Synthesis of Au–CdS Core–Shell Hetero‐Nanorods with Efficient Exciton–Plasmon Interactions

The synthesis of large lattice mismatch metal‐semiconductor core–shell hetero‐nanostructures remains challenging, and thus the corresponding optical properties are seldom discussed. Here, we report the gold‐nanorod‐seeded growth of Au–CdS core–shell hetero‐nanorods by employing Ag₂S as an interim layer that favors CdS shell formation through a cation‐exchange process, and the subsequent CdS growth, which can form complete core–shell structures with controllable shell thickness. Exciton–plasmon interactions observed in the Au–CdS nanorods induce shell thickness‐tailored and red‐shifted longitudinal surface plasmon resonance and quenched CdS luminescence under ultraviolet light excitation. Furthermore, the Au–CdS nanorods demonstrate an enhanced and plasmon‐governed two‐photon luminescence under near‐infrared pulsed laser excitation. The approach has potential for the preparation of other metal‐semiconductor hetero‐nanomaterials with complete core–shell structures, and these Au–CdS nanorods may open up intriguing new possibilities at the interface of optics and electronics.     

Preparation of Hollow Zeolite Spheres and Three‐Dimensionally Ordered Macroporous Zeolite Monoliths with Functionalized Interiors

A novel and flexible strategy involving hydrothermal transformation of guest‐incorporated zeolite‐seeded mesoporous silica spheres was proposed to prepare guest‐encapsulated hollow zeolite spheres and three‐dimensionally (3D) ordered macroporous zeolite monoliths. The guest species that were pre‐incorporated into the mesopores of silica spheres could be spontaneously encapsulated inside the formed hollow zeolite shells by consuming silica nutrition of the original mesoporous silica cores during the hydrothermal process. A wide range of guest materials with a size ranging from nanometers to micrometers, e.g., Ag and PdO nanoparticles, and mesoporous spheres of carbon and polymer of micrometer size were successfully encapsulated into both discrete hollow zeolite spheres and 3D ordered macroporous zeolite monoliths. Such materials are expected to find a variety of applications such as catalysis, adsorption, and novel microreactors for their special structures with active species inside and zeolitic porous shell outside.     

Three‐Dimensionally Ordered Macroporous Polymeric Materials by Colloidal Crystal Templating for Reversible CO2 Capture

The design and preparation of porous materials with controlled structures and functionalities is crucial to a variety of absorption‐ or separation‐relevant applications, including CO₂ capture. Here, novel functional polymeric materials with three‐dimensionally ordered macroporous (3DOM) structures are prepared by using colloidal crystals as templates using relatively simple, rapid, and inexpensive approaches. These ordered structures are used for the reversible CO₂ capture from ambient air by humidity swing. Typically, the colloidal crystal template is synthesized from polymer latex particles of poly(methyl methacrylate) (PMMA) or polystyrene (PS). To maintain the functionality of the material, it is important to prevent the porous structure collapsing, which can occur by the hydrolysis of the ester bonds in conventional crosslinkers under basic conditions. This hydrolysis can be prevented by using a water‐soluble crosslinker containing two quaternary ammonium moieties, which can be used to prepare stable porous crosslinked polymers with the monomer (vinylbenzyl)trimethylammonium chloride (VBTMACl) and using a PMMA‐based colloidal crystal template. The hydroxide‐containing monomer and dicationic crosslinker are synthesized from their chloride precursors, avoiding the ion‐exchange step which causes shrinkage of the pores. An analysis of different methods for infiltrating the monomer solution into the colloidal crystal template shows that infiltration using capillary forces leads to fewer defects than infiltration under a partial vacuum. In addition, functional macroporous films with micrometer thickness are prepared from a template of PS‐based colloidal crystals in a thin film. In general, the colloidal crystal templated materials showed improved CO₂ absorption/desorption rates and swing sizes compared to a commercially available material with similar functional groups. This work could easily be extended to create a new generation of ordered macroporous polymeric materials with tunable functionalities for other applications.     

Biopolymer Templated Glass with a Twist: Controlling the Chirality,Porosity, and Photonic Properties of Silica with Cellulose Nanocrystals

A detailed investigation of the formation and properties of mesoporous silica templated by the chiral nematic liquid crystal phase of cellulose nanocrystals (CNCs) is presented. Under appropriate conditions, CNCs co‐assemble with silica up to loadings of ≈60 wt% to give composite films with periodic chiral nanostructures. The periodicity of these films can be readily controlled to obtain materials that selectively reflect light with wavelengths ranging from ≈400–1400 nm. The co‐assembly of CNCs and silica into ordered chiral nematic structures is demonstrated to occur within a narrow window of pH and is affected by aging: a slow rate of silica condensation appears to be vital for the formation of well‐ordered materials. CNCs can be removed from the composite films by calcination or acid hydrolysis to give high surface area chiral nematic mesoporous silica (CNMS) with tunable pore diameters. The combination of mesoporosity and chiral nematic ordering in CNMS enables it to be used in a unique way for refractometric sensing applications. It is shown that, when using circular dichroism (CD) signals to monitor the chiral photonic properties of CNMS, variations in refractive index can be detected based on changes of both CD signal intensity and peak position with good sensitivity.     

Poly(ϵ‐caprolactone)‐Functionalized Carbon Nanotubes and Their Biodegradation Properties

Biodegradable poly(?‐caprolactone) (PCL) has been covalently grafted onto the surfaces of multiwalled carbon nanotubes (MWNTs) by the “grafting from” approach based on in‐situ ring‐opening polymerization of ?‐caprolactone. The grafted PCL content can be controlled easily by adjusting the feed ratio of monomer to MWNT‐supported macroinitiators (MWNT‐OH). The resulting products have been characterized with Fourier‐transform IR (FTIR), NMR, and Raman spectroscopies, transmission electron microscopy (TEM), and scanning electron microscopy (SEM). After PCL was coated onto MWNT surfaces, core/shell structures with nanotubes as the “hard” core and the hairy polymer layer as the “soft” shell are formed, especially for MWNTs coated with a high density of polymer chains. Such a polymer shell promises good solubility/dispersibility of the MWNT–PCL nanohybrids in low‐boiling‐point organic solvents such as chloroform and tetrahydrofuran. Biodegradation experiments have shown that the PCL grafted onto MWNTs can be completely enzymatically degraded within 4 days in a phosphate buffer solution in the presence of pseudomonas (PS) lipase, and the carbon nanotubes retain their tubelike morphologies, as observed by SEM and TEM. The results present possible applications for these biocompatible PCL‐functionalized CNTs in bionanomaterials, biomedicine, and artificial bones.     

Polyaniline–Silica Composite Conductive Capsules and Hollow Spheres

In this paper, we report on the preparation of monodisperse polyaniline (PANi)–silica composite capsules and hollow spheres on monodisperse core–gel‐shell template particles. An extension of the previously reported inward growth method was used. The samples were self‐stabilized without external additives. The core–gel‐shell particles were prepared by the inward sulfonation of monodisperse polystyrene particles. The introduced sulfonic acid and sulfone groups are responsible for the gel properties. The gel‐shell thickness and core size were synchronously controlled over the whole particle radius range. After aniline (ANi) monomer was preferentially absorbed in the sulfonated polystyrene shell, PANi was formed by polymerization. PANi was doped in situ with a sulfonic acid group to give the capsules a high conductivity. PANi hollow spheres were derived after the polystyrene cores were dissolved: their cavity size and shell thickness were synchronously controlled by using different core–gel‐shell particles. The PANi–silica composite capsules and hollow spheres were therefore prepared by a sol–gel process using tetraethylorthosilicate in the conducting shell. The PANi shell became more robust while maintaining the same conductivity level. Morphological results indicate that the PANi and silica formed a bicontinuous network. Fourier‐transform infrared (FTIR) spectra revealed that the hydrogen bonding in the PANi–gel shell was enhanced after the silica phase was incorporated, which could explain the high conductivity level after the silica phase was added. In a converse procedure, silica capsules and hollow spheres were prepared by a sol–gel process that incorporated tetraethylorthosilicate into the core–gel‐shell templates, which was followed by the absorption and polymerization of aniline in the silica shell thus forming PANi–silica composite capsules and hollow spheres. The silica capsules and hollow spheres thereby became conductive.     

Brilliant Pitaya‐Type Silica Colloids with Central–Radial and High‐Density Quantum Dots Incorporation for Ultrasensitive Fluorescence Immunoassays

Creating secondary nanostructures from fundamental building blocks with simultaneous high loading capacity and well‐controlled size/uniformity, is highly desired for nanoscale synergism and integration of functional units. Here a novel strategy is reported for hydrophobic quantum dots (QDs) assembley with porous templates, to form pitaya‐type fluorescent silica colloids with densely packed and intact QDs throughout the silica matrix. The mercapto‐terminated dendritic silica spheres with highly accessible central–radial pores and metal‐affinity interior surface, are adopted as a powerful absorbent host for direct immobilization of QDs from organic phase with high loading capacity. The alkylsilane mediated silica encapsulation prevents QDs' optical degradation induced by ligand exchange and favors the homogeneous silica shell formation. These multiple QD embedded silica spheres exhibit good compatibility for different colored QDs with well‐preserved fluorescence, high colloidal/optical stability, and versatile surface functionality. It is demonstrated that after integration with a lateral flow strip platform, these silica colloids provide an ultrasensitive, specific, and robust immunoassay for C‐reaction protein in clinical samples as promising fluorescent reporters.     

Surfactant‐Free,Self‐Assembled PVA‐Iron Oxide/Silica Core–Shell Nanocarriers for Highly Sensitive,Magnetically Controlled Drug Release and Ultrahigh Cancer Cell Uptake Efficiency

Surfactant‐free, self‐assembled iron oxide/silica core–shell (SAIO@SiO₂) nanocarriers were synthesized as bifunctional magnetic vectors that can be triggered for the controlled release of therapeutic agents by an external magnetic field. In addition, drug release profiles can be well‐regulated through an ultrathin layer of silica shell. The hydrophobic drug molecules were encapsulated within the iron oxide‐PVA core and then further covered with a thin‐layer silica shell to regulate the release pattern. Remote control of drug release from the SAIO@SiO₂ nanocarriers was achieved successfully using an external magnetic field where the core phase being structurally disintegrated to a certain extent while subjected to magnetic stimulus, resulting in a burst release of the encapsulated drug. However, a relatively slow and linear release restored immediately, directly after removal of the stimulus. The nanostructural evolution of the nanocarriers upon the stimulus was examined and the mechanism for controlled drug release is proposed for such a core–shell nanocarrier. Surprisingly, the surfactant‐free SAIO@SiO₂ nanocarriers demonstrated a relatively high uptake efficiency from the HeLa cell line. Together with a well‐regulated controlled release design, the nanocarriers may provide great advantages as an effective cell‐based drug delivery nanosystem for biomedical applications.     

All‐Natural Oil‐Filled Microcapsules from Water‐Insoluble Proteins

The formation and characterization of a novel class of all‐natural digestible microcapsules containing a liquid lipid core encapsulated by a water‐insoluble protein shell with tunable thickness is demonstrated. As an example of a water‐insoluble protein, zein is used—the protein of corn—which is an attractive biomaterial from a sustainable source. The microcapsules are prepared by a direct and simple method, based on the precipitation of protein from the continuous phase of an oil‐in‐(water/ethanol) emulsion onto the oil droplets without the need of any surfactant. The shell thickness can be controlled by the amount of precipitated protein. An in vitro digestion assay is performed to study the lipid hydrolysis and biodegradability. The rate of lipid hydrolysis and release of fatty acids are highly dependent on the protein shell thickness. All‐natural edible microcapsules with controlled degradation under gastrointestinal conditions can enable new applications for oral delivery systems. They may further be used as a model system for controlled release studies of lipophilic compounds and could promote the sustainable use of underutilized water insoluble proteins as functional biomaterials.     

Template‐Assisted Self‐Assembly of Spherical Colloids into Complex and Controllable Structures

Colloidal aggregates with well‐controlled sizes, shapes, and structures have been fabricated by dewetting aqueous dispersions of monodispersed spherical colloids across surfaces patterned with two‐dimensional arrays of relief structures (or templates). The capability and feasibility of this approach have been demonstrated with the organization of polymer latex or silica beads into homo‐aggregates, including circular rings; polygonal and polyhedral clusters; and linear, zigzag, and spiral chains. It was also possible to generate hetero‐aggregates in the configuration of HF and H₂O molecules that contained spherical colloids of different sizes, compositions, densities, functions, or a combination of these features. These uniform, well‐defined aggregates of spherical colloids are ideal model systems to investigate the aerodynamic, hydrodynamic, and optical properties of colloidal particles characterized by non‐spherical shapes and/or complex topologies. They can also serve as a new class of building blocks to generate hierarchically self‐assembled structures that are expected to exhibit interesting features valuable to areas ranging from condensed matter physics to photonics.     

Spherical MSU‐1 Mesoporous Silica Particles Tuned for HPLC

Among the mesoporous silica micellar templated structures (MTSs), MSU‐X silica, obtained through an N⁰I⁰ assembly between non‐ionic polyethyleneoxide‐based surfactants (N⁰) and silica neutral inorganic precursors (I⁰), exhibits a regular ordered structure with a 3D wormhole porous framework and an easily controlled pore size. These materials have been tested for applications requiring both a narrow mesopore size distribution and isotropic properties. A specific double‐step synthesis that we developed recently for MSU‐X materials has allowed us to prepare mesoporous silica particles with the required shape, size, and properties. Both the particles’ synthesis and comparative HPLC separation tests with a commercial ungrafted silica HPLC powder of identical shape and size are reported.     

Core–Shell Nanoparticle Interface and Wetting Properties

Latex colloids are among the most promising materials for broad thin film applications due to their facile surface functionalization. Yet, the effect of these colloids on chemical film and wetting properties cannot be easily evaluated. At the nanoscale, core–shell particles can deform and coalesce during thermal annealing, yielding fine‐tuned physical properties. Two different core–shell systems (soft and rigid) with identical shells but with chemically different core polymers and core sizes are investigated. The core–shell nanoparticles (NPs) are probed during thermal annealing in order to investigate their behavior as a function of nanostructure size and rigidity. X‐ray scattering allows to follow the re‐arrangement of the NPs and the structural evolution in situ during annealing. Evaluation by real‐space imaging techniques reveals a disappearance of the structural integrity and a loss of NP boundaries. The possibility to fine‐tune the wettability by tuning the core–shell NPs morphology in thin films provides a facile template methodology for repellent surfaces.     

Multiresponsive Elastic Colloidal Crystals for Reversible Structural Color Patterns

Multiresponsive elastic poly(methyl methacrylate‐butyl acrylate) (P(MMA‐BA)) copolymer nanoparticles with controlled sizes are fabricated through a one‐step method, which further serve as building blocks for the construction of multiresponsive films via self‐assembly. Taking advantage of the relatively low glass transition temperature and the core–shell structure of the copolymer nanoparticles, they possess the capacity to partially deform and fuse at room temperature under dry status, eventually resulting in the enhancement of the mechanical properties as well as the control of optical properties in the assembled ordered structures. The generated elastic films not only can control the concealment or exhibition of the designed color information, but also can rapidly respond to external stimuli such as the solvent, pH, and tensile force in a reversible fashion. These functional elastic copolymer nanoparticles have potential applications in dynamic color display, optical sensing, and anticounterfeiting.     

Porous Iron–Cobalt Alloy/Nitrogen‐Doped Carbon Cages Synthesized via Pyrolysis of Complex Metal–Organic Framework Hybrids for Oxygen Reduction

Efficient and stable nonprecious metal electrocatalysts for oxygen reduction are of great significance in some important electrochemical energy storage and conversion systems. As a unique class of porous hybrid materials, metal–organic frameworks (MOFs) and their composites are recently considered as promising precursors to derive advanced functional materials with controlled structures and compositions. Here, an “MOF‐in‐MOF hybrid” confined pyrolysis strategy is developed for the synthesis of porous Fe–Co alloy/N‐doped carbon cages. A unique “MOF‐in‐MOF hybrid” architecture constructed from a Zn‐based MOF core and a Co‐based MOF hybrid shell encapsulated with FeOOH nanorods is first prepared, followed by a pyrolysis process to obtain a cage‐shaped hybrid material consisting of Fe–Co alloy nanocrystallites evenly distributed inside a porous N‐doped carbon microshell. Of note, this strategy can be extended to synthesize many other multifunctional “nanosubstrate‐in‐MOF hybrid” core–shelled structures. Benefiting from the structural and compositional advantages, the as‐derived hybrid cages exhibit superior electrocatalytic performance for the oxygen reduction reaction in alkaline solution. The present approach may provide some insight in design and synthesis of complex MOF hybrid structures and their derived functional materials for energy storage and conversion applications.     

Hierachically Structured Hollow Silica Spheres for High Efficiency Immobilization of Enzymes

In this work, the first example of a hierarchically structured hollow silica system is reported without any chemical modification to the enzyme involved in the process. The leaching of the physically adsorbed enzyme is substantially restrained in comparison to pure hollow silica supports. The hierarchical architecture is composed of the ordered hollow silica spheres with a shell‐in‐shell structure. This rationally integrated architecture, which serves as the host for glucose oxidase immobilization, displays many significant advantages, including increases in mechanical stability, enzyme loading, and bioactivity, and a decrease in enzyme leaching compared to existing pure hollow silica matrices. This facilitates further multifarious applications for enhanced enzyme immobilization, biosensors, and biocatalysis.     

Order Mesoporous Carbon Spheres with Precise Tunable Large Pore Size by Encapsulated Self‐Activation Strategy

Order mesoporous carbon spheres (O‐MCS) have wide applications in catalysis, absorption, and energy storage/conversion due to their ordered mesoporous channels, large surface areas, and quantum effects in the nanoscale. However, realizing a precise control of large mesoporous size still remains a big challenge. Herein, an encapsulated self‐activation strategy to prepare highly ordered mesoporous carbon spheres with precise tunable large pore sizes is first reported. The large mesopore size is achieved by encapsulating mesoporous polymer sphere in compact silica shell for pyrolysis process. Moreover, the self‐activation mechanism endows the O‐MCS high surface area, large mesoporous size, and pore volume. In addition, simply increasing the amount of silica precursor will enlarge the pore sizes of O‐MCS from 3.1 to 10.0 nm with increased specific surface area from 696 to 1186 m² g^?1. The large order mesoporous structure of O‐MCS, which can facilitate diffusion of guest molecules in the channels exhibit great advantage in the adsorption and electrochemical applications.     

Luminescent Core/Shell Nanoparticles with a Rhabdophane LnPO4‐xH2O Structure: Stabilization of Ce3+‐Doped Compositions

The core/shell strategy has been successfully developed for rhabdophane lanthanide phosphate aqueous colloids. The growth of a LaPO₄‐xH₂O shell around Ce,Tb‐doped core nanoparticles increases their stability against oxidation. A bright green luminescence is thus preserved in sol–gel films whose fabrication requires silica coating and thermal treatment of the core/shell nanoparticles.     

Dimer‐Based Three‐Dimensional Photonic Crystals

The self‐assembly of polystyrene dimer‐ and spherocylinder‐shaped colloids is achieved via controlled drying on glass and silicon substrates. 3D monoclinic colloidal crystal structures are determined from scanning electron microscopy images of sections prepared using focused ion‐beam (FIB) milling. Full photonic bandgaps between the eighth and ninth bands are found for a systematic range of colloidal dimer shapes explored with respect to the degree of constituent lobe fusion and radius ratio. The pseudogap between bands 2 and 3 for spherocylinder‐based monoclinic crystals is also probed using normal incidence reflection spectroscopy.     

Yolk–Shell Hybrid Materials with a Periodic Mesoporous Organosilica Shell: Ideal Nanoreactors for Selective Alcohol Oxidation

This contribution describes the preparation of multifunctional yolk–shell nanoparticles (YSNs) consisting of a core of silica spheres and an outer shell based on periodic mesoporous organosilica (PMO) with perpendicularly aligned mesoporous channels. The new yolk–shell hybrid materials were synthesised through a dual mesophase and vesicle soft templating method. The mesostructure of the shell, the dimension of the hollow space (4～52 nm), and the shell thickness (16～34 nm) could be adjusted by precise tuning of the synthesis parameters, as evidenced by X‐ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM) and nitrogen sorption investigations. Various metal nanoparticles (e.g., Au, Pt, and Pd) were encapsulated and confined in the void space between the core and the shell using impregnation and reduction of adequate metal precursors. The selective oxidation of various alcohol substrates was then carried out to illustrate the benefits of such an architecture in catalysis. High conversion (～100%) and excellent selectivity (～99%) were obtained over Pd nanoparticles encapsulated in the hybrid PMO yolk–shell structures.     

Ordered Mesoporous C70 with Highly Crystalline Pore Walls for Energy Applications

Mesoporous materials with carbon framework structure can offer distinctive functionalities with tunable electronic or catalytic properties. Many synthetic routes including hard or soft templating approaches are developed for the fabrication of various ordered mesoporous carbon based materials which have demonstrated unique catalytic and energy storage properties. So far, most of these techniques deliver only mesoporous carbon with amorphous wall structures which limit their performance in many applications. Fullerenes exhibit unique structure and significant properties including superconductivity, electrochemical stability, and heat resistance. Herein, for the first time, the preparation of highly ordered mesoporous fullerene C₇₀ materials with tunable porous structure and controlled rod‐shaped morphology through the thermal oligomerization of fullerene C₇₀ molecules inside the mesopore channels of SBA‐15 silica as a hard template with the help of chlorinated aromatics, wherein the solubility of fullerenes is high, is reported. It is demonstrated that these metal‐free mesoporous fullerene C₇₀ framework with a high surface area and bimodal pores with multifunctionality exhibit excellent performance in the oxygen reduction reaction for fuel cells and supercapacitors. This simple strategy can also be extended to other fullerene nanostructures with different carbon atoms which can exhibit interesting physicochemical properties and find applications in catalysis and energy storage.