High-efficiency Devices Research Articles

OLUFF: a novel set of ground and excited state force field parameters of the emitting oxyluciferin species.

The modeling of the bioluminescent system of fireflies is key to understand the binding mode of the oxyluciferin/luciferase complex and its photophysical properties with the aim of developing high-efficiency devices and techniques. In this work, we present the OLUFF force field, which is able to describe the interactions to sample the conformational space of the four possible oxyluciferin emitters in both ground and excited state. This force field has been parameterized to reproduce quantum mechanical (QM) energies and geometrical parameters. Moreover, it has been validated by comparing probability distribution functions, minimized structures, infrared spectra and normal mode analysis obtained from OLUFF-based molecular dynamic (MD) simulations with their QM counterparts. Additionally, ground state simulations have also been performed using the general amber force field (GAFF) and compared with the OLUFF. It has been demonstrated that the OLUFF not only reproduces well the QM properties, but also improves the results from the GAFF.

An efficient extraction device for microplastics in marine sediments and its applications.

Microplastics, defined as small pieces of plastic with a size less than 5 millimeters, constitute a significant sink for microplastics in marine sediments. Given the potential harm to nature and human beings, accurate detection of microplastics in marine sediments is of the utmost importance. The separation of microplastics from marine sediments represents a pivotal step in the quantitative detection of microplastics. This paper presents a high-efficiency extraction device for microplastics in marine sediments, with the objective of enhancing the effectiveness and efficiency of microplastics extraction. The device employs an air pump to thoroughly mix the samples and incorporates metal perforated plate fillers to achieve efficient sedimentation, thus facilitating the separation of microplastics from the surrounding marine sediments. Subsequently, the separated microplastics are passed through a series of pore sizes of stainless steel screens and glass fibre filters via suction filtration, allowing for the collection of microplastics of varying particle sizes for subsequent identification. Following a series of method trials, the optimal extraction conditions for this device were identified. The results demonstrated its excellent extraction effectiveness and high efficiency. To verify the feasibility of this device, it was used to investigate the microplastics in the sediments of Dongzhai Harbor, Hainan. The abundance, particle size distribution, shape, and composition of microplastics in the sediments of this area were obtained, which not only validated the practicality of this microplastic extraction device but also provided significant insights for ecological and environmental protection in the region.

Integrated sensor chip of a resonant cavity light emitter and photon detector for wearable optical medicine

This work presents an integrated chip of a resonant cavity light emitter and photon detector (RCLEPD) to address the requirements of wearable optical medical devices for compact size, high efficiency, and interference resistance sensors. The optical radiation pattern and light extraction efficiency of the resonant cavity light emitting diode (RCLED) as well as the optical absorption spectrum of the resonant cavity enhanced photon detector (RCEPD) are theoretically simulated. Additionally, the wavelength selectivity of the RCEPD absorption spectrum is analyzed. Material epitaxial growth of RCLEPD was performed using metal-organic chemical vapor deposition (MOCVD), and an integrated sensing chip with an area of 2 × 2 mm2 was fabricated. Experimental results demonstrate that RCLED achieves a maximum external quantum efficiency of 10.206%, consistent with the simulation results, while maintaining a peak wavelength at 677.5 nm within a current range of 0-20 mA. Furthermore, the RCEPD exhibits a peak response wavelength at 678 nm, matching that of the RCLED. Utilizing RCLEPD as the sensor, photoplethysmography (PPG) signals are collected from the human wrist under different RCLED driving currents resulting in an average period of 977 ms which aligns with a human pulse frequency of 61 beats/min. With further processing techniques applied to PPG signals, RCLEPD is expected to be used as a sensor in wearable blood pressure and glucose monitoring devices.

Experimental and numerical study of corrugated anchors for CFRP plates

Carbon fibre reinforced polymer (CFRP) plates are promising materials for cables and prestress tendons in structural engineering for the excellent tensile performance, light in weight and anti-corrosion character. Anchoring has always been the main challenge of this high-performance material due to its anisotropy and brittleness. Corrugated anchors are high-efficiency friction-based anchorage devices. Nevertheless, premature failure of the CFRP plates can still be observed with this type of anchors, and the anchor efficiency for the corrugated anchors needs further improvement. This paper proposes a novel configuration of corrugated anchors. Experimental tests are then carried out to investigate the influence of the pre-tensioning bolt load and adhesive layer. Consequently, numerical analysis is conducted to reveal the anchoring mechanism. The results indicate the traditional corrugated anchors lead to non-uniform stress distribution in the CFRP plate, and with the proposed configuration the anchor efficiency can be increased up to 100%.

Investigation of the behaviour of tunable chalcogenide-Bismuth based perovskite BiTl (SxSe1-x)3(X = 0, 0.33, 0.67, 1): first principles calculations

Density functional theory (DFT) driven by the quantum ESPRESSO code was used in this study to investigate the structural, opto-electronic, and thermoelectric properties of ternary perovskite chalcogenide compound. This is to examine their possible use in optoelectronics and reducing the dependency on silicon and fossil fuel. The Perovskite compounds crystalize in the cubic phase with a space group Pm-3m. The volume versus energy is fitted by the Birch-Murnaghan equation of state which yielded the equilibrium lattice constant of 8.353, 8.488, 8.629 and 8.806, bulk modulus of 255.8, 242.7, 233.5 and 222.4, for BiTlS3 , BiTlS2 Se1 , BiTlS1 Se2 and BiTlSe3 . Indirect band gaps of 2.6 eV, 2.7 eV, 2.9 eV, and 3.2 eV were obtained for BiTlS3 , BiTlS2 Se1 , BiTlS1 Se2 and BiTlSe3 compounds, respectively. Also, increment in the energy from 0 eV to 10 eV resulted in optical properties fluctuation within 0 cm-1 to 1.5 × 109 cm-1 for absorption coefficient in the compounds. However, a variation from 10 eV to 20 eV moved the absorption coefficient to 4.2 × 109 cm-1 for all the compounds from visible to the UV range. Furthermore, the observed properties show that the value of figure of merit obtained is 0.125 for BiTlS3 , 0.100 for BiTlS2 Se1 , 0.068 for BiTlS1 Se2 and 0.055 for BiTlSe3 at 300 K. By adjusting the chalcogen ratio, BiTlX3 (X = S, Se) possess the tunable band gap in the whole visible light range, which is of great significance for the development of new-type, high-efficient semiconductor material and optoelectronic devices, while the low thermoelectric values predict the compounds use as sensors. The proposed results may pave the way for further investigations into the use of the perovskite compounds for optoelectronic devices.

Optimization of collection efficiency for a dual-row jet mining machine based on CFD-DEM coupling

Deep-sea mineral resources possess vast reserves; yet, the depositional environment is extremely harsh, and the mining challenges are significant. Overcoming the technical hurdles of deep-sea mining and protecting the marine environment to achieve sustainable development and utilization of seabed resources are major challenges in the field of marine resource development. In this work, we employ a coupled Computational Fluid Dynamics-Discrete Element Method (CFD-DEM) approach with the objective of enhancing the collection efficiency of deep-sea polymetallic nodules. The research focuses on adjusting and optimizing the collection parameters of a dual-jet collector. We examine the influence of the collector's jet angle and velocity on the collection efficiency. We conduct a numerical analysis of the movement characteristics of nodules, the distribution of the flow field, and the efficiency of nodule collection. The results indicate that when the rear jet angle is too small, the stripping and blocking effects on the nodules deteriorate. Conversely, when the jet angle is too large, the upwelling flow velocity decreases. The optimal collection effect is achieved with a rear jet angle of 55°. Lower jet velocities result in poorer nodule stripping, collection, and lifting. Higher jet velocities, however, increase seafloor disturbance and reduce the device's energy utilization efficiency. The collection efficiency is optimal at jet velocities ranging from 8 to 9 m/s. This research provides valuable insights for the design of high-efficiency dual-jet collector devices.

The red or orange emitters based on phenylquinoline or trifluoromethylpyridine iridium complexes with dimesitylboryl or diphenylphosphoryl fluorenyl unit

Novel complexes bis[2-(4-(7-dimesitylboryl-9,9-diethylfluoren-2-yl)phenyl)-4-phenyl- quinolyl-C2, N] iridium (acetylacetonate or 2-picolinic acid), bis[2-[4-(7-diphen- ylphosphoryl-9,9-diethylfluoren-2-yl)phenyl)-4-phenylquinolyl-C2, N]iridium (acetyl-acetonate or 2-picolinic acid), and bis[2-(7-dimesitylboryl-9, 9′-diethylfluoren-2-yl)-5-trifluoromethylpyridinto-C3, N] iridium (acetylacetonate or 2-picolinic acid) were synthesized. 7-Dimesitylboryl (DMB) or 7-diphenylphosphoryl (DPPO) 9,9-diethylfluorenyl with larger steric hindrance was introduced into 2-phenyl-4-phenylquinoline or 5-trifluoromethylpyridine iridium complex to improve the electron-injection and electron-transport abilities and to decrease intermolecular interaction, which promoted luminous efficiency and adjusted emission. The devices displayed stable electroluminescent (EL) peaks at about 620, 600 and 584 nm, which exhibited approximate CIE coordinates of (0.67, 0.33), (0.62, 0.38) and (0.58, 0.42) with maximum current (external quantum) efficiencies of 9.1 (5.7 %), 13.2 (8.7 %) and 6.4 cd/A (3.5 %). Slow decay and high efficiency of devices showed the potential red or orange emitters.

Chemically anchored black phosphorus/chromophore composite luminescent materials towards solid-state photoluminescence and electroluminescence

As a promising two-dimensional (2D) material, black phosphorus (BP) has gained great attention because of its intrinsic physicochemical characteristics. However, BP is easy to be oxidized and form various surface defects, which decreases the charge transport and makes luminescence difficult. Herein, we report a facile strategy to synthesize chemically anchored BP/chromophore composite luminescent materials by integrating 2D BP nanosheets with boron dipyrromethene (BODIPY) dyes through simple sonication reactions. Solids of BP composite materials are brightly fluorescent with 5 orders of magnitude increase of photoluminescence intensity compared with the pure solids of BP and BODIPY. 2D BP nanosheets with large specific surface area and lone pair electrons facilitate chemisorption of BODIPY by forming covalent interactions between P and B/N atoms, which not only passivates the surface of BP and eliminates the oxidation, but also prevents the aggregation caused quenching (ACQ) issue of BODIPY. Furtherly, the organic light-emitting diodes (OLEDs) based on the BP/chromophore composite luminescent materials were first successfully achieved, the electroluminescence spectra of which cover the full spectrum of red, green, and blue visible light. This work provides a brand-new approach to further design and development of high mobility and high luminous efficiency composite luminescent materials and devices based on BP.

Tailoring CoAl2O4 inversion degree-driven photocarrier separation and injection for photoelectrochemical water splitting

Highly efficient photoanodes are highly desirable for hydrogen production to construct photoelectrochemical (PEC) water oxidation devices. This work used the spinel-structured CoAl2O4 (CAO) as the cocatalysts to BiVO4(BVO), delivering the high photocurrent density of 3.85 mA/cm2 at 1.23 VRHE. Interestingly, their PEC performance depended on the CAO's inversion degree (δ). When δ = 0.2, the oxygen evolution process on CAO can cooperatively adsorb *OOH and dissociate the O2, then the *OH absorbs on the re-exposed active site again, leading to an improved charge separation on the surface. Meanwhile, the n-p heterojunction was formed at the interface of BVO/CAO, with the most robust built-in field strength at δ = 0.2, and the charge separation in bulk was greatly improved. Additionally, the CAO can also retard the photo corrosion of BVO by effectively extract and reservoir the photoholes, achieving over 10 h of long-term durability on BVO/CAO-450. This work illustrates the roles of CAO, clarifies the effect of inversion degree on PEC water oxidation, offers fresh insights into constructing highly efficient and stable OER catalysts, and provides fundamentals for developing high-efficiency PEC devices.

Interacting Emission Species among Donor and Acceptor Moieties in a Donor-Grafted Polymer Host/TADF-Guest System and Their Effects on Photoluminescence and Electroluminescence.

Thermally activated delayed fluorescence (TADF)-based electroluminescence (EL) devices adopting a host/guest strategy in their emitting layer (EML) are capable of realizing high efficiency. However, TADF emitters composed of donor and acceptor moieties as guests dispersed in organic host materials containing a donor and/or an acceptor are subject to donor-acceptor (D-A) interactions. In addition, electron delocalization between neighboring emitter molecules could form different species of aggregates. Here, we investigate the effects of intermolecular interacting emission species on the optoelectronic properties of sky-blue/green/red (sB/G/R) TADF emitters as guests using poly(biphenyl-Si/Ge) grafted with various donor moieties as hosts. We found the presence of guest/guest exciplex (Dg/Ag)*, host/guest exciplexes (Dh/Ag)*, and aggregates through the exploration of interactions between neighboring TADF guest molecules and between host and TADF-guest molecules. The nonradiative 3(Dh/Ag)* (ΔEST ≈ 0.5 eV) could increase the internal conversion rate (kIC) and reduce delayed luminescence, and both of them could cause a decrease in PLQY. The luminescence of 3(Dh/Ag)* may have a positive or negative effect on PLQY depending on its triplet energy. As the singlet and triplet energies of (aggregate)* are lower than those of (ICT)*, energy transfer from (ICT)* to (aggregate)* could occur. The low PLQY nature of (aggregate)* means that it is more likely to cause quenching in device emission. The emissions from (Dh/Ag)* and (aggregate)* are found to have increased full width at half-maximum and lead to lower emission color purity. Such intermolecular interactions should also occur in host/guest (TADF) systems and nondoped TADF emitter systems and thus are important factors for the molecular design of the TADF emitter and/or its accompanying host for high device efficiency and emission color purity.

Shortwave-Infrared Silver Chalcogenide Quantum Dots for Optoelectronic Devices.

Silver chalcogenide (Ag2X, X = S, Se, Te) semiconductor quantum dots (QDs) have been extensively studied owing to their short-wave infrared (SWIR, 900-2500 nm) excitation and emission along with lower solubility product constant and environmentally benign nature. However, their unsatisfactory photoluminescence quantum yields (PLQYs) make it difficult to obtain optoelectronic devices with high performances. To tackle this challenge, researchers have made great efforts to develop valid strategies to improve the PLQYs of SWIR Ag2X QDs by suppressing their nonradiative recombination of excitons. In this Perspective, we summarize the significant approaches of heteroatom doping and surface passivation to enhance the PLQYs of SWIR Ag2X QDs, and we conclude their application in high-efficiency optoelectronic devices. Finally, we examine the future trends and promising opportunities of Ag2X QDs with regard to their optical properties and optoelectronics. We believe that this Perspective will serve as a valuable reference for future advancement in the synthesis and application of SWIR Ag2X QDs.

Next-Generation Self-Powered Photodetectors using 2D Bismuth Oxide Selenide Crystals.

The concept of self-powered photodetectors has attracted significant attention due to their versatile applications in areas such as intelligent systems and hazardous substance detection. Among these, p-n junction and Schottky junction photodetectors are the most widely studied types; however, their fabrication processes are often complex and costly. To overcome these challenges, we focused on the emerging self-powered, ultrasensitive photodetector platform based on photoelectrochemical (PEC) principles. This platform leverages the unique properties of the emerging material bismuth oxide selenide (Bi2O2Se), which features a wide bandgap (∼2 eV) and a high absorption coefficient. We utilized chemical exfoliation to obtain thin layers of Bi2O2Se, enabling highly efficient photodetection. The device characterization demonstrated impressive performance metrics, including a responsivity of 97.1 μA W-1 and a specific detectivity of 2 × 108 cm Hz 1/2 W-1. The PEC photodetector also exhibits broad-spectrum sensitivity, from blue to infrared wavelengths, and features an ultrafast response time of ∼82 ms and a recovery time of ∼86 ms, highlighting its practical potential. Moreover, these self-powered photodetectors show excellent stability in electrochemical environments, positioning them promising candidates for integration into future high-efficiency devices.

Rapid-annealed FeSiBPCu nanocrystalline alloy with high Bs approaching 1.9 T and good bendability

To promote energy savings, high efficiency and miniaturization of power electronic devices, Fe–Si–B–P–Cu nanocrystalline soft magnetic materials with high saturation magnetization (Bs) parallel to that of the 6.5 wt% Si steel and low coercivity (Hc) are desired. In this work, 30 μm-thick Fe84Si3B10P2Cu1 and Fe84.5Si3B9.5P2Cu1 (at.%) amorphous/nanocrystalline precursor ribbons were melt-spun, which has high Fe contents comparable to that of the 6.5 wt% Si steel. These ribbons consist of an amorphous matrix and pre-existing α-Fe of approximately 28–30 nm in size possessed relatively low and similar-value activation energy of nucleation and growth in the range of 224–249 kJ/mol. Which could induce strong crystallization competition and effectively suppress coarsening of the pre-existing α-Fe. The Fe84Si3B10P2Cu1 nanocrystalline alloy obtained by rapid-annealing (∼100 °C/s) the amorphous/nanocrystalline precursor at 480 °C for 30 s (Fe84-480) exhibited a fine and uniform nanostructure containing α-Fe with small average grain size of approximately 23.1 nm and high volume fraction. The Fe84-480 alloy possessed a high Bs of approximately 1.88 T, a low Hc of 8.6 A/m, and good bendability revealed by relatively large bending fracture strain of ∼1.65%, making it a promising soft magnetic material for power electronic devices.

Challenges and opportunities in high efficiency scalable and stable perovskite solar cells

Perovskite solar cells (PSCs) are the fastest-growing photovoltaic (PV) technology and hold great promise for the photovoltaic industry due to their low-cost fabrication and excellent efficiency. To achieve commercial readiness level, the most important factor would be yield beyond 95% at the PSC module levels. The current essential requirements for PSCs are reproducibility of high efficiency devices, scalability, and stability. The reported certified high efficiency (24–26%) results are based on the use of FAPbI3 perovskites with a bandgap of Eg≈ 1.5 eV, and the typical device's active area ranges from ≈ 0.1 cm2 to a maximum of 1 cm2. However, relatively higher bandgap PSCs are essential, especially in tandem solar cell applications. Hence, optimization of higher bandgap PSCs is a necessity. As the bandgap of the perovskites increases, the efficiency goes down due to reduced JSC and increased VOC loss. Therefore, understanding the loss mechanism and corresponding solutions need to be developed. Scaling up the device's active area without compromising the fill factor and, hence, efficiency is non-trivial. So, understanding the loss mechanism in large area devices is crucial. The stability analysis reported in the literature is inconsistent, preventing data comparison and identifying various degradation factors or failure mechanisms. Moreover, how the accelerated tests would be useful in predicting the real lifetime of the solar cells is yet to be developed. So, understanding the knowledge and the technological gaps between laboratory and industry-scale production is crucial for further development. Therefore, in this review article, we discuss the challenges and opportunities for scalable and stable high efficiency PSCs.

Rational Design Dithieno[3,2-f:2',3'-h]quinoxaline-Based Polymers with Optimized Molecular Configuration and Charge Transfer for High-Performance All-Polymer Solar Cells.

Due to poor planarity and weak intermolecular interactions of acceptor units which have two-dimensional configuration, the development of related polymers is slow. In this work, we synthesized a dithieno[3,2-f:2',3'-h]quinoxaline-based unit substituted with fluorinated thiophene, which can effectively expand the area of the acceptor unit. Then, it paired with three different benzodithiophene-based donor units, and three new polymers of PQTF-BT, PQTF-BTCl and PQTF-DTCl were obtained. PQTF-BT with thiophene side chain exhibits appropriate aggregation and crystallization performance, and the PQTF-BT:PY-IT all-polymer solar cells exhibit high device efficiency of 15.54%. Meanwhile, PQTF-BTCl with chlorination strategy on thiophene side chain further enhances the open-circuit voltage of related devices. However, it has negative impact on the miscibility and charge transfer of the material, leading to a poor efficiency of 8.71% in the PQTF-BTCl:PY-IT device. To reinforce miscibility, PQTF-DTCl with expanded backbone planarity was further studied. However, the big dihedral angles of the donor side chains disrupted the effective stacking of the molecules, resulting in great recovery of device performance to 13.42%. This work provides research ideas for the design of polymers with two-dimensional configuration side chain and match selection of donor units.

Mesoporous structured MoS2 as an electron transport layer for efficient and stable perovskite solar cells.

Mesoporous structured electron transport layers (ETLs) in perovskite solar cells (PSCs) have an increased surface contact with the perovskite layer, enabling effective charge separation and extraction, and high-efficiency devices. However, the most widely used ETL material in PSCs, TiO2, requires a sintering temperature of more than 500 °C and undergoes photocatalytic reaction under incident illumination that limits operational stability. Recent efforts have focused on finding alternative ETL materials, such as SnO2. Here we propose mesoporous MoS2 as an efficient and stable ETL material. The MoS2 interlayer increases the surface contact area with the adjacent perovskite layer, improving charge transfer dynamics between the two layers. In addition, the matching between the MoS2 and the perovskite lattices facilitates preferential growth of perovskite crystals with low residual strain, compared with TiO2. Using mesoporous structured MoS2 as ETL, we obtain PSCs with 25.7% (0.08 cm2, certified 25.4%) and 22.4% (1.00 cm2) efficiencies. Under continuous illumination, our cell remains stable for more than 2,000 h, demonstrating improved photostability with respect to TiO2.

Reversing band bending at grain boundaries enables high-efficiency Cu2ZnSn(S,Se)4 solar cells

Kesterite solar cells show great potential for sustainable photovoltaic technology, attributed to their excellent semiconductor properties and earth abundant composition. However, undesirable band bending at the grain boundaries (GBs) in Cu2ZnSn(S,Se)4 (CZTSSe) films induces serious carrier recombination because of inhomogeneous distribution of S and Se in the grain interiors (GIs) and at GBs, which results in large open-circuit voltage deficit and overall poor performance of CZTSSe solar cells. Here, a robust hydrothermal sulfurization design has successfully inverted the band bending at the GBs, with advanced cathodoluminescence measurement confirming the transition of carrier collection pathways from the GBs to the GIs, thereby achieving efficient carrier collection within the GIs. Simultaneously, this design has effectively passivated the non-radiative recombination in the GIs, smoothing the way for carrier collection. Ultimately, a 13.7 % efficiency CZTSSe solar cell with 44 % improvement is realized by this process. This study discloses that reversing the band bending at GBs is practical to tailor the carrier collection, and thus pave the pathway for high-efficient photoelectronic devices.

Silicon nitride shadowed selective area growth of low defect density vertical GaN mesas via plasma-assisted molecular beam epitaxy

Ion bombardment during inductively coupled plasma reactive-ion etching and ion-implantation introduces irreparable crystalline damage to gallium nitride (GaN) power devices, leading to early breakdown and high leakage current. To circumvent this, a bi-layer selective area growth mask was engineered to grow up to 3.0 µm thick epitaxy of GaN using plasma-assisted molecular beam epitaxy as an ion-damage-free alternative to standard epitaxial processing routes. The masks and regrown architectures are characterized via SEM, conductive-atomic force microscopy (AFM), x-ray photo electron spectroscopy, Raman, and cathodoluminescence. Mask deposition conditions were varied to modulate and minimize the stress induced during thermal cycling. The resulting mesas exhibit low leakage, attributed to naturally terminated sidewalls as measured by an innovative perpendicular AFM measurement of the regrown sidewall. The regrown sidewall exhibited RMS (root mean square) roughness of 1.50 (±0.34) nm and defect density of 1.36 × 106 (±1.11 × 106) cm−2. This work provides a method to eliminate defect-inducing steps from GaN vertical epitaxial processing and stands to enhance GaN as a material platform for high-efficiency power devices.

Surface plasmon-mediated photoluminescence boost in graphene-covered CsPbBr3 quantum dots

The optical properties of graphene (Gr)-covered CsPbBr3 quantum dots (QDs) were investigated using micro-photoluminescence spectroscopy, revealing a remarkable three orders of magnitude enhancement in photoluminescence (PL) intensity compared to bare CsPbBr3 QDs. To elucidate the underlying mechanisms, we combined experimental techniques with density functional theory (DFT) calculations. DFT simulations showed that the graphene layer generates interfacial electrostatic potential barriers when in contact with the CsPbBr3 surface, impeding carrier leakage from perovskite to graphene and enhancing radiative recombination. Additionally, graphene passivates CsPbBr3 surface defect states, suppressing nonradiative recombination of photo-generated carriers. Our study also revealed that graphene becomes n-doped upon contact with CsPbBr3 QDs, activating its plasmon mode. This mode resonantly couples with photo-generated excitons in the perovskite. The momentum mismatch between graphene plasmons and free-space photons is resolved through plasmon scattering at Gr/CsPbBr3 interface corrugations, facilitating the observed super-bright emission. These findings highlight the critical role of graphene as a top contact in dramatically enhancing CsPbBr3 QDs’ PL. Our work advances the understanding of graphene-perovskite interfaces and opens new avenues for designing high-efficiency optoelectronic devices. The multifaceted enhancement mechanisms uncovered provide valuable insights for future research in nanophotonics and materials science, potentially leading to breakthroughs in light-emitting technologies.

Polarized and Directional Electroluminescence from Organic Light‐Emitting Devices by Using a Bifunctional Meta‐Electrode

AbstractOrganic light‐emitting devices (OLEDs) with polarized and directional emission are highly desired for their promising applications in optical imaging, optical communication, and immersive visual technologies. Existing implementation methods based on free space bulk optical elements suffer from significant power loss, limiting their practical applications. Here, a bifunctional meta‐electrode is proposed by integrating a metasurface consisting of Ag periodic corrugations onto the indium tin oxide (ITO) anode to simultaneously realize the functions of charge carrier injection and photon management in the OLEDs. Highly polarized and directional light emission is demonstrated while maintaining a high device efficiency using the meta‐electrode. The electroluminescence with a polarization extinction ratio of 5 is achieved by judiciously engineering the polarization‐dependent Purcell factor of the resonant cavity constructed by the meta‐electrode. Meanwhile, the directional light emission with a divergence angle of 10° can be obtained by the efficient out‐coupling of surface plasmon‐polariton mode. The light beam can be collimated in one direction by using 1D nanogratings and in two directions by using 2D nanopillars, respectively.