A multi-particle colloidal probe technique based on the atomic force microscope (AFM) was used to measure the interaction forces between individual charged latex particles with adsorbed cationic poly(amido amine) (PAMAM) dendrimers. The forces near the isoelectric point (IEP) were found to be attractive and stronger than van der Waals interactions. These additional attractions can be rationalized semi-quantitatively with a patch-charge model, which is derived from Debye-Hückel theory. However, the model predicts a larger decay constant for the attractive interaction than observed experimentally. The deviation is probably due to the disordered liquid-like structure of the experimentally investigated system and the finite size of the interacting regions. The amplitude of the attractive interaction is estimated correctly by the patch-charge model including its dependence on the ionic strength and dendrimer generation. The experimental force curves are situated between predictions for constant charge and constant potential boundary conditions. We conclude that the observed additional attractive forces are of electrostatic origin, and that charge regulation effects may play an important role.
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http://dx.doi.org/10.1039/b925812d | DOI Listing |
ACS Appl Mater Interfaces
January 2025
CAS Key Laboratory of Green Process and Engineering, Institute of Process Engineering, Chinese Academy of Sciences, Beijing 100190, China.
Maintaining human body temperature in both high and low-temperature environments is fundamental to human survival, necessitating high-performance thermal insulation materials to prevent heat exchange with the external environment. Currently, most fibrous thermal insulation materials are characterized by large weight, suboptimal thermal insulation, and inferior mechanical and waterproof performance, thereby limiting their effectiveness in providing thermal protection for the human body. In this study, lightweight, waterproof, mechanically robust, and thermal insulating polyamide-imide (PAI) grooved micro/nanofibrous aerogels were efficiently and directly assembled by electrospinning.
View Article and Find Full Text PDFAngew Chem Int Ed Engl
January 2025
Harbin Institute of Technology, School of Chemistry and Chemical Engineering, No. 92, West Dazhi Street, 150001, Harbin, CHINA.
Commercial hard carbon (HC) anode suffers from unexpected interphase chemistry rooted in the parasitic reactions between surface oxygen-functional groups and ester-based electrolytes. Herein, an innovative strategy is proposed to regulate interphase chemistry by tailoring targeted functional groups on the HC surface, where highly active undesirable oxygen-functional groups are skillfully converted into a Si-O-Si molecular layer favorable for anchoring anions. Then, an inorganic/organic hybrid solid electrolyte interphase with low interfacial charge transfer resistance and enhanced cycling durability is constructed successfully.
View Article and Find Full Text PDFJ Chem Theory Comput
January 2025
Institute for Computational Physics, University of Stuttgart, Allmandring 3, Stuttgart 70569, Germany.
The constant-pH Monte Carlo method is a popular algorithm to study acid-base equilibria in coarse-grained simulations of charge regulating soft matter systems including weak polyelectrolytes and proteins. However, the method suffers from systematic errors in simulations with explicit ions, which lead to a symmetry-breaking between chemically equivalent implementations of the acid-base equilibrium. Here, we show that this artifact of the algorithm can be corrected a-posteriori by simply shifting the pH-scale.
View Article and Find Full Text PDFChem Soc Rev
January 2025
Department of Applied Physics, The Hong Kong Polytechnic University, Hung Hom, Kowloon, Hong Kong, P. R. China.
Establishing and regulating the ferroelectric polarization in ferroelectric nano-scale catalysts has been recognized as an emerging strategy to advance water splitting reactions, with the merits of improved surface charge density, high charge transfer rate, increased electronic conductivity, the creation of real active sites, and optimizing the chemisorption energy. As a result, engineering and tailoring the ferroelectric polarization induced internal electric field provides significant opportunities to improve the surface and electronic characteristics of catalysts, thereby enhancing the water splitting reaction kinetics. In this review, an interdisciplinary and comprehensive summary of recent advancements in the construction, characterization, engineering and regulation of the polarization in ferroelectric-based catalysts for water splitting is provided, by exploiting a variety of external stimuli.
View Article and Find Full Text PDFAngew Chem Int Ed Engl
January 2025
Beihang University, 37 Xue Yuan Road, Hai Dian District, 100191, Beijing, CHINA.
Sodium-ion batteries (SIBs), endowed with relatively small Stokes radius and low desolvation energy for Na+, are reckoned as a promising candidate for fast-charging endeavors. However, the C-rate charging capability of practical energy-dense sodium-ion pouch cells is currently limited to ≤1C, due to the high propensity for detrimental metallic Na plating on the hard carbon (HC) anode at elevated rates. Here, an ampere-hour-level sodium-ion pouch cell capable of 3C charging is successfully developed via phosphorus (P)-sulfur (S) interphase chemistry.
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