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1.
Colloidal crystallization takes advantage of the strong interfacial forces and tunable interactions that organize particles into regular structures at small scales. Thus, colloidal crystallization and patterning provide a powerful and simple method to functionalize planar surfaces with applications to optical, catalytic, sensing, and cleansing materials. Nevertheless, the ability to pattern topologically more complex surfaces such as curved, confined, or soft substrates can open new avenues for novel, "intelligent", and responsive materials. We present one step in this direction by characterizing colloidal crystallization inside circular capillaries: a nearly periodic banding is observed, and the colloidal packing is dictated by confinement produced by the wedge-like region formed by a capillary confined meniscus. The packing consists of a succession of hexagonally close-packed regions, which are separated by narrow regions of "buckled phase crystals".  相似文献   

2.
A new and versatile way--using poly(dimethylsiloxane) (PDMS) sheets to layer-by-layer (LbL) transfer hexagonal-close-packed particle monolayers from preformed colloidal crystals and stack them on substrates-has been demonstrated to create colloidal crystals. This approach allows LbL control of the thickness of the resulting crystals and especially of the size and the packing structure of the particles in each layer. Furthermore, it also allows fabrication of binary colloidal crystals over large areas by deformation of the PDMS sheets during LbL transfer. Two new binary crystals-one composed of identically sized particles but in different densities and the other of a nonclose-packed monolayer of large particles and a close-packed monolayer of small particles-were created, which are hard grown by other colloidal crystallization techniques developed thus far.  相似文献   

3.
We report a new fabrication method of asymmetric colloidal clusters by using contact area lithography with site-selective growth. Nanometric surface patterns (approximately 44, 60, and 81 nm in diameter) were prepared by coating surfaces with self-assembled monolayers (SAMs; octadecyltrichlorosilane (OTS) in this study) except the contact area either between colloidal particles or between colloids and substrate. Nanoscale site-specific heterogeneous nucleation and growth of oxide materials of titanium were studied using the patterns of OTS-SAMs onto the either flat or curved surfaces of SiO2. Experimental results suggest that a combination of the large difference in the surface energy between the growing and surrounding surfaces and the diffusion-controlled growth leads to complete nanoscale site specificity. We also fabricated superstructrures of silica spheres with hemispheres of titania (<20 nm in dimension) on their surfaces and discussed the optical properties of colloidal films consisting of the monodisperse asymmetric colloidal clusters in terms of photonic band gap.  相似文献   

4.
Silicon disk arrays and silicon pillar arrays with a close-packed configuration having an ordered periodicity were fabricated by the electrochemical etching of a silicon substrate through colloidal crystals used as a mask. The colloidal crystals were directly prepared by the self-assembly of polystyrene particles on a silicon substrate. The transfer of a two-dimensional hexagonal array of colloidal crystals to the silicon substrate could be achieved by the selective electrochemical etching of the exposed silicon surfaces, which were located in interspaces among adjacent particles. The diameter of the tip of the silicon pillars could be controlled easily by changing the anodization conditions, such as current density and period of electrochemical etching.  相似文献   

5.
We present a novel and simple method to fabricate two-dimensional (2D) poly(styrene sulfate) (PSS, negatively charged) colloidal crystals on a positively charged substrate. Our strategy contains two separate steps: one is the three-dimensional (3D) assembly of PSS particles in ethanol, and the other is electrostatic adsorption in water. First, 3D assembly in ethanol phase eliminates electrostatic attractions between colloids and the substrate. As a result, high-quality colloidal crystals are easily generated, for electrostatic attractions are unfavorable for the movement of colloidal particles during convective self-assembly. Subsequently, top layers of colloidal spheres are washed away in the water phase, whereas well-packed PSS colloids that are in contact with the substrate are tightly linked due to electrostatic interactions, resulting in the formation of ordered arrays of 2D colloidal spheres. Cycling these processes leads to the layer-by-layer assembly of 3D colloidal crystals with controllable layers. In addition, this strategy can be extended to the fabrication of patterned 2D colloidal crystals on patterned polyelectrolyte surfaces, not only on planar substrates but also on nonplanar substrates. This straightforward method may open up new possibilities for practical use of colloidal crystals of excellent quality, various patterns, and controllable fashions.  相似文献   

6.
Cristobalite with ordered interstitial dual-sized mesopores was synthesized through the crystallization of silica colloidal crystals composed of monodispersed amorphous silica nanoparticles. An aqueous solution containing both a flux (Na2O) and a carbon precursor (an aqueous low-molecular weight phenolic resin) was infiltrated into the interstices of silica colloidal crystals. The organic fraction in the nanocomposite was further polymerized and subsequently carbonized in an Ar flow at 750 °C to reinforce the colloidal crystal structure. The thermal treatment resulted in the crystallization of the colloidal crystals into cristobalite while retaining the porous structure. The cristobalite-carbon nanocomposite was calcined in air to remove the carbon and create interstitial ordered mesopores in the cristobalite. The surfaces of crystalline mesoporous silica are quite different from those of various ordered mesoporous silica with amorphous frameworks; thus, the present findings will be useful for a precise understanding and control of the interfaces between the mesopores and silica networks.  相似文献   

7.
The structural rearrangements during growth of colloidal crystals were investigated using a combination of light microscopy and image analysis based on a Delaunay triangulation procedure. We followed the creation and disappearance of square lattice domains during the convection-promoted formation of colloidal monolayers by drying. We found that the concentration of square lattice domains increased with the crystal growth rate and that there is a direct relation between the concentration of square lattice domains formed at the crystal-suspension interface and the lower concentration of these domains in the colloidal monolayer; hence, the degree of rearrangement from square lattice domains to a close-packed triangular structure is not significantly affected by the crystal growth rate for colloidally stable suspensions. The colloidal stability, manipulated by the addition of salt, has a profound influence on the structural features of the growing monolayers. Particles that adhere strongly to each other, and to the substrate, tend to resist rearrangement; hence, the defect density is high in the colloidal monolayers and the structural reorganization of the square lattice domains to the more stable close-packed triangular structure occurred gradually over large distances from the crystal-suspension interface.  相似文献   

8.
Synthetic calcite single crystals,due to their strong crystal habit,tend to grow into characteristic rhombohedra.In the nature,biogenic calcite crystals form composites together with biomacromolecular materials,spurring investigations of how the growing calcite single crystals change their habit to satisfy the curvature of the organic phase.In this work,we examine calcite crystallization on a flat surface of glass slide and a curved surface of polystyrene(PS)sphere.The crystals exhibit tiny contact area onto the glass substrate that is averagely only 15% of their projected area on the substrate.In sharp contrast,the contact area greatly increase to above 75% of the projected area,once magnesium ions or agarose gel networks are introduced into the crystallization media.Furthermore,the calcite crystals form rough and step-like interfaces with a curved surface.However,the interfaces become smooth and curved as the crystals grow in presence of magnesium ions or agarose gel networks.The discrepancy between the interfacial structures implies kinetic effects of the additives on the crystallization around the surfaces. This work may provide implications for understanding the formation mechanisms of single-crystal composite materials.  相似文献   

9.
关英  张拥军 《高分子学报》2017,(11):1739-1752
Poly(N-isopropylacrylamide)(PNIPAM)微凝胶粒子是一种软的胶体粒子.和单分散的SiO_2、PS、PMMA等硬的胶体粒子一样,单分散的PNIPAM微凝胶粒子也可以自组装成为高度有序的胶体晶体.微凝胶粒子软物质的特性及其对外部刺激的响应性赋予其不同于硬球的组装行为.微凝胶胶体晶体的高度有序结构及其刺激响应性使其在诸多领域有重要用途.本文分别介绍了三维及二维微凝胶胶体晶体组装的研究进展,并对已开发的基于微凝胶胶体晶体的应用进行了总结.  相似文献   

10.
The mechanism of action of additives that control the sedimentation of paraffin crystals after their crystallization in model diesel oil has been studied by means of a new experimental approach. The chemical analysis of the crystals and detailed measurements of the sedimentation phenomenon give new insights into this complex process. Thus, the wax antisettling additives used for preventing wax crystal sedimentation adsorb at the surfaces of wax particles and provide them with enhanced colloidal stability. The settling rate is not related to the size of the crystals or the viscosity of the liquid medium, but to the ability of the additives to prevent the aggregation of wax crystals. The reported methodology makes it possible to investigate the fundamental mechanisms, but also to evaluate structure-activity relationships of the various additives used in the petroleum industry.  相似文献   

11.
DNA is a powerful and versatile tool for nanoscale self-assembly. Several researchers have assembled nanoparticles and colloids into a variety of structures using the sequence-specific binding properties of DNA. Until recently, however, all of the reported structures were disordered, even in systems where ordered colloidal crystals might be expected. We detail the experimental approach and surface preparation that we used to form the first DNA-mediated colloidal crystals, using 1 mum diameter polystyrene particles. Control experiments based on the depletion interaction clearly indicate that two standard methods for grafting biomolecules to colloidal particles (biotin/avidin and water-soluble carbodiimide) do not lead to ordered structures, even when blockers are employed that yield nominally stable, reversibly aggregating dispersions. In contrast, a swelling/deswelling-based method with poly(ethylene glycol) spacers resulted in particles that readily formed ordered crystals. The sequence specificity of the interaction is demonstrated by the crystal excluding particles bearing a noninteracting sequence. The temperature dependence of gelation and crystallization agree well with a simple thermodynamic model and a more detailed model of the effective colloidal pair interaction potential. We hypothesize that the surfaces yielded by the first two chemistries somehow hinder the particle-particle rolling required for annealing ordered structures, while at the same time not inducing a significant mean-force interaction that would alter the self-assembly phase diagram. Finally, we observe that particle crystallization kinetics become faster as the grafted-DNA density is increased, consistent with the particle-particle binding process being reaction, rather than diffusion limited.  相似文献   

12.
Surface modification of colloidal silica with ferrocenyl-grafted polymer and colloidal crystallization of the particles in organic solvent were studied. Poly(methyl methacrylate-co-vinylferrocene)-grafted silica never formed colloidal crystals in polar solvent, such as acetone, acetonitrile, ethanol and N,N-dimethylformamide (DMF), while poly(methyl methacrylate-co-ferrocenyl acrylate)-grafted silica gave colloidal crystallization in DMF. The particles prepared by grafting of poly(N,N-dimethylacrylamide-co-vinylferrocene), with vinylferrocene (Vfc) mole fraction of 1/13 and 1/23, were observed to give the crystallization in ethanol and DMF over particle volume fraction of 0.058. Further, silica modified with copolymer of Vfc and N-vinyl-2-pyrrolidone, N-vinylcarbazole or N-isopropylacrylamide formed colloidal crystals in ethanol and DMF. Especially, poly(N-isopropylacrylamide-co-Vfc)-grafted silica, which was composed of the highest mole fraction of vinylferrocene, 1/3, afforded colloidal crystallization in ethanol over particle volume fraction of 0.053. Relatively high polar vinylferrocene copolymer grafting of silica resulted in colloidal polymerization in organic solvents.  相似文献   

13.
Monolayers of 1,1'-bi-2-naphthol (BN) derivatives, of which the two naphthalene rings are twisted along the carbon(1)-carbon(1') single bond, were studied for their conformational effect on the growth of pentacene crystals on their monolayer surface. BN monolayers with H and Br at 6,6'-positions (H-BN and Br-BN) were prepared by immersion-coating in toluene solution of the corresponding BNSiCl2. Pentacene was thermally evaporated onto the H-BN and Br-BN monolayers, silica, octadecylsilyl (ODTS) SAM, and a micropattern of H-BN and ODTS SAM. Pentacene crystals were also grown on the SAMs of 1-naphthylsilyl(NPh), phenylsilyl(Ph), and diphenylsilyl (DPh) groups, which are aromatic and have contact angle values similar to those of the the BN monolayers. AFM images of the crystals at the early stage of growth indicated that the BN monolayers suppressed the nucleation while facilitating the growth of nuclei to larger crystals. The low nucleation density and high growth rate are accounted for by the amorphous nature of the twisted BN monolayer surface where the intermolecular interaction between neighboring adsorbates is likely to be suppressed. The results offer new insights into designing surfaces for controlling the crystallization kinetics of organic materials.  相似文献   

14.
The biomimetic synthesis of patterned mineral thin films, based on a combination of the microcontact printing technique and a novel crystallization process called the polymer-induced liquid-precursor (PILP) process, is demonstrated. The PILP process enables the deposition of smooth and continuous calcitic mineral films (up to 1500 nm in thickness) under low-temperature and aqueous-based processing conditions. The films are formed by deposition of colloidal droplets composed of a liquid-phase mineral precursor that is induced by a polymeric process-directing agent (polyaspartate or polyacrylate salts). The droplets can be preferentially deposited onto patterned substrates templated with self-assembled monolayers (SAMs) of alkanethiolate on gold. The droplets coalesce to form an amorphous mineral film, which then transforms (solidifies and crystallizes) while retaining the shape of the patterned template, providing a means for patterning the location and morphology of two-dimensional calcite crystals. A vertical substrate experiment supports the premise that the calcite films are created by adsorption of colloidal droplets from solution, rather than heterogeneous nucleation and growth of an amorphous phase on the SAMs. Large single-crystalline domains, on the order of 50-100 microm, can be "molded" into nonequilibrium morphologies by constraining the mineral precursor to a chemically defined "compartment". Biominerals are well recognized for their elaborate nonequilibrium molded crystal morphologies, and increasing evidence suggests that many biominerals are formed from an amorphous precursor that is stabilized by polyanionic proteins. The biomimetic system examined here, which consists of a polyanionic process-directing agent in combination with a functionalized organic template, offers a practical tool for generating complex inorganic structures such as those found in biominerals.  相似文献   

15.
Rigidity (G) of colloidal crystals in organic solvents of acetonitrile and nitrobenzene has been measured by reflection spectroscopy in sedimentation equilibrium. The colloidal spheres used are the silica spheres (136 nm in diameter) modified on their surfaces with polymers, poly(maleic anhydride-co-styrene) [P(MA-ST)], poly(methyl methacrylate) (PMMA), or polystyrene (PST). Log G increases linearly with the slope of unity as log N (number density of colloidal spheres) increases. The mean values of the b-factor, which is the fluctuation parameter in crystal lattices and should be smaller than 0.1 according to the Lindeman's rule, are 0.045±0.003, 0.039±0.007, and 0.038±0.003 for P(MA-ST)/SiO2, PMMA/SiO2, and PST/SiO2, respectively. These values are larger than that of colloidal crystals of mother silica spheres in the deionized aqueous suspension, 0.028. These results support the important role of the excluded volume effects from the polymer layers formed around the silica surfaces. However, contribution of the excluded volume effects from the electrical double layers formed around the spheres in the organic solvents is also effective in the colloidal crystallization. Electronic Publication  相似文献   

16.
The structure, crystal growth kinetics and rigidity of colloidal crystals of core–shell-type latex spheres (diameters 280–330 nm) with differences in shell rigidity have been studied in aqueous suspension, mainly by reflection spectroscopy. The suspensions were deionized exhaustively for more than 2 years using mixed-bed ion-exchange resins. The five kinds of core–shell spheres examined form colloidal crystals, where the critical sphere concentrations, c, of crystallization (or melting) are high and range from 0.01 to 0.06 in volume fraction. Nearest-neighbor intersphere distances in the crystal lattice agree satisfactorily with values calculated from the sphere diameter and concentration. The crystal growth rates are between 0.1 and 0.3 s–1 and decrease slightly as the sphere concentration increases, indicating that the crystal growth rates are from the secondary process in the colloidal crystallization mechanism, corresponding to reorientation from metastable crystals formed in the primary process and/or Ostwald-ripening process. The rigidities of the crystals range from 2 to 200 Pa, and increase sharply as the sphere concentration increases. The g factor, the parameter for crystal stability, is around 0.02 irrespective of the sphere concentration and/or the kind of core–shell sphere. There are no distinct differences in the structural, kinetic and elastic properties among the colloidal crystals of the different core–shell-type spheres, showing that the internal sphere structure does not affect the properties of the colloidal crystals. The results show that colloidal crystals form in a closed container owing to long-range repulsive forces and the Brownian movement of colloidal spheres surrounded by extended electrical double layers and that their formation is not influenced by the rigidity and internal structure of the spheres.  相似文献   

17.
In this communication, we demonstrate that chiral self-assembled monolayers can be used for polymorphism control of chiral crystals. We studied the crystallization of DL-glutamic acid on chiral self-assembled monolayers and showed that crystallization of DL-glutamic acid on the chiral SAMs resulted in stabilization of the metastable conglomerate form.  相似文献   

18.
Superhydrophobic bionic surfaces with hierarchical micro/nano structures were synthesized by decorating single-walled or multiwalled carbon nanotubes (CNTs) on monolayer polystyrene colloidal crystals using a wet chemical self-assembly technique and subsequent surface treatment with a low surface-energy material of fluoroalkylsilane. The bionic surfaces are based on the regularly ordered colloidal crystals, and thus the surfaces have a uniform superhydrophobic property on the whole surface. Moreover, the wettability of the bionic surface can be well controlled by changing the distribution density of CNTs or the size of polystyrene microspheres. The morphologies of the synthesized bionic surfaces bear much resemblance to natural lotus leaves, and the wettability exhibited remarkable superhydrophobicity with a water contact angle of about 165 degrees and a sliding angle of 5 degrees.  相似文献   

19.
Colloidal crystallization kinetics is studied in the shear flow of a suspension of colloidal silica spheres (110 nm in diameter), using a continuously-circulating type of stopped flow cell system. The crystallization rate from a suspension containing a small amount of nuclei and/or single crystals is high compared with that from a suspension containing no nuclei and/or single crystals. Crystal growth takes place at shear rates smaller than 3.4 s–1 and at sphere concentrations higher than a volume fraction of 0.004.  相似文献   

20.
Zeolite A suspensions with a monomodal, narrow particle size distribution have been prepared. The suspended particles in a TMAOH water solution at pH 9 are negatively charged with a zeta potential of −43 mV. Modification of the external surface of the zeolite particles by a silylation reaction produces particles that, when they are suspended in water, are positively charged and have a zeta potential of +40 mV.The suspensions of the negatively or positively charged particles can be used for the preparation of adsorbed layers of particles on oppositely charged substrates by electrostatic attraction. This deposition process leads to a high coverage of the substrate with well-adhered particles. The cubic morphology of the zeolite particles results in preferential orientation after deposition. The particles are oriented with their {h 0 0} planes (cube faces) parallel and perpendicular to the substrate (out-of-plane orientation). The particles are randomly oriented with respect to the direction perpendicular to the substrate (in-plane orientation). Although, under optimized conditions, the coverage is high and only one adsorption cycle is necessary, the particles are not closely packed.Alternately, the zeolite particle suspensions can be used to deposit close-packed arrays of particles by convective particle transport during dip coating on substrates bearing the same charge as the zeolite particles. Using monodispersed zeolite A suspensions and slow speed dip coating close-packed hexagonal colloidal crystals were prepared. The type of colloidal crystal deposits formed range from continuous sublayers, monolayers, or multilayers to isolated discoidal clusters consisting of few zeolite particles. Factors affecting the deposited layer(s) structure are particle concentration of the suspension and withdrawal speed. In addition to close packing, the layers prepared by dip coating exhibit preferred orientation with the particle faces lying parallel and perpendicular to the substrate surface. Moreover, this second route of precursor film formation by colloidal crystallization leads to domains of well-aligned zeolite particles in three dimensions, i.e. with their faces parallel to each other. The oriented domains span the length of several particles; however, low angle boundaries and other defects during colloidal crystallization prevent the formation of macroscopically three-dimensionally ordered zeolite particles.The precursor layers were subjected to secondary growth in order to prepare continuous intergrown films. Secondary growth proceeds initially by local epitaxy on the deposited particles. Later in the process, deposition proceeds by incorporation of particles from solution along with re-nucleation on the growing film. The intergrown films have predominately [h 0 0] out-of-plane orientation; however, after extended secondary growth treatment a population of [h h h] grains appears on the surface of the regrown films.  相似文献   

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