Yifeng Shi

Ordered Mesoporous Metallic MoO2 Materials with Highly Reversible Lithium Storage Capacity

Highly ordered mesoporous crystalline MoO(2) materials with bicontinuous Ia3d mesostructure were synthesized by using phosphomolybdic acid as a precursor and mesoporous silica KIT-6 as a hard template in a 10% H(2) atmosphere via nanocasting strategy. The prepared mesoporous MoO(2) material shows a typical metallic conductivity with a low resistivity ( approximately 0.01Omega cm at 300 K), which makes it different from all previously reported mesoporous metal oxides materials. Primary test found that mesoporous MoO(2) material exhibits a reversible electrochemical lithium storage capacity as high as 750 mA h g(-1) at C/20 after 30 cycles, rendering it as a promising anode material for lithium ion batteries.

Fabrication of Ag@SiO2@Y2O3:Er Nanostructures for Bioimaging: Tuning of the Upconversion Fluorescence with Silver Nanoparticles

We demonstrated that the nanostructures comprising silver cores and dense layers of Y(2)O(3):Er separated by a silica shell are an excellent model system to study the interaction between upconversion materials and metals in nanoscale. This architecture allows for versatile control of the Y(2)O(3):Er-metal interaction through control of the silica dielectric spacer thickness and the metal-core size. Finally, the nanoparticles are potentially interesting as fluorescent labels in, for instance (single particle), imaging experiments or bioassays which require low background or tissue penetrating wavelengths.

Mesoporous Multifunctional Upconversion Luminescent and Magnetic "Nanorattle" Materials for Targeted Chemotherapy

Nanorattles consisting of hydrophilic, rare-earth-doped NaYF(4) shells each containing a loose magnetic nanoparticle were fabricated through an ion-exchange process. The inner magnetic Fe(3)O(4) nanoparticles are coated with a SiO(2) layer to avoid iron leaching in acidic biological environments. This multifunctional mesoporous nanostructure with both upconversion luminescent and magnetic properties has excellent water dispersibility and a high drug-loading capacity. The material emits visible luminescence upon NIR excitation and can be directed by an external magnetic field to a specific target, making it an attractive system for a variety of biological applications. Measurements on cells incubated with the nanorattles show them to have low cytotoxicity and excellent cell imaging properties. In vivo experiments yield highly encouraging tumor shrinkage with the antitumor drug doxorubicin (DOX) and significantly enhanced tumor targeting in the presence of an applied magnetic field.

Ordered mesoporous non-oxide materials

Ordered mesoporous inorganic non-oxide materials attract increasing interest due to their plenty of unique properties and functionalities and potential applications. Lots of achievements have been made on their synthesis and structural characterization, especially in the last five years. In this critical review, the ordered mesoporous non-oxide materials are categorized by compositions, including non-oxide ceramics, metal chalcogenides, metal nitrides, carbides and fluorides, and systematically summarized on the basis of their synthesis approaches and mechanisms, as well as properties. Two synthesis routes such as hard-templating (nanocasting) and soft-templating (surfactant assembly) routes are demonstrated. The principal issues in the nanocasting synthesis including the template composition and mesostructure, pore surface chemistry, precursor selection, processing and template removal are emphatically described. A great number of successful cases from the soft-templating method are focused on the surfactant liquid-crystal mesophases to synthesize mesostructured metal chalcogenide composites and the inorganic-block-organic copolymer self-assembly to obtain non-oxide ceramics (296 references).

Designed synthesis of mesoporous solids via nonionic-surfactant-templating approach

The continual needs for improved performances in applications derived by diversified compositions and mesostructures have pushed forward the development of mesoporous solids. The nonionic-surfactant-templating approach has been a critical route in this advancement. A large number of nonionic surfactants widely used in industries and featured with low cost, low toxicity, bio-degradation and ordered microdomains can be utilized as effective templates to the design and synthesis of abundant mesoporous solids. This feature article provides recent reports on the use of nonionic surfactant self-assembly as examples to fabricate high-quality ordered mesoporous solids which illustrates advances in synthesis and understanding of formation mechanisms. It includes the selection of surfactants, a summary of the effects of synthetic parameters, the current understanding of the synthetic pathways and related mechanisms with some emphasis on evaporation induced self-assembly (EISA), as well as the design and synthesis on the microscale (atomic and molecular compositions) and mesoscale (mesostructures). Preliminary applications of mesoporous solids particularly in optical devices, electrodes and biomaterials are also presented.

Fluorescence Upconversion Microbarcodes for Multiplexed Biological Detection: Nucleic Acid Encoding

Fluoride rare-earth-doped upconversion microbarcodes have been successfully developed for multiplexed signaling and nucleic-acid encoding. This kind of novel barcode material can be used for rapid and sensitive analysis of nucleic acids and antigens, which would have many potential applications in clinical, food, and environment detection.

Container Effect in Nanocasting Synthesis of Mesoporous Metal Oxides

We report a general reaction container effect in the nanocasting synthesis of mesoporous metal oxides. The size and shape of the container body in conjunction with simply modifying the container opening accessibility can be used to control the escape rate of water and other gas-phase byproducts in the calcination process, and subsequently affect the nanocrystal growth of the materials inside the mesopore space of the template. In this way, the particle size, mesostructure ordering, and crystallinity of the final product can be systemically controlled. The container effect also explain some of the problems with reproducibility in previously reported results.

Anionic surfactant induced mesophase transformation to synthesize highly ordered large-pore mesoporous silica structures

Successive mesophase transformation induced by an anionic surfactant such as sodium dioctyl sulfosuccinate (AOT) has been demonstrated to fabricate four kinds of large pore mesoporous silica materials in a triblock copolymer F127 surfactant assembly system. The transformation of the highly ordered mesostructures from face-centered cubic (space group Fmm) to body-centered Imm then towards two-dimensional (2-D) hexagonal p6m and eventually to cubic bicontinuous Iad symmetries has been achieved by tuning the amount of AOT and 1,3,5-trimethylbenzene (TMB). Characterization by small-angle X-ray scattering (SAXS), powder X-ray diffraction (XRD), transmission electron microscopy (TEM) and N2 sorption isotherms reveals that all mesoporous silica structures have highly ordered regularity in large domains and possess high surface areas, large pore volumes and uniform pore sizes. The expansion of hydrophobic volume in the amphiphilic Pluronic F127 surfactant associated with AOT and TMB molecules in an acidic media is attributed to the observed mesophase transformation. A further swelling of the surfactant micelles can be achieved by adding TMB molecules into the mixed AOT and F127 surfactants system due to their synergistic solubility enhancement, which gives rise to a long-range ordered 2-D hexagonal mesoporous silica structure with very large cell parameter (a = 16.5 nm) and pore size (∼12 nm). The understanding of the blend–surfactant assembly mechanism will lead to a more rational approach for economical and large-scale production of mesoporous materials with controllable structures.

Magnetic Permanently Confined Micelle Arrays for Treating Hydrophobic Organic Compound Contamination

Magnetic permanently confined micelle arrays (Mag-PCMAs) have been successfully synthesized as sorbents for hydrophobic organic compound (HOC) removal from contaminated media. The synthesis of Mag-PCMAs involves coating a silica/surfactant mesostructured hybrid layer on the negatively charged Fe(3)O(4) microparticles to create a core/shell structure. The surfactant, 3-(trimethoxysily)propyl-octadecyldimethyl-ammonium chloride (TPODAC), has a reactive endgroup -Si(OCH(3))(3) on its hydrophilic groups, which allows the surfactant micelles to permanently anchor on the silica framework through covalent bonding. This unique structural property avoids surfactant loss during application and allows for sorbent regeneration. The isotherms and kinetics of four representative HOCs (atrazine, diuron, naphthalene, and biphenyl) onto Mag-PCMAs were determined, and the regeneration and reusability of Mag-PCMAs for diuron removal was also investigated. As a proof of principle for application of Mag-PCMAs for soil-washing, the use of Mag-PCMAs for removal of diuron from a contaminated soil was also demonstrated. All of the results showed that Mag-PCMAs are reusable sorbents for fast, convenient, and highly efficient removal of HOCs from contaminated media.

Rare‐Earth Upconverting Nanobarcodes for Multiplexed Biological Detection

Since the decoding of the human genome, the need to obtain more and more molecular information from smaller and smaller samples is intensifying. Biosystem-analysis, disease diagnosis, and biomedical studies all require the tracking of spatio-temporal information from multiple targets, involving proteins, genes, lipids and glycans for target pattern recognition and system definition. Multiplexed assays are therefore required in order to complement advances in genomics and proteomics, and to allow a large number of nucleic acids and proteins to be rapidly screened.[1–4]