Intercalation-based inorganic materials that change their colours upon ion insertion/extraction lay an important foundation for existing electrochromic technology. However, using only such inorganic electrochromic materials, it is very difficult to achieve the utmost goal of full-colour tunability for future electrochromic technology mainly due to the absence of structural flexibility. Herein, we demonstrate an ultracompact asymmetric Fabry-Perot (F-P) nanocavity-type electrochromic device formed by using partially reflective metal tungsten as the current collector and reflector layer simultaneously; this approach enables fairly close matching of the reflections at both interfaces of the WO3 thin layer in device form, inducing a strong interference. Such an interference-enhanced device that is optically manipulated at the nanoscale displays various structural colours before coloration and, further, can change to other colours including blue, red, and yellow by changing the optical indexes (n, k) of the tungsten oxide layer through ion insertion.

The past few decades have witnessed a substantial increase in terahertz (THz) research. Utilizing THz waves to transmit communication and imaging data has created a high demand for phase and amplitude modulation. However, current active THz devices, including modulators and switches, still cannot meet THz system demands. Double-channel heterostructures, an alternative semiconductor system, can support nanoscale two-dimensional electron gases (2DEGs) with high carrier concentration and mobility and provide a new way to develop active THz devices. In this Letter, we present a composite metamaterial structure that combines an equivalent collective dipolar array with a double-channel heterostructure to obtain an effective, ultrafast, and all-electronic grid-controlled THz modulator. Electrical control allows for resonant mode conversion between two different dipolar resonances in the active device, which significantly improves the modulation speed and depth. This THz modulator is the first to achieve a 1 GHz modulation speed and 85% modulation depth during real-time dynamic tests. Moreover, a 1.19 rad phase shift was realized. A wireless free-space-modulation THz communication system based on this external THz modulator was tested using 0.2 Gbps eye patterns. Therefore, this active composite metamaterial modulator provides a basis for the development of effective and ultrafast dynamic devices for THz wireless communication and imaging systems.

The ability of plasmonic nanostructures to harvest photons beyond the traditional band-to-band photovoltaic conversion of semiconductors has stimulated intensive research activities in hot electron. As an emerging strategy for energyharvesting, photodetection and photocatalysis, realization of broadband and efficient plasmonic absorption with easily constructed metal-semconductor (M-S) nanosystems is essential for improving its photoelectric efficiency, while minimizing the cost and complexity of fabrication. Here, we report an approach for near-infrared (NIR) photodetection by combining the randomly and densely packed photonic nanostructures with ultrathin plasmonic coatings. Relying on the Au covered disordered silicon nanoholes (SiNHs) M-S platform, the efficient plasmonic absorption, strong field localization and together with random nature facilitate the broadband photon-energy conversion from both photoelectric hot electron ejection and photothermal hot electron relaxation. Spectral-and time-resolved studies reveal that the proposed Au-SiNHs device is capable of tracking fastvarying NIR signals via hot electron emission process, with a photoresponsivity around 1.5−13 mA/W at wavelengths ranging from 1100 to 1500 nm. With a detailed theoretical analysis based on phenomenological model, different loss mechanisms involved in the hot electron related photoelectric process were described quantitatively and a large improvement potential was identified in the proposed hot electron harvesting platform. In addition, we demonstrated that the closely distributed random voids and tips in the Au-SiNHs structures enable the formation of a substantial amount of hot-spots that can significantly elevate the local temperature through the relaxation of the nonejected hot electrons and, therefore, generate the obvious photothemal mediated photoresponse under voltage driven conditions.

The Jones matrix is a useful tool to deal with polarization problems, and its number of degrees of freedom (DOFs) that can be manipulated represents its polarization-controlled capabilities. A metasurface is a planar structure that can control light in a desired manner, which, however, has a limited number of controlled DOFs (≤4) in the Jones matrix. Here, we propose a metasurface design strategy to construct a Jones matrix with six DOFs, approaching the upper-limit number of a 2D planar structure. We experimentally demonstrate several polarization functionalities that can only be achieved with high (five or six) DOFs of the Jones matrix, such as polarization elements with independent amplitude and phase tuning along its fast and slow axes, triple-channel complex-amplitude holography, and triple sets of printing-hologram integrations. Our work provides a platform to design arbitrary complex polarization elements, which paves the way to a broader exploitation of polarization optics.