Interfacial Effects Research Articles

Strong and weak interface synergistic enhance the mechanical and microwave absorption properties of alumina

Multifaceted balance makes the design of ceramics difficult but is urgently needed. This work purposes to grow uniform edge-rich graphene (ERG) on alumina (Al2O3/ERG) in-situ, then constructs a discontinuous conductive, strengthening and toughening network of crosslinked ERG by mixing Al2O3/ERG with Al2O3 and sintering. Under the guarantee of the tight-bound covalent interface, ERG and doping Al2O3 strengthen and toughen the ceramic by synergistic effect of weak and strong interface. And doping Al2O3 interrupts the conductive network of ERG to improve the impedance matching and endow material with moderate electromagnetic wave (EMW) loss capacity. The optimal flexural strength and fracture toughness of the composite ceramic reach 333.04 MPa and 12.43 MPa⋅m1/2, respectively. Meanwhile, it can absorb 80 % or more of the incident EMW in X-band with a matching thickness of 2 mm. This work takes full advantage of ERG to prepare load-bearing EMW absorbing ceramics, which expands the idea for material design.

Internal heating and distribution in electromagnetic Powell-Eyring [formula omitted]/glycerin hybridized nanomaterial with radiation and wall slip conditions

The synergistic influences of the hybridization of molybdenum disulfide (MoS2) and graphene oxide (GO) nanoparticles on electromagnetic radiation absorption and augmentation of thermal conductivity coupled with the industrial demand for an enhanced non-Newtonian working fluid spurred this study. Therefore, the study examines the radiative properties and thermal behaviour of hybridized MoS2 and GO nanoparticle systems dispersed in a glycerin Powell-Eyring fluid with wall slip conditions. A theoretical mathematical setup is modelled for the nanoparticle thermophysical characteristics with viscous dissipation and heat generation under the influence of the electromagnetic Riga plate. The model is transformed into an invariant dimensionless form and solved utilizing the pseudo-spectral collocation technique. The effect of fluid rheology, nanoparticle concentration, and fluid-wall slip conditions interface on radiative heat transfer and thermal propagation is investigated. The results reveal momentous augments in radiation absorption and thermal conductivity of about 4.13% to 10.22% due to MoS2 and GO hybridized nanoparticles. Also, it was found that thermal transport is enhanced close to the solid boundary wall slip, leading to an improve heat distribution rate. Hence, this study contributes to the interplay complexity between external stimuli, fluid dynamics, and nanoparticle morphology in thermal systems, offering insights into the advanced materials synthesis, thermal management systems, and optimization and design of nanoparticle fluid enhancement applications.

Interfacial lignin glued cellulose/aramid nanofiber membranes: Combing toughness, stability, and dye rejection performances

Nanoscale cellulose-based membranes have been considered as perfect candidates for organic dye separation attributed to their sustainability, high aspect ratio, and nanoscale designation. However, as natural polysaccharide, nanocellulose still suffers from drawbacks like brittleness and vulnerability. In this work, the tough and stable lignocellulose nanofibers (LCNFs) based composite membranes were fabricated by introducing lignin modified aramid nanofibers (DANFs) as reinforcing agents. Being benefit from the interfacial lignin bridging effects, the noncovalent interactions (e.g., H-bond and π-π stacking) between LCNFs and DANFs strengthened, and the resultant composite membranes presented enhanced tensile strength (∼186.9 MPa, 6.3 time higher than LCNFs membranes), toughness (∼9.28 MJ/m3, 105 time higher than LCNFs membranes), Young’s modulus (∼8.43 GPa, 4.6 time higher than LCNFs membranes), as well as the optimized stabilities (in organic, acidic and alkali conditions). Combing all these advantages, the composite membranes demonstrated promising dye rejection performances toward methyl violet (a reject rate of ∼98.54 % and a flux of ∼29.76 L•m−2•h−1•bar−1), and can removal 63.08 % of methyl violet after 10 recycles. Thus, this research paves a simple and efficient way to made strong LCNFs-based separation membranes that are suitable as dye separator in harsh environments.

AgNWs self-assembly along coaxially electrospun SEBS-PVP core-sheath fibers for stretchable conductive membranes with low interfacial losses

In this paper, core-sheath fibers with poly(styrene-ethylene/butylene-styrene) triblock copolymer (SEBS) as the core layer and polyvinylpyrrolidone (PVP) of different molecular weights as the sheath layer were prepared by coaxial electrospinning. Amphiphilic triblock copolymers were added to the SEBS core layer, and the fusion of incompatible SEBS-PVP at the core-sheath interface was further promoted by appropriate solvent post-treatment. Polydopamine (PDA) was in situ polymerized on the surface of SEBS-PVP fibers, so that silver nanowires (AgNWs) with high aspect ratios were conformally self-assembled along the fibers to form good interfacial bonding, so that the SEBS-PVP/AgNW composite membrane has high conductivity and exhibits good interfacial transfer effect in cyclic stretching under large strain. Based on core-sheath nanofibers and self-assembly, the excellent interfacial transfer gives SEBS-PVP/AgNW low viscoelastic loss, integrated large tensile strain sensing and stable Joule heating effect, which is conducive to the development and application of multifunctional stretchable electronics.

Quantifying Heterogeneous Interface Effect of Fe3O4(111)/C for Enhanced Low-Frequency Electromagnetic Wave Absorption

How to tailor electromagnetic parameters of multi-component materials is the fundamental issues for low-frequency electromagnetic wave absorbers (EMA). However, there remains a challenge to accurately elucidate the impact of respective components at heterogeneous interfaces on the EMAs, not to mentioning the further quantitative contribution of the interfacial effect to the electromagnetic loss. In this paper, we for the first time separated the Fe3O4(111)/C heterogeneous interface of Fe3O4@C via a controllable interfacial separation strategy, meanwhile ensuring the consistent microstructure and the ratio of each component, as well as the unchanged macroscopic structure of the particles. Once all potential influences on electromagnetic parameters have been independently studied, the unique difference in heterogeneous interfaces enabled us to quantitatively evaluate the effect of them on electromagnetic parameters. Both experimental and density functional theory (DFT) calculation results consistently demonstrate that the Fe3O4(111)/C heterointerface increases carrier concentration and conductivity, thereby enhancing the imaginary part of the dielectric constant. Very distinguished from traditional interfacial polarisation mechanism presented in previous publications, this study introduces a novel interfacial loss mechanism primarily characterized by conductivity loss, which is rigorously investigated in a quantitative way. This discovery offers a novel approach for designing controllable heterogeneous interfaces and manipulating electromagnetic parameters in multicomponent EMAs.

Phase-Regulated built-in electric field intensity mediates reconstructing for efficient water oxidation

The uncontrollable dynamic surface reconstruction of oxygen evolution reaction (OER) catalysts poses a significant impact on the activity and stability of the catalysts. To tackle this issue, a phase-controlled strategy is utilized to fabricate various CoxSy/layered double hydroxides (LDH) heterojunction with adjustable built-in electric field (BIEF) strength. The BIEF formed at the interface leads to an accumulation of OH– on the electron-deficient region of CoxSy side, facilitating its reconstruction and exposing more active sites. Furthermore, it enhances the bond energy of M−O in the electron-rich LDH, reducing LDH reconstruction and enhancing stability. The asymmetrical distribution of interface charges induced by the BIEF effectively modulates the d-band center of the metal sites, optimizing the adsorption/desorption of reaction intermediates. As a result, the designed Co3S4/LDH demonstrates outstanding OER activity and stability. This study introduces a novel approach to regulate the reconstruction of heterogeneous catalysts by leveraging interface effects driven by the BIEF.

Interface effects of polycrystalline Fe2O3 thin films on Pt

Interface effects of polycrystalline Fe2O3 thin films on Pt

Unveiling Intrinsic Bulk Photovoltaic Effect in Atomically Thin ReS2.

The bulk photovoltaic effect (BPVE) offers a promising avenue to surpass the efficiency limitations of current solar cell technology. However, disentangling intrinsic and extrinsic contributions to photocurrent remains a significant challenge. Here, we fabricate high-quality, lateral devices based on atomically thin ReS2 with minimal contact resistance, providing an optimal platform for distinguishing intrinsic bulk photovoltaic signals from other extrinsic photocurrent contributions originating from interfacial effects. Our devices exhibit large bulk photovoltaic performance with intrinsic responsivities of ∼1 mA/W in the visible range, without the need for external tuning knobs such as strain engineering. Our experimental findings are supported by theoretical calculations. Furthermore, our approach can be extrapolated to investigate the intrinsic BPVE in other noncentrosymmetric van der Waals materials, paving the way for a new generation of efficient light-harvesting devices.

Bifunctional MoO3-x/CuS Heterojunction Nanozyme-Driven "Turn-On" SERS Signal for the Sensitive Detection of Cerebral Infarction Biomarker S100B.

The use of nanozymes has become a promising auxiliary approach to "turn on" surface-enhanced Raman scattering (SERS) signals for the label-free detection of disease markers. Nevertheless, there are still major challenges to develop bifunctional nanomaterials with both excellent enzyme-like activity and high SERS performance. To this end, a novel Z-scheme MoO3-x/CuS heterojunction was first constructed as a powerful "two-in-one" substrate, which can not only catalyze leucomalachite green (LMG) to SERS-active malachite green (MG) but also serve as an efficient substrate to amplify the SERS signal of catalysate. Due to the strong interfacial coupling effect between the MoO3-x and CuS nanomaterial, which promoted the separation and transport of carriers in the heterojunction, the MoO3-x/CuS heterojunction showed higher peroxidase-like activity compared to individual components and the previously reported heterojunction nanozymes. Inspired by these results, a sandwich-type SERS immunoassay for the detection of the cerebral infarction biomarker S100 calcium-binding protein (S100B) was proposed based on the output signal of MG at 1620 cm-1. Furthermore, introducing the antifouling material chitosan on the surface of the MoO3-x/CuS heterojunction can effectively resist nonspecific protein adsorption and significantly improve the detection accuracy of the immunoassay. Therefore, the SERS immunoassay based on the MoO3-x/CuS heterojunction realized highly sensitive and selective detection of S100B in the concentration range of 0.001 to 100 ng/mL, with a low limit of detection of 0.47 pg/mL. The developed method has been successfully used for the accurate detection of S100B in clinical serum. The results showed that the level of S100B in the serum of cerebral infarction patients can be distinguished from those of healthy individuals and intracranial tumor patient controls. In addition, the acquired values of S100B in the serum of cerebral infarction patients based this strategy were well consistent with the results of electrochemiluminescence (ECL) detection with a relative error of less than ±7.3. It is expected that this work may open up a paradigm for improving detection sensitivity and accuracy for the early diagnosis and treatment monitoring of cerebral infarction in the clinic.

Preparation of antishrinkage and high strength poly(butylene adipate-co-terephthalate) microcellular foam via in situ fibrillation of polylactide

High-expansion-ratio microcellular poly (butylene adipate-co-terephthalate) (PBAT) foams exhibit severe shrinkage, which hinders their industrial applications. This study provides a facile method to prepare low-shrinkage, high-compressive-strength and high-resilience PBAT foam. CEPBAT/PLA blends (CE = chain extender, PLA = polylactide) were prepared via in situ fibrillation to obtain CEPBAT/PLA-S (CEPBAT/PLA containing PLA spherical phase) foam containing PLA spheres and CEPBAT/PLA-F (CEPBAT/PLA containing PLA fiber phase) foam with PLA nanofibers. The effects of the PLA nanofibers and spheres on the antishrinkage and compression strength of the PBAT foams were studied. The PLA nanofibers exhibited a higher specific surface area than the PLA spheres and a supporting network structure for the PBAT foam, thereby improving its melt strength. As a result, the antishrinkage performance and compression strength of CEPBAT/PLA-F improved by 100 % and 180 %, respectively, compared with the neat PBAT foam after aging for 144 h. However, the permanent deformation of CEPBAT/PLA-F increased only slightly after ten compression cycles. CEPBAT/PLA-F showed better antishrinkage performance, compression strength, and resilience than CEPBAT/PLA-S owing to the interface effect of the PLA nanofibers, whose nanolinear network structure provides enhancement and a larger deformation range under pressure to reduce plastic deformation.

Interface Engineering Induced by Low Ru Doping in Ni/Co@NC Derived from Ni-ZIF-67 for Enhanced Electrocatalytic Overall Water Splitting.

Electrochemical water splitting is a promising approach for hydrogen evolution reactions (HER); however, the oxygen evolution reaction (OER) remains a major bottleneck due to its high energy requirements. High-performance electrocatalysts capable of facilitating HER, OER, and overall water splitting (OWS) are highly needed to improve OER kinetics. In this work, we synthesized a trimetallic heterostructure of Ru, Ni, and Co incorporated into N-doped carbon (denoted as Ru/Ni/Co@NC) by first synthesizing Ni/Co@NC from Ni-ZIF-67 polyhedrons via high-temperature carbonization, followed by Ru doping using the galvanic replacement method. Benefiting from increased active surface sites, modulated electronic structure, and enhanced interfacial synergistic effects, Ru/Ni/Co@NC exhibited exceptional electrocatalytic performance for both HER and OER processes. The optimized Ru/Ni/Co@NC catalyst, with a minimal Ru mass ratio of ∼2.07%, demonstrated significantly low overpotential values of 34 mV for HER and 174 mV for OER at a current density of 10 mA/cm2 with corresponding Tafel slope values of 33.42 and 34.39 mV/dec, respectively. Further, the optimized catalyst was loaded onto carbon paper and used as anode and cathode materials for alkaline water splitting. Interestingly, a low cell voltage of just 1.44 V was obtained. The enhanced electrolytic performance was further elaborated by density functional theory (DFT) calculations, which confirmed that Ru doping in Ni/Co introduced additional active sites for H*, enhancing adsorption/desorption abilities for HER (ΔGH* = -0.30 eV), lowering water dissociation barrier (ΔGb = 0.49 eV) and reducing the energy barrier for the rate-determining step of OER (O* → OOH*) to 1.62 eV in an alkaline environment. These findings reflect the significant potential of ZIF-67-based catalysts in energy conversion and storage applications.

Helmet Continuous Positive Airway Pressure for Acute Bronchiolitis Respiratory Failure in a Pediatric Ward: Is It a Replicable Experience?

(1) Background: Helmet Continuous Positive Airway Pressure (H-CPAP) has primarily been used in intensive care settings to treat moderate-to-severe bronchiolitis in infants. We aim to report on the feasibility of H-CPAP for selected infants with bronchiolitis in a pediatric ward. (2) Methods: A retrospective, observational, consecutive case series was studied of 26 patients who received H-CPAP on the pediatric ward from October 2022 to February 2023, including a description of patient outcomes and costs. (3) Results: Of 130 infants with bronchiolitis admitted to Bambino Gesù Hospital in Rome, 34 were hospitalized for moderate to severe bronchiolitis, and 26 began H-CPAP on the ward. Among the 26 pediatric patients who received H-CPAP on the ward, 4 out of 26 (15%) required transfer to the PICU within the first hours of care due to clinical deterioration. No problems with the H-CPAP interface or side effects attributable to H-CPAP were reported. Pharmacological sedation with a single dose of dexmedetomidine was required for 15/26 patients (57%) following failure of non-pharmacological anxiety reduction strategies. After introducing H-CPAP in our pediatric ward, we achieved total cost savings of approximately EUR 147,120. (4) Conclusions: Treatment with H-CPAP for infants with bronchiolitis may be feasible in non-intensive care settings with trained staff, appropriate monitoring, and rapid access to pediatric intensive care.

BiOBr/SnO2/ZnO Catalyst With Interfacial Effect Enhanced Photocatalytic Degradation of Organic Dye

ABSTRACTBiOBr nanosheets were loaded onto SnO2 quantum dots, ZnO nanosheets, and SnO2/ZnO‐2 (SZ‐2) to form different heterojunction photocatalysts by sonochemistry, respectively. The photocatalytic activity of the prepared photocatalysts was evaluated by degrading the target dye Rhodamine B (RhB). The results showed that the degradation efficiency of BiOBr/SnO2/ZnO (BSZ) for RhB reached 97.5% at 80 min. The significant increase in catalytic activity of BSZ was attributed to the synergistic and interfacial effects among the three materials. Combined with the radical trapping experiments, it can be concluded that the catalytic mechanism of BSZ as a dual Z‐type heterojunction.

Lead-Free Hybrid Perovskite: An Efficient Room-Temperature Spin Generator via Large Interfacial Rashba Effect.

Two-dimensional (2D) hybrid organic-inorganic perovskite (HOIP) shows great potential for developing flexible and wearable spintronic devices by serving as spin sources via the bulk Rashba effect (BRE). However, the practical application of BRE in 2D HOIP faces huge challenges, particularly due to the toxicity of lead, which is crucial for achieving large spin-orbit coupling, and the restrictions in 2D HOIP candidates to meet specific symmetry-breaking requirements. To overcome these obstacles, we designed a strategy to exploit the interfacial Rashba effect (IRE) of lead-free 2D HOIP (C6H5CH2CH2NH3)2CuCl4 (PEA-CuCl), manifesting as an efficient spin generator at room temperature. IRE of PEA-CuCl originates from the large orbital hybridization at the interface between PEA-CuCl and adjacent ferromagnetic layers. Spin-torque ferromagnetic resonance measurements further quantify a large Rashba effective field of 14.04 Oe per 1011 A m-2, surpassing those of lead-based HOIP and traditional all-inorganic heterojunctions with noble metals. Our lead-free 2D HOIP PEA-CuCl, which harnesses large IRE for spin generation, is efficient, nontoxic, and economic, offering huge promise for future flexible and wearable spintronic devices.

Phonon-charge carrier dynamics via grain-boundary phase in equilibrium reaction of higher manganese silicide/CNF hybrid composites

Higher manganese (TE) silicide (HMS), an eco-friendly, low-cost, and earth-abundant p-type thermoelectric material, exposes a Nowotny chimney-ladder crystal structure, obeying the 14th-electron rule. Here, a hybrid composite of a carbon nanofiber (CNF) and HMS was synthesized by vacuum melting followed by spark plasma sintering, and its thermoelectric performance were demonstrated. The incorporation of CNF with HMS notably enhances the Seebeck coefficient and decline the thermal conductivity without significantly affecting the carrier concentration and electrical conductivity due to the interfacial energy filtering effect. A maximum Seebeck coefficient of 307 μV/K was recorded for the 0.5% CNF composite with HMS, leading to accomplish a high-power factor of 1755.63 μW/mK2 at 803 K. Also, interfaces, grain boundaries, and dislocations leading to the high magnitude of strain, confirmed from HR-TEM and strain analysis, leads to decrease in lattice thermal conductivity to 1.95 W/mK. As a result, HMS attains the peak zT value of 0.64, suggesting that carbon-based composites are a promising way to boost the thermoelectric performance of HMS-based compounds.

Silicate Derived from Phaeodactylum tricornutum for Removal of Polystyrene: Interfacial Effects of Living Organism and Its Derivatives with Nanoplastics.

The deposition of nanoplastics in the environment poses a direct threat to human health through the food chain. There is an urgent need to investigate how they can be effectively removed from water. In this work, the toxic effects of nanopolystyrene (PS) at different concentrations on Phaeodactylum tricornutum (PT) were investigated. The results show that PS affects the cell activity of PT through cell wall adhesion and shading effect and hinders the transmission of light energy, thus inhibiting the growth of PT. Considering that living PT is not suitable for the removal of heterogeneous aggregation of PS, magnesium silicate (MS) was obtained by calcination of PT biomass based on retaining salt. The maximum adsorption capacity of PS by MS was 40.85 mg g-1, which was 10 times higher than that of conventional adsorbents. The presence of competitive anions significantly affects the removal of PS. The application in real water bodies and the reusability of the adsorbents were also verified. By characterizing the materials before and after adsorption, it is found that the adsorption mechanism mainly includes electrostatic attraction, hydrogen bonding, π-π interaction, and complexation between Si-O bond and PS. This study explains the toxic effect of nano-PS on PT and innovatively develops a biomass derivative from diatoms, which provides a novel and feasible strategy for environmental remediation.

Efficient Molecular Rectification in Metal-Molecules-Semimetal Junctions.

Molecular rectification is expected to be observed in metal-molecule-metal tunnel junctions in which the resonance levels responsible for their transport properties are spatially localized asymmetrically with respect to the leads. Yet, effects such as electrostatic screening and formation of metal induced gap states reduce the magnitude of rectification that can be realized in such junctions. Here we suggest that junctions of the form metal-molecule(s)-semimetal mitigate these interfacial effects. We report current rectification in junctions based on the semimetal bismuth (Bi) with high rectification ratios (>102) at 1.0 V using alkanethiols, molecules for which rectification has never been observed. In addition to the alleviation of screening and surface states, the efficient rectification is argued to be related to symmetry breaking of the applied bias in these junctions because of a built-in potential within the Bi lead. The significance of this built-in potential and its implications for the future and other applications are discussed.

Preparation of unique corn-stalk-like MnO₂/CoNi nanowires via in situ epitaxial attachment growth for monitoring environmental pollutant hydrazine

This paper presents the synthesis of a novel corn-stalk-like MnO₂/CoNi oxide composite using an in situ epitaxial attachment growth strategy, in which CoNi oxide nanosheets are anchored onto MnO₂ nanowires. The one-dimensional MnO₂ nanowires, with their large specific surface area, serve as a support to enhance the electronic conductivity of the CoNi oxides. Hexamethylenetetramine (HMTA) is employed as an alkaline linking agent, playing a key role in shaping the CoNi oxide nanosheets and ensuring their successful growth on the MnO₂ nanowires. The MnO₂/CoNi oxide composite-based electrochemical sensor exhibits excellent synergistic and interfacial effects, promoting electron transfer and charge migration. This composite material shows outstanding electrocatalytic performance for hydrazine detection, with a broad linear range (0.48−6106.58 μM), low detection limit (0.286 μM, S/N = 3), and high sensitivity (0.037 μA μM⁻1). Moreover, when tested for hydrazine detection in water samples, the sensor achieved a recovery rate of 95.7–105 %, highlighting its high sensitivity and rapid response in practical applications.

Suppression of Initial Degradation via an Interfacial Charge-Induced Overshooting Effect in Solution-Processed Organic Light-Emitting Diodes.

As the chemical stability of organic materials in organic light-emitting diodes (OLEDs) greatly impacts devices' lifetime, a thoughtful and advanced design of materials and device structures is necessary. In our work, we have achieved lifetime enhancement at its initial stage for solution-processed OLEDs. This improvement was realized through the implementation of a double electron transporting layer (dETL) composed of 2-[4-(9,10-dinaphthalen-2-yl-anthracen-2-yl)-phenyl]-1-phenyl-1H-benzoimidazole (ET) and hydroxyquinolinolato-lithium (Liq). A giant surface potential was generated at the surface of a constituent electron transport layer (ETL) that contained a higher concentration of Liq with high polarity. This giant surface potential simultaneously promoted the injection of trapped/accumulated electrons through the interface within dETL and the injection of holes from the anode, generating more exciton recombination events and ultimately enhancing efficiency by 133.0% and lifetime LT95 (luminance dropped by 5%) by 300% with an overshooting effect. Additionally, the degradation at the emitting layer was mitigated by shifting the degradation zone to the dETL, which was evidenced by laser desorption/ionization-time-of-flight (LDI-TOF) mass spectroscopy.

Competition between Disentanglement Effect and Interfacial Effect Determines the Chain Relaxation Dynamics of Entangled Ultrathin Polystyrene Films

Competition between Disentanglement Effect and Interfacial Effect Determines the Chain Relaxation Dynamics of Entangled Ultrathin Polystyrene Films