Light Absorption Research Articles

Phase change materials encapsulated in a novel hybrid carbon skeleton for high-efficiency solar-thermal conversion and energy storage

Phase change materials (PCMs) with high energy density and stationary transition temperature are now considered promising solar energy storage mediums. However, their intrinsic poor light absorption, thermal conductivity and stability severely impede their potential applications. In this study, a novel carbonized hybrid aerogel (CHA) structure was firstly constructed by incorporating MXene and carbon nanofibers (CNFs) into a continuous phase polyamic acid salt (PAAS) aqueous solution, followed by directional freezing, vacuum drying, imidization, and carbonization processes. Finally, the composite PCMs (CPCMs) were fabricated by vacuum impregnation of PCMs into the CHAs. The CPCM, of which CHA consists of 20 wt% MXene and 10 wt% CNF@PDA, demonstrates high solar-thermal conversion efficiency (>91 %), improved thermal conductivity of 0.40 W·m−1·K−1, great thermal stability (enthalpy loss < 0.19 % after 100 cycling tests with no obvious leakage). The introduction of MXene and CNFs endows PCM with broader light absorption spectrum range. The skeleton matrix embedded with bonded MXene sheets and CNFs provides more thermal pathways, light absorption sites and carrying capacity, improves the thermal conductivity, solar-thermal conversion property and stability of PCM. In addition, CPCM also exhibits outstanding EMI SE (95 dB). The multifunctional and high-performance CPCMs shows potential to realize the effective capture and utilization of solar energy. This work provides a new strategy to construct stable and multifunctional hybrid carbon skeleton for high-efficiency solar-thermal conversion and energy storage.

Optimization of Cu2O Thickness to Enhance Photocatalytic Properties of Electrodeposited Cu2O/FTO Photoanode

Currently, n-type cuprous oxide (Cu2O) is a promising material as photocatalyst because of its energy gap of 2 eV that absorbs visible light up to a wavelength of 600 nm. As a photoelectrode, the thickness of Cu2O is crucial, where the improper thickness may worsen the photocatalytic properties. This work aimed to enhance the photocatalytic properties of Cu2O electrodeposited on fluorine-doped tin oxide (FTO), called Cu2O/FTO, by optimizing the Cu2O thickness. The thickness of Cu2O was controlled by adjusting the deposition time in the electrochemical deposition of Cu2O/FTO. By changing the deposition time from 5 to 45 min, the morphology of Cu2O changed from a leaf-like shape to an irregular facet shape with highly dense coverage, and the average thickness increased from 370 to 1100 nm. The increasing Cu2O thickness resulted in the increasing light absorption. The Cu2O/FTO demonstrated anodic photocurrent, which increased with the Cu2O thickness up to a threshold value of 1000 nm (35 min deposition time). At a thickness of 1000 nm, Cu2O/FTO achieved the highest photocurrent (150 and 58 µA under irradiation of 365 and 470 nm, respectively) due to the highly dense morphology and high absorption. In addition, with a thickness of 1000 nm, the charge diffusion was still good. Further, the increase of Cu2O film thickness higher than 1000 nm caused low photocatalytic properties even though the morphology was highly dense, and the absorption was the highest. This condition could be due to the relatively too-high resistance of Cu2O that caused poor charge diffusion. Copyright © 2024 by Authors, Published by BCREC Publishing Group. This is an open access article under the CC BY-SA License (https://creativecommons.org/licenses/by-sa/4.0).

Oxygen vacancy engineering of ultra-small CuWO4 nanoparticles for boosting photocatalytic organic pollutant degradation.

Nanomaterials have attracted great interest in the field of photocatalytic degradation due to their larger specific surface area and efficient charge/mass transfer ability, which are beneficial for enhancing photocatalytic activity. However, the bandgap of photocatalysts would increase with the size reduction, weakening the photoabsorption ability. Thus the relationship between the size of catalysts and photoactivity should be balanced to achieve optimal photocatalytic performance. Herein, ultra-small CuWO4 nanoparticles (ca. 39 nm) with moderate oxygen vacancies (CuWO4-OVs) were synthesized by the cascade strategy (ligand confinement@fast calcination). The introduction of oxygen vacancies offset the deficiency of light absorption ability caused by the small size effect. Besides, oxygen vacancies could provide more reaction active sites, conducive to the adsorption and activation of dye molecules and H2O. Degradation experiments reveal that the optimized photocatalyst CuWO4-OVs 350 shows outstanding photocatalytic activity, and the removal ratio of methylene blue (MB) reaches over 90.26% in 70 min, exceeding that of pure CuWO4-air (37.66%). Additionally, the degradation performance of CuWO4-OVs 350 surpasses most of the other CuWO4-based photocatalytic systems. More importantly, the photocatalytic degradation activity of CuWO4-OVs 350 could remain at 88.26% even after five cycles, and high photostability was achieved. This work affords constructive inspiration for synergistic photoactivity enhancement and increase of catalyst reaction active sites to achieve eminent photocatalytic degradation performance.

All-dielectric grating-assisted absorption enhancement in a subwavelength mercury cadmium telluride layer for infrared photodetectors

Light absorption enhancement in a 1.5 μm thick mercury–cadmium–telluride (Hg0.762Cd0.238Te, MCT) layer at room temperature utilizing 1D dielectric grating at mid-wave infrared (MWIR) wavelengths (3–5 μm) has been theoretically investigated. The optimized dielectric grating facilitates light diffraction and scattering into the MCT-absorbing waveguiding layer resulting in an increased lateral optical path. The light absorption was improved from ∼37.5% to ∼71% (TE) and ∼70% (TM) at normal incidence. With enhanced absorption, the photocarrier generation rate in the thin layer would be comparable to a bulk 5 μm thick MCT layer. A ∼3× reduction in the MCT layer thickness without compromising absorption has the potential for realizing infrared photodetectors with improved sensitivity at conventional operating temperatures and/or elevated operating temperatures.

Photo Switchable 4D Printing Remotely Controlled Responsive and Mimetic Deformation Shape Memory Polymer Nanocomposites

AbstractPhoto‐triggered shape morphing structures can be found in myriads of areas. Utilizing light as a switch can effectively control and regulate the precise deformation of structures. However, the integration of photo‐switching functions in shape‐morphing structures with complex geometries remains a challenge. Here, photoswitchable digital light processing based 4D printing high‐resolution and highly complex geometries, based on UV curable WO2.9 nanoparticle doped shape memory polymer nanocomposites is reported, which are highly deformable (stretchability up to ≈1000% at rubbery state) and fatigue resistant (repeatedly loaded &gt;1200 times at ambient temperature). The presence of just trace WO2.9 nanoparticles (&lt;0.20 wt.‰) contributes to the controlled photothermal property of nanocomposite via selective absorption of light, which enables reversibly photoswitchable (&gt;50 times), spatial and remote control of 4D printing shape morphing structures. These findings offer a promising approach to expanding the applications of photo‐triggered shape‐morphing structures.

Two-Dimensional Sc2CCl2/XSe2(X=Mo, Pt) van der Waals heterojunctions: Promising photocatalytic hydrogen evolution materials.

This paper presents a study on two newly constructed two-dimensional van der Waals heterojunctions, Sc2CCl2/MoSe2 and Sc2CCl2/PtSe2, using density-functional theory. The study includes a systematic investigation of their geometrical structure, electronic properties, and optical properties. The results indicate that both heterojunctions are thermodynamically, kinetically, and mechanically stable. Additionally, Bader charge analysis reveals that both heterojunctions exhibit typical type II band properties. However, the band gap of the Sc2CCl2/MoSe2 heterojunction is only 1.18 eV, which is insufficient to completely cross the reduction and oxidation (REDOX) potential of 1.23 eV, whereas the band gap of Sc2CCl2/PtSe2 heterojunction is 1.49 eV, which is theoretically capable for water decomposition. The subsequent calculation of the Sc2CCl2/PtSe2 heterojunction demonstrate excellent hole carrier mobility and high efficiency light absorption in the visible light range, facilitating the separation of photogenerated electrons and holes. More importantly, Sc2CCl2/PtSe2 vdW type II heterojunction can achieve full water decomposition from pH 1 to pH 4, and its thermodynamic feasibility is confirmed by Gibbs free energy results. The aim of this study is to develop materials and analyses that will result in optoelectronic devices that are more efficient, stable, and sustainable.

Role of Pyramidal Low-Dimensional Semiconductors in Advancing the Field of Optoelectronics

Numerous optoelectronic devices based on low-dimensional nanostructures have been developed in recent years. Among these, pyramidal low-dimensional semiconductors (zero- and one-dimensional nanomaterials) have been favored in the field of optoelectronics. In this review, we discuss in detail the structures, preparation methods, band structures, electronic properties, and optoelectronic applications (photocatalysis, photoelectric detection, solar cells, light-emitting diodes, lasers, and optical quantum information processing) of pyramidal low-dimensional semiconductors and demonstrate their excellent photoelectric performances. More specifically, pyramidal semiconductor quantum dots (PSQDs) possess higher mobilities and longer lifetimes, which would be more suitable for photovoltaic devices requiring fast carrier transport. In addition, the linear polarization direction of exciton emission is easily controlled via the direction of magnetic field in PSQDs with C3v symmetry, so that all-optical multi-qubit gates based on electron spin as a quantum bit could be realized. Therefore, the use of PSQDs (e.g., InAs, GaN, InGaAs, and InGaN) as effective candidates for constructing optical quantum devices is examined due to the growing interest in optical quantum information processing. Pyramidal semiconductor nanorods (PSNRs) and pyramidal semiconductor nanowires (PSNWRs) also exhibit the more efficient separation of electron-hole pairs and strong light absorption effects, which are expected to be widely utilized in light-receiving devices. Finally, this review concludes with a summary of the current problems and suggestions for potential future research directions in the context of pyramidal low-dimensional semiconductors.

Modifying electronic and optical properties of violet phosphorus through variable fluorine coverage.

We present a comprehensive investigation of the electronic properties of fluorinated monolayer violet phosphorus using first-principles calculations. Our results reveal a strong dependence of the electronic properties on the different fluorine coverages of fluorination. As the fluorine coverage increases, monolayer violet phosphorus undergoes a significant transition from a wide direct bandgap semiconductor to a narrow indirect bandgap semiconductor. Moreover, both semi-fluorinated and fully fluorinated monolayer violet phosphorus exhibit advantageous semiconducting characteristics, with a tunable bandgap of 0.50 ~ 1.04 eV under biaxial strain ranging from -6% to 6%. Notably, the fully fluorinated monolayer violet phosphorus demonstrates a higher coefficient of light absorption within the visible range. Therefore, our findings highlight the tunability of monolayer violet phosphorus properties through the absorption of various fluorine coverages, providing valuable insights for the design and development of novel semiconductor devices based on this material.

Modulation of Sulfur Vacancies in ZnIn2S4/MXene Schottky Heterojunction Photocatalyst Promotes Hydrogen Evolution

AbstractThe sustainable production of hydrogen utilizing solar energy is a pivotal strategy for reducing reliance on fossil fuels. ZnIn2S4 (ZIS), as a typical metal sulfide semiconductor, has received extensive attention in photocatalysis. Although the introduction of sulfur (S) vacancies in ZIS to enhance photocatalytic hydrogen production by creating defect energy levels has been explored, detailed studies on the control and modulation of S‐vacancies in ZIS are sparce. This study demonstrates that while moderate levels of S‐vacancies can enhance hydrogen evolution, excessive vacancies may hinder the process, underscoring the importance of S‐vacancy modulation. Guided by theoretical calculations, We have designed and synthesized ZIS with modulated S‐vacancies to realize favorable hydrogen adsorption‐free energy and integrated in a Schottky‐heterojunction with MXene co‐catalysts for enhanced hydrogen evolution. The optimized hydrogen evolution performance of ZnIn2S4/MXene (ZMX) reaches 14.82 mmol g−1 h−1 under visible light irradiation, surpassing many reported ZnIn2S4‐based photocatalysts. The enhanced performance is ascribed to widened light absorption and enhanced carrier transportation realized by S‐vacancy modulation and the co‐catalytic effect. Femtosecond ultrafast absorption (fs‐TA) spectra and other in‐situ/ex‐situ characterizations further prove an efficient separation and transfer in an as‐prepared ZMX catalyst. These findings open up new perspectives for designing catalysts with vacancy modulation.

Gap type effect on photocatalytic degradation using newly hydrotalcite nanoposite precursor synthesized by hydrothermal method

&lt;p&gt;A novel technique involving hydrothermal synthesis was employed to prepare nanocomposite precursors of lamellar double hydroxide based basic mixed oxides. This method extended ongoing research on iron-impregnated hydrotalcite-supported nanomaterials. The iron-based Fe/MgAl-h nanocomposite was prepared via dry impregnation, introducing a known % by weight of Fe (NO3)3.9H2O metal salt into the hydrothermally synthesized MgAl-h structure. For comparative analysis, the photocatalytic performance of Fe/MgAl-h was compared with the coprecipitation-synthesized Fe/MgAl-c after calcination at 400°C, using various characterization techniques. Structural examination revealed a double-layered hydroxyl structure and the presence of iron oxide phase Fe2O3 in Fe/MgAl-h400. Optical assessments indicated an indirect band gap energy of 1.89 eV for solid Fe/MgAl-h400, which is suitable for visible light absorption. Photocatalytic experiments for methylene blue (MB) dye degradation in aqueous solution were performed under artificial irradiation with a tungsten lamp as the visible light source, mirroring the conditions of Fe/MgAl-c400. Using 50 mg/L MB concentration and 0.5 g/L catalyst quantity, increased MB removal efficiency with time was observed. A comparative study of hydrothermal and coprecipitation synthesis methods showed decreased photodegradation for the hydrothermally prepared solid. Fe/MgAl-h400 and Fe/MgAl-c400 exhibited reaction efficiencies of approximately 46% and 67%, respectively, possibly attributed to their distinct indirect and direct band gap characteristics. Moreover, a wider band gap in a semiconductor material offers several advantages for the degradation of dyes.&lt;/p&gt;&#x0D;

Development of a Plasmonic Light Management Architecture Integrated within an Interface Passivation Scheme for Ultrathin Solar Cells

In response to climate and resource challenges, the transition to a renewable and decentralized energy system is imperative. Ultrathin Cu(In,Ga)Se2 (CIGS)‐based solar cells are compatible with such transition due to their low material usage and improved production throughput. Despite the benchmark efficiency of CIGS technology, ultrathin configurations face efficiency drops arising from increased rear interface recombination and incomplete light absorption. Dielectric passivation schemes address rear interface recombination, but achieving simultaneous electrical and optical gains is crucial for thinning down the absorber. Plasmonic nanoparticles emerge as a solution, enhancing light interaction through resonant scattering. In the proposed architecture, the nanoparticles are encapsulated within a dielectric rear passivation layer, combining effective passivation and light trapping. A controlled deposition and encapsulation of individualized nanoparticles is achieved by an optimized process flow using microfluidic devices and nanoimprint lithography. With the developed plasmonic and passivated architecture, a 3.7 mA cm−2 short‐circuit current density and a 23 mV open‐circuit voltage improvements are obtained, leading to an almost 2% increase in light‐to‐power conversion efficiency compared to a reference device. This work showcases the developed architecture potential to tackle the electrical and optical downfalls arising from the absorber thickness reduction, contributing to the dissemination of ultrathin technology.

Significant contribution of fractal morphology to aerosol light absorption in polluted environments dominated by black carbon (BC)

In recent years, researchers have emphasized the use of fractal aggregate morphology instead of the core-shell morphology in global climate models for estimating black carbon (BC) forcing. This study confirms that fractal morphology plays an important role in reducing the overestimation of aerosol light absorption calculations in the case of an urban polluted environment. During periods of high anthropogenic BC emissions at Delhi, the particle light absorption is overestimated by 50 to 200% by assumptions of both external mixing and internal core-shell mixing. While incorporating the aggregate morphology model into light absorption simulations is beneficial in such cases, it comes with a high computational burden. To address this, we propose a metric known as morphology index (MI). This index distributes the weightage between the two extreme cases of core-shell and fractal aggregate to obtain accurate particle light absorption. Long-range transported aerosols were estimated to have an MI of 0.78, and fresh local emissions had an MI of 0.48. A BC-based aerosol classification approach was developed to determine the most relevant particle size mode for light absorption. The method is based on patterns found between the correlations of the BC mass concentrations and aerosol number concentrations at the different particles sizes (BC-size correlation spectra). BC-size correlation spectra are introduced as a concept that may be used (i) independently to understand the size-dependent heterogeneous distribution of aerosol light absorption and (ii) in conjunction with MI to accurately model the optical properties of aerosols in different BC regimes.

Construction of 2D/2D BCNS/Ti3C2 heterojunction with boron-doped g-C3N4 and Ti3C2 MXene for enhanced photocatalytic water splitting

Graphitic carbon nitride (g-C3N4) has attracted great interest in photocatalytic water splitting. However, the poor photogenerated charge carriers transfer and the insufficient driving force for oxygen evolution reaction limit its practical application. In this work, boron-doped g-C3N4 nanosheets (BCNS) have been synthesized by calcining a mixture of g-C3N4 and NaBH4. The synthesized BCNS were then combined with Ti3C2 MXene using electrostatic self-assembly to construct a 2D/2D BCNS/Ti3C2 heterojunction. The resultant BCNS retained the original framework of g-C3N4, while the optimized band structure of BCNS induced prominently enhanced visible light absorption, accelerated charge carriers separation, and the increased driving force for water oxidation compared to pure g-C3N4. Density functional theory further proved that BCNS can enhance the driving force for photocatalytic O2 evolution. Moreover, the construction of 2D/2D face-to-face BCNS/Ti3C2 heterojunction was carried out to further enhance photocatalytic performance due to the intimate contact interface and the accelerated separation and transfer of photogenerated charge carriers. As a result, the 2D/2D BCNS/Ti3C2 hetrojunction exhibited a dramatically improved photocatalytic water-splitting performance compared to pristine g-C3N4. This integrated engineering strategy, involving non-metal element doping and 2D/2D heterojunction construction, might provide a unique paradigm for the rational design of efficient photocatalysts for photocatalytic water splitting.

Exploring Electron Transfer Mechanism in Synergistic Interactional Reduced Polyoxometalate-Based Cu(I)-Organic Framework for Photocatalytic Removal of U(VI).

Photocatalytic reduction of U(VI) is a promising method for removing uranium containing pollutants. However, using polyoxometalate-based metal-organic frameworks (POMOFs) for photoreduction of U(VI) is rare, and the relevant charge transfer pathway is also not yet clear. In this article, we demonstrate a highly efficient strategy and revealed a clearly electron transfer pathway for the photoreduction of U(VI) with 99% removal efficiency by using a novel POMOF, [Cu(4,4'-bipy)]5·{AsMo4VMo6VIV2VO40(VIVO)[VIVO(H2O)]}·2H2O (1), as catalyst. The POMOF catalyst was constructed by the connection of reduced {AsMo10V4} clusters and Cu(I)-MOF chains through Cu-O coordination bonds, which exhibits a broader and stronger light absorption capacity due to the presence of reduced {AsMo10V4} clusters. Significantly, the transition of electrons from Cu(I)-MOF to {AsMo10V4} clusters (Cu → Mo/V) greatly inhibits the recombination of photogenerated carriers, thereby advancing electron transfer. More importantly, the {AsMo10V4} clusters are not only adsorption sites but also catalytically active sites. This causes the fast transfer of photogenerated electrons from Mo/V to UO22+(Mo/V → O → U) via the surface oxygen atoms. The shorter electron transmission distance between catalytic active sites and UO22+ achieves faster and more effective electron transport. All in all, the highly effective photocatalytic removal of U(VI) using the POMOF as a catalyst is predominantly due to the synergistic interaction between Cu(I)-MOFs and reduced {AsMo10V4} clusters.

Enhanced visible‐light‐driven photocatalytic application for water purification and hydrogen evolution by large‐sized nanofilm‐constructed hierarchical porous g‐C3N4/SiO2

AbstractThe large‐sized nanofilm‐constructed hierarchical porous SiO2 (LNCHPS) is successfully prepared by the dual templating approach and subsequently used as the support for g‐C3N4. A series of characterization techniques are conducted to evaluate the structure and property of the as‐prepared materials. The LNCHPS possesses two sets of explicated successive pass‐through macropores (0.5–1.0 µm) with large specific surface area. In addition, the macropore wall is constructed by uniform mesoporous nanofilms with the thickness ranging from 35 to 50 nm. Then, the photocatalytic property is investigated by degradations towards Rhodamine B (RhB) under simulated sunlight, in which experiments have been performed through controlling the g‐C3N4 loading contents, solution pH values, and photocatalyst dosages. The apparent rate constant of g‐C3N4/LNCHPS could reach 0.03 min−1 under optimum conditions, showing 6.0 times that of the bulk g‐C3N4. In addition, g‐C3N4/LNCHPS also exhibits significantly enhanced performance in H2 evolution (39.9 µmol h−1) compared to that of the bulk g‐C3N4. High light absorption and utilization, enhanced adsorption capability and quick electron hole separation can render this fine structure excellent photocatalytic performance. Our work enables a facile route for large‐scale preparation of g‐C3N4/LNCHPS for addressing the wastewater treatment and hydrogen energy production simultaneously.

Mo-modified BiOI0.5Cl0.5 composites preparation for antibiotic removal

Photocatalytic technology has the advantages of high efficiency, mild reaction conditions, low cost, and minimal secondary contamination in antibiotic degradation. Bismuth oxyhalides(BiOX) has garnered considerable attention and application as a photocatalyst, due to its suitable band gap and light capture capability. In this study, we successfully synthesized the BiOI0.5Cl0.5 (BCI) material through hydrothermal treatment. Furthermore, Molybdenum (Mo) atoms were diffused into the composite to form Mo-doped Mo@BiOI0.5Cl0.5. Various techniques were employed to characterize the structures, chemical compositions, and morphologies of the obtained materials.The photocatalytic performance of the obtained materials was investigated, revealing that MBCI-3 exhibited superior performance in the photocatalytic degradation of contaminants. Over a span of 20 min, 100% of rhodamine B and 86.0% of tetracycline were successfully removed from water. The enhancement in photocatalytic performance can be attributed to the alteration in the band gap of the BCI complex, leading to improved light absorption, while the incorporation of Mo atoms expedites electron transfer. Finally, the role of h+ and O2•- radicals in photocatalytic degradation was verified through radical trapping experiments.

Measurement of light absorption by chromophoric dissolved organic matter (CDOM) using a type-II liquid capillary waveguide: assessment of an achievable accuracy.

Measurement of light absorption by chromophoric dissolved organic matter (CDOM) using a type-II liquid capillary waveguide: assessment of an achievable accuracy.

External Electric Field Control of Exciton Motion in Porphyrin-Based Metal Organic Frameworks.

Porphyrins are excellent light-harvesting complexes. Presently they are unsuitable for photovoltaic applications, as their excellent light absorbance is compensated to a large extent by their poor transport properties, where most excitons are lost by recombination. Arranging porphyrins in regular, strongly bound, lattices of surface-anchored metal-organic frameworks (PP-SURMOFs) may facilitate charge carrier dissociation, but does not significantly enhance the conductive properties. In most cases, photogenerated excitons traverse undirected, Brownian motion through a hopping process, resulting in a substantial diffusion length to reach electrodes, leading to significant exciton loss through recombination. Here, we propose to guide exciton diffusion indirectly by an external electric field. We show that electric fields, even as strong as 1 V∙nm-1, do not affect the HOMO-LUMO gap of the porphyrins. However, fields of 0.1 V∙nm∙1 and even less demonstrate a notable Stark effect, with slight band gap reductions, for some PP-SURMOFs. When applied as an electric field gradient, for instance, via the substrate, it creates a unidirectional hopping pathway for the excitons. Consequently, we expect a significant reduction of exciton diffusion length leading to increased utilization of photogenerated excitons as they reach the electrodes. This strategy holds promise for integrating photoactive molecules in photovoltaic and photocatalytic applications.

Tailoring Charge Flow in Carbon-Defective Cu-MOF with Pd Nanoparticles: A Boost for Visible Light Organic Photoelectrochemical Transistor in Bioanalysis.

The photoactive material was of significant importance in organic photoelectrochemical transistor (OPECT) bioanalysis as it influences the photoinduced voltage and the μC* product, resulting in a varying sensor sensitivity. The utilization of metal-organic frameworks (MOFs) as photoactive materials in OPECT analysis is promising, yet it remains a grand challenge due to the inherently narrow light absorption range and high electron-hole recombination rate. Herein, Pd NPs were encapsulated as electron acceptors into the Cu-MOF using a double-solvent method, followed by pyrolysis at the proper temperature. After pyrolysis, Cu-MOF transformed into a carbon defect-rich composite of CuO and Cu2O while retaining its high porosity and structural morphology. The resulting carbon defect-rich pyrolysis Cu-MOF (p-Cu-MOF) served as an active support, facilitating the separation of electrons and holes. The photoelectrons trigger the electron transfer of adjacent active metal components and the formation of a Schottky junction between Pd and the MOFs. This effect induces the electron donation from the MOFs. Moreover, Pd/pyrolysis Cu-MOF exhibits significantly higher visible light absorption, better water stability, and higher electrical conductivity compared to Cu-MOF and Pd/Cu-MOF. An OPECT sensor was fabricated by utilizing Pd/p-Cu-MOF as the photoactive material and poly(3,4-ethylenedioxythiophene):poly(styrenesulfonate) (PEDOT:PSS) as the channel material on an integrated laser-etched FTO. The aptamer was used as the recognition element, enabling sensitive and efficient detection of residual isocarbophos.

Wavelength‐Linearly‐Dependent and Polarization‐Sensitive Perfect Absorbers based on Optically Anisotropic Germanium Selenide (GeSe)

AbstractPerfect absorbers, widely utilized in solar energy‐harvesting devices, optical communications, sensors, displays, and filters, achieve 100% light absorption. However, perfect absorbers employing micro/nanostructures encounter challenges such as high cost and complexity in simulation and fabrication. Here, novel wavelength‐linearly‐dependent and polarization‐sensitive perfect absorbers utilizing optically anisotropic germanium selenide (GeSe) are proposed. A simple and cost‐effective GeSe‐SiO2‐Si multilayered optical thin film is constructed and optimized to achieve destructive interference, leading to perfect absorption. The operating wavelength can be linearly tuned from 900 nm to 1300 nm by adjusting the GeSe thickness from 125 nm to 200 nm. Leveraging the significant optical anisotropy, the polarization angle is introduced as an additional parameter to dynamically and finely control the operating wavelength, enabling the creation of polarization‐sensitive perfect absorbers. Experimental results validate the feasibility of fabricating and dynamically modulating the proposed wavelength‐linearly‐dependent and polarization‐sensitive perfect absorbers. This study introduces a novel approach for designing and fabricating reconfigurable perfect absorbers utilizing low‐symmetry materials, facilitating mass production and on‐chip integrated systems.