Interfacial Properties Research Articles

Interfacial Metal Chlorides as a Tool to Enhance Charge Carrier Dynamics, Electroluminescence, and Overall Efficiency of Organic Optoelectronic Devices.

Interface engineering is the key to optimizing optoelectronic device performance, addressing challenges like reducing potential barriers, passivating interface traps, and controlling recombination of charges. Metal fluorides such as lithium fluoride are employed in interface modification within organic devices due to their strong dipole characteristics but carry health risks, high processing costs, and minimal impact on interface traps in organic electronics. Hence, this study investigates alternative metal chloride (MC) nanocrystals (sodium, cesium, rubidium, and potassium chlorides) that exhibit a strong dipole moment and are readily processable with the aim of reducing the influence of interface traps. Interfacial properties are assessed via various techniques, including electron paramagnetic resonance, X-ray/ultraviolet photoelectron spectroscopy, capacitance-voltage measurements, and density functional theory calculations. In organic light-emitting diodes (OLEDs), the influence of MC on charge transfer, trap density, and light emission properties is evaluated. MCs in ZnO:PEIE nanocomposites (NCs) show improved charge transport, accelerated trapping/detrapping in ZnO:PEIE NCs, and a 50% reduction in active traps in NaCl-based devices versus the reference without MCs. RbCl-, CsCl-, and NaCl-based OLEDs exhibit substantial reductions in the potential barrier between the electron injection layer and the metal contact (Al) from 4.43 to 2.93, 3.02, and 4 eV, respectively, accompanied by enhancements of 35, 27, and 25% in electroluminescence intensity.

Identifying the Role of Interfacial Long-Range Order in Regulating the Solid Electrolyte Interphase in Lithium Metal Batteries.

The self-assembled monolayer (SAM) technique, known for its customizable molecular segments and active end groups, is widely recognized as a powerful tool for regulating the interfacial properties of high-energy-density lithium metal batteries. However, it remains unclear how the degree of long-range order in SAMs affects the solid electrolyte interphase (SEI). In this study, we precisely controlled the hydrolysis of silanes to construct monolayers with varying degrees of long-range order and investigated their effects on the SEI nanostructure and lithium anode performance. The results indicate that the degree of long-range order in SAMs significantly influences the decomposition kinetics of the carbon-fluorine bond in lithium bis(trifluoromethanesulfonyl)imide (LiTFSI), promoting the formation of a LiF-rich SEI and profoundly affecting the long-term stability of the highly sensitive anode during electrochemical processes. These findings provide new insights and directions for the molecular design of SAMs tailored for long-lasting lithium metal interfaces.

Cold Sintered ZnO-Polystyrene (PS) Composites with Modified Interfacial Structures and Properties.

Lightweight and integrated electronic devices with high performance have become an inevitable trend in the development of power electronic systems. However, it is challenging to obtain lightweight and miniaturized varistors due to the low threshold electric field. Herein, (1 - x)ZnO-xPS composites with a high threshold electric field are prepared through a cold sintering process at 220 °C for 50 min, utilizing lightweight PS to modulate the grain boundary structures of ZnO varistors. With PS content ≤1.5 wt %, the relative densities of cold sintered composites exceed 95%. PS thin layers with a thickness of 2-10 nm are distributed at the grain boundaries of ZnO, forming the Schottky barrier, which triggers nonlinear current-voltage responses. With the addition of PS, the threshold electric field is dramatically enhanced from 135 to 2703 V·mm-1, higher than that of commercial ZnO varistors, which is further demonstrated by the electric field simulation of the Finite Element Method. The interfacial resistance obtained from impedance analysis increases with the increase of the PS content, and the activation energy of (1 - x)ZnO-xPS composites is higher than that of pure ZnO ceramics. This study provides a promising approach for the development of lightweight and cost-effective varistor materials.

Extremely Ultrahigh Stretchable Starch‐Based Hydrogels with Continuous Hydrogen Bonding

AbstractNatural polysaccharides‐based hydrogels have drawn extensive attention yet have been plagued by less desirable stretchability due to their inherent nature. Here, ultra‐stretchable starch‐based hydrogels (amylopectin/polyacrylamide, AAM) are developed by constructing reversible intramolecular physical interactions. This strategy endows the hydrogel with exceedingly ultrahigh deformation due to a continuous hydrogen bonding network. It can be stretched from less than 0.5 to >300 cm without breakage that the elongation exceeds 600 times the original length. The elongation collected by the universal testing machine reaches up to 36 000% without breakage outperforming previous reports and demonstrating extraordinary stretchability. Furthermore, an interwoven structure of hydrogen bonding interaction and trace covalent bonds make the stress of hydrogel reach 0.28 MPa, accompanied by an ultra‐high strain of 22 500% and significant toughness (47 MJ·m−3). The hydrogel displays high transparency (≈93%), low‐temperature resistance, moisturizing property, and extraordinary interfacial adhesion property. Intriguingly, the aqueous precursor can act as inks to prepare various forms of hydrogel within minutes through the facile writing or drawing method. This hydrogel verifies strong potential in both fields of human motion sensor (After long‐term or low‐temperature conditions) and energy storage. This study will facilitate the progress of ultra‐stretchable or multifunctional hydrogels.

Utilizing Binary Phase Segregation and Extrusion to Enhance the Electronic Properties of Graphene Nanocomposites.

Our goal in this study is to incorporate graphene nanoplatelets (GNPs) in a polymer blend of poly(lactic acid) (PLA) and isotactic polypropylene (iPP) to facilitate the dispersion of GNPs and use the morphology of phase segregation to create a pathway for concentrating GNPs to achieve percolation with lower GNP concentration. Investigating the interfacial properties between PLA/GNPs and iPP/GNPs, we noticed that iPP has a lower contact angle on GNPs compared to PLA on GNPs. This showed a great potential that the GNP are easily confined in iPP rather than in PLA domains or at the PLA/PP interfaces. Utilizing this property, as the PLA content increases, the iPP content decreases, resulting in a reduction of the available space for GNPs. This decrease in space leads to a higher chance for GNPs to accumulate together. Furthermore, through careful control of the concentration in the immiscible blend of PLA/PP, it is possible to achieve a bicontinuous structure. This structure facilitates the creation of a pathway for the fillers, allowing for the use of minimal GNPs while achieving optimal electrical conductivity properties. The PLA/PP/GNPs can be oriented by the shear forces coming from the nozzle that produce a higher performance.

Origins of synergy in multilipid lubrication

Lipid bilayers, ubiquitous in living systems, form lubricious boundary layers in aqueous media, with broad relevance for biolubrication, especially in mechanically stressed environments such as articular cartilage in joints, as well as for modifying material interfacial properties. Model studies have revealed efficient lubricity by single-component lipid bilayers; synovial joints, however (e.g. hips and knees), comprise over a hundred different lipids, raising the question of whether this is natural redundancy or whether it confers any lubrication benefits. Here, we examine lubrication by progressively more complex mixtures of lipids representative of those in joints, using a surface forces balance at physiologically relevant salt concentrations and pressures. We find that different combinations of such lipids differ very significantly in the robustness of the bilayers to hemifusion under physiological loads (when lubrication breaks down), indicating a clear lubrication synergy afforded by multiple lipid types in the bilayers. Insight into the origins of this synergy is provided by detailed molecular dynamics simulations of potential profiles for the formation of stalks, the essential precursors of hemifusion, between bilayers of the different lipid mixtures used in the experiments. These reveal how bilayer hemifusion-and thus lubrication breakdown-depends on the detailed lipid bilayer composition, through the corresponding separation into domains that are better able to resist stalk formation. Our results shed light on the role of lipid-type proliferation in biolubrication synergy, point to improved treatment modalities for common joint diseases such as osteoarthritis, and indicate how lipid-based interfacial modification in a materials context may be optimized.

Interfacial Proton Precompensation: Suppressing Deprotonation-Driven Lattice Collapse for Enhanced Efficiency and Stability in Perovskite Solar Cells.

The chemical property of the buried interface plays a crucial role in improving the performance and stability of perovskite solar cells (PSCs). The SnO2/perovskite interface prepared from SnO2 alkaline hydrogel with high proton affinity triggers directional migration and irreversible reactions of protons, exacerbating the disintegration of perovskite crystal. In this study, we proposed proton precompensation strategy to suppress the deprotonation effect of the buried interface and improve the durability of the devices. By modulating the chemical environment and surface energy state of the buried interface, the domain-limiting and spontaneous compensation of protons in formamidinium (FA+) under Coulomb force were achieved, thereby stabilizing the perovskite crystal structure. The stability of target perovskite films under UV illumination and heating at 85 °C was significantly enhanced. As a result, the devices can retain around 90% of their initial power conversion efficiency (PCE) after 1000 h of continuous irradiation at the maximum power point (MPP). Moreover, due to the reduction of defect content at the buried interface and the improvement of conductivity and carrier mobility by the precompensation treatment, the interfacial energy loss and non-radiative recombination were substantially diminished. The target PSC devices exhibited much higher PCE of 25.55% than the control devices (23.03%).

Effects of Absorption on the Tribological Properties of Carbon Fiber Reinforced Polyamide-6 Composites Manufactured by Fused Deposition Modeling

Abstract The present work studied the water absorption behavior of polymeric composite materials fabricated using 3D printing technology, as well as its effect on their tribological properties. Polyamide-6 was selected as the base matrix material. Short and continuous carbon fibers are used as the reinforced material. The results showed that the moisture absorption would impair the mechanical properties of polymer matrix and interface bonding between the fiber and the matrix. As a result, the tensile strength of the fiber reinforced polymer composites (FRPCs) decreases with water absorption. Nevertheless, the effects of moisture absorption on the wear properties of FRPCs are more complicated, which are depending on the fiber length and sliding conditions. With the short fiber reinforcements, moisture absorption deteriorated the wear resistance under all the testing conditions. With the increase of moisture level, more severe fiber damage/removal was observed, associated with the higher wear loss. With a relative high volume fracture of continuous carbon fiber (∼35 vol%), however, the wear resistance of the FRPC increased with moisture level, especially under a relatively low load. Based on microscopic observations, it was proposed that water inside FRPC specimens is able to provide the lubricating and cleaning effects, which contribute to a lower friction and smooth worn surfaces. The work provides new insights into designing and selecting printed polymer materials, subjected to different loading conditions.

Interfacial Proton Precompensation: Suppressing Deprotonation‐Driven Lattice Collapse for Enhanced Efficiency and Stability in Perovskite Solar Cells

The chemical property of the buried interface plays a crucial role in improving the performance and stability of perovskite solar cells (PSCs). The SnO2/perovskite interface prepared from SnO2 alkaline hydrogel with high proton affinity triggers directional migration and irreversible reactions of protons, exacerbating the disintegration of perovskite crystal. In this study, we proposed proton precompensation strategy to suppress the deprotonation effect of the buried interface and improve the durability of the devices. By modulating the chemical environment and surface energy state of the buried interface, the domain‐limiting and spontaneous compensation of protons in formamidinium (FA+) under Coulomb force were achieved, thereby stabilizing the perovskite crystal structure. The stability of target perovskite films under UV illumination and heating at 85 °C was significantly enhanced. As a result, the devices can retain around 90% of their initial power conversion efficiency (PCE) after 1000 h of continuous irradiation at the maximum power point (MPP). Moreover, due to the reduction of defect content at the buried interface and the improvement of conductivity and carrier mobility by the precompensation treatment, the interfacial energy loss and non‐radiative recombination were substantially diminished. The target PSC devices exhibited much higher PCE of 25.55% than the control devices (23.03%).

Impact of metal deposition on the optical and interface properties of NiO: growth and characterization of NiO/metal thin bilayer films

Abstract Since transparent conductive oxides (TCOs) provide electrical conductivity together with optical transparency, they have found wide applications in optoelectronic devices and photovoltaics. Among the TCOs, nickel oxide (NiO) is challenging due to its inherent trade-off between transparency and electrical conductivity. To address this challenge, one effective approach is to deposit a metal layer onto NiO thin films. In this work, NiO, NiO/Au, NiO/Ag, and NiO/Cu thin films are prepared by sputtering and thermal evaporation techniques on glass substrates and fully characterized finding the proper film for optoelectronic applications. The electrical and optical properties of the fabricated films are examined by four-point probe measurements and optical spectrometry. According to the obtained results, the NiO/Au, NiO/Ag, and NiO/Cu bilayers show sheet resistance of 200, 338, and 925 Ω sq−1 respectively while their optical bandgaps vary from 3.2 to 3.76 eV. These findings provide valuable insights into the performance of these films, making them potentially viable choices for various optoelectronic applications.

Interfacial adhesion enhancement in high‐modulus carbon fiber/poly (ether ether ketone) composites: through the flexible macromolecule‐grafted‐carbon nanotubes sizing treatment

AbstractIn this study, a flexible macromolecule‐grafted‐carbon nanotube (t‐CTN‐SPEEK) is developed and utilized as bridge to enhance the interfacial properties of high‐modulus carbon fiber (HM‐CF) reinforced poly (ether ether ketone) (PEEK) composites. With t‐CTN‐SPEEK sizing, the wettability of HM‐CF is enhanced, thereby promoting better resin wetting. The increased roughness induced by the t‐CTNs‐SPEEK on the surface of the HM‐CF affords improved mechanical interlocking among interface. Additionally, SPEEK enhances the interfacial compatibility of the composites. Thus, after the t‐CTN‐SPEEK sizing treatment, the composite exhibits the best interfacial shear strength (IFSS), as evaluated using the interfacial strength evaluation instrument. This paper also discusses in detail the interfacial strengthening mechanism after sizing and presents a promising approach to enhancing the interfacial properties of HM‐CF composites.

Densifying Conduction Networks of Vertically Aligned Carbon Fiber Arrays with Secondary Graphene Networks for Highly Thermally Conductive Polymer Composites

AbstractThermally conductive polymer composites hold great potential for thermal management applications in the electronics industry, but achieving metal‐like thermal conductivity (>200 W m−1 K−1) remains challenging due to the inevitable phonon scattering and the thermal resistance at filler‐filler and filler‐matrix interfaces. Herein, an efficient approach is presented to overcome this long‐standing barrier by designing a densified interconnecting filler framework, featuring a macro‐level carbon fiber (CF) array welded with a high‐quality, self‐assembled graphene network. In this framework, vertically aligned continuous CFs function as primary through‐plane thermal conduction paths, minimizing phonon scattering and thermal resistance. Meanwhile, the secondary graphene network interconnects the CFs into a more integrated and densified framework while introducing supplementary thermal conduction paths. Following polymer backfilling, the resulting epoxy nanocomposite exhibits an unprecedented through‐plane thermal conductivity of 262 W m−1 K−1 at a filler loading of 23.3 vol%, establishing a new benchmark among the thermally conducting polymer composites. When employed as a thermal interface material, this composite offers a 68.2% enhancement in cooling efficiency compared to standard commercial counterparts. Furthermore, the functional composite presents excellent Joule heating and interfacial adhesion properties, making it promising for thermal interface healing and multifunctional thermal management applications in complex environments.

Controllable Graphene/MoS2 Heterointerfaces by Perpendicular Surface Functionalization.

Surface chemistry and interface interactions profoundly influence the properties of two-dimensional (2D) materials and heterostructures. Therefore, developing methods to precisely control surfaces and interfaces is crucial for harnessing the properties and functions of 2D materials and heterostructures. Here, we developed a facile approach to tuning the interface distance and properties of graphene/MoS2 heterostructures (G/MoS2) by varying the functional groups attached to the surface of graphene bottom layer. We systematically investigated how different functionalized graphene bottom layers affect the interlayer distance, coupling between the interlayers, and optical properties of resulting G/MoS2 heterostructures. Our findings indicate that both the size and electron-withdrawing/donating properties of functional groups are pivotal in regulating charge transport properties, with size playing a particularly decisive role. Our approach demonstrates an efficient and flexible pathway to regulate the interlayer spacing and charge transport, highlighting the potential of engineering interface chemistry in optimizing properties of van der Waals heterostructures.

Exploring the multi-scale evolution mechanism of the ultra-high-temperature mechanical behaviour of carbon/carbon composites

The microstructure and mechanical properties of Carbon/Carbon (C/C) composites were investigated after ultra-high-temperature heat treatment (HTT) in the range of 30 – 2950 °C. The evolutionary mechanisms of the mechanical behaviour were explained at three scales: graphene sheets, carbon fibre (CF) monofilaments and the C/C composites. The results displayed that the tensile strength of CF monofilaments decreases monotonically as the HTT increases, while C/C composites present a tendency to decrease and then increase, demonstrating that CF/matrix interfacial properties play a decisive role in the tensile properties. Obvious microstructure change of C/C composites after HTT at 2700 °C was observed, meanwhile the high temperature tensile strength (measured at 2000 °C and 2500 °C) for the composites treated at temperature beyond 2600 °C was higher than that of room temperature. The high-temperature mechanical properties of C/C composites were regulated by the competing mechanisms of the graphite crystallite structure and the skin-core structure of CF monofilament, the CF/matrix interfacial strength and the porosity of C/C composites.

Enhancing the Interfacial Properties of Polyethylene-Based Carbon Fiber Composites Through Low-Temperature Thermally Reduced Graphene

Enhancing the Interfacial Properties of Polyethylene-Based Carbon Fiber Composites Through Low-Temperature Thermally Reduced Graphene

Three‐Dimensional Imaging of the Structural Phase Transition in a Single Vanadium Dioxide Nanocrystal

Vanadium dioxide (VO2) is a strongly correlated material that exhibits a number of structural phase transitions (SPT) near to room temperature of considerable utility for various technological applications. When reduced to the nanoscale, a foreknowledge of surface and interface properties of VO2 during the SPT can facilitate the development of devices based on VO2. Herein, it is shown that Bragg coherent X‐ray diffractive imaging (BCDI) combined with machine learning is an effective means to recover three‐dimensional images of a single VO2 nanocrystal during a temperature‐induced SPT from a room‐temperature monoclinic phase to a high‐temperature rutile phase. The findings reveal the coexistence of multiple phases within the nanocrystal throughout the transition, along with missing density which indicates the presence of a newly formed rutile phase.

Numerical model of curved composite tiles under low-velocity impact loading

In recent years, composite structures have seen widespread application across diverse industries, including automotive and aerospace, owing to their favourable strength-to-weight ratio. However, these structures, particularly high-pressure vessels, are susceptible to extreme loadings such as impact forces, resulting in visible and latent damage, ultimately leading to catastrophic failures. Hence, it is imperative to assess such damages diligently. Given the cost implications associated with experimental investigations, numerical methodologies emerge as a potent means for conducting relevant analyses. This paper will introduce a numerical model approach to conducting virtual tests to assess curved carbon fibre composite tiles subjected to low-velocity impact. The primary focus of this study is to consider the impact-induced delamination on composite tiles through a numerical model. The composite tiles are conducted to 90J impact loading. Specifically, the study evaluates filament winding structures’ interface properties (shear resistance) variability during manufacturing. Notably, the parameter of shear resistance significantly impacts the anticipation of intralaminar damage (delamination) after impact loading. Three-point bending tests were performed to calibrate the composite material’s shear interface properties, followed by low-velocity impact tests on the curved composite tiles. The findings indicate that the shear resistance values, which ranged from 14.25 MPa to 60 MPa, play a critical role in predicting delamination, with lower shear resistance leading to increased damage areas. The results underscore the importance of accurately calibrating interface properties to enhance the predictive accuracy of numerical models for curved composite structures under impact loading.

Microstructure Evolution and Mechanical Properties of Ta-Cladded Ni-Cr-Mo Low Alloyed Steel via Explosive Welding

The effects of welding variables (stand-off distance and explosive thickness) on the interfacial microstructure evolution and mechanical properties of explosively welded Ta alloy to Ni-Cr-Mo low alloyed steel have been investigated. Regardless of welding conditions (a stand-off distance of 3-5 mm and explosive thickness of 40-80 mm), the Ta/steel interface consistently exhibited a wavy configuration. This wavy interface facilitated the formation of vortex, resulting in strong interlocking. The height of the vortex increased with a larger stand-off distance at a fixed explosive thickness of 60 mm. Similarly, increasing the explosive thickness at a stand-off distance of 3 mm also resulted in a greater vortex height. The explosive weldability window, plotting the collision angle (<i>β</i>) against the collision point velocity (<i>v<sub>c</sub></i>), was successfully established for the dissimilar Ta and steel plates. The upper limit prediction with <i>N</i>=0.11, as proposed by Wittman, best matched the experimental results. This guided the determination of the optimal condition, which was a standoff distance of 3 mm and an explosive thickness of 40 mm. A vortex melted zone (VMZ) was identified, which resulted from the dynamic intermixing of Ta and steel, combined with localized melting caused by high-energy collisions and heat accumulation. The VMZ surrounded by a highly deformed Ta alloy, showed the highest hardness. Near the interface on the steel side, a fine recrystallized grain structure was observed. No significant inter-diffusion was detected at the wavy Ta/steel interface. The tension-shear properties of the wavy interface, which was subjected to loading parallel to interface, showed a good balance of strength and ductility, confirming the soundness of Ta/steel interface.

Surface‐Interface Engineering of Electrocatalysts for Two‐Electron Water Oxidation Reaction to Produce H2O2

AbstractElectrochemical two‐electron water oxidation reaction (2e− WOR) driven by renewable energy offers an attractive route to produce H2O2, while the corresponding electrocatalyst still requires further improvement for the activity, selectivity, and the resulting H2O2 yield. Surface‐interface engineering of electrocatalysts has great potential to advance 2e− WOR performance. This review provides a succinct yet comprehensive insight into the functional mechanisms of surface‐interfacial properties affecting 2e− WOR performance on electrocatalyst. The Gibbs free energy theoretical framework related to surface electronic structure and interfacial reactive kinetics mechanism related to electrolyte, electrode–electrolyte interface structure, and interfacial microenvironment properties are firstly discussed. Afterward, various surface‐interface engineering strategies toward high performance electrocatalysts including the regulation of surface electronic structure, the electrode–electrolyte interface structure, and the interfacial microenvironment have been overviewed. Rational manipulations of the above surface‐interfacial engineering strategies are critical to design highly efficient 2e− WOR electrocatalysts, leading to the development of the green H2O2 production.

Rubisco at interfaces II: Structural reassembly enhances oil-water interface and emulsion stabilization

Rubisco is the most abundant protein on earth and has gained extensive attentions as a novel food ingredient, such as an emulsifier. Extraction methods can significantly affect its molecular structures and consequently influence its oil-water interface and emulsion stabilization properties. This work aims to elucidate the role of the Rubisco molecular structure in stabilizing the oil-water interface and the multiphase system of emulsions. Ultrafiltration (mild) and acid precipitation-alkaline redispersion (extensive) were used to extract Rubisco from spinach leaves. Protein molecular properties were characterized by size exclusion chromatography (SEC), circular dichroism (CD), and fluorescence spectrometry. Subsequently, the oil-water interfacial properties, including the adsorption and rheological behavior in both small and large dilatational and shear deformations, and the emulsion stabilization properties of Rubisco were investigated. We found that acid precipitation-alkaline redispersion produced a Rubisco extract (RA) with extensive structural reassembling, compared to the one produced by ultrafiltration (RU), for which nativity was mostly retained. RA had two-fold higher surface hydrophobicity than RU, and this caused RA to adsorb faster to the oil-water interface and developed a stiffer solid-like interface (Gi’ = 26 ± 3 mN/m) than RU (Gi’ = 15 ± 2 mN/m), which was also more resistant to density changes in large dilatational deformations. Consequently, RA displayed higher emulsifying activity and emulsion stability to coalescence during bulk shear and storage. Additionally, structural reassembly resulted in a higher value of the zeta potential of RA, which made the emulsion more stable against flocculation, compared to RU. Our study demonstrates that structural reassembly might be a useful strategy to improve the behavior of plant proteins in oil-water interface and emulsion stabilization, and may stimulate the development of new plant protein-stabilized emulsion-based products.