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Silvio O. Rizzoli

Publications and source records attributed to Silvio O. Rizzoli.

2 recordsLinked to original sources

Mitigating Measurement-Induced Training Instability in Hybrid Quantum Neural Networks for Protein Classification

Hybrid Quantum Neural Network (QNN) classifiers produce logits as expectation values of quantum measurement operators. For standard Pauli measurements, these outputs are intrinsically bounded to the interval [-1,1]. When such bounded logits are used directly with the cross-entropy loss applied to softmax-normalized logits for multi-class classification, the loss function operates in a regime of weak sensitivity to logit differences. As a consequence, parameter gradients are suppressed, leading to unstable optimization in variational quantum classifiers (VQCs). In this work, we identify this effect as measurement-induced logit contraction, a previously uncharacterized source of trainability degradation in hybrid QNNs. To address this limitation, we introduce a learnable scaling parameter, termed Quantum Measurement Temperature (QMT), which rescales quantum measurement outputs prior to the loss. Unlike post-hoc calibration, QMT acts during training and compensates for the physically imposed bounds on quantum measurement outputs. This rescaling increases gradient magnitude and variance, thereby improving loss sensitivity. The proposed mechanism is architecture-agnostic and does not modify the quantum ansatz, circuit depth, or measurement operators. Experiments on fluorescence microscopy images and a six-class variant of Fashion MNIST demonstrate that QMT consistently enhances logit separation, strengthens gradients, stabilizes training across random initializations, and improves classification accuracy, relative to unscaled measurement readouts. These results demonstrate that QMT enables stable and reliable training of hybrid QNNs for practical applications.

cs.LG↗

Super-resolution Live-cell Fluorescence Lifetime Imaging

Super-resolution Structured Illumination Microscopy (SR-SIM) enables fluorescence microscopy beyond the diffraction limit at high frame rates. Compared to other super-resolution microscopy techniques, the low photon fluence used in SR-SIM makes it readily compatible with live-cell imaging. Here, we combine SR-SIM with electro-optic fluorescence lifetime imaging (EOFLIM), adding the capability of monitoring physicochemical parameters with 156 nm spatial resolution at high frame rate for live-cell imaging. We demonstrate that our new SIMFLIM technique enables super-resolved multiplexed imaging of spectrally overlapping fluorophores, environmental sensing, and live-cell imaging.

physics.optics↗