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Hua Chun Zeng

Publications and source records attributed to Hua Chun Zeng.

At least 19 recordsLinked to original sources

Template-free parallel one-dimensional assembly of gold nanoparticles.

In this work, we have identified key process parameters to generate parallel unidirectional 1D assemblies of gold nanoparticles with the assistance of organic surfactants. By controlling the surfactant population, metal particle size, and amount of solvent for dispersion, the length of nanoparticle chains and their interchain space can be further tailored. In principle, the general findings of this work can also be extended to large-scale 1D organization of other transition/noble metal nanoparticles using simple organic surfactants.

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Fabrications of hollow nanocubes of Cu(2)O and Cu via reductive self-assembly of CuO nanocrystals.

In this work, a template-free synthetic approach for generating single-crystalline hollow nanostructures has been described. Using the small optical band-gap cuprous oxide Cu(2)O as a model case, we demonstrate that, instead of normally known spherical aggregates, primary nanocrystalline particles can first self-aggregate into porous organized solids with a well-defined polyhedral shape according to the oriented attachment mechanism, during which chemical conversion can also be introduced. In contrast to the spherical aggregates, where the nanocrystallites are randomly joined together, the Cu(2)O nanocrystallites in the present case are well organized, maintaining a definite geometric shape and a global crystal symmetry. Due to the presence of intercrystallite space, hollowing and chemical conversion can also be carried out in order to create central space and change the chemical phase of nanostructured polyhedrons. It has been revealed that Ostwald ripening plays a key role in the solid evacuation process. Using this synthetic strategy, we have successfully prepared single-crystal-like Cu(2)O nanocubes and polycrystalline Cu nanocubes with hollow interiors. For the first time, we demonstrate that nanostructured polyhedrons of functional materials with desired interiors can be synthesized in solution via a combination of oriented attachment and Ostwald ripening processes.

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Asymmetric ZnO nanostructures with an interior cavity.

As a next level of nanofabrication of inorganic materials, free-standing asymmetric nanostructures with an interior space are highly desirable for new applications. In this work, we demonstrate a wet synthesis scheme for bullet-head-like nanostructures of wurtzite zinc oxide (ZnO). The synthesized asymmetric nanostructures are single crystalline, and each has an interior space. In addition to the exterior geometric anisotropy, it is found that the interior space is located at the upper part of the ZnO nanostructures; a new type of structural anisotropy has thus been revealed. On the basis of the present findings, in principle, this synthetic architecture should be applicable to other II-VI compound semiconductors through stabilizing two or more sets of crystallographic planes in solution media. The possibility of dimerization and higher ordered coupling/growth of the ZnO nanostructures has also been addressed.

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Semiconductor rings fabricated by self-assembly of nanocrystals.

Three types of nonlinear organization schemes for creating ringlike semiconductors have been elucidated with the self-assembly of nanocrystals in aqueous phase under one-pot conditions. The synthetic architecture is based on morphological controls of primary nanocrystals which possess an intrinsic hexagonal symmetry. As most semiconducting materials have similar hexagonal (or cubic) crystal symmetries, in principle, the self-assembling processes revealed in this work should be extendable to other semiconductor nanocrystals.

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Deposition method for preparing SERS-active gold nanoparticle substrates.

Surface-enhanced Raman scattering or SERS, discovered some 20 years ago, has recently become a promising tool for routine biofluid assays in a clinical setting. Many attempts have been made to produce cheap and reproducible SERS-active substrates. In this study, we report on the fabrication of SERS-active substrates through the convective assembly of gold (Au) particles on electrostatically charged glass slides. We show that, by a proper control of the initial particle concentration in an evaporating Au suspension droplet, it is possible to obtain a closely packed colloidal film capable of generating SERS activity. Finally, AFM and SERS measurements of the resulting films reveal comparability in performance with previous silane-immobilized Au colloidal films. The minimum electromagnetic enhancement factor of our films is estimated to be about 2 x 10(4).

Colloids↗

Reduction and reconstruction of Co3O4 nanocubes upon carbon deposition.

We describe a synthetic investigation on the formation of carbon nanofibers using a preshaped free-standing metal-oxide catalyst (single-crystal cobalt oxide (Co(3)O(4)) nanocubes). In reacting with acetylene (C(2)H(2)) vapor, Co(3)O(4) nanocubes are reduced and reconstructed into metallic cobalt. The resultant metal catalyst with a 2-fold symmetry leads to a bilateral base growth for carbon nanofibers. Our findings indicate that an understanding of catalyst-assisted chemical vapor deposition (CVD) mechanisms can be acquired, when the shape, size, and crystal orientation of pristine metal catalysts are made known to the CVD process. By tracing their evolutional changes in structure and composition, the shape-designed model catalysts may offer new opportunities for mechanistic investigations on the chemical reactivity of nanoparticles, general catalyst-assisted material synthesis, and metal intercalation chemistry.

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Large-scale synthesis of high-quality ultralong copper nanowires.

The present difficulties in synthesis of one-dimensional copper are short length, nonlinear morphology, polydispersivity, poor crystallinity, low yield, and process complexity. In this work, we demonstrate that high-quality ultralong copper nanowires (90-120 nm in diameter, 40-50 microm in length; aspect ratio >350-450) can be synthesized in large scale with a facile aqueous reduction route at low cost. The prepared copper nanowires can also be used as starting solid precursor for fabrication of polycrystalline oxide nanotubes via direct oxidation in air.

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Formation of colloidal CuO nanocrystallites and their spherical aggregation and reductive transformation to hollow Cu2O nanospheres.

In this work, we demonstrate that cuprous oxide Cu(2)O nanospheres with hollow interiors can be fabricated from a reductive conversion of aggregated CuO nanocrystallites without using templates. A detailed process mechanism has been revealed: (i) formation of CuO nanocrystallites; (ii) spherical aggregation of primary CuO crystallites; (iii) reductive conversion of CuO to Cu(2)O; and (iv) crystal aging and hollowing of Cu(2)O nanospheres. In this template-free process, Ostwald ripening is operative in (iv) for controlling crystallite size in shell structures and thus for precisely tuning the optical band gap energy (E(g)) of resultant semiconductor nanostructures. For the first time, a wealth of colorful Cu(2)O hollow nanospheres (outer diameters in 100-200 nm), with variable E(g) in the range of 2.405-2.170 eV, has been fabricated via this novel chemical route. Considering their unique hollow structure and facile tuning in band gap energy, the prepared Cu(2)O hollow spheres can be potentially useful for harvesting solar energy in the visible range. Possibility of fabrication of Cu-Cu(2)O nanocomposites has also been discussed.

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Synthetic architectures of TiO2/H2Ti5O11.H2O, ZnO/H2Ti5O11.H2O, ZnO/TiO2/H2Ti5O11.H2O, and ZnO/TiO2 nanocomposites.

Although synthetic investigations of inorganic nanomaterials had been carried out extensively over the past decade, few of them have been devoted to fabrication of complex nanostructures that comprise multicomponents/phases (i.e., composite nanobuilding blocks), especially in the area of structural/morphological architecture. In this work, nanobelts of a protonated pentatitanate (H(2)Ti(5)O(11).H(2)O) were synthesized hydrothermally for the first time. Two technologically important transition-metal-oxides TiO(2) and ZnO were then grown respectively or sequentially onto the surface of the as-prepared nanobelts in aqueous mediums. With a main emphasis on organizational manipulation, the present investigation examines general issues of morphological complexity, synthetic interconvertibility, and material combinability related to fabrication of inorganic nanocomposites. Using this model material system, we demonstrate that complex binary and tertiary composite building blocks of TiO(2)/H(2)Ti(5)O(11).H(2)O, ZnO/H(2)Ti(5)O(11).H(2)O, ZnO/TiO(2)/H(2)Ti(5)O(11).H(2)O, and ZnO/TiO(2) can be architected stepwise in solution. Structural features of these nanocomposites have also been addressed.

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Symmetric and asymmetric Ostwald ripening in the fabrication of homogeneous core-shell semiconductors.

Two methodic concepts, symmetric and asymmetric Ostwald ripening, are elucidated by solution-route syntheses of oxide and sulfide semiconductors. While the original shape of a crystallite aggregate forms the exterior appearance, the preorganization of the crystallites determines the ultimate interior space structure of the aggregate upon Ostwald ripening. Further investigations on the design of crystallite preorganization and control of the solution process will allow the construction of complex architectures, including nonspherical configurations.

Colloids↗

Fabrication of ZnO "dandelions" via a modified Kirkendall process.

We report that in addition to the fabrication of hollow nanomaterials, the Kirkendall-type diffusion can also be utilized in synthetic nanoarchitecture, through which low-dimensional nanobuilding blocks can be designed and organized chemically into complex geometrical conformations. Our approach may provide a new chemical alternative to materials self-organization. In principle, a great variety of inorganic "dandelions" and their nanocomposites can be tailored and fabricated through this type of total synthetic architecture.

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Self-generation of tiered surfactant superstructures for one-pot synthesis of Co3O4 nanocubes and their close- and non-close-packed organizations.

Self-generation of ionic organic capping from nonionic surfactant polyoxyethylene (20) sorbitan trioleate (Tween-85) has been realized for the controlled synthesis of single crystalline Co(3)O(4) quantum dots (3.0-5.7 nm) in cubic morphology from related layered hydroxide precursors at 80-95 degrees C. With chemical modification of hydrophobic functional groups on the surface of Co(3)O(4) nanocubes; furthermore, various nanocube-containing micellar superstructures can be further assembled through hydrophobic interactions between Tween-85 molecules and the surface coating under "one-pot" conditions. In particular, square arrangements, spherical domains, and line-assemblies of the prepared Co(3)O(4) nanocubes and their inter-transformations have been attained for the first time by manipulating intersurfactant-interactions. Hydrolysis of Tween-85 and the resultant tiered surfactant superstructures have been investigated with FTIR/UV-vis/EA/TGA/DTA/XPS methods, and the capping species has been identified to be alkylated oleic carboxylate anions derived from Tween-85. Pronounced quantum confinement effects have been observed with the prepared Co(3)O(4) nanocubes, and the optical band gap energies determined are 3.95 and 2.13 eV, respectively, for O(2-)--> Co(2+) and O(2-)--> Co(3+) charge-transfer processes.

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Mesoscale organization of CuO nanoribbons: formation of "dandelions".

A two-tiered organizing scheme with multiple-length scales for construction of dandelion-like hollow CuO microspheres has been elucidated: (1) mesoscale formation of rhombic building units from smaller nanoribbons via oriented aggregation and (2) macroscopic organization of these units into the CuO microspheres. This self-assembly concept may also be applicable to other metal oxides by creating geometric constraints for constructional units.

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Room temperature solution synthesis of monodispersed single-crystalline ZnO nanorods and derived hierarchical nanostructures.

In this work, we report a room temperature wet-chemical approach to synthesize highly regulated, monodispersed ZnO nanorods and derived hierarchical nanostructures. In particular, ZnO has been prepared into single-crystalline conical or prismatic nanorods, and various hierarchical structures such as hexagonally branched, reversed umbrella-type, and cactus-like ZnO nanostructures comprising individual c-oriented nanorods. Depending on the synthetic conditions used, the diameter of nanorods can be controlled with a size down to 10-30 nm, while the aspect ratio can be controlled up to 50-100. Various preparative parameters, such as initial reactant concentrations, solvents, ligands, surfactants, precursor salts, and reaction time, have been systematically examined. Due to slow reactions at room temperature, excellent crystallinity and high morphological yield (100% in most cases) have been achieved via tuning the synthetic parameters. Our photoluminescence and UV measurements also confirm the attained crystal perfection and size uniformity.

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