Chemical Research in Chinese Universities ›› 2025, Vol. 41 ›› Issue (5): 1106-1113.doi: 10.1007/s40242-025-5050-8

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Integration of Periodic External Fields in Dissipative Particle Dynamics Simulation for Designing Stimuli-responsive Triblock Copolymer Materials

ZHANG Kuo1,2, LI Bingyu1,3, SHI Rui1, GAO Huimin1, LU Zhongyuan1   

  1. 1. State Key Laboratory of Supramolecular Structure and Materials, Institute of Theoretical Chemistry, College of Chemistry, Jilin University, Changchun 130023, P. R. China;
    2. School of Materials Science & Engineering, Jilin Institute of Chemical Technology, Jilin 132022, P. R. China;
    3. College of Medical Laboratory, Dalian Medical University, Dalin 116044, P. R. China
  • Received:2025-03-30 Accepted:2025-05-06 Online:2025-10-01 Published:2025-09-26
  • Contact: GAO Huimin, E-mail: gaohuimin@jlu.edu.cn;LU Zhongyuan, E-mail: luzhy@jlu.edu.cn E-mail:gaohuimin@jlu.edu.cn;luzhy@jlu.edu.cn
  • Supported by:
    This work was supported by the National Key Research and Development Program of China (No. 2022YFB3707300), the National Natural Science Foundation of China (No. 22003019), the Free Exploration of Basic Research Program through a Jilin Provincial Science and Technology Development Plan Project, China (No. YDZJ202301ZYTS322), the Dalian Science and Technology Star Program, China (No. 2022RQ084), and the Natural Science Foundation of Liaoning Province, China (No. 2022-BS-241).

Abstract: The development of functionally accurate stimuli-responsive materials based on the principle of dissipative self-assembly (DSA) poses significant challenges within polymer chemistry, a field critical for elucidating the fundamental mechanisms underpinning the specific functions of living organisms. Based on the dissipative particle dynamics simulations, this study proposes a novel approach to driving the DSA process of polymer solutions through the application of periodic external fields, thereby modulating enthalpy changes. We aim to design stimuli-responsive materials capable of dynamically transitioning between non-equilibrium three-dimensional (3D) nanogels and steady-state spherical micelles or layered structures. Our findings indicate that the formation of the dissipative structure of the 3D gel is contingent upon the frequency of the external field exceeding a critical threshold, which instigates high-frequency oscillations of the conformational transitions of the polymer block copolymer. Concurrently, we observe that the power of the external field predominantly influences the formation rate of the dissipative structure; specifically, higher external field power correlates with accelerated formation kinetics. Moreover, the design principle outlined in this research is applicable to polymer concentrations ranging from 20% to 40%, effectively streamlining the experimental procedure by obviating the requirement for precise concentration control. This investigation offers valuable insights into the design of biomimetic stimui-responsive materials and contributes to a deeper understanding of the mechanisms, by which external fields facilitate DSA processes in polymer systems.

Key words: Block copolymer, Dissipative self-assembly, Dissipative particle dynamics simulation, Stimuli-responsive material