PubMed Health⌕ Search

Biomedical subjects

Nanfeng Zheng

Publications and source records attributed to Nanfeng Zheng.

At least 19 recordsLinked to original sources

A general synthetic strategy for oxide-supported metal nanoparticle catalysts.

Despite recent exciting progress in catalysis by supported gold nanoparticles, there remains the formidable challenge of preparing supported gold catalysts that collectively incorporate precise control over factors such as size and size-distribution of the gold nanoparticles, homogeneous dispersion of the particles on the support, and the ability to utilize a wide range of supports that profoundly affect catalytic performance. Here, we describe a synthetic methodology that achieves these goals. In this strategy, weak interface interactions evenly deposit presynthesized organic-capped metal nanoparticles on oxide supports. The homogeneous dispersion of nanoparticles on oxides is then locked in place, without aggregation, through careful calcination. The approach takes advantage of recent advances in the synthesis of metal and oxide nanomaterials and helps to bring together these two classes of materials for catalysis applications. An important feature is that the strategy allows metal nanoparticles to be well dispersed on a variety of oxides with few restrictions on their physical and chemical properties. Following this synthetic procedure, we have successfully developed efficient gold catalysts for green chemistry processes, such as the production of ethyl acetate from the selective oxidation of ethanol by oxygen at 100 degrees C.

Journal Article↗

One-step one-phase synthesis of monodisperse noble-metallic nanoparticles and their colloidal crystals.

A variety of metallic nanoparticles with a narrow size distribution have been synthesized in a facile one-phase method in which amine-borane complexes are applied as reducing agents. It is particularly striking that large colloidal crystals with sizes up to tens of micrometers can directly form from the reaction mixtures without any further treatment. By using the synthetic route described, large-scale syntheses of both mono- and alloyed metallic nanoparticles with a narrow size distribution can be easily achieved.

Journal Article↗

Metal-chelate dye-controlled organization of Cd32S14(SPh)40(4-) nanoclusters into three-dimensional molecular and covalent open architecture.

Chalcogenide II-VI nanoclusters are usually prepared as isolated clusters and have defied numerous efforts to join them into covalent open-framework architecture with conventional templating methods such as protonated amines or inorganic cations commonly used to direct the formation of porous frameworks. Herein, we report the first templated synthesis of II-VI covalent superlattices from large II-VI tetrahedral clusters (i.e., [Cd32S14(SPh)38]2-). Our method takes advantage of low charge density of metal-chelate dyes that is a unique match with three-dimensional II-VI semiconductor frameworks in charge density, surface hydrophilicity-hydrophobicity, and spatial organization. In addition, metal-chelate dyes also serve to tune the optical properties of resulting dye semiconductor composite materials.

Journal Article↗

One-dimensional assembly of chalcogenide nanoclusters with bifunctional covalent linkers.

Even though different approaches have been developed to achieve various 1D assemblies of nanocrystals, few studies have been done on the assembly of crystallographically well-defined chalcogenide nanoclusters. Here, by using bifunctional organic ligands as the directional linker, a series of one-dimensional assemblies of semiconducting chalcogenide nanoclusters have been prepared and characterized. The synthetic method allows for the preparation of differently sized tetrahedral nanoclusters that are joined together with organic linkers of different length and rigidity. Multiple linking modes between nanoclusters and organic ligands are revealed in four different assemblies that also exhibit size-dependent optical properties.

Journal Article↗

Crystalline superlattices from single-sized quantum dots.

Despite the recent progress toward the synthesis of monodisperse semiconducting nanocrystals, it remains a challenge to prepare quantum dot structures with a precise number of atoms. Here, we report synthesis, crystal structure, and optical properties of a family of cadmium sulfide nanocrystal superlattices assembled through single-sized semiconducting clusters. Clusters of various sizes have been made. The largest cluster determined from single-crystal analysis has a total of 138 metal-chalcogen sites. It is the largest known single-sized II-VI quantum dot and is also the first one with more than 100 metal-chalcogen sites. X-ray powder diffraction (XRD) and optical absorption studies indicate the presence of even larger single-sized quantum dots (>200 metal-chalcogen sites). These clusters consist of cubic zinc blende-type core and hexagonal wurtzite-type corners and can exist in up to five isomeric forms that differ only in the position of the hexagonal-cubic interface.

Journal Article↗

Na5(In4S)(InS4)3.6H2O, a zeolite-like structure with unusual SIn4 tetrahedra.

A hydrated sodium indium sulfide, Na5(In4S)(InS4)3.6H2O, has been prepared by hydrothermal synthesis. This material contains a tetrahedral sulfur site coordinated to four trivalent indium ions, an unusual bonding pattern not previously observed in open framework chalcogenides. The structure is related to the perovskite (CaTiO3) type with simultaneous substitutions of Ti by SIn4, O by InS4, and Ca2+ by [Na5(H2O)6]5+. It is a wide-gap semiconductor and shows photocatalytic activity under UV light for hydrogen generation from aqueous solution without use of any cocatalyst.

Journal Article↗

The interface chemistry between chalcogenide clusters and open framework chalcogenides.

One of the most exciting recent developments concerning molecular architectures is the emerging field of crystalline chalcogenide superlattices that bridges two traditional but distinct areas of research: chalcogenide clusters and porous materials. By combining synthetic and structural concepts in these two areas, many crystalline solids containing spatially organized chalcogenide clusters have been created that exhibit varied properties ranging from microporosity, fast ion conductivity, and photoluminescence to narrow and tunable electronic band gaps. The potential applications of these materials extend beyond traditional areas such as acid catalysis or adsorption-based separation to include shape- or size-selective photocatalysis, solid-state ionics, and electrochemistry.

Journal Article↗

Tetrahedral chalcogenide clusters and open frameworks.

By integrating porosity with electrical or optical properties, microporous chalcogenides may have unique applications. Here we review recent advances and discuss concepts in the synthesis and crystal structure of tetrahedral clusters and their frameworks. These chalcogenides can be viewed as trivalent metal chalcogenides doped with tetra-, di-, or monovalent metal cations. Low-valent cations help to increase the cluster size, while high-valent cations have the opposite effect.

Journal Article↗

Synthetic design of crystalline inorganic chalcogenides exhibiting fast-ion conductivity.

Natural porous solids such as zeolites are invariably formed with inorganic cations such as Na(+) and K(+) (refs 1, 2). However, current research on new porous materials is mainly focused on the use of organic species as either structure-directing or structure-building units; purely inorganic systems have received relatively little attention in exploratory synthetic work. Here we report the synthesis of a series of three-dimensional sulphides and selenides containing highly mobile alkali metal cations as charge-balancing extra-framework cations. Such crystalline inorganic chalcogenides integrate zeolite-like architecture with high anionic framework polarizability and high concentrations of mobile cations. Such structural features are particularly desirable for the development of fast-ion conductors. These materials demonstrate high ionic conductivity (up to 1.8 x 10(-2) ohm(-1) cm(-1)) at room temperature and moderate to high humidity. This synthetic methodology, together with novel structural, physical and chemical properties, may lead to the development of new microporous and open-framework materials with potential applications in areas such as batteries, fuel cells, electrochemical sensors and photocatalysis.

Journal Article↗

Templated assembly of sulfide nanoclusters into cubic-C3N4 type framework.

Here we report a new type of nanocluster superlattice in which each four-connected cluster ([M4In16S31],6- M = Fe, Co, Zn, and Cd) alternates with a three-connected sulfur anion (S2-) to form a rare and yet theoretically important non-centrosymmetric and non-interpenetrating (3,4)-connected net topologically identical to that of the hypothetical cubic carbon nitride type net. These materials have a ring size consisting of 16 tetrahedral atoms. Because of the large cluster size and the elimination of structural intergrowth, the volume fraction of the inorganic framework is as low as 38%. A strong photoluminescent emission has also been observed.

Journal Article↗

Nonaqueous synthesis and selective crystallization of gallium sulfide clusters into three-dimensional photoluminescent superlattices.

A low-temperature, nonaqueous synthesis approach is described that produces a series of gallium sulfide and polysulfide three-dimensional superlattices from binary Ga-S and ternary Zn-Ga-S supertetrahedral clusters. The diversity of superlattices is achieved by modifying the cluster size, the cluster composition, and the inter-cluster linkage mode. Both pure T3 (Ga10S186-) (denoted as UCR-7GaS) and pure T4 (Zn4Ga16S3310-) (denoted as UCR-5ZnGaS) superlattices with ring sizes of 18 and 24 tetrahedral atoms have been made. Of particular interest is the synthesis of the T3-T4 hybrid superlattice (denoted as UCR-19) with an odd ring size of 21 tetrahedral atoms. Another unprecedented feature is the occurrence of the -S-S-S- polysulfide linkage between supertetrahedral clusters in UCR-18. The fluorescent emission wavelength of these materials ranges from 440 to 500 nm and fills the previously observed gap between open-framework oxides and indium sulfides. A comparative study shows that open-framework gallium sulfides are more thermally stable than indium sulfides. They can also undergo ion exchange. It is suggested here that supertetrahedral clusters of different types coexist in a solution and can be selectively crystallized out with a proper choice of structure-directing agents.

Journal Article↗

Microporous and photoluminescent chalcogenide zeolite analogs.

Crystalline semiconducting sulfide and selenide zeolite analogs were synthesized that possess four-connected, three-dimensional tetrahedral networks built from tetravalent (M4+ = Ge4+ or Sn4+, where M = meta) and trivalent (M3+ = Ga3+ or In3+) cations. Microporous materials were obtained in all four combinations of M4+ and M3+, and some of them were thermally stable up to at least 380 degrees C. These materials exhibit framework topologies with pore size ranging from 12 to 24 tetrahedral atoms, high surface area, high framework charge density and ion exchange capacity, and tunable electronic and optical properties.

Journal Article↗

Pushing up the size limit of chalcogenide supertetrahedral clusters: two- and three-dimensional photoluminescent open frameworks from (Cu(5)In(30)S(54))(13-) clusters.

Direct band gap copper indium chalcogenides are of great technological importance in part because of their high photovoltaic conversion efficiency. Covalent superlattices constructed from copper indium chalcogenide clusters are of particular interest because they may combine open framework architecture with semiconducting properties. Here two photoluminescent covalent superlattices built from core-shell type copper indium sulfide supertetrahedral clusters are reported. Each cluster consists of 35 metal cations and is so far the largest known supertetrahedral cluster with a metal-to-metal distance of 1.6 nm. In addition, this is the first example of supertetrahedral clusters in heterometallic copper indium chalcogenides. The preparation of these large clusters has narrowed down the size gap between colloidal nanoclusters and small supertetrahedral clusters and revealed new possibilities in the construction of nanoporous semiconducting superlattices with tunable pore size. Through the combination of metal ions with different oxidation states to provide both overall and local charge neutrality, an effective approach has been demonstrated in the rational synthesis of chalcogenide open framework materials with large and unprecedented supertetrahedral clusters.

Journal Article↗