Abstract:Fabrication of block copolymer (BCP) template-assisted nano-catalysts has been a subject of immense interest in the field of catalysis and polymer chemistry for more than two decades now. Different methods, such as colloidal route, on-substrate methods, bulk self-assembly approaches, combined approaches, and many others have been used to prepare such nano-catalysts. The present review focuses on the advances made in this direction using diblock, triblock, and other types of BCP self-assembled structures. It wi… Show more
“…Block copolymers composed of more than one species of monomer linked by chemical bonds have also been used as chiral assemblies. 35 The morphologies of block copolymers depend on the thermal equilibrium condition with respect to the volume fraction of monomer blocks. Thus, various morphologies, such as lamellae and cylinders, and even chiral geometries, like gyroid, 36,37 spiral, 38–40 toroid, 41 and helix, can be obtained by exploiting phase separation and reconstructions of block copolymers.…”
Section: Part 1 3d Self-assembly For Fabrication Of Chiral Metamaterialsmentioning
Artificial chiral structures have possible applications in the field of enantioselective signal sensing. Advanced nanofabrication methods enable a large diversity in geometric structures and broad selectivity of materials, which can...
“…Block copolymers composed of more than one species of monomer linked by chemical bonds have also been used as chiral assemblies. 35 The morphologies of block copolymers depend on the thermal equilibrium condition with respect to the volume fraction of monomer blocks. Thus, various morphologies, such as lamellae and cylinders, and even chiral geometries, like gyroid, 36,37 spiral, 38–40 toroid, 41 and helix, can be obtained by exploiting phase separation and reconstructions of block copolymers.…”
Section: Part 1 3d Self-assembly For Fabrication Of Chiral Metamaterialsmentioning
Artificial chiral structures have possible applications in the field of enantioselective signal sensing. Advanced nanofabrication methods enable a large diversity in geometric structures and broad selectivity of materials, which can...
“…Block copolymers (BCPs) have gained remarkable attention as crucial materials for controlling the spatial positioning of various types as well as multiple types of nanoparticles. − For example, Haridas and Basu have demonstrated the fabrication of hybrid arrays comprising CdSe QDs and AuNPs using BCP thin films as templates. Lü et al have demonstrated a quick and efficient way to precisely control the dispersion and localization of QDs in BCP micelles via coordination interaction.…”
In the present work, we report the fabrication and characterization of well-defined core-satellite nanostructures. These nanostructures comprise block copolymer (BCP) micelles, containing a single gold nanoparticle (AuNP) in the core and multiple photoluminescent cadmium selenide (CdSe) quantum dots (QDs) attached to the micelle's coronal chains. The asymmetric polystyrene-block-poly(4-vinylpyridine) (PS-b-P4VP) BCP was employed to develop these core-satellite nanostructures in a series of P4VP-selective alcoholic solvents. The BCP micelles were first prepared in 1-propanol and subsequently mixed with AuNPs, followed by gradual addition of CdSe QDs. This method resulted in the development of spherical micelles that contained a PS/Au core and a P4VP/CdSe shell. These core-satellite nanostructures, developed in different alcoholic solvents, were further employed for the time-resolved photoluminescence analysis. It was found that solvent-selective swelling of the core-satellite nanostructures tunes the distance between the QDs and AuNPs and modulates their Forster resonance energy transfer (FRET) behavior. The average lifetime of the donor emission varied from 12.3 to 10.3 nanoseconds (ns) with the change in the P4VP-selective solvent within the core-satellite nanostructures. Furthermore, the distances between the donor and acceptor were also calculated using efficiency measurements and corresponding Forster distances. The resulting core-satellite nanostructures hold promising potential in various fields, such as photonics, optoelectronics, and sensors that utilize the FRET process.
“…Among these, self-assembly of rod-rod BCPs was rarely studied because of severe polymerization conditions. Spherical micelles and vesicles could be easily obtained via self-assembly of coil-coil BCPs, showing extensive applications as templates, 5,6 catalysts, 7,8 nanoreactors, 9,10 etc. However, the phase region of the nonspherical morphologies is extremely narrow, 11 which restricts some morphology-dependent applications in biomedicine, [12][13][14] stimuliresponsive materials, [15][16][17][18][19] controlled drug delivery systems, 20,21 and so on.…”
Anisotropic polymeric nanoparticles (NPs) have attracted considerable attention due to their morphology-dependent applications in the fields of nanocatalysts, drug delivery and sensors. By introducing liquid crystalline (LC) driving force into NPs, the region of non-spherical shapes in phase diagrams can be broadened effectively, which attracts great interest of many researchers. LC mesogens can be easily introduced to monomers, such as acrylates and methacrylates, as side groups connected by spacers with tunable length, and then side-chain LC polymers can be acquired after polymerization accordingly. Among these polymers, amphiphilic block copolymers (BCPs) have been widely studied, attributed to their property of spontaneous assembly into NPs under appropriate conditions. In this review, based on traditional solution self-assembly and polymerization-induced self-assembly, the recent research into side-chain LC BCP NPs is elaborated in terms of the aspects of the types of LC mesogens, LC phases, morphologies and functionalities. Finally, we summarize recent progress, and prospect the development trend in the future.
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