ABSTRACT
Fluorescence microscopy in the second near-infrared optical window (NIR-II, 1000-1350 nm) has become a technique of choice for non-invasive in vivo imaging. The deep penetration of NIR light in living tissue, as well as negligible tissue autofluorescence within this optical range, offers increased resolution and contrast with even greater penetration depths. Here, we present a custom-built spinning-disc confocal laser microscope (SDCLM) that is specific to imaging in the NIR-II. The SDCLM achieves a lateral resolution of 0.5 ± 0.1 µm and an axial resolution of 0.6 ± 0.1 µm, showing a ~17% and ~45% enhancement in lateral and axial resolution, respectively, compared to the corresponding wide-field configuration. We furthermore showcase several applications that demonstrate the use of the SDCLM for in situ, spatiotemporal tracking of NIR particles and bioanalytes within both synthetic and biological systems.
ABSTRACT
We create a six-qubit linear cluster state by transforming a two-photon hyperentangled state in which three qubits are encoded in each particle, one in the polarization and two in the linear momentum degrees of freedom. For this state, we demonstrate genuine six-qubit entanglement, persistency of entanglement against the loss of qubits, and higher violation than in previous experiments on Bell inequalities of the Mermin type.