Shaped zeolite nanocrystals and larger zeolite particles with three-dimensionally ordered mesoporous (3DOm) features hold exciting technological implications for manufacturing thin, oriented molecular sieve films and realizing new selective, molecularly accessible and robust catalysts. A recognized means for controlled synthesis of such nanoparticulate and imprinted materials revolves around templating approaches, yet identification of an appropriately versatile template has remained elusive. Because of their highly interconnected pore space, ordered mesoporous carbon replicas serve as conceptually attractive materials for carrying out confined synthesis of zeolite crystals. Here, we demonstrate how a wide range of crystal morphologies can be realized through such confined growth within 3DOm carbon, synthesized by replication of colloidal crystals composed of size-tunable (about 10-40 nm) silica nanoparticles. Confined crystal growth within these templates leads to size-tunable, uniformly shaped silicalite-1 nanocrystals as well as 3DOm-imprinted single-crystal zeolite particles. In addition, novel crystal morphologies, consisting of faceted crystal outgrowths from primary crystalline particles have been discovered, providing new insight into constricted crystal growth mechanisms underlying confined synthesis.

Abstract:Due to its exceptionally outstanding electrical, mechanical and thermal properties, graphene is being explored for a wide array of applications and has attracted enormous academic and industrial interest.Graphene and its derivatives have also been considered as promising nanoscale fillers in gas barrier application of polymer nanocomposites (PNCs). In this review, recent research and development of the utilization of graphene and its derivatives in the fabrication of nanocomposites with different polymer matrices for barrier application are explored. Most synthesis methods of graphene-based PNCs are covered, including solution and melt mixing, in situ polymerization and layer-by-layer process.Graphene layers in polymer matrix are able to produce a tortuous path which works as a barrier structure for gases. A high tortuosity leads to higher barrier properties and lower permeability of PNCs. The influence of the intrinsic properties of these fillers (graphene and its derivatives) and their state of dispersion in polymer matrix on the gas barrier properties of graphene/PNCs are discussed. Analytical modeling aspects of barrier performance of graphene/PNCs are also reviewed in detail. We also discuss and address some of the work on mixed matrix membranes for gas separation.

Anisotropic II-VI semiconductor nanocrystals and nanoparticles have become important building blocks for (potential) nanotechnological applications. Even though a wide variety of differently shaped nanoparticles of this class can be prepared, the underlying mechanisms are mostly not fully understood. This Review article provides a brief overview of the currently studied shape-evolution mechanisms and the most prominent synthesis methods for such particles, with an aim to provide a fundamental understanding on how different morphologies evolve, and to function as a tool to aid in the preparation of specific nanocrystals.

MCM-22(P), the precursor to zeolite MCM-22, consists of stacks of layers that can be swollen and exfoliated to produce catalytically active materials. However, the current swelling procedures result in significant degradation of crystal morphology along with partial loss of crystallinity and dissolution of the crystalline phase. Fabrication of polymer nanocomposites and coatings with MCM-22 for separation, barrier, and other applications requires a swelling method that does not alter drastically the crystal morphology and layer structure and preserves the high aspect ratio of the layers. Here, we demonstrate such a method by swelling MCM-22(P) at room temperature. The low-temperature process does not disrupt the framework connectivity present in the parent MCM-22(P) material. By extensive washing with water, the swollen material, MCM-22(PS-RT), evolves to a new ordered layered structure. Interestingly, the swelling procedure is reversible and the swollen material can be restored back to MCM-22(P) by acidification of the sample. The swollen material can also be pillared to produce an MCM-36 analogue. It can also be exfoliated, and layers can be incorporated in a polymer matrix to make nanocomposites.

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Size- and shape-dependent property modifications of semiconductor nanocrystals have been a subject of intense interest because of their potential for future engineering devices. The bandgap and related optical-property tuning of these materials are mainly governed by the nature of their band edges. In addition, fusing one type of nanocrystal over another enables further control of material properties that are dependent on the relative alignments of their energy levels. On a molecular scale, the synthesis of supramolecular compounds has inspired advances in theories for photoinduced charge transfer. Heterostructured nanocrystals potentially provide a nanoscale analog of such systems. A method for preparing heterostructured nanocrystals of complex morphologies showing photoinduced charge separation is presented. It is shown that the energy and lifetime of the charge-transfer photoluminescence band can be tuned by changing the relative alignment of band edges in CdSe/CdTe heterostructure nanorods. The long-lived charge transfer states in these type II semiconductors may make them attractive for photovoltaic applications.

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This article reviews recent developments in the microfluidic preparation of different types of particles made of polymeric and inorganic materials. We discuss control of the particle sizes, morphologies, shapes, and structures in terms of various features of microfluidic synthesis.