Nonequilibrium relaxation of soft responsive colloids
Metadatos
Mostrar el registro completo del ítemEditorial
AIP publishing
Fecha
2024-09-03Referencia bibliográfica
López Molina, J. et. al. J. Chem. Phys. 161, 094902 (2024). [https://doi.org/10.1063/5.0221903]
Patrocinador
Deutsche Forschungsgemeinschaft (DFG) via the Research Unit FOR 5099 “Reducing complexity of nonequilibrium systems” and Project No. 430195928; State of Baden Württemberg through bwHPC and the DFG through Grant No. INST 39/963-1 FUGG (bwForCluster NEMO); Grant No. PID2022-136540NB-I00 funded by No. MCIN/AEI/10.13039/501100011033, ERDF A way of making Europe; Spanish Ministerio de Ciencia e Innovación, Programa Estatal de Investigación Científica, Técnica y de Innovación 2021–2023 (Project No. PID2022-136540NB-00) and program Visiting Scholars funded by the Plan Propio of the University of Granada (Project No. PPVS2018-08); Student fellowship (No. FPU21/03568) supported by the Spanish Ministerio de UniversidadesResumen
Stimuli-responsive macromolecules display large conformational changes during their dynamics, sometimes switching between states. Such a
multi-stability is useful for the development of soft functional materials. Here, we introduce a mean-field dynamical density functional theory
for a model of responsive colloids to study the nonequilibrium dynamics of a colloidal dispersion in time-dependent external fields, with a
focus on the coupling of translational and conformational dynamics during their relaxation. Specifically, we consider soft Gaussian particles
with a bimodal size distribution between two confining walls with time-dependent (switching-on and off) external gravitational and osmotic
fields. We find a rich relaxation behavior of the systems in excellent agreement with particle-based Brownian dynamics computer simulations.
In particular, we find time-asymmetric relaxations of integrated observables (wall pressures, mean size, and liquid center-of-mass) for activation/
deactivation of external potentials, respectively, which are tunable by the ratio of translational and conformational diffusion time scales.
Our work thus paves the way for studying the nonequilibrium relaxation dynamics of complex soft matter with multiple degrees of freedom
and hierarchical relaxations.