Few-layer Graphene Research Articles

Enhanced Optoelectronic Properties of Few-Layer Graphene for Transparent Conducting Electrode: Density Functional Theory Perspective

The challenge in utilizing graphene for transparent conducting electrodes (TCE) is to increase the electronic conductivity without significantly decreasing its transmittance. Forming a few-layer structure is an effective way to modify the electronic properties of graphene. In this paper, we used the density functional theory (DFT) method to study the effect of the number of few-layer graphene (FLG) layers on the electronic conductivity and transmittance. We find that increasing the number of layers leads to an increase in electronic conductivity. On the other hand, a decrease in transmittance was observed when the number of layers was increased. Based on the performance analysis, the optoelectronic properties of FLG with more than three layers were better than those of conventional TCE materials, such as indium tin oxide (ITO) and aluminium-doped zinc oxide (AZO). The calculated electronic conductivity and transmittance of a 4-layer FLG were 2.23×1019 (1/Ω.m.s) and 95.69%, respectively. This finding can be used as guidance for experimental research in developing graphene-based TCE materials. Keywords: density functional theory, electronic conductivity, few-layer graphene, transmittance

Hydrogen and Solid Carbon Production via Methane Pyrolysis in a Rotating Gliding Arc Plasma Reactor.

Plasma-induced methane pyrolysis is a promising hydrogen production method. However, few studies have focused the decomposition of pure methane as a discharge gas. Herein, a rotating gliding arc reactor was used for the conversion of methane (discharge gas and feedstock) into hydrogen and solid carbon. Methane conversion, gaseous product selectivity, and energy usage efficiency(specific energy requirement for hydrogen production(SER)) were investigated as functions of operating parameters, e.g., specific energy input(SEI), residence time, and reactor design. SEI was positively(almost linearly)correlated with methane conversion and hydrogen yield and negatively correlated with SER. Conversion and efficiency of energy usage increased when reactor designs providing higher thermal densities were used. With the increasing flow rate of methane at constant SEI, the reaction volume and, hence, the residence time of the gas inside the reaction zone increased, which resulted in methane conversion and hydrogen selectivity enhancement. The solid carbon featured four distinct domains, namely graphitic carbon, turbostratic carbon, few-layer graphene, and amorphous carbon, which indicated a nonuniform temperature distribution in the reaction zone. But it seems that graphitic carbon dominates amorhphous one. This study highlights the potential of rotating gliding arc plasma systems for efficient methane conversion into hydrogen and valuable solid carbon products.

Two-photon absorption and negative nonlinear refraction in few-layer graphene nanosheets suspensions via liquid-phase exfoliation

Two-photon absorption and negative nonlinear refraction in few-layer graphene nanosheets suspensions via liquid-phase exfoliation

Strain engineering for the interfacial thermal resistance of few-layer graphene with porous defects

As electronic devices continue to advance toward higher integration, thermal management issues have become a bottleneck, limiting device performance at the nanoscale. In this study, we reveal the bistable structural characteristics of circular hole defects in few-layer graphene, exhibiting both adhered and separated states, through molecular dynamics simulations. We propose a mechanical model that considers the interplay between the bending energy and cohesive energy to determine the critical size of the hole defect, at which the structure transits between the adhered and separated states. We further demonstrate that strain engineering can adjust the interfacial thermal resistance by more than fivefolds, which drives the structure transit between bistable states. The strain effect on the interfacial thermal resistance of the structure can be accurately described using analytical models. These findings illustrate that strain engineering is an effective method for precisely controlling the interfacial thermal resistance in few-layer graphene and provide new insights into possible thermal switch applications.

Improving thermal conductivity of phthalonitrile composite through constructing three-dimensional graphene networks and interfacial engineering

Achieving high thermal conductivity for polymer composite with low filler loading is still a challenge. Here, phthalonitrile (APN)/few-layer graphene (FLG) composite with high thermal conductivity was successfully prepared by constructing three dimensional (3D) thermally conductive pathways. Such 3D structure was formed by hot compressing APN@FLG core-shell structures. The results showed that the thermal conductivity of APN@FLG composites with only 30 wt% of FLG was up to 11.4Wm−1K−1, which was 57 times to that of the pristine resin (0.2 Wm−1K−1). Such high thermal conductivity was attributed to the 3D connected thermally conductive networks. Furthermore, benefited from the high thermal stability of APN matrix, the as-prepared composite also showed high T5 (temperature of mass losing 5 %) of higher than 500 °C. The composite with both high thermal conductivity and heat resistance are expected to be an idea candidate for high temperature thermal management applications.

Direct graphene growth on low-alloy and mild steel surfaces controlled by carbon solubility and surface microstructural transformations during chemical vapor deposition

This study demonstrates for the first time, graphene grown directly on the iron-rich surfaces of bulk 8620 low-alloy and 1018 mild steel by chemical vapor deposition, a key step toward developing thin graphene coatings with strong graphene-steel bonding. Low growth temperatures of 660 °C–680 °C, were used to manipulate the steel's carbon solubility, confining carbon diffusion and microstructural transformations to the surface regions, with the bulk relatively unchanged. For 1018, a growth temperature of 680 °C resulted in a multilayer graphene coating with 80 % coverage. The alloying elements in 8620 improved graphene formation by influencing the surface microstructure transformations at these growth temperatures, with graphene coverage up to 95 %. The surface microstructure for 8620 affected graphene formation, seen in growths at 660 °C where a few-layer graphene coating formed from a cementite surface layer, and for growths at 680 °C where multi-layer graphene covered a pearlite dominant surface microstructure. Contact angle measurements confirmed the hydrophobicity of the graphene coating and electrochemical testing by potentiodynamic polarization and electrochemical impedance spectroscopy confirmed the 101 mV improvement to corrosion potential and an increase in impedance up to 18.23 kΩ. These detailed results regarding the direct growth of graphene as a coating layer on highly oxidation-sensitive steel surfaces suggest that this process is achievable through manipulating carbon solubility at the steel's surface by controlling temperature, alloy composition and surface microstructure transformations. These methods could be leveraged in developing protective graphene coatings for various iron-based alloys.

Applicability of few layer graphene derived from annoni grass biomass on the mechanical properties of cement mortars

In this work, we report the potential applicability of few layer graphene (FLG) synthesized from annoni grass (AG) biomass (Eragrostis plana Nees) by investigating its impact on the flexural and compression strength of cement mortars. For this purpose the AG biomass was collected and burnt at the temperature of 400 °C per 60 min, obtaining the AG ash (AGA). For FLG production, the AGA was mixture with the chemical reagent potassium hydroxide (KOH) and burnt at the temperature and time of 850 °C and 60 min, respectively. For the mechanical properties analysis, a reference sample (A0-without FLG) and samples with different percentage of FLG were prepared, specifically 0.02 % (A1), 0.03 % (A2), 0.05 % (A3), 0.07 % (A4) and 0.1 % (A5). Statistical analysis (Analysis of Variance, ANOVA) of the mechanical properties demonstrates a maximum flexural and compression strength in sample A2. The flexural and compression strength increase 25.2 % and 10.1 % compared to the reference mortar. These results indicate that the FLG produced from AG not only improves the mechanical properties of mortars but also presents significant environmental benefits, because AG is considered an invasive pest of agricultural fields of the southern region of Brazil. Therefore, with its removal from the fields it would be contributing to environmental preservation.

Evolution of morphology and electrical properties under controlled flow in polypropylene/polystyrene co-continuous blends containing interfacially localized carbonaceous nanoparticles

This study investigates the evolution of morphology and electrical properties of polypropylene (PP)/polystyrene (PS) blend nanocomposites under controlled steady shear flow. These nanocomposites contain either few-layer graphene (FLG) or a mixture of FLG and multi-walled carbon nanotubes (MWCNT), prepared via a conventional melt-mixing. Composites were created by premixing FLG or FLG/MWCNT with either PP [PP/PS/FLG or PP/PS/(FLG+MWCNT)] or PS [PS/PP/FLG or PS/PP/(FLG+MWCNT)] at a PP/PS ratio inducing co-continuous morphology. Results showed a significant reduction in the percolation threshold (PT) for PS/PP/FLG composites, with an 81% decrease compared to PS/FLG. When FLG was premixed with PS, PT required only 2 wt. % FLG, compared to 5.9 wt. % in PP/PS/FLG. Steady shear deformation disrupted the electrical network in both PP/PS/FLG and PS/PP/FLG composites. However, the PS/PP/FLG composites exhibited greater stability in electrical conductivity at lower FLG concentrations (above 3 wt. %) compared to the PP/PS/FLG composites (above 6 wt. %). The applied shear did not affect the co-continuous morphology of the blend-based composites containing 1 wt. % or more of FLG. Additionally, the synergistic effects of the hybrid FLG/MWCNT mixture on the electrical conductivity and rheological properties of both PP/PS/(FLG+MWCNT) and PS/PP/(FLG+MWCNT) composites were evaluated. The incorporation of MWCNT into both PP/PS/FLG and PS/PP/FLG composites significantly enhanced the formation of a hybrid electrical network structure, leading to a further reduction in the percolation threshold concentration of FLG. Specifically, in PP/PS/FLG composites, PT decreased from 5.9 to 1–3 wt. % of FLG, while in PS/PP/FLG composites, PT dropped from 2 to 1 wt. % of FLG.

Graphene functionalized nanoencapsulated composite phase change material based nanofluid for battery cooling: An experimental investigation

The graphene-nano encapsulated composite phase change material (GnePCM) based nanofluid holds great potential as a coolant for batteries in electric vehicles. The current work focuses on the synthesis and study of the cooling performance of GnePCM-based nanofluid. Few layered graphene (FLG) was synthesized via the liquid phase exfoliation method. Mini-emulsion polymerization was adopted to encapsulate composite PCM (octadecane: paraffin wax) within polystyrene shell and distribute these nanoballs across the graphene flakes of FLG to obtain GnePCM. Differential Scanning Calorimetry (DSC) was used to optimize the composition of composite PCM based on the melting range and latent heat. GnePCM was characterized by Scanning Electron Microscope (SEM), Transmission Electron Microscopy (TEM), DSC, Fourier Transform Infrared (FTIR) spectroscopy, and Raman Spectroscopy. Nanofluid was made by mixing GnePCM slurry with the base fluid (ethylene glycol − water mixture) and its thermo-physical properties were estimated. The analysis of thermal conductivity and specific heat capacity showed a 14.7 % and 56 % increase for the nanofluid compared to the base fluid. The optimal concentration of nanofluid for maximum stability was 10 % v/v based on zeta potential measurements. The heat transfer studies and pressure drop studies were conducted on a set of 10 cylindrical heaters, mimicking a 18,650 battery cell pack. The nanofluid could potentially achieve a maximum reduction of 5 °C in average surface temperatures of the cells as compared to the base fluid. The enhanced cooling efficiency of nanofluid could be related to the increased thermal conductivity and heat capacity of GnePCM, as well as the absorption of latent heat during its melting process. Enhancement in heat transfer parameters was found to be more prominent at lower flow rates for the nanofluids. The results reveal that the flow rate and power input play a significant role in the cooling performance of the nanofluid. Due to the increased viscosity of the nanofluid, a slight increase in the pressure drop and pumping power was observed at higher flow rates, as compared to base fluid.

Corrosion resistance and wear behavior of CoCrFeNiMn@Gr high entropy alloy-based composite coatings prepared by laser cladding

In this study, we utilize laser cladding to apply a CoCrFeNiMn HEA with 2 wt.% few-layer graphene (Gr) coating onto the surface of Q235B mild steel. Alcohol stirring method was used for HEA and Gr preparation of composite powder. Raman spectroscopy and energy dispersion spectroscope (EDS) indicate the successful mixing of HEA and Gr powders, with Gr adhering to the surface of the HEA powder in a lamellar structure. The X-ray diffraction (XRD), scanning electron microscope (SEM), EDS, and Electron backscatter diffraction (EBSD) analyses revealed that grain refinement and the formation of fine carbide-hard phases in the HEA/Gr coating improve microhardness and wear resistance. The average Schmidt factors of the coating decreased from 0.47 to 0.45 with the addition of Gr, indicating enhanced resistance to plastic deformation and anisotropy. Nanoindentation experiments demonstrated that the HEA/Gr coatings exhibit superior resistance to plastic deformation, effectively enhancing the coating’s durability against spalling under stress and wear conditions. The microhardness of the HEA/Gr coating increased by 99.25%, and the wear rate decreased by 86.31% compared to the HEA coating alone. The open circuit potential (OCP), linear polarization curve, Tafel curves, electrochemical impedance spectroscopy (EIS), and Mott-Schottky tests all indicated that the HEA/Gr coating possesses superior corrosion resistance. X-ray Photoelectron Spectroscopy (XPS) results suggest that the passivation film of the HEA/Gr coating, which contains more oxides and less hydroxide, is more protective and denser, thereby slowing the corrosion rate.

Unveiling graphite anodic expansion: Insights from electrochemical techniques, mass spectrometry, and kinetic modelling

Anodic expansion of graphite at different pH has been studied by coupling a mass spectrometer to an electrochemical cell. The mass spectrometry technique permits to follow the electrochemical gasification of graphite as well as the reaction products formed from the electrolyte. The current and mass spectrometry signals suggest that the neutral medium is the least aggressive for expansion. In addition, chronoamperometric expansion of graphite at different potentials has been carried out using the neutral medium. This experimental approach permits to get detailed information about the reaction mechanism that produces graphene-oxide based materials. The effect of potential and electrolyte concentration have been studied, and it has been observed that the degree of oxidation of the graphene oxide material obtained can be controlled. In addition, a kinetic model based on a phase-moving boundary has been used to describe the chronoamperometric experiments. Two types of graphene oxide materials have been obtained with the anodic synthesis and have been classified as few-layer graphene oxide (FLGO) and graphene oxide quantum dots (GOQDs). The physicochemical and electrochemical properties of both products have been studied.

Investigation of Electrochemical Fingerprints for Buzhong Yiqi Tang Extract Granules Using Diamond-Graphene Composite Electrode

This study presents a novel electrochemical fingerprinting method for Buzhong Yiqi Tang extract granules using a diamond-graphene composite electrode. The electrode was fabricated through chemical vapor deposition of graphene on high-pressure high-temperature synthetic diamond, resulting in a few-layer graphene coating as confirmed by Raman spectroscopy (I₂D/IG ratio ≈ 1.2) and XPS analysis (78% sp² C-C signal). Cyclic voltammetry revealed four anodic and three cathodic peaks, while differential pulse voltammetry provided enhanced resolution with eight distinct oxidation peaks. The method demonstrated high sensitivity (LODs 0.08-0.15mg/mL) and good linearity (R² > 0.995) over a concentration range of 0.5-10mg/mL. Comparison of fingerprints from individual herb extracts (Astragalus membranaceus, Panax ginseng, and Glycyrrhiza uralensis) elucidated the origins of major peaks in the Buzhong Yiqi Tang profile. Principal component analysis of fingerprints successfully differentiated between samples from three manufacturers, accounting for 87.3% of total variance. Strong correlations (r > 0.92) were observed between key DPV peak intensities and HPLC-determined concentrations of traditional chemical markers. The rapid analysis time, minimal sample preparation, and holistic representation of multiple electroactive components make this approach a promising complement to existing chromatographic methods for quality assessment of traditional Chinese medicine formulations.

A simple lable-free aptasensor based on liquid exfoliated graphene modified electrode for chloramphenicol detection in milk

Antibiotic residues in animal derived foods considered as one of the most serious food contamination poses significant risks to human health. Conventional methods for antibiotic residue detection rely on expensive and bulky instruments, complicated sample pretreatment and time-consuming, thus limiting their applications. Consequently, developing miniaturized and low-cost analytical technology for ultrasensitive monitoring and accurate evaluation of antibiotic residues in foods is of great significance. Herein, a simple and label-free electrochemical sensing platform for the highly sensitive detection of chloramphenicol (CAP) in milk was demonstrated by employing aptamer specific for CAP as a biological recognition element and liquid exfoliated graphene (LEG) modified indium tin oxide electrode (LEG/ITO) as substrate. LEG is believed to be the most economic few-layer graphene with remarkable electrical properties and larger specific surface area not only promotes electron transfer but also provides a large number of binding sites for aptamers to be assembly immobilized via the π–π stacking of DNA bases. Under optimal experimental factors, the aptasensor displayed a wider linear range for detecting CAP (1 fM ∼ 100 nM), accompanied by a limit of detection (LOD) (1 fM), as well as satisfactory performance with specificity, reproducibility, and stability. In addition, the designed strategy allowed the direct analysis of actual milk samples and the recovery rates were from 97.92 % to 103.34 %, rendering a ideal sensing strategy for quantitative determination of various analytes in food by adapting the specific aptamer.

Influence of exfoliation method of graphene on physical properties of graphene/High Density Polyethylene nanocomposites: Semiconductor‐like electrical conductivity, glass transition, and melting temperature

AbstractDespite the wide range of applications of polyethylene (PE), many efforts are being made to improve its properties with carbon allotropes such as graphene. The addition of graphene can improve the electrical, thermal, and mechanical properties of this polymer. Through the present study, the effects of exfoliated graphene nanoplatelets (XGNPs) and few‐layer graphene (FLG) on the electrical conductivity and thermal properties of high‐density polyethylene (HDPE) were investigated. XGNPs were synthesized by ultrasonication of graphite nanoplatelets, and FLG was synthesized by shear exfoliation of flake graphite. Finally, HDPE powder particles were coated with dispersed XGNPs and FLG. Then XGNPs/HDPE nanocomposites and FLG/HDPE nanocomposites were fabricated by compression molding. The morphology, structural, electrical, and thermal properties of the graphite, graphene, PE, and nanocomposites were observed and comparatively studied by transmission electron microscopy, field emission scanning electron microscope, x‐ray diffraction (XRD), Raman spectroscopy, and conductivity measurements. The graphene's D, G, and 2D bands were revealed by Raman spectroscopy of nanocomposites and verified the existence of the graphene in the polymer matrix. XRD revealed that the graphene did not affect the original crystalline structure of the HDPE matrix, and the Fourier‐transform infrared spectroscopy revealed that the nanocomposite was obtained without the formation of any functional groups. The electrical properties of the nanocomposites were comparatively studied. After adding XGNPs (7 wt%), volumetric electrical conductivity in a sample reached from 10−16 to 10−3 S/m. The highest volumetric conductivity, 1.1 × 10−2 S/m, that is, semiconductor‐like conductivity, was achieved after adding 7 wt% of FLG. The glass transition temperatures (Tg), melting temperatures (Tm), and thermal stability were investigated by differential scanning calorimetry and TGA, respectively, and it was concluded that Tg and Tm increase by adding the graphene. This study shows that shear exfoliation of graphene is the best and the most facile method to prepare mass‐scale graphene for the production of graphene/polyolefin nanocomposites.Highlights Two types of graphene were produced by using sonication and shear‐exfoliation. HDPE powders were coated with two types of graphene and then hot pressed. The method of (G) preparation is crucialparameter on electrical conductivity. In the sample containing 7 wt% (XGNPs), the highest conductivity is 10−3 S/m. In the sample containing 7 wt% (FLG), the highest conductivity is 10−2 S/m.

Mutant amplitude modulation behavior of MIS-like structure of few-layer graphene/SiO2/p-Si in 500–750 GHz band

Graphene has great application potential in the field of electromagnetic modulation field because of its excellent physical and electronic properties. Studies have demonstrated that the properties of graphene films with different layers are also different due to the difference in energy band structure. Nowadays, the modulation mechanism of monolayer graphene (MLG) and bilayer graphene (BLG) has been gradually discovered, but for graphene with more than three layers, the mechanism of whether it is tunable remains to be explored, especially on the proving from an experimental perspective. In this study, the CVD-prepared highly homogeneous few-layer graphene (FLG) film was combined with SiO2 nanolayers and P-doped Si substrate to form an MIS-like capacitor structure, a unique electromagnetic behavior of mutant amplitude modulation exhibited by FLG film was found, which was different from that of mono- and bi-layers of graphene. The results show that the structure exhibits obvious modulation behavior in the ultra-wideband frequency of 500–750 GHz and the bias of 0.9 V, up to 3.1 dB. This study makes a new supplement to a gap in the EM modulation system of graphene series material.

On the study of proximity magnetism in van der Waals graphene/CuCrP2S6 heterostructure via the anomalous Hall effect

Recently, several experimental works have appeared in the literature where induced magnetism in single- and few-layer graphene (SL-gr and FL-gr) interfaced with layered van der Waals materials was investigated via the application of the anomalous Hall effect (AHE). In most of these works, it is suggested that the observation of the AHE in such systems can be explained by a magnetic exchange interaction appearing at the interface between graphene and the underlying magnetic insulator. Considering the recently studied FL-graphene/bulk-CuCrP2S6 system as an example, our careful and rigorous analysis of recent experimental and theoretical data presented in the literature shows that the claimed observation of the AHE and magnetic proximity effect in this system is not supported. Moreover, the theoretically calculated electronic structures of the studied system contain serious errors and flaws that cannot be considered as an accurate description of such an interface and cannot be taken as solid support for the proposed proximity effect.

Green conversion of waste polyester into few-layer graphene for interfacial solar-driven evaporation and hydroelectric electricity generation

The coupling of solar-driven interfacial evaporation with hydrovoltaic technology is emerged as a hopeful approach to alleviate energy crisis and freshwater shortage. However, constructing low-cost evaporators with high-performance freshwater and electricity co-generation and unveiling the co-generation mechanism remain a grand challenge. Herein, we report the green transformation of waste poly(ε-caprolactone) into graphene through a salt-assisted carbonization strategy and build a flexible bi-functional graphene-based evaporator for freshwater and electricity co-generation. The graphene exhibits a typical wrinkled structure with curved edges and is composed of 7–8 discontinuous layers with rich oxygen-containing groups. The graphene-based evaporator exhibits excellent sunlight absorption (98%), photo-to-thermal conversion property, good water transport ability, low water evaporation enthalpy, and low thermal conductivity of 0.06 W m−1 K−1. The evaporator not only exhibits a notable water evaporation rate (2.92 kg m−2 h−1), but also achieves the maximum output voltage of 310 mV, surpassing many previously reported evaporators/generators. The result of molecular dynamics simulation proves the diffusion difference between H+ and OH− in water and graphene, which eventually leads to the voltage generation. Not only will this work help to improve the upcycling of waste plastics and achieve carbon neutrality, but it will also open an avenue for co-generation of freshwater and electricity.

Correlation study of graphitic shell encapsulated nickel: A multi-spectroscopic approach

Graphite-encapsulated metal nanoparticles hold great potential across various applications due to their unique combination of metal and graphitic properties. While Raman spectroscopy is widely used to assess the graphitic shells, metrics derived from prominent Raman bands often prove unreliable when analyzing such structures with a large number of heterogeneous flakes and are mostly applicable to few-layer graphene. However, researchers continue to face challenges in identifying reliable metrics that accurately reflect two key properties of graphitic shells: thickness and degree of graphitization. In this study, graphitic shells were synthesized via plasma-enhanced chemical vapor deposition (PECVD) at low temperatures (500 °C), seeded by nickel nano-islands. A full-factorial experiment was designed to explore a diverse sample space by varying two key input factors: the initial thickness of the nickel seeding film and the duration of carbon deposition. Using resource-intensive surface characterization techniques (SEM, EDS, XPS, and AFM), we verified encapsulation efficiency and morphology, identifying strong correlations between the input factors and properties of the shells. To gain insights into structural characteristics, we employed conventional spectroscopy techniques (Raman, UV–Vis-nIR transmission, and Transient Absorption Spectroscopy), introducing 107 metrics derived from spectral data. Principal Component Analysis (PCA) aligned the input factors, and their corresponding shell properties, with the first two principal components. Accordingly, we identified the most relevant metrics including new candidates derived from less prominent Raman bands. Additionally, inter-metric correlations enable interchangeable use of spectroscopy techniques. This study marks the first multi-spectroscopic correlation analysis of graphitic shells and provides a novel framework for evaluating their properties.

Supercapacitor electrodes based on Ru/RuO2 decorated on N,S-doped few-layer graphene

Innovatively designed flexible and high-performance shape memory polymer supercapacitors are promising next-generation energy storage devices for portable and wearable electronics. Therefore, thermally induced smart shape memory polymer polyurethane was synthesized using polycaprolactone/poly(ethylene glycol)/hexamethylene diisocyanate (PCL/PEG/HDI) in which the incorporation of PEG successfully assisted in lowering the transition temperature. The resulting polymer exhibits a remarkable transition temperature of 50 °C and a shape recovery ratio of 100 % at a strain of 300 %. The smart polymer was coated with a silver paste to ease the electron flow followed by coating with the electrode. Hybrid electrode materials are prepared in two stages. Initially, a few layers of holey-graphene were synthesized, where BET surface area reveals the presence of pores that are tuned by isothermal treatments in O2-atmosphere. Subsequently, active hybrid electrode materials nanostructured Ru/RuO2 decorated N, S-doped few layers of holey graphene were synthesized using hydrothermal methods. Here, nitrogen and sulfur doping in the basal or edge plane served as catalysts and metal coordination sites, facilitating the uniform distribution of ruthenium nanoparticles on the graphene. It is further confirmed by the density function theory (DFT) calculation using the adsorption energy. The optimized hybrid electrode material demonstrates a specific capacitance of 1297 mFcm−2 at a current density of 2 mAcm−2. A flexible-shape memory polymer supercapacitor exhibits a notable device-specific capacitance of 189 mFcm−2 at a current density of 1 mAcm−2, a high energy density of 45 µWhcm−2 at a power density of 0.25 mWcm−2, with 81 % of specific capacitance retention after eight shape programming and recovery cycle. Excellent shape recoverability and robust electrochemical performance make the as-fabricated symmetric supercapacitors a promising candidate for integration in flexible electronic applications.

Van der Waals integrated single-junction light-emitting diodes exceeding 10% quantum efficiency at room temperature.

The construction of miniaturized light-emitting diodes (LEDs) with high external quantum efficiency (EQE) at room temperature remains a challenge for on-chip optoelectronics. Here, we demonstrate microsized LEDs fabricated by a dry-transfer van der Waals (vdW) integration method using typical layered Ruddlesden-Popper perovskites (RPPs). A single-crystalline layered RPP nanoflake is used as the active layer and sandwiched between two few-layer graphene contacts, forming van der Waals LEDs (vdWLEDs). Strong electroluminescence (EL) emission with a low turn-on current density of ~20 pA μm-2 and high EQE exceeding 10% is observed at room temperature, which sets the benchmark for the EQE of vdWLEDs ever recorded. Such efficient EL emission is attributed to the inherent multiple quantum well structure and high photoluminescence quantum yield (~35%) of RPPs and a low charge injection barrier of ~0.10 eV facilitated by the Fowler-Nordheim tunneling mechanism. These findings promise a scalable pathway for accessing high-performance miniaturized light sources for on-chip optical optoelectronics.