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Using organic photodetectors for multispectral sensing is attractive due to their unique capabilities to tune spectral response, transmittance, and polarization sensitivity. Existing methods lack tandem multicolor detection and exhibit high spectral cross talk. We exploit the polarization sensitivity of organic photodetectors, together with birefringent optical filters to design single-pixel multispectral detectors that achieve high spectral selectivity and good radiometric performance. Two different architectures are explored and optimized, including the Solc-based and multitwist-retarder-based organic photodetectors. Although the former demonstrated a higher spectral resolution, the latter enables a more compact sensor as well as greater flexibility in device fabrication. 

Simultaneous spectral and polarimetric imaging enables versatile detection and multimodal characterization of targets of interest. Current architectures incorporate a 2×2 pixel arrangement to acquire the full linear polarimetric information causing spatial sampling artifacts. Additionally, they suffer from limited spectral selectivity and high color crosstalk. Here, we demonstrate a bio-inspired spectral and polarization sensor structure based on integrating semitransparent polarization-sensitive organic photovoltaics (P-OPVs) and liquid crystal polymer (LCP) retarders in a tandem configuration. Color tuning is realized by leveraging the dynamic chromatic retardation control of LCP films, while polarization sensitivity is realized by exploiting the flexible anisotropic properties of P-OPVs. The structure is marked by its ultra-thin design and its ability to detect spectral and polarimetric contents along the same optical axis, thereby overcoming the inherent limitations associated with conventional division-of-focal plane sensors. 

Channeled spectropolarimetry measures the spectral dependence of the polarization states of light. This technique is marked by its snapshot feature, in that the complete polarization states can be determined simultaneously from a single intensity spectrum. However, without athermalization, it suffers from high sensitivity to temperature, which in turn, degrades the polarimetric reconstruction accuracy. In this paper, we present a calibration technique for a fiber-based channeled spectropolarimetry that leverages phase-shifting interferometry to accurately demodulate the retarders' phase, thereby improving the accuracy of the acquired Stokes parameters. Additionally, it enables robust spectropolarimetric performance that is insensitive to environmental perturbations. Experimental results demonstrate that calibrations using phase-shifting interferometry improve the Stokes reconstruction results by approximately a factor of 3 when compared to the reference beam calibration method. 

Combining hyperspectral and polarimetric imaging provides a powerful sensing modality with broad applications from astronomy to biology. Existing methods rely on temporal data acquisition or snapshot imaging of spatially separated detectors. These approaches incur fundamental artifacts that degrade imaging performance. To overcome these limitations, we present a stomatopod-inspired sensor capable of snapshot hyperspectral and polarization sensing in a single pixel. The design consists of stacking polarization-sensitive organic photovoltaics (P-OPVs) and polymer retarders. Multiple spectral and polarization channels are obtained by exploiting the P-OPVs’ anisotropic response and the retarders’ dispersion. We show that the design can sense 15 spectral channels over a 350-nanometer bandwidth. A detector is also experimentally demonstrated, which simultaneously registers four spectral channels and three polarization channels. The sensor showcases the myriad degrees of freedom offered by organic semiconductors that are not available in inorganics and heralds a fundamentally unexplored route for simultaneous spectral and polarimetric imaging. 

Abstract Photodetectors that can sense not only light intensity but also light's polarization state add valuable information that is beneficial in a wide array of applications. Polymer semiconductors are an attractive material system to achieve intrinsic polarization sensitivity due to their anisotropic optoelectronic properties. In this report, the thermomechanical properties of the polymer semiconductors PBnDT‐FTAZ and P(NDI2OD‐T2) are leveraged to realize bulk heterojunction (BHJ) films with record in‐plane alignment. Two polymer blends with distinct weight average molar masses (Mw) are considered and either a strain‐ or rub‐alignment process is applied to align the polymer blend films. Optimized processing yields films with dichroic ratios (DR) of over 11 for the highMwsystem and nearly 17 for the lowMwsystem. Incorporating the aligned films into photodetectors results in a polarized photocurrent ratio of 15.25 with corresponding anisotropy ratio of 0.88 at a wavelength of 530 nm, representing the highest reported photocurrent ratio for photodiodes that can operate in a self‐powered regime. The demonstrated performance showcases the ability of polymer semiconductors to achieve BHJ films with exceptional in‐plane polymer alignment, enabling high performance polarization sensitive photodetectors for incorporation into novel device architectures.