Spectroscopy is a cornerstone in the field of optics. Conventional spectrometers generally require two elements. The first provides wavelength selectivity, for example, diffraction grating or Michelson interferometer. The second is a detector (or detector array). Many applications would benefit from very small and lightweight spectrometers. This motivates us to investigate what may be regarded as an ultimate level of miniaturization for a spectrometer, in which it consists solely of a detector array. We demonstrate a chip containing 24 pixels, each comprising a silicon nanowire (Si NW) array photodetector formed above a planar photodetector. The NWs are structurally colored, enabling us to engineer the responsivity spectra of all photodetectors in the chip. Each pixel thus combines wavelength selectivity and photodetection functions. We demonstrate the use of our chip to reconstruct the spectrum of an unknown light source impinging upon it. This is achieved by an algorithm that takes as its inputs the measured photocurrents from the pixels and a library of their responsivity spectra.

We computationally reconstruct short- to long-wave infrared spectra using an array of plasmonic metasurface filters. We illuminate the filter array with an unknown spectrum and measure the optical power transmitted through each filter with an infrared microscope to emulate a filter-detector array system. We then use the recursive least squares method to determine the unknown spectrum. We demonstrate our method with light from a blackbody. We also demonstrate it with spectra generated by passing the light from the blackbody through various materials. Our approach is a step towards miniaturized spectrometers spanning the short- to long-wave infrared based on filter-detector arrays.

Although many nanoscale materials such as quantum dots and metallic nanocrystals exhibit size dependent optical properties, it has been difficult to incorporate them into optical or electronic devices because there are currently no methods for precise, large‐scale deposition of single nanocrystals. Of particular interest is the need to control the orientation of single nanocrystals since the optical properties are usually strongly anisotropic. Here a method based on electrophoretic deposition (EPD) is reported to precisely assemble vertically oriented, single gold nanorods. It is demonstrated that the orientation of gold nanorods during deposition is controlled by the electric dipole moment induced along the rod by the electric field. Dissipative particle dynamics simulations indicate that the magnitude of this dipole moment is dominated by the polarizability of the solution phase electric double layer around the nanorod. The resulting vertical gold nanorod arrays exhibit reflected colors due to selective excitation of the transverse surface plasmon mode. The EPD method allows assembly of arrays with a density of over one million, visually resolvable, vertical nanorods per square millimeter.

The assembly of nanoscale materials into arbitrary, organized structures remains a major challenge in nanotechnology. Herein, we report a general method for creating 2D structures by combining top-down lithography with bottom-up chemical assembly. Under optimal conditions, the assembly of gold nanoparticles was achieved in less than 30 min. Single gold nanoparticles, from 10 to 100 nm, can be placed in predetermined patterns with high fidelity, and higher-order structures can be generated consisting of dimers or trimers. It is shown that the nanoparticle arrays can be transferred to, and embedded within, polymer films. This provides a new method for the large-scale fabrication of nanoparticle arrays onto diverse substrates using wet chemistry.