Absorption In Devices Research Articles

Highly Tunable Light Absorber Based on Topological Interface Mode Excitation of Optical Tamm State.

Optical absorbers based on Tamm plasmon states are known for their simple structure and high operational efficiency. However, these absorbers often have limited absorption channels, and it is challenging to continuously adjust their light absorption rates. Here, we propose a Tamm plasmon state optical absorber composed of a layered stack structure consisting of one-dimensional topological photonic crystals and graphene nano-composite materials. Using the four-by-four transfer matrix method, we investigate the structural relationship of the absorber. Our results reveal that topological interface states (TISs) effectively excite the optical Tamm state (OTS), leading to multiple absorption peaks. This expands the number of absorption channels, with the coupling number of the TIS determining the transmission quality of these channels-a value further adjustable by the period number of the photonic crystals. Tuning the filling factor, refractive index, and thickness of the graphene nano-composite material allows for a wide range of control over the device's absorption rate, from 0 to 1. Additionally, adjusting the defect layer thickness, incident angle, and Fermi energy enables us to control the absorber's operational bandwidth and the switching of its absorption effect. This work presents a new approach to expanding the tunability of optoelectronic devices.

Tunable bandwidth terahertz perfect absorption device based on vanadium dioxide phase transition control.

Utilizing the phase transition principle of VO2, this paper presents a tunable ultra-wideband terahertz perfect absorption device with simple structure and tunability. The proposed broadband terahertz perfect absorption device is a three-layer structure with a metal reflective layer, a silicon dioxide dielectric layer and a VO2 layer from bottom to top. It was found that the terahertz perfect absorption device's absorption could be dynamically adjusted from 1.2% to 99.9% when changing from an insulated to a metallic state. With the VO2 in the metallic state, the terahertz perfect absorption device has an absorption efficiency of more than 90% in 4.00 to 10.08 THz's ultra-broadband range and near-perfect absorption is achieved in the ranges of 4.71 THz to 5.16 THz and 7.74 THz to 8.06 THz. To explain the working principle of this terahertz perfect absorption device, this paper utilizes wave interference's principle, theory of impedance matching and electric field analysis. Compared to previously reported terahertz metamaterial devices, the vanadium dioxide device proposed in this paper is significantly optimized in terms of tunable range and absorption bandwidth. In addition, the terahertz perfect absorption device is polarization insensitive and maintains good absorptivity over a wide-angle incidence range. This tunable ultra-wideband terahertz perfect absorption device could have applications in the fields of modulation, stealth devices, and thermal emission devices.

Design and performance analysis of a mid-infrared broadband thermally tunable metamaterial absorption device based on the phase-change effect.

We propose a structurally simple, innovative, and multifunctional mid-infrared broadband thermally tunable metamaterial absorption device. The absorption device consists of a three-layer structure, from bottom to top: Ti substrate, SiO2 dielectric layer, and patterned VO2 layer. Through temperature control, the average absorption intensity of the absorption device can vary between 0.08 and 0.94. The absorption device's absorption mechanism is rooted in the thermal phase-change characteristics exhibited by the topologically patterned VO2. When the temperature is below 340 K, VO2 is in a dielectric state, resulting in near-total reflection performance in the mid-infrared range. When the temperature is above 340 K, VO2 undergoes a dielectric-to-metal transition, enabling the absorption device to achieve an average absorption rate of 94.12% in the ultra-wideband range of 6.26 μm-20.96 μm in the mid-infrared. This absorption range completely covers the atmospheric window wavelengths of 8 μm-14 μm, demonstrating high practical value. We explain the working mechanism of the absorption device from the perspective of the electromagnetic field. Subsequently, we study the variations in the absorption curve of the absorption device at different temperatures of VO2 and use the changes in the electric field at the same wavelength under different temperatures to explain the variations in absorption. Compared to previous work, our structure has only three layers in a single unit, making it easy to process and produce. Additionally, the absorption device's operating bandwidth and average absorption rate in the mid-infrared range have been significantly improved. Furthermore, the absorption device exhibits substantial incident angle tolerance and polarization insensitivity. We believe that this design has broad application potential in future optothermal conversion, infrared stealth, and thermal radiation.

Advancing perovskite solar cell performance: Enhanced efficiency and stability through superimposed PbS QDs

This study investigates enhancing efficiency in thin-film photovoltaic devices by incorporating varying-sized superimposed PbS colloidal quantum dots (CQDs). These CQDs offer tunable near-infrared absorption, multiple exciton generation effects, and solution processability, rendering them promising for improved performance. Superimposing QDs of different sizes extends the device's absorption spectrum beyond conventional limits, utilizing tailored absorption coefficients for broader sunlight wavelength utilization and increased solar energy conversion efficiency. Each QD group exhibits a unique absorption coefficient, with a peak at its central wavelength from the Schrödinger equation solution. Spectral analysis reveals strategic enhancement in light absorption across visible and near-infrared regions, broadening the perovskite absorption range beyond 800 nm. These QDs enhance both infrared and visible spectra, improving light harvesting. Summing the absorption of single QD groups creates a continuous spectrum, enhancing perovskite film stability and morphology. Rigorous optical analysis and comprehensive electrical modeling investigate charge carrier interactions within the photovoltaic framework. The study verifies around 24 % efficacy enhancement compared to QD-absent configurations, surpassing uniformly dispersed QDs by 11 %. Optical and electrical analyses yield a short-circuit current of 26.7 mA/cm2, open-circuit voltage of 1.13 V, fill factor of 0.88, and overall efficiency of 25.12 % in superimposed configurations. Results underscore the significance of varied QD dimensions and layered structures for enhanced absorption, offering a promising route for advancing thin-film solar technology. The study showcases the potential of PbS CQDs with varying radii in photovoltaics, contributing to improved efficiency and stability, with implications for the future of solar energy technology.

High efficient perovskite solar cells enhancement via photosystem I proteins

AMX3 (A, M, and X are, respectively, organic cation, metal cation, and halogen anion)-type hybrid Perovskite Solar Cells (PeSCs) initiated a promising new generation of Solar Cells (SCs). Photovoltaics utilizing lead Halide Perovskites (HPe) absorbers swiftly have enhanced Power Conversion Efficiencies (PCEs). Furthermore, for materials used in fabricating process of SCs and Solar Energy Conversion (SEC), using bio-photonic systems has shown great promise. Accordingly, plants' photosynthetic organs have attracted tremendous attention. SEC in the photosynthesis organs of plants has indicated a substantial potential towards the advancement of green renewable energy technologies. The maximum absorption spectrum wavelengths of the principal member of photosynthetic components, the photosystem I (PS1) protein complex, are 430 nm and 665 nm. Hence, they act as a complementary mechanism in PeSCs in which the absorption spectrum infirmity is at the 665 nm wavelength area. In the present research, we enhance the PeSCs via using the photosystem1 protein complex and present their positive obtained results. The device's absorption spectrum and external quantum efficiency (EQE) show advantageous ameliorates. Hereupon, the PCE of the PeSCs, is optimized from 17.84% to 18.63%.

Tunable Resonant‐Photopyroelectric Detector Using Chalcogenide−Metal−Fluoropolymer Nanograting

AbstractPyroelectric detectors are often broadband and require external filters for wavelength‐specific applications. This paper reports a tunable, narrowband, and lightweight pyroelectric infrared detector built upon a flexible membrane of As2S3−Ag−P(VDF‐TrFE) with subwavelength grating, which is capable of both on‐chip filtering and photopyroelectric energy conversion. The top surface of this hybrid membrane is a corrugated As2S3−Ag film contributing to narrowband light absorption in the near‐infrared (NIR) regime, and the bottom part is a polyvinylidene fluoride‐trifluoroethylene (PVDF‐TrFE) membrane for the conversion of the absorbed light to an electrical signal. Uniquely, applying a bias voltage to the PVDF‐TrFE membrane enables the tuning of the device's absorption and pyroelectric characteristics owing to the piezoelectrically induced mechanical bending. The resonator exhibited a resonant absorption coefficient of 80% and a full‐width‐half‐maximum of 15 nm within the NIR, a responsivity of 1.4 mV mW−1, and an equivalent noise power of 13 µW Hz−1/2 at 1560 nm. By applying a 15‐V bias to the PVDF‐TrFE membrane, the absorption coefficient decreased to 18% due to the change in the grating period and incident angle. The narrowband and tunable features of the As2S3−Ag−P(VDF‐TrFE) pyroelectric detector will benefit a variety of potential applications in sensors, optical spectroscopy, and imaging.

Enhancement of the Photorefractive Response Time in a Polymeric Composite Photosensitized with CdTe Nanoparticles

Because of their enhanced spectral response, photorefractive polymeric composites photosensitized with semiconductor nanocrystals are emerging as an important class of materials. Despite their promising characteristics, however, several deficiencies persist. Relatively low diffraction efficiencies and slow response times have prevented these materials from reaching their full potential. In this work we demonstrate the ability to enhance a composite's response time by nearly 1 order of magnitude without significantly ceding diffraction efficiency through judicious selection of semiconductor material. By replacing the commonly employed cadmium selenide nanocrystals with those of cadmium telluride, the response time was enhanced from 1.05 s to 171 ms. Moreover, through careful control of the photorefractive device's absorption characteristics, this augmentation in response time is accompanied by a relatively small decrease in internal diffraction efficiency from 24% to 20%.