent interactions at the microscopic level. This review gives a brief introduction of the hierarchical peptide self-assembly process and focuses on the roles of various non-covalent interactions in the sub-processes based on recent simulation, experimental, and theoretical studies.展开更多
An interesting order-order transition between two different complex nanostructures was observed in a new liquid crystalline linear coil-coil-rod ABC triblock copolymer（tri BCP）. First, the ABC tri BCP, poly（dimethy...An interesting order-order transition between two different complex nanostructures was observed in a new liquid crystalline linear coil-coil-rod ABC triblock copolymer（tri BCP）. First, the ABC tri BCP, poly（dimethylsiloxane）-bpolystyrene-b-poly{2,5-bis[（4-methoxyphenyl）oxycarbonyl]styrene}（PDMS-b-PS-b-PMPCS）, was synthesized through sequential atom transfer radical polymerization. The degrees of polymerization of PDMS, PS, and PMPCS blocks are 58, 159, and 106, and the corresponding volume fractions of PDMS, PS, and PMPCS are 0.09, 0.29, and 0.62, respectively. The phase behaviors of the PDMS-b-PS diblock copolymer precursor and the final triblock copolymer were studied by smallangle X-ray scattering, one-dimensional wide-angle X-ray scattering, and transmission electron microscopy experiments. The PDMS-b-PS precursor self-assembles into hexagonally packed cylinders with a relatively small periodic size after thermal annealing. When the triblock copolymer is annealed at a relatively low temperature（120 ○C） at which the PMPCS block is in the amorphous state, the tri BCP forms core-shell hexagonally packed cylinders（CSH） with a relativly large periodic size. After the tri BCP is annealed above 140 ○C at which the PMPCS block transforms to the liquid crystalline（LC） phase, the nanophase-separated structure transforms to a three-phase four-layer lamellar structure（LAM-3P4L）. Thus, accompanied with the transition of the PMPCS blocks from the amorphous state to the LC phase, the order-order transition from CSH to LAM-3P4 L occurs in the PDMS-b-PS-b-PMPCS ABC tri BCP.展开更多
Here,we use two important biomaterials,protein and DNA,to construct self-assembled linear nanostructures through Watson-Crick base-paring of DNAs.We apply a simple magnetic separation method to purify traptavidin-DNA ...Here,we use two important biomaterials,protein and DNA,to construct self-assembled linear nanostructures through Watson-Crick base-paring of DNAs.We apply a simple magnetic separation method to purify traptavidin-DNA co njugates,and demonstrate synthesis of linear arrays of traptavidinDNA conjugates via the step-growth polymerization approach with pre-determined DNA sequences.Using the traptavidin-DNA array as a template,we assemble gold nanoparticles to form linear plasmonic nanostructures in a programmable manner.The traptavidin-DNA conjugates thus provide a convenient platform for one-dimensional assembly of biotinylated nanomaterials for many biomedical applications from drug delivery to bio-sensing.展开更多
In order to exploit the outstanding physical properties of one-dimensional （1D） nanostructures such as carbon nanotubes and semiconducting nanowires and nanorods in future technological applications, it will be nece...In order to exploit the outstanding physical properties of one-dimensional （1D） nanostructures such as carbon nanotubes and semiconducting nanowires and nanorods in future technological applications, it will be necessary to organize them on surfaces with precise control over both position and orientation. Here, we use a 1D rigid DNA motif as a model for studying directed assembly at the molecular scale to lithographically patterned nanodot anchors. By matching the inter-nanodot spacing to the length of the DNA nanostructure, we are able to achieve nearly 100% placement yield. By varying the length of single-stranded DNA linkers bound covalently to the nanodots, we are able to study the binding selectivity as a function of the strength of the binding interactions. We analyze the binding in terms of a thermodynamic model which provides insight into the bivalent nature of the binding, a scheme that has general applicability for the controlled assembly of a broad range of functional nanostructures.展开更多
Bottom-up approach to constructing low-dimensional nanostructures on surfaces with terminal alkynes has drawn great interest because of its potential applications in fabricating advanced functional nanomaterials. The ...Bottom-up approach to constructing low-dimensional nanostructures on surfaces with terminal alkynes has drawn great interest because of its potential applications in fabricating advanced functional nanomaterials. The diversity of the achieved products manifests rich chemistry of terminal alkynes and hence careful linking strategies and proper controlling methodologies are required for selective preparations of high-quality target nanoarchitectures. This review summarizes various on-surface linking strategies for terminal alkynes, including non-bonding interactions as well as organometallic and covalent bonds, and presents examples to show effective control of surface assemblies and reactions of terminal alkynes by variations of the precursor structures, substrates and activation modes. Systematic studies of the on-surface linkage of terminal alkynes may help efficient and predictable preparations of surface nanomaterials and further understanding of surface chemistry.展开更多
基金Project (2012CB932800) supported by the National Basic Research Program of ChinaProject (2012M521330) supported by China Postdoctoral Science Foundation
文摘The fabrication of a new type of one-dimensional Au-Ag porous nanotube（NPT） structure was presented based on a facile combination of nanocrystal growth and surface modification.Ag nanowires with various diameters were firstly served as the chemical plating templates via a polyol-process.Then,one-dimensional（1D） Au-Ag porous nanostructures with tailored structural features could be prepared by controlling the individual steps involved in this process,such as nanowire growth,surface modification,thermal diffusion,and dealloying.Structural characterizations reveal these Au-Ag porous nanotubes,non-porous nanotubes and porous nanowires possess novel nano-architectures with multimodal open porosity and excellent structural continuity and integrity,which make them particularly desirable as novel 1D nanocarriers for biomedical,drug delivery and sensing applications.
基金The authors acknowledge the support from the National Major Project of Fundamental Research:Nanomaterials and Nanostructures(Grant No.2005CB623603)the National Natural Science Foundation of China(Grant Nos.10304018,10574131)Special Fund for President Scholarship,Chinese Academy of Sciences.
文摘One-dimensional （1D） nanomaterials and nanostructures have received much attention due to their potential interest for understanding fundamental physical concepts and for applications in constructing nanoscale electric and optoelectronic devices. Zinc sulfide （ZnS） is an important semiconductor compound of Ⅱ-Ⅵ group, and the synthesis of 1D ZnS nanomaterials and nanostructures has been of growing interest owing to their promising application in nanoscale optoelectronic devices. This paper reviews the recent progress on 1D ZnS nanomaterials and nanostructures, including nanowires, nanowire arrays, nanorods, nanobelts or nanoribbons, nanocables, and hierarchical nanostructures etc. This article begins with a survey of various methods that have been developed for generating 1D nanomaterials and nanostructures, and then mainly focuses on structures, synthesis, characterization, formation mechanisms and optical property tuning, and luminescence mechanisms of 1D ZnS nanomaterials and nanostructures. Finally, this review concludes with personal views towards future research on 1D ZnS nanomaterials and nanostructures.
文摘The synthesis of one-dimensional （1D） semiconductor nanostructures has been studied intensively for a wide range of materials due to their unique structural and physical properties and promising potential for future technological applications. Among various strategies for synthesizing 1D semiconductor nanostructures, solution-phase synthetic routes are advantageous in terms of cost, throughput, modulation of composition, and the potential for large-scale and environmentally benign production. This article gives a concise review on the recent developments in the solution-phase synthesis of ID semiconductor nanostructures of different compositions, sizes, shapes, and architectures. We first introduce several typical solution-phase synthetic routes based on controlled precipitation from homogeneous solutions, including hydrothermal/solvothermal process, solution-liquid-solid （SLS） process, high-temperature organic-solution process, and low-temperature aqueous-solution process. Subsequently, we discuss two solution-phase synthetic strategies involving solid tem- plates or substrates, such as the chemical transformation of 1D sacrificial templates and the oriented growth of 1D nanostructure arrays on solid substrates. Finally, prospects of the solution-phase approaches to 1D semiconductor nanostructures will be briefly discussed.
基金the National Natural Science Foundation of China under grant Nos.10674138 and 20571022.
文摘Aluminum nitride （AIN） nanowires, serrated nanoribbons, and nanoribbons were selectively obtained through a simple chloride assisted chemical vapor deposition process. The morphologies of the products could be controlled by adjusting the deposition position and the flux of the reactant gas. The morphologies and structures of the AIN products were investigated in detail. The formation mechanism of the as-prepared different morphologies of AIN one-dimensional （ID） nanostructures was discussed on the basis of the experimental results.
基金financial support of the National Natural Science Foundation of China (No. 21302058)the financial support of the Key Basic Research Project of Shanghai Science and Technology Commission (No. 13JC1402200)
文摘We designed and constructed a new family of 608 dendritic dipyridyl donors, from which two novel triangular metallodendrimers were successfully prepared via coordination-driven self-assembly.Inspired by the existence of multiple intermolecular interactions（e.g., p–p stacking and CH–p interactions） imposed by the DMIP-functionalized poly（benzyl ether） dendrons, their hierarchical selfassembly behaviors were studied in various mixed solvents by using scanning electron microscopy（SEM）. Interestingly, it was found that the morphologies of the obtained metallodendrimers were highly depended on the dendron generation. For example, the first-generation metallodendrimer was able to hierarchically self-assemble into the spherical nanostructures in various mixed solvents. However, the nanofibers were observed for the second-generation metallodendrimer under the similar conditions.Furthermore, the driven force for the formation of such ordered nanostructures was investigated by using1 H NMR and fluorescence spectroscopy.
基金the National Natural Science Foundation of China(Grant Nos.12004137,62071200,and 12104236)Shandong Provincial Natural Science Foundation of China(Grant Nos.ZR2020QA052,ZR2020ZD28,ZR2021MA040,and ZR2021MA060).
文摘Searching for one-dimensional(1D)nanostructure with ferromagnetic(FM)half-metallicity is of significance for the development of miniature spintronic devices.Here,based on the first-principles calculations,we propose that the 1D CrN nanostructure is a FM half-metal,which can generate the fully spin-polarized current.The ab initio molecular dynamic simulation and the phonon spectrum calculation demonstrate that the 1D CrN nanostructure is thermodynamically stable.The partially occupied Cr-d orbitals endow the nanostructure with FM half-metallicity,in which the half-metallic gap(?s)reaches up to 1.58 eV.The ferromagnetism in the nanostructure is attributed to the superexchange interaction between the magnetic Cr atoms,and a sizable magnetocrystalline anisotropy energy(MAE)is obtained.Moreover,the transverse stretching of nanostructure can effectively modulate?s and MAE,accompanied by the preservation of half-metallicity.A nanocable is designed by encapsulating the CrN nanostructure with a BN nanotube,and the intriguing magnetic and electronic properties of the nanostructure are retained.These novel characteristics render the 1D CrN nanostructure as a compelling candidate for exploiting high-performance spintronic devices.
基金supported by the Strategic Priority Research Program of Chinese Academy of Sciences(XDB36000000)National Natural Science Foundation of China(22073022,11874130,12074086,22173025)+3 种基金the Support by the DNL Cooperation Fund,CAS(DNL202016)China Postdoctoral Science Foundation(2022M710925)Beijing Municipal Natural Science Foundation(1222030)the CAS Instrument Development Project(No.Y950291).
文摘In recent years,one-dimensional(1D)nanomaterials have raised researcher's interest because of their unique structur-al characteristic to generate and confine the optical signal and their promising prospects in photonic applications.In this re-view,we summarized the recent research advances on the spectroscopy and carrier dynamics of 1D nanostructures.First,the condensation and propagation of exciton-polaritons in nanowires(NWs)are introduced.Second,we discussed the properties of 1D photonic crystal(PC)and applications in photonic-plasmonic structures.Third,the observation of topological edge states in 1D topological structures is introduced.Finally,the perspective on the potential opportunities and remaining chal-lenges of 1D nanomaterials is proposed.
基金supported by an NSF CAREER Award(CMMI-1454293)a Grant-In-Aid(GIA)program/a start-up fund at the University of Minnesota,Twin Cities+2 种基金Parts of this work were carried out in the Characterization Facility,University of Minnesota,a member of the NSF-funded Materials Research Facilities Network(www.mrfn.org)via the MRSEC programA portion of this work was also carried out in the Minnesota Nano Center which receives partial support from the NSF through the NNCI programthe 3M Science and Technology Fellowship
文摘Grain coalescence has been applied in many areas of nanofabrication technology, including modification of thinfilm properties, nanowelding, and self-assembly of nanostructures. However, very few systematic studies of selfassembly using the grain coalescence, especially for threedimensional(3D) nanostructures, exist at present. Here, we investigate the mechanism of plasma triggered grain coalescence to achieve the precise control of nanoscale phase and morphology of the grain coalescence induced by exothermic energy. Exothermic energy is generated through etching a silicon substrate via application of plasma. By tuning the plasma power and the flow rates of reactive gases, different etching rates and profiles can be achieved, resulting in various morphologies of grain coalescence. Balancing the isotropic/anisotropic substrate etching profile and the etching rate makes it possible to simultaneously release 2D nanostructures from the substrate and induce enough surface tension force,generated by grain coalescence, to form 3D nanostructures.Diverse morphologies of 3D nanostructures have been obtained by the grain coalescence, and a strategy to achieve self-assembly, resulting in desired 3D nanostructures, has been proposed and demonstrated.
基金National Natural Science Foundation of China(Nos.50433020,50403022 and 50520150165)the developing program of Changjiang Scholar and Innovation Team from Education Department of China under Grant No.IRT0651.
文摘An asymmetrical perylene diimide 3, N-（4-methoxyphenyl）-N＇-（4-nitrophenyl）-perylene-3,4,9,10-tetracarboxylic diimide, was synthesized, and its self-assembly and dissociation behaviors in chloroform was studied in detail by UV-vis and fluorescence spectroscopies. The resulting unique helical nanostructures from 3 were proposed to be self-assembled via the cooperative actions of π-π stacking, steric hindrance and electrophile-nucleophile type pairing.
文摘The self-assembling behavior of random copolymers of sodium 2-(acrylamido)-2-methylpropanesulfonate (AMPS)and hydrophobic comonomers possessing dodecyl groups linked by various spacer bonds was discussed with a focus on theeffect of the spacer. The characterization of association behavior of such polymers in water using quasielastic light scattering,capillary electrophoresis, NMR relaxation, various fluorescence, and viscoelastic methods was described. These copolymersform a variety of self-assembled nanostructures depending on the type of the spacer. Random copolymers of AMPS and N-dodecylmethacrylamide show a strong preference for intrapolymer self-association even in concentrated aqueous solutionsforming single-macromolecular self-assemblies (unimolecular micelles). In contrast, random copolymers of AMPS anddodecyl methacrylate are prone to undergo interpolymer associations yielding multipolymer micelles. In random copolymersof AMPS and a methacrylate substituted a nonionic surfactant (HO(CH_2CH_2O)_(25)C_(12)H_(25)) (C_(12)E_(25)), dodecyl groups are muchless restricted by the polymer backbone because they are linked via a long, flexible hydrophilic spacer. Thus, the polymer-bound C_(12)E_(25) surfactant moieties form micelles similar to those formed by discrete surfactants, but they are bridged bypolymer chains forming a network structure.
基金the Nationnal Natural Science Foundation of China (No. 50342016).
文摘Iron（Ⅲ）-doped nanostructure TiO2-coated SiO2 （TiO2/SiO2） particles were prepared using the layer-by-layer assembly technique and their photocatalytic property was studied. TiO2 colloids were synthesized employing the sol-gel method with TiChas a precursor. The samples were characterized by Fourier transform infrared spectroscopy （FTIR）, SEM, EDS, XPS, and XRD. The experimental results show that TiO2 nanopowders on the surface of SiO2 particles are well distributed, the amount of TiO2 is increased with the adding of coating layers, the pure anatase-TiO2 coating layers are synthesized at 500℃, and the photocatalytic activity of Fe^3＋-doped TiO2/SiO2 is higher than that of undoped TiO2/SiO2.
基金supported by the National Key Research and Development Program of China(No.2016YFB0601100)the Fundamental Research Funds for the Central Universities(No.FRFBD-16-008A)
文摘The peony-like CuO micro/nanostructures were fabricated by a facile hydrothermal approach. The peony- like CuO micro/nanostructures about 3 -5μm in diameter were assembled by CuO nanoplates. These CuO nanoplates, as the building block, were self-assembled into multilayer structures under the action of ethidene diamine, and then grew into uniform peony-like CuO architecture. The novel peony-like CuO micro/nanostructures exhibit a high cycling stability and improved rate capability. The peony-like CuO microJnanostructures electrodes show a high reversible capacity of 456 mAhJg after 200 cycles, much higher than that of the commercial CuO nanocrystals at a current 0.1 C. The excellent electrochemical performance of peony-like CuO micro/nanostructures might be ascribed to the unique assembly structure, which not only provide large electrode/electrolyte contact area to accelerate the lithiation reaction, but also the interval between the multilayer structures of CuO nanoplates electrode could provide enough interior space to accommodate the volume change during Li insertion and de-insertion process,
基金National Natural Science Foundation of China(No.10774053)Hubei Province Nature Science Foundation of China(No.2007ABB008)Programs Foundation of Ministry of Education of China(No.20070487038)
文摘One-dimensional(1D) GaN nanomaterials exhibiting various morphologies and atomic structures were prepared via ammoniation of either Ga_2O_3 nanoribbons, Ga_2O_3 nanorods or Ga nanowires filled into carbon nanotubes(CNTs). The 1D GaN nanomaterials transformed from Ga_2O_3 nanoribbons consisted of numerous GaN nanoplatelets having the close-packed plane, i.e.(0002)2H or(111)3C parallel to the axes of starting nanoribbons. The 1D GaN nanomaterials converted from Ga_2O_3 nanorods were polycrystalline rods covered with GaN nanoparticles along the axes. The 1D GaN nanomaterials prepared from Ga nanowires filled into CNTs displayed two dominant morphologies:(i) single crystalline Ga N nanocolumns coated by CNTs, and(ii) pure single crystalline Ga N nanowires. The cross-sectional shape of Ga N nanowires were analyzed through the transmission electron microscopy(TEM) images. Formation mechanism of all-mentioned 1D GaN nanomaterials is then thoroughly discussed.
基金financially supported by the National Natural Science Foundation of China(Nos.21504053 and 91527304)the Recruitment Program of Global Experts(No.15Z127060012)
文摘Structural DNA nanotechnology, an emerging technique that utilizes the nucleic acid molecule as generic polymer to programmably assemble well-defined and nano-sized architectures, holds great promise for new material synthesis and constructing functional nanodevices for different purposes. In the past three decades, rapid development of this technique has enabled the syntheses of hundreds and thousands of DNA nanostructures with various morphologies at different scales and dimensions. Among them, discrete three-dimensional （3D） DNA nanostructures not only represent the most advances in new material design, but also can serve as an excellent platform for many important applications. With precise spatial addressability and capability of arbitrary control over size, shape, and function, these nanostructures have drawn particular interests to scientists in different research fields. In this review article, we will briefly summarize the development regarding the synthesis of discrete DNA 3D nanostructures with various size, shape, geometry, and topology, including our previous work and recent progress by other groups. In detail, three methods majorly used to synthesize the DNA 3D objects will be introduced accordingly. Additionally, the principle, design rule, as well as pros and cons of each method will be highlighted. As functions of these discrete 3D nanostructures have drawn great interests to researchers, we will further discuss their cutting-edge applications in different areas, ranging from novel material synthesis, new device fabrication, and biomedical applications, etc. Lastly, challenges and outlook of these promising nanostructures will be given based on our point of view.
基金supported by the Innovation Program of Shanghai Municipal Education Commission(No.12ZZ067)Shanghai Pujiang Program(No.11PJ1400200)+1 种基金the Research Fund for the Doctoral Program of Higher Education of China(No.20120075120018)the Fundamental Research Funds for the Central Universities
文摘A facile approach for constructing diverse architectures of unmodified C60 was developed via simple evaporation of pure C60 solution in CS2 under various poor solvent atmospheres. Diverse architectures such as belts, sheets, and starfishes were successfully constructed under different experimental conditions. C60 belts obtained under EtOH atmosphere were confirmed to be a face-centered cubic （fcc） structure. The solvent atmospheres not only slowed clown the evaporation speed, but also could reorganize the self-assembly of C60 by partially re-dissolving the initially formed architectures. This concept represents a novel method for preparation of nanostructures of C60 and could also be applied for controlling of the self-assembly of other functional organic molecules.
基金supported by the National Natural Science Foundation of China(Grant Nos.21373270 and 11504431)the Fundamental Research Funds for Central Universities of China(Grant No.15CX02025A)
文摘Under appropriate physicochemical conditions, short peptide fragments and their synthetic mimics have been shown to form elongated cross-fl nanostructures through self-assembly. The self-assembly process and the resultant peptide nanos- tructures are not only related to neurodegenerative diseases but also provide inspiration for the development of novel bionanomaterials. Both experimental and theoretical studies on peptide self-assembly have shown that the self-assembly process spans multiple time and length scales and is hierarchical, β-sheet self-assembly consists of three sub-processes from the microscopic to the mesoscopic level： β-sheet locking, lateral stacking, and morphological transformation. De- tailed atomistic simulation studies have provided insight into the early stages of peptide nanostructure formation and the interplay between different non-covalent interactions at the microscopic level. This review gives a brief introduction of the hierarchical peptide self-assembly process and focuses on the roles of various non-covalent interactions in the sub-processes based on recent simulation, experimental, and theoretical studies.
基金supported by the National Natural Science Foundation of China(Nos.20874003 and 21174006)
文摘An interesting order-order transition between two different complex nanostructures was observed in a new liquid crystalline linear coil-coil-rod ABC triblock copolymer（tri BCP）. First, the ABC tri BCP, poly（dimethylsiloxane）-bpolystyrene-b-poly{2,5-bis[（4-methoxyphenyl）oxycarbonyl]styrene}（PDMS-b-PS-b-PMPCS）, was synthesized through sequential atom transfer radical polymerization. The degrees of polymerization of PDMS, PS, and PMPCS blocks are 58, 159, and 106, and the corresponding volume fractions of PDMS, PS, and PMPCS are 0.09, 0.29, and 0.62, respectively. The phase behaviors of the PDMS-b-PS diblock copolymer precursor and the final triblock copolymer were studied by smallangle X-ray scattering, one-dimensional wide-angle X-ray scattering, and transmission electron microscopy experiments. The PDMS-b-PS precursor self-assembles into hexagonally packed cylinders with a relatively small periodic size after thermal annealing. When the triblock copolymer is annealed at a relatively low temperature（120 ○C） at which the PMPCS block is in the amorphous state, the tri BCP forms core-shell hexagonally packed cylinders（CSH） with a relativly large periodic size. After the tri BCP is annealed above 140 ○C at which the PMPCS block transforms to the liquid crystalline（LC） phase, the nanophase-separated structure transforms to a three-phase four-layer lamellar structure（LAM-3P4L）. Thus, accompanied with the transition of the PMPCS blocks from the amorphous state to the LC phase, the order-order transition from CSH to LAM-3P4 L occurs in the PDMS-b-PS-b-PMPCS ABC tri BCP.
基金supported by the Brain Research Program(No.2016M3C7A1904987)through the National Research Foundation of Korea(NRF)。
文摘Here,we use two important biomaterials,protein and DNA,to construct self-assembled linear nanostructures through Watson-Crick base-paring of DNAs.We apply a simple magnetic separation method to purify traptavidin-DNA co njugates,and demonstrate synthesis of linear arrays of traptavidinDNA conjugates via the step-growth polymerization approach with pre-determined DNA sequences.Using the traptavidin-DNA array as a template,we assemble gold nanoparticles to form linear plasmonic nanostructures in a programmable manner.The traptavidin-DNA conjugates thus provide a convenient platform for one-dimensional assembly of biotinylated nanomaterials for many biomedical applications from drug delivery to bio-sensing.
文摘In order to exploit the outstanding physical properties of one-dimensional （1D） nanostructures such as carbon nanotubes and semiconducting nanowires and nanorods in future technological applications, it will be necessary to organize them on surfaces with precise control over both position and orientation. Here, we use a 1D rigid DNA motif as a model for studying directed assembly at the molecular scale to lithographically patterned nanodot anchors. By matching the inter-nanodot spacing to the length of the DNA nanostructure, we are able to achieve nearly 100% placement yield. By varying the length of single-stranded DNA linkers bound covalently to the nanodots, we are able to study the binding selectivity as a function of the strength of the binding interactions. We analyze the binding in terms of a thermodynamic model which provides insight into the bivalent nature of the binding, a scheme that has general applicability for the controlled assembly of a broad range of functional nanostructures.
基金jointly supported by National Natural Science Foundation of China (NSFC) (Nos. 91527303, 21333001)
文摘Bottom-up approach to constructing low-dimensional nanostructures on surfaces with terminal alkynes has drawn great interest because of its potential applications in fabricating advanced functional nanomaterials. The diversity of the achieved products manifests rich chemistry of terminal alkynes and hence careful linking strategies and proper controlling methodologies are required for selective preparations of high-quality target nanoarchitectures. This review summarizes various on-surface linking strategies for terminal alkynes, including non-bonding interactions as well as organometallic and covalent bonds, and presents examples to show effective control of surface assemblies and reactions of terminal alkynes by variations of the precursor structures, substrates and activation modes. Systematic studies of the on-surface linkage of terminal alkynes may help efficient and predictable preparations of surface nanomaterials and further understanding of surface chemistry.
