As a glass-forming liquid is cooled, the dynamics of its constituent particles changes
from being liquid-like to more solid-like. The solidity of the resulting glassy material is
believed to be due to a cage-formation process, whereby the motion of individual
particles is increasingly constrained by neighbouring particles. This process begins at
the temperature (or particle density) at which the glass-forming liquid first shows
signs of glassy dynamics; however, the details of how the cages form remain
unclear1–4. Here we study cage formation at the particle level in a two-dimensional
colloidal suspension (a glass-forming liquid). We use focused lasers to perturb the
suspension at the particle level and monitor the nonlinear dynamic response of
the system using video microscopy. All observables that we consider respond
non-monotonically as a function of the particle density, peaking at the density at
which glassy dynamics is first observed. We identify this maximum response as being
due to cage formation, quantified by the appearance of domains in which particles
move in a cooperative manner. As the particle density increases further, these local
domains become increasingly rigid and dominate the macroscale particle dynamics.
This microscale rheological deformation approach demonstrates that cage
formation in glass-forming liquids is directly related to the merging of such domains,
and reveals the first step in the transformation of liquids to glassy materials1,5.