Self-oscillating synchronematic colloids.

Self-oscillators that sustain periodic dynamics under constant input are ubiquitous in natural and engineered systems, where their interactions enable spatiotemporal coordination among many individual units. New forms of organization can emerge when these self-oscillating units are free to move and rotate, linking their spatial arrangement and orientation with their oscillation frequencies and phases. Here, we report experiments and simulations on populations of Quincke colloids that behave as self-oscillating units characterized by position, orientation, frequency, and phase. Hydrodynamic interactions among these colloids drive temporal synchronization and spatial alignment of their phases and orientations, giving rise to a new form of collective order that we term synchronematic. Within finite-size crystalline clusters, these non-reciprocal interactions promote global synchronization and circular alignment, with a collective frequency that increases with cluster size. Using the theory of weakly coupled oscillators, we derive a reduced-order model that captures the coupled evolution of phase and orientation and explains how synchronematic order depends sensitively on the particle configuration. Our results establish Quincke colloids as a model system for active oscillatory matter and reveal fundamental principles by which synchronization, alignment, and structure co-emerge-offering a framework for designing adaptive, frequency-tunable materials.