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Gel formation is described by a nonequilibrium self-assembly (SA) mechanism which considers the presence of precursors. Assuming that nonequilibrium structures appear and are maintained by entropy production, we developed a mesoscopic nonequilibrium thermodynamic model that describes the dynamic assembly of the structures. In the model, the evolution of the structures from the initially inactivated building blocks to the final agglomerates is governed by kinetic equations of the Fokker-Planck type. From these equations, we get the probability densities which enable one to know the measurable quantities such as the concentrations of the different components and the dynamic structure factor obtained in light-scattering experiments. Our results obtained are in very good agreement with the experiments. The model proposed can in general be used to analyze the kinetics of formation of nonequilibrium SA structures usually found in biomedicine and advanced materials.
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http://dx.doi.org/10.1021/acs.jpcb.8b02320 | DOI Listing |
Mater Today Bio
August 2025
School of Chemical Engineering, Kunming University of Science and Technology, Kunming, 650500, China.
Evaporation-driven self-assembly of colloidal particles in a sessile drop can construct simple structures in various scenarios. However, the non-equilibrium self-assembly process, dominated by internal capillary flow and solute- or thermal-induced Marangoni flow, cannot guarantee the precise positioning of the particles. One can exert forces on individual suspended particles by introducing external field manipulation, which enables the construction of precise deposits and even 3D structures.
View Article and Find Full Text PDFACS Appl Mater Interfaces
August 2025
State Key Laboratory of Cryogenic Science and Technology, Technical Institute of Physics and Chemistry, Chinese Academy of Sciences, Beijing 100190, China.
Harnessing liquid metal behavior at solid interfaces opens pathways for functional material fabrication and soft-matter device integration. Leveraging the distinct wettability of liquid gallium (Ga) on solid indium (In) and silicon substrates, we propose a facile dewetting-based method for realizing the self-assembly of interfacial patterns. Nonequilibrium eutectic-type Ga liquid and In film systems are constructed, and the self-assembled behaviors of the "feather" and "cell" patterns at the interface under the effect of surface tension-driven dewetting and oxide film-induced wetting have been disclosed.
View Article and Find Full Text PDFJ Chem Phys
August 2025
Université Paris-Saclay, CNRS, Laboratoire de Physique des Solides, 91405 Orsay, France.
We report the experimental observation of a square crystalline phase in a vibrated binary mixture of spherical grains. This structure spontaneously forms from a disordered state, consistently with predictions obtained in an equilibrium system with similar geometrical properties under conservative dynamics. By varying the area fraction, we also observe stable coexistence between a granular fluid and an isolated square crystal.
View Article and Find Full Text PDFJ Am Chem Soc
August 2025
School of Automation and Intelligent Sensing, School of Electronic Information and Electrical Engineering, Shanghai Jiao Tong University, Shanghai 200240, China.
Living cells exhibit dynamic adaptability through ATP-fueled processes that are crucial for tissue development and immune responses. Conventional methods for controlling cell assembly lack the nonequilibrium, reversible behavior of natural systems. Here, we present an ATP-dissipative DNA assembly system that leverages DNA's programmability to enable adaptive, hierarchical structures with spatiotemporal control.
View Article and Find Full Text PDFJ Chem Phys
July 2025
Departament de Física de la Matèria Condensada, Universitat de Barcelona, Martí i Franquès 1, 08028 Barcelona, Spain.
Many biological and nanotechnological processes rely on the self-assembly of tubular structures. For this reason, theoretical models that offer insights into this process and ways to control its final outcome are essential. In this work, we study the conditions under which tubules are self-assembled spontaneously from free subunits in solution and explore the possible formation pathways using classical nucleation theory and an elastic model in the stretching-dominated regime.
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