Structural colors arising from all-dielectric nanostructures are very promising for high-resolution color nanoprinting and high-density optical storage. However, once the all-dielectric nanostructures are fabricated, their optical performances are usually static or change slowly, significantly limiting the practical applications in advanced displays. Herein, we experimentally demonstrate the real-time tunable colors with microfluidic reconfigurable all-dielectric metasurfaces. The metasurface is composed of an array of TiO nanoblocks, which are embedded in a polymeric microfluidic channel. By injecting solutions with a different refractive index into the channel, the narrow band reflection peak and the corresponding distinct colors of a TiO metasurface can be precisely controlled. The transition time is as small as 16 ms, which is orders of magnitude faster than the current techniques. By varying the lattice size of TiO metasurfaces, the real-time tunable colors are able to span the entire visible spectrum. Meanwhile, the injection and ejection of solvent have also shown the capability of the erasion and the restoration of information encoded in TiO metasurfaces. The combination of all-dielectric nanostructures with microfluidic channels shall boost their applications in functional color display, banknote security, anticounterfeiting, and point-of-care devices.

The long-dreamed-of capability of monitoring the molecular machinery in living systems has not been realized yet, mainly due to the technical limitations of current sensing technologies. However, recently emerging quantum sensors are showing great promise for molecular detection and imaging. One of such sensing qubits is the nitrogen−vacancy (NV) center, a photoluminescent impurity in a diamond lattice with unique roomtemperature optical and spin properties. This atomic-sized quantum emitter has the ability to quantitatively measure nanoscale electromagnetic fields via optical means at ambient conditions. Moreover, the unlimited photostability of NV centers, combined with the excellent diamond biocompatibility and the possibility of diamond nanoparticles internalization into the living cells, makes NV-based sensors one of the most promising and versatile platforms for various life-science applications. In this review, we will summarize the latest developments of NV-based quantum sensing with a focus on biomedical applications, including measurements of magnetic biomaterials, intracellular temperature, localized physiological species, action potentials, and electronic and nuclear spins. We will also outline the main unresolved challenges and provide future perspectives of many promising aspects of NV-based bio-sensing.

Mechanical stretching has been an effective way to achieve widely tunable optical response in artificial nanostructures. However, the typical stretchable optical devices produce exactly the reverse effects for two orthogonal linear polarizations, significantly hindering their practical applications in many emerging systems. Herein, we demonstrate an approach for a mechanically tunable all-dielectric metasurface with polarization insensitivity and full-spectrum response in the visible range from 450 to 650 nm. By embedding a TiO2 metasurface in a polydimethylsiloxane substrate and stretching it in one direction, we find that the distinct reflection colors of two orthogonal linear polarizations can be tuned across the entire visible spectrum simultaneously. Encryption and display of information have also been realized with the same technique. The corresponding calculations show that the spectral responses of light with polarizations perpendicular and parallel to the strain are determined by two different mechanisms, that is, the near-field mutual interaction and the grating effects. This research shall shed light on stretchable and wearable photonics.