Photonic quantum information processing, one of the leading platforms for quantum technologies critically relies on optical quantum interference to produce an indispensable effective photon–photon interaction. However, such an effective interaction is fundamentally limited to bunching due to the bosonic nature of photons and the restricted phase response from conventional unitary optical elements. Here we propose and experimentally demonstrate a new degree of freedom in the optical quantum interference enabled by a non-unitary metasurface. Due to the unique anisotropic phase response that creates two extreme eigen-operations, we show dynamical and continuous control over the effective interaction of two single photons such that they show bosonic bunching, fermionic antibunching or arbitrarily intermediate behaviour, beyond their intrinsic bosonic nature. This quantum operation opens the door to both fundamental quantum light–matter interaction and innovative photonic quantum devices for quantum communication, quantum simulation and quantum computing.

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Cell–cell adhesions are often subjected to mechanical strains of different rates and magnitudes in normal tissue function. However, the rate-dependent mechanical behavior of individual cell–cell adhesions has not been fully characterized due to the lack of proper experimental techniques and therefore remains elusive. This is particularly true under large strain conditions, which may potentially lead to cell–cell adhesion dissociation and ultimately tissue fracture. In this study, we designed and fabricated a single-cell adhesion micro tensile tester (SCAµTT) using two-photon polymerization and performed displacement-controlled tensile tests of individual pairs of adherent epithelial cells with a mature cell–cell adhesion. Straining the cytoskeleton–cell adhesion complex system reveals a passive shear-thinning viscoelastic behavior and a rate-dependent active stress-relaxation mechanism mediated by cytoskeleton growth. Under low strain rates, stress relaxation mediated by the cytoskeleton can effectively relax junctional stress buildup and prevent adhesion bond rupture. Cadherin bond dissociation also exhibits rate-dependent strengthening, in which increased strain rate results in elevated stress levels at which cadherin bonds fail. This bond dissociation becomes a synchronized catastrophic event that leads to junction fracture at high strain rates. Even at high strain rates, a single cell–cell junction displays a remarkable tensile strength to sustain a strain as much as 200% before complete junction rupture. Collectively, the platform and the biophysical understandings in this study are expected to build a foundation for the mechanistic investigation of the adaptive viscoelasticity of the cell–cell junction.

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