Strong Interlayer Research Articles

Scalable ultrastrong MXene films with superior osteogenesis.

Titanium carbide MXene flakes have promising applications in aerospace, flexible electronic devices and biomedicine owing to their superior mechanical properties1 and electrical conductivity2 and good photothermal conversion3, biocompatibility4 and osteoinductivity5. It is highly desired yet very challenging to assemble MXene flakes into macroscopic high-performance materials in a scalable manner. Here we demonstrate a scalable strategy to fabricate high-performance MXene films by roll-to-roll-assisted blade coating (RBC) integrated with sequential bridging, providing good photothermal conversion and osteogenesis efficiency under near-infrared irradiation. MXene flakes were first bridged with silk sericin by hydrogen bonding and then assembled into macroscopic films using a continuous RBC process, followed by ionic bridging to freeze their aligned structure. The resultant large-scale MXene films with strong interlayer interactions are highly aligned and densified, exhibiting high tensile strength (755 MPa), toughness (17.4 MJ m-3) and electromagnetic interference (EMI) shielding capacity (78,000 dB cm2 g-1), as well as good ambient stability, photothermal conversion and bone regeneration performance. The proposed strategy not only paves a feasible way for realizing the practical applications of MXene in the fields of flexible EMI shielding materials and bone tissue engineering but also provides an avenue for the high-performance and scalable assembly of other two-dimensional flakes.

S-Modified Graphitic Carbon Nitride with Double Defect Sites For Efficient Photocatalytic Hydrogen Evolution.

Graphitic carbon nitride (gC3N4) is an attractive photocatalyst for solar energy conversion due to its unique electronic structure and chemical stability. However, gC3N4 generally suffers from insufficient light absorption and rapid compounding of photogenerated charges. The introduction of defects and atomic doping can optimize the electronic structure of gC3N4 and improve the light absorption and carrier separation efficiency. Herein, the high efficiency of carbon nitride photocatalysis for hydrogen evolution in visible light is achieved by an S-modified double-deficient site strategy. Defect engineering forms abundant unsaturated sites and cyano (─C≡N), which promotes strong interlayer C─N bonding interactions and accelerates charge transport in gC3N4. S doping tunes the electronic structure of the semiconductors, and the formation of C─S─C bonds optimizes the electron-transfer paths of the C─N bonding, which enhances the absorption of visible light. Meanwhile,C≡N acts as an electron trap to capture photoexcited electrons, providing the active site for the reduction of H+ to hydrogen. The photocatalytic hydrogen evolution efficiency of SDCN (1613.5µmolg-1h-1) is 31.5 times higher than that of pristine MCN (51.2µmolg-1h-1). The charge separation situation and charge transfer mechanism of the photocatalysts are investigated in detail by a combination of experimental and theoretical calculations.

Efficient Li+/Mg2+ separation by two-dimensional montmorillonite membrane with stable channel structure through ion exchange and metal–organic coordination strategy

Two-dimensional (2D) nanochannel membranes stacked by nanosheets are promising membrane separation materials. However, intrinsic swelling properties of 2D membrane have emerged as a significant challenge to establish stable nanochannels and achieve high separation performance. Inspired by the natural ion exchange property of montmorillonite (MMT), we constructed a two-dimensional MMT membrane with robust nanochannels by exchanging Fe3+ into interlayer of the membrane, and further achieved efficient separation of Li+/Mg2+ through coordination manipulation of tannic acid (TA) and Fe3+. Swelling was dramatically prevented by strong interlayer interaction between exchanged Fe3+ and nanosheets resulting in a 32-fold increase in anti-swelling properties. Furthermore, experiments and simulations revealed that TA could rapidly chelate with Fe3+ to form a dense hydrophilic functional layer on the membrane interface, which endowed MMT membranes with enhanced mechanical strength, cation transport and recognition, as well as anti-fouling properties. Consequently, the resulting MMT membranes showed the Li+/Mg2+ selectivity as high as 9.98 with a fast Li+ permeation rate (0.108 mol m-2h−1), which exceeded most of the previously reported membranes. This study proposed a novel strategy to diminish the trade-off effect among stability, ion flux, and selectivity of membranes, and inspired the development of next-generation ion selective separation membranes.

A bio-inspired Janus hydrogel patch facilitates oral ulcer repair by combining prolonged wet adhesion and lubrication

Oral ulcers, the most common type of mucosal lesion, are both highly prevalent and prone to recurrence. In the persistently moist environment of the oral cavity, current therapeutic patches face challenges such as short adhesion time, disruption by food particles and bacteria, and oral movements. To address these challenges, we develop a Janus patch, named ANSB, inspired by the multi-layered and asymmetric structure of natural mucosa, featuring a long-lasting adhesive layer and a lubricating layer. By eliminating the salivary barrier and leveraging covalent crosslinking between tissue surface amine groups and N-hydroxysuccinimide ester (NHS), the adhesive layer—composed of gelatin and acrylic acid—achieves rapid (≤ 30 s), strong (≥ 45 kPa), and durable (≥ 8 h) adhesion to wet buccal tissues. Furthermore, the efficient lubricating effect (COF = 0.02 ± 0.003) provided by zwitterions renders the lubricating layer of ANSB highly similar to natural mucosal tissue, effectively preventing bacterial invasion, secondary damage, and unintended adhesion. Additionally, the strong interlayer bonding and complementary mechanical properties are confirmed, resulting in a unified performance characterized by rapid wet adhesion, hydration lubrication, and enhanced mechanical strength. Importantly, ANSB treatment demonstrates a long-term protective barrier and superior therapeutic effects in rat oral ulcers, inhibiting pseudomembrane formation and accelerating tissue regeneration without causing secondary damage. Consequently, this distinctive Janus patch, characterized by prolonged adhesion, efficient lubrication, and simple preparation, holds significant potential for clinical oral ulcer treatment. Statement of SignificanceOral ulcers, with healing impeded by secondary injury and bacterial invasion due to the absence of protective barriers, are highly prevalent and recurrent. However, sustaining therapeutic materials and physical barriers in the highly dynamic and moist oral environment poses a considerable challenge. In this study, a Janus patch (ANSB) that integrated a soft wet adhesive layer and a tough lubricating layer was developed to reconstruct a new protective barrier thus preventing external stimuli such as secondary damage and bacterial infiltration. This innovative patch with high therapeutic potential for oral ulcers may offer a new way for ulcer treatment based on barrier protection.

Boosting photothermal conversion through array aggregation of metalloporphyrins in bismuth-based coordination frameworks.

Materials capable of efficiently converting near-infrared (NIR) light into heat are highly sought after in biotechnology. In this study, two new three-dimensional (3D) porphyrin-based metal-organic frameworks (MOFs) with a sra-net, viz. CoTCPP-Bi/NiTCPP-Bi, were successfully synthesized. These MOFs feature bismuth carboxylate nodes interconnected by metalloporphyrinic spacers, forming one-dimensional (1D) arrays of closely spaced metalloporphyrins. Notably, the CoTCPP-Bi exhibits an approximate Co⋯C distance of 3 Å, leading to enhanced absorption of NIR light up to 1400 nm due to the presence of strong interlayer van der Waals forces. Furthermore, the spatial arrangement of the metalloporphyrins prevents axial coordination at the centers of porphyrin rings and stabilizes a CoII-based metalloradical. These characteristics promote NIR light absorption and non-radiative decay, thereby improving photothermal conversion efficiency. Consequently, CoTCPP-Bi can rapidly elevate the temperature from room temperature to 190 °C within 30 seconds under 0.7 W cm-2 energy power from 808 nm laser irradiation. Moreover, it enables solar-driven water evaporation with an efficiency of 98.5% and a rate of 1.43 kg m-2 h-1 under 1 sun irradiation. This research provides valuable insights into the strategic design of efficient photothermal materials for effective NIR light absorption, leveraging the principles of aggregation effect and metalloradical chemistry.

Perovskite quantum dots/WSe2 mixed-dimensional van der Waals heterostructure for photoelectric enhancement and polarization sensitivity

The performance of some heterostructures based devices is limited by strong interlayer coupling and limited electronic structure modulation. Meanwhile, the detection of polarized light holds great significance in future photoelectric fields such as cryptography. In this work, zero-dimensional/two-dimensional (0D/2D) mixed-dimensional van der Waals heterostructure (MvdWH) polarization-sensitive photodetector composed of solution-synthesized CH3NH3PbI3(MAPbI3) perovskite quantum dots (QDs) and chemical vapor deposition (CVD)-grown WSe2 was designed, forming a type II band structure. The MvdWH effectively enhance the carrier transmission rate, and improve the efficiency of charge separation, realizing an ultra-high responsiveness of 217.8 A/W and an ultrasensitive photodetectivity of 2.56 × 1011 Jones under 633 nm illumination. The device shows ultra-fast response times of 4.5/4.9 μs, which is due to the introduction of 0D QDs will shorten the electron transport path and reduces trap-mediated non-radiative recombination. Further, the in-plane anisotropy of MAPbI3 QDs was identified by angle-resolved absorption spectroscopy and angle-resolved polarization Raman spectroscopy, respectively. The MAPbI3/WSe2 device exhibits polarization-sensitive optoelectronic detection with an anisotropy ratio of 1.71, and powerful polarization-sensitive imaging ability, implying that MAPbI3 QDs endows the device with polarization detection and imaging capabilities. These results indicate that the construction of 0D/2D MvdWH opens a new avenue for ultrasensitive and polarization-sensitive photodetection, which depicts opportunities for designing multifunctional, high-performance imaging optoelectronic devices.

Dissolution process and mechanism of montmorillonite in oxalic acid and sulfuric acid media at various pH levels

The dissolution of silicate minerals plays a crucial role in many natural geological processes. In order to better comprehend the reaction mechanisms and dissolution characteristics of montmorillonite in different acidic systems, the effects of interfacial reactions of montmorillonite with oxalic and sulfuric acid solutions at various pH levels on the ionic dissolution, crystal structure, and micro-morphology were studied, and the morphology of aluminum and saturation index of secondary mineral were simulated. It was shown that the dissolution amounts of Mg2+, Al3+ and Si4+ in montmorillonite structure decreased with the increase of pH value, which reflected the dependence of montmorillonite dissolution on the pH value of solution. The dissolution percentages of Mg2+, Al3+ and Si4+ after the reaction of montmorillonite with oxalic acid solution were greater than those in sulfuric acid solution, and the highest dissolution rate of Al3+, indicated that both ligands and protons attacked the surface sites of montmorillonite and accelerated the dissolution of ions. Moreover, oxalate ligands exerted specific binding effects on Al3+ ions. While reacting with oxalate and sulfate, the tetrahedral, octahedral and interlayer cations of montmorillonite exhibited the non-stoichiometric and inconsistent dissolution. The oxalate ligands have a strong complexation effect on Al3+, so that Al3+ in oxalate solution exists in the form of aluminum oxalate complex, which reduces the effective concentration of Al3+ in solution and promotes the dissolution of Al3+ in montmorillonite structure. The Mg2+ ions settled at octahedral substitution sites possessed weak stability, while those from the interlayer featured strong interlayer interchangeability, demonstrating the dissolution percentage up to 10.85 % and 8.62 % even in oxalic and sulfuric acid solutions at pH of 6.5. All secondary mineral phases in the solution were undersaturated, making the montmorillonite dissolution difficult to balance. Montmorillonite has a high cation exchange capacity, which makes it have a strong buffer capacity to exogenous acids. This study helps to explain the dissolution process of montmorillonite in inorganic and organic acid solutions at different pH value.

Quenched Pair Breaking by Interlayer Correlations as a Key to Superconductivity in La_{3}Ni_{2}O_{7}.

The recent discovery of superconductivity in La_{3}Ni_{2}O_{7} with T_{c}≃80 K under high pressure opens up a new route to high-T_{c} superconductivity. This material realizes a bilayer square lattice model featuring a strong interlayer hybridization unlike many unconventional superconductors. A key question in this regard concerns how electronic correlations driven by the interlayer hybridization affect the low-energy electronic structure and the concomitant superconductivity. Here, we demonstrate using a cluster dynamical mean-field theory that the interlayer electronic correlations (IECs) induce a Lifshitz transition resulting in a change of Fermi surface topology. By solving an appropriate gap equation, we further show that the leading pairing instability, s± wave, is enhanced by the IECs. The underlying mechanism is the quenching of a strong ferromagnetic channel, resulting from the Lifshitz transition driven by the IECs. Based on this picture, we provide a possible reason of why superconductivity emerges only under high pressure.

Flexible and high-strength MXene/polyimide nanofiber aerogel membranes achieving infrared stealth through combined thermal control and low emissivity

The development of high-performance infrared stealth materials has been a long-standing goal for scientists. Despite their excellent performance, these materials are challenging to fabricate. In this work, a simple water immerse-stacking assembly process is employed to transform two-dimensional nanofiber membranes into three-dimensional aerogel membranes. Directional freezing from different directions induced varied orientations in the polyimide nanofibers (PINF), leading not only to unique anisotropic microstructures and thermal conductivities but also to synergistic enhancements in thermal insulation and mechanical properties. By vacuum-assisted filtration, MXene is embedded into the PINF membrane, resulting in a low emissivity of 0.283 and strong interlayer bonding of the MXene/PINF aerogel membrane without affecting the high and low-temperature resistance, the tensile strength, and the flexibility. Inspired by the art of origami, two types of MXene/PINF aerogel membrane bags are developed. When using one of the bags to cover an object at 130.2 °C, the thermal radiation temperature decreases to 28.9 °C. This study provides a promising approach for designing flexible, high-strength, and efficient infrared stealth composite materials, paving the way for further research and applications.

Van Hove Singularity-Enhanced Raman Scattering and Photocurrent Generation in Twisted Monolayer-Bilayer Graphene.

Twisted monolayer-bilayer graphene (TMBG) has recently emerged as an exciting platform for exploring correlated physics and topological states with rich tunability. Strong light-matter interaction was realized in twisted bilayer graphene, boosting the development of broadband graphene photodetectors from the visible to infrared spectrum with high responsivity. Extending this approach to the case of TMBG will help design advanced quantum nano-optoelectronic devices because of the reduced symmetry of the system. Here, we observe the formation of van Hove singularities (VHSs) in TMBG by monitoring the significant enhancement of the Raman intensity of the G peak and the intensity ratio of G and 2D peaks. The strong interlayer coupling also leads to the appearance of twist-angle-dependent Raman R and R' peaks in TMBG. Furthermore, the constructed graphene photodetectors from 13.5°-TMBG show significantly enhanced photoresponsivity (∼31 folds of monolayer graphene and ∼15 folds of trilayer graphene) when the energy of incident photons matches the interval energy between the two VHSs in the conduction and valence bands. Our findings establish TMBG as a tunable platform for investigating the light-matter interaction and designing high-performance graphene photodetectors with combined high responsivity and high selectivity.

Conductive three-layer-stacked polycrystalline graphene intercalated with FeCl3

Graphene has attracted attention as a new transparent conductive film (TCF) because of its transparency, stability, strength, and versatility. However, it has a higher resistance than conventional TCFs. Recently, vapor transport intercalation with doping effect materials has been investigated to reduce the resistivity of graphene. Studies have revealed a correlation between the stacking structure and the intercalation efficiency, which favors smaller interactions between the graphene layers. In this study, polycrystalline graphene, which consists of small domains, grown by chemical vapor deposition is stacked in three layers using a layer-by-layer method, and the graphene layers are intentionally randomly stacked to suppress the interlayer interactions. Intercalation of FeCl3, which has p-type doping effects, into randomly stacked three-layer graphene (3LG) significantly reduces the sheet resistance (Rs) of 3LG from 500 to 41 Ω/sq. Interestingly, Raman mapping of the G peak shift of FeCl3 intercalated into randomly stacked 3LG indicates that in-plane intercalation proceeds homogeneously, even though strong interlayer interactions such as AB stacking are observed in some parts of 3LG. This study reveals that a randomly stacked polycrystalline graphene layer is advantageous for intercalation.

De novo contrived three-in-one oriented graft molecule for high-performance GO nanofiltration membranes with ultra-low friction 2D nanochannels

The realistic application promotion of two-dimensional graphene oxide (GO) membranes is hampered by the trade-off between permeance and stability due to the mismatching nanochannel structure and wall chemistry enabled by the current decoration strategy. To address this, we de novo contrive a three-in-one oriented graft molecule, 1-(3-aminopropyl)-2,3-dimethylimidazolium bromide. In this compound, amino groups can reduce GO while acting as covalently grafting sites, thereby expanding the graphene region and decreasing the molecular transport resistance. Imidazolium cation moieties can interact with oxygen-containing groups of GO to enhance membranes’ anti-swelling ability. The whole molecules act as pillars to maintain the interlayer spacing. The modified GO (AIMGO) membranes show one-order-of-magnitude permeance improvements over GO membranes, with equally promising rejections. Furthermore, AIMGO membranes display ideal stability, remaining intact after 20-day water and ethanol immersion, unlike rapidly swollen GO membranes. AIMGO membranes are effective in the realistic pharmaceutical area achieving a separation factor of 9.8, with ethanol permeance of 513 L m−2 h−1 bar−1, which far exceeds the state-of-the-art polymeric membranes for drug purification. Herein, we highlight the rational combination of wide interlayer distance, low wall friction, and strong interlayer interactions to establish an efficient pathway for overcoming the permeance-stability trade-off in GO membranes and other two-dimensional membranes.

The frustrated bilayer Ising model: A cluster mean-field approach

We investigate the Ising model on the bilayer square lattice with antiferromagnetic interactions between first-(J1) and second-neighbors (J2) inside each layer and a perpendicular antiferromagnetic interaction (Jp) between layers. The roles of frustration and interlayer interactions on the thermal phase transitions are described within a variational cluster mean-field (CMF) approach. For J2/J1<1/2, the model exhibits a Néel antiferromagnetic (AF) ground state and, for J2/J1>1/2, a stripe antiferromagnetic (SAF) ground state takes place. In the absence of interlayer interactions, a tricritical point is found in the phase boundary between SAF and paramagnetic (PM) phases. Our CMF calculations show that the ordering temperature of both AF and SAF phases is enhanced by the interlayer couplings. We also show that, at different levels of frustration, in the strong-interlayer-coupling limit, the ordering temperature is twice the one in the absence of interlayer interactions. At the weak-interlayer-coupling limit, a linear dependence of the ordering temperature with the interlayer interaction is observed, which indicates a shift exponent ϕ=1. Our investigation revealed that the model exhibits tricriticality at all strengths of the interlayer interactions, but the coupling coordinate of the tricritical point (J2/J1)t exhibits a minimum at a finite strength of Jp/J1. However, in the strong interlayer coupling limit, the coupling coordinate of the tricritical point is the same as in the decoupled (Jp=0) limit. Therefore, our CMF study reveals a persistent tricriticality in the frustrated bilayer Ising model.

Covalent triazine framework nanosheets for photo-enhanced uranium extraction

Uranium extraction is the cornerstone of the sustainable development of the nuclear industry. Although a variety of porous framework materials for uranium extraction have been explored over the past few decades, almost all of them have been limited to bulk powder materials. In particular, due to the strong interlayer π-π interaction, the specific recognition sites and photocatalytic active centers of bulk two-dimensional framework materials are severely buried, resulting in the inability to exploit the optimal performance of the materials. In this study, a novel hydroquinone modified covalent triazine frame nanosheets (H-CTF-NSs) is reported for the first time, which is designed for specific extraction and photocatalytic reduction of uranium. The densely distributed hydroquinone and triazine units in the H-CTF-NSs synergistically form high-affinity binding sites, and the ultrathin nanosheets facilitate the exposure of binding sites and catalytically active centers, and accelerate the diffusion of uranyl ions, it is ideally suited as an advanced platform for the selective extraction and efficient reduction of U(VI). Remarkably, H-CTF-NSs demonstrated an unprecedented uranium extraction capacity of 3230.3 mg/g, which is almost 1.71 times that of its bulk counterpart H-CTF, making it one of the best uranium-trapping photocatalysts known to date.

Large-scale 2D heterostructures from hydrogen-bonded organic frameworks and graphene with distinct Dirac and flat bands

The current strategies for building 2D organic-inorganic heterojunctions involve mostly wet-chemistry processes or exfoliation and transfer, leading to interface contaminations, poor crystallizing, or limited size. Here we show a bottom-up procedure to fabricate 2D large-scale heterostructure with clean interface and highly-crystalline sheets. As a prototypical example, a well-ordered hydrogen-bonded organic framework is self-assembled on the highly-oriented-pyrolytic-graphite substrate. The organic framework adopts a honeycomb lattice with faulted/unfaulted halves in a unit cell, resemble to molecular “graphene”. Interestingly, the topmost layer of substrate is self-lifted by organic framework via strong interlayer coupling, to form effectively a floating organic framework/graphene heterostructure. The individual layer of heterostructure inherits its intrinsic property, exhibiting distinct Dirac bands of graphene and narrow bands of organic framework. Our results demonstrate a promising approach to fabricate 2D organic-inorganic heterostructure with large-scale uniformity and highly-crystalline via the self-lifting effect, which is generally applicable to most of van der Waals materials.

Infrared Photodetector Based on van der Waals MoS2/MoTe2 Hetero‐Bilayer Modulated by Photogating

AbstractPhotodetectors based on 2D hetero‐bilayers can overcome the bandgap limitations of individual 2D monolayers and operate at relatively long wavelengths. However, ultra‐low light absorptions within hetero‐bilayers result in extremely weak photoresponsivity. Here, an infrared photodetector based on the MoS2/MoTe2 type‐II hetero‐bilayer is demonstrated to reach a photoresponsivity of 0.55 A W−1 at 1550 nm, well beyond energy band cut‐offs of monolayer MoS2 and MoTe2, primarily resulted from the photogating effect. Raman and photoluminescence (PL) spectroscopy reveal strong interlayer couplings in the hetero‐bilayer, and a broad PL peak around 1550 nm is observed that is ascribed to interlayer transitions of carriers. The photodetector showcases a broadband detection capability from 1100 to 1700 nm, with a peak at 1550 nm corresponding to the interlayer absorption. Electrical characterization of the hetero‐bilayer‐based field‐effect transistor and kelvin probe force microscopy reveal efficient interlayer hole transfer. The highly responsive MoS2/MoTe2 infrared photodetector offers a large photo‐gain of ≈103 and a time constant of 130 ms. The research illuminates how interlayer transitions affect 2D hetero‐bilayer‐based photodetectors and advances the utilization of layered semiconductor heterostructures.

Strong interlayer magnetic exchange coupling in La3Ni2O7−δ revealed by inelastic neutron scattering

After several decades of studies of high-temperature superconductivity, there is no compelling theory for the mechanism yet; however, the spin fluctuations have been widely believed to play a crucial role in forming the superconducting Cooper pairs. The recent discovery of high-temperature superconductivity near 80 K in the bilayer nickelate La3Ni2O7 under pressure provides a new platform to elucidate the origins of high-temperature superconductivity. We perform elastic and inelastic neutron scattering studies on a polycrystalline sample of La3Ni2O7−δ at ambient pressure. No magnetic order can be identified down to 10 K. The absence of long-range magnetic order in neutron diffraction measurements may be ascribed to the smallness of the magnetic moment. However, we observe a weak flat spin-fluctuation signal in the inelastic scattering spectra at ∼ 45 meV. The observed spin excitations could be interpreted as a result of strong interlayer and weak intralayer magnetic couplings for stripe-type antiferromagnetic orders. Our results provide crucial information on the spin dynamics and are thus important for understanding the superconductivity in La3Ni2O7.

Earth-Abundant Kaolinite Nanoplatelet Gel Electrolytes for Solid-State Lithium Metal Batteries.

Lithium-ion batteries are the leading energy storage technology for portable electronics and vehicle electrification. However, demands for enhanced energy density, safety, and scalability necessitate solid-state alternatives to traditional liquid electrolytes. Moreover, the rapidly increasing utilization of lithium-ion batteries further requires that next-generation electrolytes are derived from earth-abundant raw materials in order to minimize supply chain and environmental concerns. Toward these ends, clay-based nanocomposite electrolytes hold significant promise since they utilize earth-abundant materials that possess superlative mechanical, thermal, and electrochemical stability, which suggests their compatibility with energy-dense lithium metal anodes. Despite these advantages, nanocomposite electrolytes rarely employ kaolinite, the most abundant variety of clay, due to strong interlayer interactions that have historically precluded efficient exfoliation of kaolinite. Overcoming this limitation, here we demonstrate a scalable liquid-phase exfoliation process that produces kaolinite nanoplatelets (KNPs) with high gravimetric surface area, thus enabling the formation of mechanically robust nanocomposites. In particular, KNPs are combined with a succinonitrile (SN) liquid electrolyte to form a nanocomposite gel electrolyte with high room-temperature ionic conductivity (1 mS cm-1), stiff storage modulus (>10 MPa), wide electrochemical stability window (4.5 V vs Li/Li+), and excellent thermal stability (>100 °C). The resulting KNP-SN nanocomposite gel electrolyte is shown to be suitable for high-rate rechargeable lithium metal batteries that employ high-voltage LiNi0.8Co0.15Al0.05O2 (NCA) cathodes. While the primary focus here is on solid-state batteries, our strategy for kaolinite liquid-phase exfoliation can serve as a scalable manufacturing platform for a wide variety of other kaolinite-based nanocomposite applications.

High‐performance electromagnetic shielding composite materials based on carbon nanotubes and Sandwich laminate structures

AbstractCarbon fiber‐reinforced composite materials exhibit excellent mechanical and electromagnetic shielding capabilities. However, they have some drawbacks, such as high cost and significant reflection losses. In order to address these shortcomings, this study set out to design a sandwich‐structured composite material and produce a composite material designed for electromagnetic shielding using Vacuum Assisted Resin Transfer Molding (VARTM) technology. This composite material promotes the “absorption‐reflection‐reabsorption” process of electromagnetic waves, significantly enhancing its shielding effectiveness, achieving up to 59.4 dB of shielding effect in the 8.2–12.4 GHz (X‐band) range. The study also employed carbon nanotubes (CNTs) matrix doping to modify the composite material, significantly reducing reflection losses. When the amount of carbon nanotubes added reaches 0.6 wt%, the overall SE can be increased by 18%. Additionally, the introduction of CNTs significantly improves the flexural strength and tensile strength of the composite material; at a 0.6 wt% CNT content, the average tensile strength increased from 526.4 to 600.9 MPa, indicating good interfacial interactions between CNTs and epoxy resin. This work provides valuable insights for the preparation of high‐performance electromagnetic shielding materials, with profound theoretical and practical significance.Highlights Observations through SEM and CT scanning techniques reveal that Vacuum Assisted Resin Transfer Molding (VARTM) technology facilitates strong interlayer bonding between carbon fibers, glass fibers, and copper wires, alongside effective epoxy resin adhesion, thus enhancing the mechanical properties. The sandwich structure's impedance mismatch characteristic facilitates an efficient “absorption‐reflection‐reabsorption” process of electromagnetic waves. Additionally, the incorporation of Carbon Nanotubes (CNTs) enhances the absorption mechanism, reducing reflection losses. Incorporating CNTs further boosts both flexural and tensile strengths, attributed to improved interfacial interactions inhibiting crack formation.

Dynamical chiral Nernst effect in twisted Van der Waals few layers

The Nernst effect is a fundamental thermoelectric conversion phenomenon that was deemed to be possible only in systems with magnetic field or magnetization. In this work, we propose a novel dynamical chiral Nernst effect that can appear in two-dimensional van der Waals materials with chiral structural symmetry in the absence of any magnetic degree of freedom. This unconventional effect is triggered by time variation of an out-of-plane electric field, and has an intrinsic quantum geometric origin linked to not only the intralayer center-of-mass motion but also the interlayer coherence of electronic states. We demonstrate the effect in twisted homobilayer and homotrilayer transition metal dichalcogenides, where the strong twisted interlayer coupling leads to sizable intrinsic Nernst conductivities well within the experimental capacity. This work suggests a new route for electric control of thermoelectric conversion.