Search for: All records

Light fields carry a wealth of information, including intensity, spectrum, and polarization. However, standard cameras capture only the intensity, disregarding other valuable information. While hyperspectral and polarimetric imaging systems capture spectral and polarization information, respectively, in addition to intensity, they are often bulky, slow, and costly. Here, we have developed an encoding metasurface paired with a neural network enabling a normal camera to acquire hyperspectro-polarimetric images from a single snapshot. Our experimental results demonstrate that this metasurface-enhanced camera can accurately resolve full-Stokes polarization across a broad spectral range (700 to 1150 nanometer) from a single snapshot, achieving a spectral sensitivity as high as 0.23 nanometer. In addition, our system captures full-Stokes hyperspectro-polarimetric video in real time at a rate of 28 frames per second, primarily limited by the camera’s readout rate. Our encoding metasurface offers a compact, fast, and cost-effective solution for multidimensional imaging that effectively uses information within light fields. 

Transition metals have been explored extensively for non-enzymatic electrochemical detection of glucose. However, to enable glucose oxidation, the majority of reports require highly alkaline electrolytes which can be damaging to the sensors and hazardous to handle. In this work, we developed a non-enzymatic sensor for detection of glucose in near-neutral solution based on copper-nickel electrodes which are electrochemically modified in phosphate-buffered saline (PBS). Nickel and copper were deposited using chronopotentiometry, followed by a two-step annealing process in air (Step 1: at room temperature and Step 2: at 150 °C) and electrochemical stabilization in PBS. Morphology and chemical composition of the electrodes were characterized using scanning electron microscopy and energy-dispersive X-ray spectroscopy. Cyclic voltammetry was used to measure oxidation reaction of glucose in sodium sulfate (100 mM, pH 6.4). The PBS-Cu-Ni working electrodes enabled detection of glucose with a limit of detection (LOD) of 4.2 nM, a dynamic response from 5 nM to 20 mM, and sensitivity of 5.47 ± 0.45 μA cm−2/log10(mole.L−1) at an applied potential of 0.2 V. In addition to the ultralow LOD, the sensors are selective toward glucose in the presence of physiologically relevant concentrations of ascorbic acid and uric acid spiked in artificial saliva. The optimized PBS-Cu-Ni electrodes demonstrate better stability after seven days storage in ambient compared to the Cu-Ni electrodes without PBS treatment.