Understanding and controlling polyelectrolyte adsorption onto carbon nanotubes is a fundamental challenge in nanotechnology. Polyelectrolytes have been shown to stabilize nanotube suspensions through adsorbing onto the nanotube surface, and polyelectrolyte-coated nanotubes are emerging as building blocks for complex and addressable self-assembly. Conventional wisdom suggests that polyelectrolyte adsorption onto nanotubes is driven by specific chemical or van der Waals interactions. We develop a simple mean-field model and show that ion-image attraction significantly effects adsorption onto conducting nanotubes at low salt concentrations. Our theory suggests a simple strategy to selectively and reversibly functionalize carbon nanotubes on the basis of their electronic structures, which in turn modify the ion-image attraction.
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http://dx.doi.org/10.1021/acs.jpcb.7b11398 | DOI Listing |
J Colloid Interface Sci
January 2025
State Key Laboratory of Integrated Optoelectronics, College of Electronic Science and Engineering, Jilin University, Changchun 130012 PR China. Electronic address:
Polyelectrolytes have shown promise as sensitive material for high-performance humidity sensors in recent years. How to obtain fast recovery and high sensitivity polyelectrolyte humidity sensors is a great challenge. A kind of poly(ionic liquid)s (PILs) humidity sensors modified by zwitterionic polymers (partially zwitterionic PILs, named PZPILs) were prepared in this work.
View Article and Find Full Text PDFBiomolecules
December 2024
Faculty of Chemical and Pharmaceutical Technologies and Biomedical Preparations, D. Mendeleev University of Chemical Technology of Russia, Miusskaya pl. 9, Moscow 125047, Russia.
The objective of this study was to compare the properties of core-shell nanoparticles with a PLGA core and shells composed of different types of polymers, focusing on their structural integrity. The core PLGA nanoparticles were prepared either through a high-pressure homogenization-solvent evaporation technique or nanoprecipitation, using poloxamer 188 (P188), a copolymer of divinyl ether with maleic anhydride (DIVEMA), and human serum albumin (HSA) as the shell-forming polymers. The shells were formed through adsorption, interfacial embedding, or conjugation.
View Article and Find Full Text PDFLangmuir
January 2025
State Key Laboratory of Digital Medical Engineering, School of Biological Science and Medical Engineering, Southeast University, Nanjing 210096, People's Republic of China.
The protein carrier and encapsulation system based on polyelectrolytes plays crucial roles in drug research and development. Traditional methods such as isothermal titration calorimetry and molecular dynamics simulation have illuminated parts of this complex relationship. However, they fall short of capturing the full picture of the interaction during the carrier's fabrication and protein loading dynamics.
View Article and Find Full Text PDFInt J Biol Macromol
January 2025
Department of Polymer Science and Technology University of Calcutta, 92 A.P.C. Road, Kolkata 700009, West Bengal, India. Electronic address:
Sodium alginate (SA) was grafted to poly (acrylonitrile-co‑sodium acrylate-co-acrylic acid). The grafted copolymer was crosslinked with N. N, methylene bis acrylamide (MBA).
View Article and Find Full Text PDFLangmuir
December 2024
Division of Chemistry and Chemical Engineering, California Institute of Technology, Pasadena, California 91125, United States.
Aqueous polyelectrolytes are effective mineralization inhibitors due to their ability to template onto crystal surfaces and chelate ions in solution. These additives have been shown to alter the morphology of calcium carbonate crystals, making them promising candidates for biological and industrial applications. However, while key to designing more effective mineralization inhibitors, the molecular mechanisms governing the interactions between polyelectrolytes and crystal surfaces remain poorly understood.
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