Light detection and quantification is fundamental to the functioning of a broad palette of technologies. While expensive avalanche photodiodes and superconducting bolometers are examples of detectors achieving single-photon sensitivity and time resolutions down to the picosecond range, thermoelectric-based photodetectors are much more affordable alternatives that can be used to measure substantially higher levels of light power (few kW/cm2). However, in thermoelectric detectors, achieving broadband or wavelength-selective performance with high sensitivity and good temporal resolution requires careful design of the absorbing element. Here, combining the high absorptivity and low heat capacity of a nanoengineered plasmonic thin-film absorber with the robustness and linear response of a thermoelectric sensor, we present a hybrid detector for visible and near-infrared light achieving response times of the order of 100 milliseconds, almost four times shorter than the same thermoelectric device covered with a conventional absorber. Furthermore, we show an almost two times higher light-to-electricity efficiency upon replacing the conventional absorber with a plasmonic absorber. With these improvements, which are direct results of the efficiency and ultra-small thickness of the plasmonic absorber, this hybrid detector constitutes an ideal component for various medium-intensity light sensing applications requiring spectrally tailored absorption coatings with either broadband or narrowband characteristics.

Organic compounds present a powerful platform for nanotechnological applications. In particular, molecules suitable for optical functionalities such as single photon generation and energy transfer have great promise for complex nanophotonic circuitry due to their large variety of spectral properties, efficient absorption and emission, and ease of synthesis. Optimal integration, however, calls for control over position and orientation of individual molecules. While various methods have been explored for reaching this regime in the past, none satisfies requirements necessary for practical applications. Here, we present direct non-contact electrohydrodynamic nanoprinting of a countable number of photostable and oriented molecules in a nanocrystal host with subwavelength positioning accuracy. We demonstrate the power of our approach by writing arbitrary patterns and controlled coupling of single molecules to the near field of optical nanostructures. Placement precision, high yield and fabrication facility of our method open many doors for the realization of novel nanophotonic devices.

Investigating biological and synthetic nanoscopic species in liquids, at the ultimate resolution of single entity, is important in diverse fields. Progress has been made, but significant barriers need to be overcome such as the need for intense fields, the lack of versatility in operating conditions and the limited functionality in solutions of high ionic strength for biological applications. Here, we demonstrate switchable electrokinetic nanovalving able to confine and guide single nano-objects, including macromolecules, with sizes down to around 10 nanometres, in a lab-on-chip environment. The nanovalves are based on spatiotemporal tailoring of the potential energy landscape of nano-objects using an electric field, modulated collaboratively by wall nanotopography and by embedded electrodes in a nanochannel system. We combine nanovalves to isolate single entities from an ensemble, and demonstrate their guiding, confining, releasing and sorting. We show on-demand motion control of single immunoglobulin G molecules, quantum dots, adenoviruses, lipid vesicles, dielectric and metallic particles, suspended in electrolytes with a broad range of ionic strengths, up to biological levels. Such systems can enable nanofluidic, large-scale integration and individual handling of multiple entities in applications ranging from single species characterization and screening to in situ chemical or biochemical synthesis in continuous on-chip processes.

Nanostructured metal-insulator-metal (MIM) metasurfaces supporting gap-plasmons (GPs) show great promise due to their ability to manipulate or concentrate light at the nanoscale, which is of importance to a broad palette of technologies. The interaction between individual, proximal GP nanoresonators, reaching the point of first electrical connection, can have unexpected, important consequences and remains unexplored. Here we study the optical properties of a GP-metasurface in the limit of diminishing spacing between GP nanocavities and show that it maintains its nanoresonator array character, with negligible GP interaction, even at extremely close proximity between cavities. Then, at the point where inter-cavity electrical connection is first established, the surface abruptly transforms into a patterned metal-insulator-metal waveguide. We report detailed experimental evidence and explain the underlying physics through computational modeling and based on the properties and inherent symmetries of the electromagnetic field of the investigated metasurface. The novel phenomenon explored here can have a host of potential applications in the field of active plasmonic metamaterials, plasmonic photocatalysis and ultra-sensitive sensors.

Understanding and controlling the individual behavior of nanoscopic matter in liquids, the environment in which many such entities are functioning, is both inherently challenging and important to many natural and man-made applications. Here, we transport individual nano-objects, from an assembly in a biological ionic solution, through a nanochannel network and confine them in electrokinetic nanovalves, created by the collaborative effect of an applied ac electric field and a rationally engineered nanotopography, locally amplifying this field. The motion of so-confined fluorescent nano-objects is tracked, and its kinetics provides important information, enabling the determination of their particle diffusion coefficient, hydrodynamic radius, and electrical conductivity, which are elucidated for artificial polystyrene nanospheres and subsequently for sub–100-nm conjugated polymer nanoparticles and adenoviruses. The on-chip, individual nano-object resolution method presented here is a powerful approach to aid research and development in broad application areas such as medicine, chemistry, and biology.