Towards a Multi-Pixel Photon-to-Digital Converter for Time-Bin Quantum Key Distribution.

We present an integrated single-photon detection device custom designed for quantum key distribution (QKD) with time-bin encoded single photons. We implemented and demonstrated a prototype photon-to-digital converter (PDC) that integrates an 8 × 8 single-photon avalanche diode (SPAD) array with on-chip digital signal processing built in TSMC 65 nm CMOS. The prototype SPADs are used to validate the QKD functionalities with an array of time-to-digital converters (TDCs) to timestamp and process the photon detection events.

Mitotic waves in an import-diffusion model with multiple nuclei in a shared cytoplasm.

Nuclei import and export proteins, including cell cycle regulators. These import-export processes are modulated periodically by the cell cycle, for example due to the periodic assembly and breakdown of the nuclear envelope. As such, replicated DNA can be segregated between the two daughter cells and the proteins that were localized in the nucleus are free to diffuse throughout the cytoplasm.

3D Photon-to-Digital Converter for Radiation Instrumentation: Motivation and Future Works.

Analog and digital SiPMs have revolutionized the field of radiation instrumentation by replacing both avalanche photodiodes and photomultiplier tubes in many applications. However, multiple applications require greater performance than the current SiPMs are capable of, for example timing resolution for time-of-flight positron emission tomography and time-of-flight computed tomography, and mitigation of the large output capacitance of SiPM array for large-scale time projection chambers for liquid argon and liquid xenon experiments. In this contribution, the case will be made that 3D photon-to-digital converters, also known as 3D digital SiPMs, have a potentially superior performance over analog and 2D digital SiPMs.

Synchronization in reaction-diffusion systems with multiple pacemakers.

Spatially extended oscillatory systems can be entrained by pacemakers, regions that oscillate with a higher frequency than the rest of the medium. Entrainment happens through waves originating at a pacemaker. Typically, biological and chemical media can contain multiple pacemaker regions, which compete with each other.

Nuclei determine the spatial origin of mitotic waves.

Traveling waves play an essential role in coordinating mitosis over large distances, but what determines the spatial origin of mitotic waves remains unclear. Here, we show that such waves initiate at pacemakers, regions that oscillate faster than their surroundings. In cell-free extracts of eggs, we find that nuclei define such pacemakers by concentrating cell cycle regulators.