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    Nonreciprocal transverse optical binding forces in dielectric-metal heterodimers

    Xiao-Yong Duan1,2,*, Yu Wang1, Bin-Jie Gao2, Jun-Xiang Zhang2, and Li-Gang Wang2,†

    • 1College of Mechanical Engineering, Jiaxing University, Jiaxing 314001, China
    • 2Zhejiang Key Laboratory of Micro-nano Quantum Chips and Quantum Control, School of Physics, Zhejiang University, Hangzhou 310058, China

    • *Contact author: xyduan@zjxu.edu.cn
    • †Contact author: lgwang@zju.edu.cn

    Phys. Rev. B 112, 085101 – Published 4 August, 2025

    DOI: https://doi.org/10.1103/7wn7-kq98

    Abstract

    Reciprocal optical binding forces between identical particles enable micron- and nanosized multiparticles to form a variety of stable static configurations. In general, the equilibrium interparticle distances are fixed and difficult to regulate. However, we demonstrate analytically that these distances can be continuously varied and even abruptly altered in dielectric-metal heterodimers driven by nonreciprocal transverse optical binding forces. These distances are crucial for determining the stable center of mass and configuration of the heterodimer. Specifically, the stability and equilibrium distances depend on the particle size and incident wavelength and can be tuned through the interplay between electric dipolar, magnetic dipolar, and electric-magnetic dipolar coupling components of the optical binding force. Moreover, the nonreciprocal nature of the binding force drives diverse nonequilibrium translations of the entire dimer as well as the attraction and repulsion of two particles. Importantly, the equilibrium distances, overall stability, and dynamics of the heterodimer can be modulated by the polarized angle of incident light. The results provide perspectives for the dynamical optical manipulation of multiparticle systems, shape-changing nanorobots, and phase-change arrays.

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