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Under the influence of electric fields, the chains in polyelectrolyte brushes can stretch and collapse, which changes the structure of the brush. Copolymer brushes with charged and uncharged monomers display a similar behavior. For pure polyelectrolyte and random copolymer brushes, the field-induced structure changes only the density of the brush and not its local composition, while the latter could be affected if charges are distributed inhomogeneously along the polymer backbone. Therefore, we systematically study the switching behavior of gradient polyelectrolyte brushes in electric fields for different solvent qualities, grafting densities, and charges per chain via coarse-grained molecular dynamics simulations. Similar to random copolymers and pure polyelectrolytes, these brushes show a mixed-phase transition: intermediate states between fully stretched and collapsed are characterized by a bimodal chain-end distribution. Additionally, we find that the total charge of the brush plays a key role in the critical field required for a complete transition. Finally, we find that gradient polyelectrolyte brushes are charge-enriched at the brush-solvent interface under stretched conditions and charge-depleted under collapsed conditions, allowing for control over the local composition and thus the surface charge of the brush due to the inhomogeneous charge along the grafted chains.
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http://dx.doi.org/10.1021/acs.langmuir.3c03127 | DOI Listing |
Int J Mol Sci
August 2025
Center for Chemical Engineering, ITMO University, 197101 St. Petersburg, Russia.
The self-consistent field Poisson-Boltzmann framework is applied for analysis of equilibrium partitioning of ampholytic protein-like nanocolloids between buffer solution and weak (pH-sensitive) versus strong polyelectrolyte (polyanionic) brushes with the same net charge per unit area. The position-dependent nanocolloid net charge and the insertion freeenergy profiles are derived as a function of pH and ionic strength in the solution. It is demonstrated that, similar to strong polyelectrolyte brushes, pH-sensitive brushes are capable of the uptake of nanocolloids in the vicinity of the isoelectric point, that is, when the net charge of the colloid in the buffer has either the opposite or the same sign as the ionized monomer units of the brush.
View Article and Find Full Text PDFAdv Mater
July 2025
Department of Molecules and Materials, MESA+ Institute, University of Twente, Enschede, 7500 AE, The Netherlands.
Polyelectrolyte brushes are stimulus-responsive coatings that change surface properties such as friction, adhesion, and interaction with biomolecules. Brush coatings are becoming increasingly available with improving synthesis and fabrication methods, but their use in real-world applications is trailing behind. With their stimulus-controlled properties, brushes can fulfill a variety of functions when they are applied in a broad spectrum of use cases ranging from tunable lubrication to ionic current rectification.
View Article and Find Full Text PDFLangmuir
August 2025
State Key Laboratory of Chemical Engineering, School of Chemical Engineering, East China University of Science and Technology, Shanghai 200237, P.R. China.
Stimuli-responsive spherical polyelectrolyte brushes (SPBs) have been of great interest for many enticing applications, yet their responsive functions are usually realized at the equilibrium state upon manually switching the external pH value or ionic strength, showing limited autonomous behaviors. Herein, we report on SPBs bearing autonomous responsive behaviors enabled by a chemically fueled reaction network. SPBs comprising poly(acrylic acid) (PAA) brush layers are employed.
View Article and Find Full Text PDFJ Colloid Interface Sci
December 2025
Jiangsu Key Laboratory for Biomaterials and Devices, School of Biological Science and Medical Engineering, Southeast University, Nanjing 210096, PR China; Jiangsu Key Laboratory for Cardiovascular Information and Health Engineering Medicine, Institute of Clinical Medicine, Nanjing Drum Tower Hospita
Prussian blue nanozymes (PBNZ) have emerged as promising biomedical agents due to their enzyme-mimetic activities, photothermal properties, and magnetic resonance imaging (MRI) contrast capabilities. However, their practical utility is limited by aggregation tendencies arising from high surface energy. Here, we present a strategy employing spherical polyelectrolyte brushes (SPB) as nanoreactors to synthesize satellite-structured SPB@PBNPs with well-defined dimensions (15-19 nm) and low crystallinity.
View Article and Find Full Text PDFJ Phys Chem B
June 2025
Department of Mechanical Engineering, University of Maryland, College Park, Maryland 20742, United States.
Deciphering the correct mechanisms governing certain phenomena in polyelectrolyte (PE) brush grafted systems, revealed through atomistic simulations, is an extremely challenging problem. In a recent study, our all-atom molecular dynamics (MD) simulations revealed a nonlinearly large electroosmotic (EOS) flow (in the presence of an applied electric field) in nanochannels grafted with PMETAC [poly(2-(methacryloyloxy)ethyl trimethylammonium chloride] brushes. Given the lack of any formal procedure that would have directed us to identify the correct factors responsible for such an occurrence, we needed to devote several months to unraveling the involved mechanisms.
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