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Colloidal colorimetric microsensors enable the in-situ detection of mechanical strains within materials. Enhancing the sensitivity of these sensors to small scale deformation while enabling reversibility of the sensing capability would expand their utility in applications including biosensing and chemical sensing. In this study, we introduce the synthesis of colloidal colorimetric nano-sensors using a simple and readily scalable fabrication method. Colloidal nano sensors are prepared by emulsion-templated assembly of polymer-grafted gold nanoparticles (AuNP). To direct the adsorption of AuNP to the oil-water interface of emulsion droplets, AuNP (≈11nm) are functionalized with thiol-terminated polystyrene (PS, M = 11k). These PS-grafted gold nanoparticles are suspended in toluene and subsequently emulsified to form droplets with a diameter of ≈30µm. By evaporating the solvent of the oil-inwater emulsion, we form nanocapsules (AuNC) (diameter < 1µm) decorated by PS-grafted AuNP. To test mechanical sensing, the AuNC are embedded in an elastomer matrix. The addition of a plasticizer reduces the glass transition temperature of the PS brushes, and in turn imparts reversible deformability to the AuNC. The plasmonic peak of the AuNC shifts towards lower wavelengths upon application of uniaxial tensile tension, indicating increased inter-nanoparticle distance, and reverts back as the tension is released.
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http://dx.doi.org/10.1002/smll.202300361 | DOI Listing |
Nano Lett
August 2025
Faculty of Physics and Astronomy, Adam Mickiewicz University, Uniwersytetu Poznanskiego 2, Poznan 61-614, Poland.
Nanocomposites assembled from polymer-grafted plasmonic nanoparticles (PGNs) can combine strong light-matter interactions with soft-matter functionalities and a high degree of translational symmetry. This work explored the potential of gold nanoparticles (16 nm diameter) grafted with polystyrene chains (degree of polymerization, ≈ 63) as building blocks for acoustoplasmonic metasurfaces. We have decorated inorganic surfaces─crystalline silicon and SiO glass─with PGN monolayers and explored their surface acoustic waves with micro-Brillouin Light Scattering (μ-BLS) at various photon energies.
View Article and Find Full Text PDFACS Nano
April 2025
Materials Science and Engineering Division, Materials Measurement Laboratory, National Institute of Standards and Technology, Gaithersburg, Maryland 20899, United States.
Polymer chain stretching enables the plastic and elastic properties that make polymers unique and valuable engineering materials. Despite its importance, polymer chain orientation in amorphous regions remains very challenging to measure by conventional techniques because it is an intrinsically molecule-scale phenomenon lacking long-range order that is frequently heterogeneous across length scales of ≈ (1 to 100) nm. Polarized resonant soft X-ray scattering (P-RSoXS) is an emerging technique that has recently achieved the measurement of amorphous chain orientation with ≈2 nm spatial resolution.
View Article and Find Full Text PDFMacromol Rapid Commun
March 2025
Leibniz-Institut für Polymerforschung Dresden e.V., Hohe Straße 6, D-01069, Dresden, Germany.
Gold nanoparticles represent nanosized colloidal entities with high relevance for both basic and applied research. When gold nanoparticles are functionalized with polymer-molecule ligands, hybrid nanoparticles emerge whose interactions with the environment are controlled by the polymer coating layer: Colloidal stability and structure formation on the single particle level as well as at the supracolloidal scale can be enabled and engineered by tailoring the composition and architecture of this polymer coating. These possibilities in controlling structure formation may lead to synergistic and/or emergent functional properties of such hybrid colloidal systems.
View Article and Find Full Text PDFSoft Matter
December 2024
Institute for Materials Chemistry and Engineering, Kyushu University, 744 Motooka, Nishi-ku, Fukuoka 819-0395, Japan.
Given that the hydration water of polymer matrices may differ from that of outermost polymer surfaces, processes at biomaterial-biofluid interfaces and role of hydration water therein cannot be adequately examined using most conventional characterization methods. To bridge this gap, a gold substrate was herein modified with linear and cyclic poly(2-methoxyethyl acrylate) to prepare -PMEA and -PMEA surfaces, respectively, as models for the outermost surfaces of blood-contacting medical devices. Both surfaces suppressed the adhesion of human platelets but differed in the adhesion behaviors of normal and tumor cells despite having the same areal density of fixed-end units.
View Article and Find Full Text PDFACS Appl Mater Interfaces
November 2024
Department of Materials Science and Engineering, University of Pennsylvania, Philadelphia, Pennsylvania 19104, United States.
Designing a functional surface that selectively adsorbs nanoparticles based on their size and shape is essential for developing an advanced adsorption-based, postsynthesis nanoparticle separation device. We demonstrate selective adsorption of larger nanoparticles from solution onto a polyelectrolyte brush by tuning the salt concentration. Specifically, a positively charged polyelectrolyte brush is created by converting pyridine groups of poly(2-vinylpyridine) to -methylpyridinium groups using methyl iodide.
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