Search results for "Copolymer"

showing 10 items of 1003 documents

Origin of enhanced efficiency and stability in diblock copolymer-grafted Cd-free quantum dot-based light-emitting diodes

2021

The efficiency and operational lifetime of quantum dot (QD) based light-emitting diodes (QLEDs) are essentially affected by the electron–hole charge balance. Although various methods have been reported to improve the charge balance, these methods cause issues at the same time, such as increasing a driving voltage and complicating a device structure. In this work, we introduce hybrid InP/ZnSeS/ZnS QDs, in which the oleic acid ligands are substituted with semiconducting diblock copolymer units possessing hole-transporting carbazole groups, to facilitate hole injection and to reduce electron leakage. As a result, the efficiency and the operational lifetime were improved by 1.4-fold and 4-fold,…

Materials sciencePhotoluminescencebusiness.industryCarbazole02 engineering and technologyGeneral Chemistry010402 general chemistry021001 nanoscience & nanotechnology01 natural sciences0104 chemical sciencesDielectric spectroscopylaw.inventionchemistry.chemical_compoundchemistryQuantum dotlawMaterials ChemistryCopolymerOptoelectronics0210 nano-technologybusinessQuantumLight-emitting diodeDiodeJournal of Materials Chemistry C
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Blend scaffolds with polyaspartamide/polyester structure fabricated via TIPS and their RGDC functionalization to promote osteoblast adhesion and prol…

2019

Target of this work was to prepare a RGDC functionalized hybrid biomaterial via TIPS technique to achieve a more efficient control of osteoblast adhesion and diffusion on the three-dimensional (3D) scaffolds. Starting from a crystalline poly(l-lactic acid) (PLLA) and an amorphous alpha,beta-poly(N-2-hydroxyethyl) (2-aminoethylcarbamate)-d,l-aspartamide-graft-polylactic acid (PHEA-EDA-g-PLA) copolymer, blend scaffolds were characterized by an appropriate porosity and pore interconnection. The PHEA-EDA-PLA interpenetration with PLLA improved hydrolytic susceptibility of hybrid scaffolds. The presence of free amino groups on scaffolds allowed to tether the cyclic RGD peptide (RGDC) via Michael…

Materials sciencePolyesters0206 medical engineeringBiomedical EngineeringBiocompatible Materialscyclic RGDC02 engineering and technologyPeptides CyclicPLLACell LineBiomaterialsMiceHydrolysischemistry.chemical_compoundCell AdhesionCopolymerAnimalsCell adhesionMaleimideporous scaffoldCell ProliferationOsteoblastsTissue ScaffoldsMetals and AlloysBiomaterialPHEA021001 nanoscience & nanotechnology020601 biomedical engineeringPolyesterChemical engineeringchemistryCeramics and CompositesMichael reactionSurface modificationTIPSPeptides0210 nano-technology
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Phase behavior of low-functionality, telechelic star block copolymers.

2010

We apply state-of-the-art, Grand Canonical Monte Carlo simulations to determine the self-organization and phase behavior of solutions of block copolymer stars. The latter consist of f AB-block copolymers with N monomers each, which contain a solvophilic block A and solvophobic block B, and which are tethered on a common center on their A-side. We vary the degree of polymerization N and the relative composition of the block copolymer arms and investigate the interplay between macrophase and microphase separation in the system. Preliminary results of the effect of increasing the number of arms, f of the stars are also presented.

Materials sciencePolymer scienceStar (graph theory)Degree of polymerizationchemistry.chemical_compoundStarsMonomerchemistryChemical physicsPhase (matter)Block (telecommunications)CopolymerPhysical and Theoretical ChemistrySolvophobicFaraday discussions
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Toward Photopatternable Thin Film Optical Sensors Utilizing Reactive Polyphenylacetylenes

2013

Substituted polyphenylacetylenes featuring reactive pentafluorophenyl (PFP) ester moieties are synthesized. Parts of the reactive PFP groups are then converted with a mono ortho-nitrobenzyl-protected diamine in variable ratios. Thin films are prepared from these copolymers and irradiated with UV light (λ = 365 nm), resulting in crosslinking of the irradiated areas and hence enabling a photopatterning. We found that during the photocrosslinking process, the excess of PFP ester moieties is stable and remained intact, enabling a subsequent post-polymerization modification step with amines. Noteworthy, this subsequent modification with amines results in a dramatically shift in the UV-vis absorp…

Materials sciencePolymers and PlasticsAbsorption spectroscopyPolymersUltraviolet RaysConjugated systemPhotochemistrylaw.inventionchemistry.chemical_compoundlawDiamineSpectroscopy Fourier Transform InfraredPolymer chemistryMaterials ChemistryCopolymerIrradiationAminesThin filmchemistry.chemical_classificationOrganic ChemistryOptical DevicesEstersPolymerPhotochemical ProcesseschemistryAlkynesPhotolithographyMacromolecular Rapid Communications
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Polyelectrolyte Brushes Grafted at the Air/Water Interface

1997

A new approach for the study of grafted polyelectrolytes is investigated:  monolayers at the air/water interface of block copolymers consisting of a liquid hydrophobic and a polyelectrolyte block. ...

Materials sciencePolymers and PlasticsAir water interfaceOrganic ChemistryPolyelectrolyteInorganic ChemistryChemical engineeringBlock (telecommunications)MonolayerPolymer chemistryMaterials ChemistryCopolymerPolyelectrolyte brushesAmphiphilic copolymerMacromolecules
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Shear-aligned block copolymer monolayers as seeds to control the orientational order in cylinder-forming block copolymer thin films

2016

We study the dynamics of coarsening of a cylinder-forming block copolymer thin film deposited on a prepatterned substrate made of a well-ordered block copolymer monolayer. During thermal annealing the shear-aligned bottom layer drives extinction of the disclinations and promotes a strong orientational correlation, disturbed only by dislocations and undulations along the cylinders of the minority phase. The thin film bilayer system remains stable during annealing, in agreement with self-consistent field theory results that indicate that although the thickness of a stack of two monolayers is not at the optimum thickness condition, it is very close to equilibrium. Phase field simulations indic…

Materials sciencePolymers and PlasticsAnnealing (metallurgy)Ciencias Físicas02 engineering and technology010402 general chemistry01 natural sciencesInstabilityCylinder (engine)law.inventionInorganic ChemistrylawMonolayerTHIN FILMSMaterials ChemistryCopolymerExternal fieldThin filmComposite materialBilayerOrganic Chemistry021001 nanoscience & nanotechnologyCOPOLYMERS0104 chemical sciencesCrystallographyORIENTATIONAL ORDER0210 nano-technologyCIENCIAS NATURALES Y EXACTASFísica de los Materiales Condensados
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Highly Ordered Nanoporous Thin Films from Photocleavable Block Copolymers

2011

Poly(styrene-block-ethylene oxide) with an o-nitrobenzyl ester photocleavable junction (PS-hν-PEO) was synthesized by a combined RAFT polymerization and “click chemistry“ approach and represents the first report utilizing this method for the synthesis of photocleavable block copolymers. After solvent annealing, highly ordered thin films were prepared from PS-hν-PEO. Following a very mild UV exposure and successive washing with water, PS-hν-PEO thin films were transformed into highly ordered nanoporous thin PS films with pore diameters of 15–20 nm and long range ordering (over 2 μm × 2 μm). Afterwards the pores were filled with PDMS by spin-coating in combination with capillary forces. After…

Materials sciencePolymers and PlasticsAnnealing (metallurgy)NanoporousOrganic ChemistryOxideInorganic Chemistrychemistry.chemical_compoundchemistryChemical engineeringPolymer chemistryMaterials ChemistryClick chemistryCopolymerReversible addition−fragmentation chain-transfer polymerizationNanodotThin filmMacromolecules
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Poly(N-isopropylacrylamide) and Copolymers: A Review on Recent Progresses in Biomedical Applications.

2017

The innate ability of poly(N-isopropylacrylamide) (PNIPAAm) thermo-responsive hydrogel to copolymerize and to graft synthetic polymers and biomolecules, in conjunction with the highly controlled methods of radical polymerization which are now available, have expedited the widespread number of papers published in the last decade—especially in the biomedical field. Therefore, PNIPAAm-based hydrogels are extensively investigated for applications on the controlled delivery of active molecules, in self-healing materials, tissue engineering, regenerative medicine, or in the smart encapsulation of cells. The most promising polymers for biodegradability enhancement of PNIPAAm hydrogels are probably…

Materials sciencePolymers and PlasticsBiocompatibilityPolymersRadical polymerizationthermo-responsive polymerBiocompatibilitatBioengineeringNanotechnology02 engineering and technologyReviewmacromolecular substances010402 general chemistry01 natural sciencesBiomaterialslcsh:Chemistrychemistry.chemical_compoundbiocompatibility:Enginyeria química [Àrees temàtiques de la UPC]Tissue engineeringlcsh:General. Including alchemybiodegradabilityPolymer chemistryCopolymerlcsh:Inorganic chemistrycopolymerspoly(N-isopropylacrylamide)lcsh:Sciencechemistry.chemical_classificationOrganic Chemistry4D-printingtechnology industry and agriculturePolymer021001 nanoscience & nanotechnologylcsh:QD146-1973. Good health0104 chemical sciencesCopolímerschemistrylcsh:QD1-999Self-healing hydrogelsPoly(N-isopropylacrylamide)lcsh:Q0210 nano-technologyEthylene glycollcsh:QD1-65Gels (Basel, Switzerland)
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Carbanions on Tap – Living Anionic Polymerization in a Microstructured Reactor

2008

The paper describes the living anionic polymerization of styrenes to homo- and diblock copolymers in continuous flow, using a microstructured mixing set-up ("microreactor"). Reaction times and experimental effort are significantly reduced compared to classical batch methods that often require stringent reaction conditions and strict drying of the apparatus by "break-seal" and "high vacuum" techniques. In continuous flow, residual impurities can be removed by purging the reactor with monomer and initiator solution before polymer samples are collected at the device outlet on a scale of up to 200 g.h -1 . Facile molecular weight adjustment is achieved by variation of the flow rates of initiato…

Materials sciencePolymers and PlasticsBulk polymerizationOrganic ChemistryDispersitySolution polymerizationCondensed Matter Physicschemistry.chemical_compoundMonomerAnionic addition polymerizationPolymerizationchemistryPolymer chemistryMaterials ChemistryCopolymerPhysical and Theoretical ChemistryLiving anionic polymerizationMacromolecular Chemistry and Physics
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Synthesis of block copolymers with poly(methyl methacrylate): P(B-b-MMA), P(EB-b-MMA), P(S-b-B-b-MMA) and P(S-b-EB-b-MMA)

1993

Well-defined diblock copolymers poly(butadiene-b-methyl methacrylate) (=P(B-b-MMA)) and triblock copolymers poly(styrene-b-butadiene-b-methyl methacrylate) (=P(S-b-B-b-MMA)) have been prepared by sequential anionic polymerization in THF. The synthesis of P(B-b-MMA) and P(S-b-B-b-MMA) was most efficient in the presence of lithium alkoxides. By this method side reactions are suppressed and the polymerization can be performed at higher temperatures. The resulting triblock copolymers have narrow molecular weight distribution. The 1,2-PB midblock was quantitatively hydrogenated with tosylhydrazide to enhance thermal stability. Alternatively the hydrogenation can be performed at elevated pressure…

Materials sciencePolymers and PlasticsButanoneGeneral ChemistryCondensed Matter PhysicsMethacrylatePoly(methyl methacrylate)chemistry.chemical_compoundAnionic addition polymerizationchemistryPolymerizationvisual_artAlkoxidePolymer chemistryMaterials ChemistryCopolymervisual_art.visual_art_mediumMolar mass distributionPolymer Bulletin
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