UNIST · 재료과학
Kang Hee Ku 교수의 연구실은 블록코폴리머를 활용한 나노입자 설계와 형태 제어를 핵심으로 하며, 상전이, 표면 에너지 조절, 외부 자극 반응성 등을 통해 기능성 입자 및 스마트 재료를 개발하고 있습니다. 특히 에멀젼을 이용한 증발 유도 조립을 통해 삼각형, 두꺼비상, 라즈베리 모양의 패치드 입자나, 광학적·화학적 자극에 반응하는 형태 변화 입자를 정밀하게 제조합니다. 이는 나노소재의 기계적·광학적·물리화학적 특성을 제어하는 데 기여합니다.
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Abstract Colloidal particles with controlled shape and internal structure have attracted great attention due to their novel morphologies and various potential applications. Among the diverse synthetic strategies toward anisotropically shaped polymer particles, facile and accurate engineering of such structures remains challenging. This review highlights the synthetic approaches to manipulate the shape of polymer particles driven by phase separation in emulsions upon solvent evaporation. And, spe
The tuning of interfacial properties at selective and desired locations on the particles is of great importance to create the novel structured particles by breaking the symmetry of their surface property. Herein, a dramatic transition of both the external shape and internal morphology of the particles of polystyrene-b-poly(4-vinylpyridine) (PS-b-P4VP) was induced by precise positioning of size-controlled Au nanoparticle surfactants (Au NPs). The size-dependent assembly of the Au NPs was localize
A series of porous block copolymer (BCP) particles with controllable morphology and pore sizes was fabricated by tuning the interfacial behavior of BCP droplets in oil-in-water emulsions. A synergistic adsorption of polystyrene-b-poly(4-vinylpyridine) (PS-b-P4VP) BCPs and sodium dodecyl sulfate (SDS) to the surface of the emulsion droplet induced a dramatic decrease in the interfacial tension and generated interfacial instability at the particle surface. In particular, the SDS concentration and
We report a simple and practical method for creating colloidal patchy particles with a variety of three-dimensional shapes via the evaporation-induced assembly of polystyrene-b-poly(4-vinylpyridine) (PS-b-P4VP) block copolymer (BCP) in an oil-in-water emulsion. Depending on the particle volume, a series of patchy particles in the shapes of snowmen, dumbbells, triangles, tetrahedra, and raspberry can be prepared, which are then precisely tuned by modulating the interfacial interaction at the part
We report a simple and robust strategy to prepare pH-responsive biphasic Janus particles composed of polystyrene/poly(2-vinylpyridine) (PS/P2VP) homopolymers that are able to control the reversible formation, breakage, and switching of Pickering emulsions depending on their geometry- and pH-dependent hydrophilic–lipophilic balance. The chemical stability of these PS/P2VP Janus particles was tuned through the incorporation of cross-linkable benzophenone units along the backbone of the homopolymer
Self-assembly of block copolymers (BCPs) in evaporative emulsion provides a simple and effective route for the preparation of anisotropic particles with controlled shape and size. Understanding of thermodynamic phenomena associated with the bending/stretching of the BCP chains confined within the particles is necessary to enable precise control of the shape and microstructure of the particles. Herein, we report the systematic design of shape-anisotropic diblock copolymer (dBCP) particles based o
Multicolor emitting microspheres with three dimensionally controlled nanostructures are produced via a simple and efficient method. Location control and separation of the quantum dots (QDs) within the microspheres are achieved by a supramolecular assembly of block copolymer micelles to control the Förster resonance energy transfer efficiency between the different-colored QDs. As a service to our authors and readers, this journal provides supporting information supplied by the authors. Such mater
The effect of aspect ratio (AR) of nanorod surfactants on the shape and internal morphology of block copolymer (BCP) particles was systemically investigated using CuPt nanorods with different AR values ranging from 1 to 15. The positioning of the nanorods in the BCP particles was dependent strongly on their AR values, and it enabled the modulation of the interfacial properties at selective locations on the BCP particles, thus producing interesting morphological transition of the BCP particles.
Interface engineering of evaporative emulsion droplets containing block copolymers (BCPs) provides an effective route to generate nonspherical particles. Here, we demonstrate the impact of length-controlled nanorods (NRs) on the interfacial properties of BCP emulsions to produce anisotropic BCP particles. A series of lamellae- and cylinder-forming polystyrene-b-poly(4-vinylpyridine) (PS-b-P4VP) and a series of NRs with different lengths (l) are coassembled, and selective arrangement of the NRs o
Dynamically reconfigurable oil-in-water (o/w) Pickering emulsions are developed, wherein the assembly of particles (i.e., platinum-on-carbon and iron-on-carbon particles) can be actively controlled by adjusting interfacial tensions. A balanced adsorption of particles and surfactants at the o/w interface allows for the creation of inhomogeneity of the particle distribution on the emulsion surface. Complex Pickering emulsions with highly controllable and reconfigurable morphologies are produced in
Photoactive shape-changing particles offer a promising platform for smart materials with tunable properties at high spatiotemporal resolutions. Herein, a series of spiropyran-based surfactants with different alkyl spacer lengths are developed to achieve photoactive, shape-changing particles through confined self-assembly of polystyrene-block-poly(4-vinylpyridine) (PS-b-P4VP) within an evaporative emulsion. The length of the alkyl chain spacer between the spiropyran headgroup and ionic chain-end
ABSTRACT Combining the functionality of nanoparticles (NPs) with the processability of polymers offers great promise for designing novel materials. In particular, NPs with tailored surface properties can effectively modify the interface between two distinct fluids and/or different polymer matrices which allows them to function as efficient surfactants. The efficiency of NP surfactants is strongly affected by their size and shape, which influences their adsorption energy to the interface, and the
Co-assembly of block copolymers (BCPs) and organic/inorganic additives affords the design of various hierarchical nanostructures. In this work, we investigate the shape-changing capabilities of poly(styrene-block-2-vinylpyridine) (PS-b-P2VP) BCP particles upon quaternization with a series of bromoalkyl benzene additives with different alkyl spacer lengths. The bromoalkyl benzene additives exhibit different hydrolyzing and quaternizing behaviors depending on their chemical structures. When benzyl
Diblock copolymer (dBCP) particles capable of dynamic shape and color changes have gained significant attention due to their versatility in programmable shapes and intricate nanostructures. However, their application in photonic systems remains limited due to challenges in achieving a sufficient number of defect-free photonic layers over a tens-of-micrometer scale. In this study, we present a pioneering demonstration of photonic dBCP particles featuring over 300 axially stacked photonic layers w
Multiphase microscale emulsions are a material platform that can be tuned and dynamically configured by a variety of chemical and physical phenomena, rendering them inexpensive and broadly programmable optical transducers. Interface engineering underpins many of these sensing schemes but typically focuses on manipulating a single interface, while engineering of the multiphase junctions of complex emulsions remains underexplored. Herein, multiphilic triblock copolymer surfactants are synthesized