0000000000241059

AUTHOR

Johannes S. Haataja

0000-0002-4523-4199

showing 5 related works from this author

Template-Free Supracolloidal Self-Assembly of Atomically Precise Gold Nanoclusters : From 2D Colloidal Crystals to Spherical Capsids

2016

We report supracolloidal self-assembly of atomically precise and strictly monodisperse gold nanoclusters involving p-mercaptobenzoic acid ligands (Au102-pMBA44) under aqueous conditions into hexagonally packed monolayer-thick two-dimensional facetted colloidal crystals (thickness 2.7 nm) and their bending to closed shells leading to spherical capsids (d ca. 200 nm), as controlled by solvent conditions. The 2D colloidal assembly is driven in template-free manner by the spontaneous patchiness of the pMBA ligands around the Au102-pMBA44 nanoclusters preferably towards equatorial plane, thus promoting inter-nanocluster hydrogen bonds and high packing to planar sheets. More generally, the findin…

Materials scienceta221DispersityNanotechnology02 engineering and technology010402 general chemistry01 natural sciencesCatalysissupramolecular chemistryNanoclustersColloidgoldnanoclusterssupramolekulaarinen kemiaGold nanoclustersta116colloid self-organizationTemplate freeAqueous solutionvetysidoksetta114Hydrogen bondColloidal self-assemblyGeneral ChemistryGeneral MedicineColloidal crystal021001 nanoscience & nanotechnology0104 chemical scienceshydrogen bondscolloidal crystalsSelf-assembly0210 nano-technology
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Rational design of ABC triblock terpolymer solution nanostructures with controlled patch morphology

2016

Block copolymers self-assemble into a variety of nanostructures that are relevant for science and technology. While the assembly of diblock copolymers is largely understood, predicting the solution assembly of triblock terpolymers remains challenging due to complex interplay of block/block and block/solvent interactions. Here we provide guidelines for the self-assembly of linear ABC triblock terpolymers into a large variety of multicompartment nanostructures with C corona and A/B cores. The ratio of block lengths NC/NA thereby controls micelle geometry to spheres, cylinders, bilayer sheets and vesicles. The insoluble blocks then microphase separate to core A and surface patch B, where NB co…

Materials scienceNanostructureScienceta221ChemieGeneral Physics and AstronomyNanotechnology02 engineering and technology010402 general chemistry01 natural sciencesMicelleGeneral Biochemistry Genetics and Molecular BiologyArticleCopolymer[CHIM]Chemical SciencesLamellar structureSoft matterMultidisciplinaryta114VesicleBilayerQGeneral Chemistry021001 nanoscience & nanotechnology0104 chemical sciencesChemical engineeringPolymersome0210 nano-technology
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Hidden Structural Features of Multicompartment Micelles Revealed by Cryogenic Transmission Electron Tomography

2014

The demand for ever more complex nanostructures in materials and soft matter nanoscience also requires sophisticated characterization tools for reliable visualization and interpretation of internal morphological features. Here, we address both aspects and present synthetic concepts for the compartmentalization of nanoparticle peripheries as well as their in situ tomographic characterization. We first form negatively charged spherical multicompartment micelles from ampholytic triblock terpolymers in aqueous media, followed by interpolyelectrolyte complex (IPEC) formation of the anionic corona with bis-hydrophilic cationic/neutral diblock copolymers. At a 1:1 stoichiometric ratio of anionic a…

Electron Microscope TomographyMaterials sciencePolymersProton Magnetic Resonance Spectroscopyta221electron tomographyGeneral Physics and AstronomyIonic bondingNanoparticleNanotechnology02 engineering and technology010402 general chemistry01 natural sciencesMicelleCopolymerGeneral Materials ScienceSoft matterMicellesta218ta214ta114interpolyelectrolyte complexesGeneral EngineeringCationic polymerization021001 nanoscience & nanotechnology0104 chemical sciencesChemical engineeringChromatography GelCryo-electron tomographySelf-assembly0210 nano-technologyACS Nano
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Hierarchical Self-Assembly of Halogen-Bonded Block Copolymer Complexes into Upright Cylindrical Domains

2017

Summary Self-assembly of block copolymers into well-defined, ordered arrangements of chemically distinct domains is a reliable strategy for preparing tailored nanostructures. Microphase separation results from the system, minimizing repulsive interactions between dissimilar blocks and maximizing attractive interactions between similar blocks. Supramolecular methods have also achieved this separation by introducing small-molecule additives binding specifically to one block by noncovalent interactions. Here, we use halogen bonding as a supramolecular tool that directs the hierarchical self-assembly of low-molecular-weight perfluorinated molecules and diblock copolymers. Microphase separation …

Materials scienceBlock copolymerGeneral Chemical Engineering116 Chemical sciencesSupramolecular chemistryNanotechnologyblock copolymer02 engineering and technologyhierarchical self-assembly010402 general chemistry01 natural sciencesBiochemistryMicelleArticleSDG9: Industry innovation and infrastructuresupramolecular complexesMaterials ChemistryCopolymerEnvironmental ChemistryNon-covalent interactionsMoleculeLamellar structureta116chemistry.chemical_classificationHalogen bondta114Biochemistry (medical)General Chemistry021001 nanoscience & nanotechnology0104 chemical sciencesblock copolymerschemistryChemical engineeringIndustry innovation and infrastructure [SDG9]nanofabricationhalogen bondSettore CHIM/07 - Fondamenti Chimici Delle TecnologieSelf-assembly0210 nano-technology
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Reversible Supracolloidal Self-Assembly of Cobalt Nanoparticles to Hollow Capsids and Their Superstructures

2017

| openaire: EC/FP7/291364/EU//MIMEFUN The synthesis and spontaneous, reversible supracolloidal hydrogen bond-driven self-assembly of cobalt nanoparticles (CoNPs) into hollow shell-like capsids and their directed assembly to higher order superstructures is presented. CoNPs and capsids form in one step upon mixing dicobalt octacarbonyl (Co2CO8) and p-aminobenzoic acid (pABA) in 1,2-dichlorobenzene using heating-up synthesis without additional catalysts or stabilizers. This leads to pABA capped CoNPs (core ca. 5nm) with a narrow size distribution. They spontaneously assemble into tunable spherical capsids (d≈50-200nm) with a few-layered shells, as driven by inter-nanoparticle hydrogen bonds th…

Hydrogen bondingta221Nanoparticlechemistry.chemical_element02 engineering and technology010402 general chemistry01 natural sciencesCatalysischemistry.chemical_compoundColloidCapsidsDicobalt octacarbonylta116ta114ChemistryHydrogen bondColloidal self-assemblyGeneral ChemistryGeneral Medicine021001 nanoscience & nanotechnology0104 chemical sciencesSolventCrystallographyElectron tomographycobalt nanoparticlesMagnetic nanoparticlesnanoparticlesSelf-assembly0210 nano-technologyCobaltSuperparamagnetismAngewandte Chemie
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