Guiding nitrogen doped vanadium pentoxide nanoclusters on cobalt sulfide nano-flakiness as stable seamless interface anode toward highly energy density and durable asymmetric supercapacitors.

Interaction of the interface-heterostructures is crucial to rapid ionic conductivity and highly energy density of electrode materials toward supercapacitors. Herein, a novel anode heterostructure is synthesized using cobalt sulfide (CoS) nanoflowers as a substrate for composite nitrogen doped vanadium pentoxide (denoted as N-V2O5@CoS) by combination of hydrothermal and calcination method. As expected, the N-V2O5@CoS electrode possesses superhigh specific surface area that significantly enhances the specific capacitance, and its unique porous interconnected structure not only reduces the volume effect during the cycles, but also greatly enhances the conductivity of electron transfer. The as-prepared N-V2O5@CoS electrode has a specific capacitance of up to 2413.6F/g at a current density of 1 A/g, and can still maintain 87.51 % of the initial capacitance after 5,000 cycles at a high current density of 10 A/g. More importantly, the partial density of states (PDOS) ares obtained through theoretical calculations reveal that the interaction of heterogeneous interfaces is contributed by the p-orbitals of C, O and S and d-orbitals of V and Co. In addition, asymmetric supercapacitor (ASC) with N-V2O5@CoS as the positive electrode and activated carbon (AC) as the negative electrode has a high voltage of 1.7 V, which achieves an outstanding energy density of 71.6 W h kg-1 at a power density of 849.8 W kg-1, showing excellent cycle stability (retain 90.6 % of the initial capacitance after 10,000 charge/discharge cycles). This paper offers novel paradigm for the doping of metal oxides and the development of heterostructures, which provides support for their use as advanced energy storage materials.

Lattice Strain Regulated by Hetero/homo Atom Interface Merging on NiMo Nanocluster for High-performance Hydrogen Production.

Lattice strain engineering represents a cutting-edge approach capable of delivering enhanced performance across various applications. The lattice strain can affect the performance of electrochemical catalysts by changing the binding energy between the surface-active sites and intermediates. In this work, lattice strain is regulated through a homo/heterogeneous atomic interface merging. The strong lattice strain and electronic interactions between Ni and Mo facilitated the reaction kinetic of HER. The prepared NiMo/SSM exhibiting excellent HER catalytic performance with 70 mV overpotential at the current density of 10 mA cm-2 and long-term stability. The method of controlling lattice strain through hetero/homo atom interface merging provides a new strategy for designing high-performance alkaline HER electrocatalysts.

Crystalline-Amorphous IrOx Supported on Perovskite Nanotubes for pH-Universal OER.

Designing catalysts with desirable oxygen evolution reaction (OER) performance under pH-universal conditions is of great significance to promote the development of hydrogen production. Herein, we successfully synthesized a crystalline-amorphous IrOx supported on perovskite oxide nanotubes to obtain IrOx@La0.6Ca0.4Fe0.8Ni0.2O3 with superior OER performance in whole pH media. The overpotential of the IrOx@La0.6Ca0.4Fe0.8Ni0.2O3 catalyst in media of pH 14, 7.2, and 1 has been demonstrated to be 120, 400, and 143 mV, respectively, with no significant element dissolution as well as double-layer capacitance decay after the durability test. Through comparative experiments with IrOx@CNT and the physical mixture of IrOx and La0.6Ca0.4Fe0.8Ni0.2O3, it is found that the strong metal-support interaction (SMSI) in IrOx@La0.6Ca0.4Fe0.8Ni0.2O3 makes IrOx exist in an amorphous state rich in Ir3+, which is closely associated with the surface-active species Ir-OH. Through the regulation of Ir by a perovskite oxide support at the heterointerface, the reaction breaks through the limitation of the adsorbate evolution mechanism (AEM) and converts to a lattice-oxygen-mediated mechanism (LOM), which was fully demonstrated by the addition of the probe tetramethylammonium cation (TMA+), a LOM reaction intermediate, to the electrolyte. This work fills the research gap of perovskite oxide supported Ir-based catalysts with heterogeneous structures, providing an excellent strategy for the structural design of efficient pH-universal OER catalysts for hydrogen production systems.

Mechanical and Electrical Conductivity Properties of Graphene/Cu Interfaces: A Theoretical Insight.

For graphene/copper (Gr/Cu) composites, achieving high-quality interfaces between Gr and Cu (strong interfacial bonding strength and excellent electron transport performance) is crucial for enabling their widespread applications in electronic devices. This study employs first-principles calculations and the nonequilibrium Green's function method to systematically investigate the mechanical and electrical conductivity properties of Cu(111)/Gr/Cu(111) interfaces with various stacking sequences and different forms of Gr. For these interface systems, the binding energy, separation work, charge transfer, and electrical conductivity across the interface were obtained. The results show that the top-fcc interface exhibits superior interfacial properties, characterized by relatively high binding energy (-3.00 eV/C atom) and separation work (≥0.78 J/m2), a small interfacial distance (2.85 Å), and enhanced electron transport capacity (2.12 G0/nm2). A bilayer form of Gr significantly reduces electronic conductance across the Gr/Cu interface by nearly 2.46 orders of magnitude. Furthermore, point defects in Gr, especially single-vacancy defects, disrupt the traditional trade-offs between mechanical and electrical performance, simultaneously enhancing mechanical performance by 7.50-124.36% and electrical performance by 33.02%. Additionally, stress mechanisms have been proposed to further enhance the interfacial electrical conductivity of Gr/Cu composites. The present study provides a theoretical basis for exploring the engineering applications of Gr/Cu composite materials.

Construction of 0-dimensional silver quantum dot/MoSe2@MXene/3-dimensional porous copper foam composite electrodes with heterogeneous interfaces for synergistic electrocatalytic degradation of antibiotics.

This study proposes a novel and efficient Ag quantum dots (QDs)/MoSe2@two-dimensional transition metal carbide/nitride (MXene)/copper foam (CF) composite electrode to address the challenge of electrocatalytic degradation of antibiotics in water. The electrode formed a unique electron donor-acceptor system by loading Ag QDs and heterostructured nanosheets on CF, significantly facilitating charge transfer and segregation at the interface. The catalytically active sites at the edges and defective locations of MoSe2 in conjunction with the two-dimensional MXene structure, which formed an efficient electron transfer channel, promoted the electron transfer from the interior to the surface and accelerated the hydrogen adsorption and reduction reactions. Moreover, the charge redistribution at the interface of Ag QDs and MoSe2@MXene formed interfacial dipoles, increasing the active sites on the catalyst surface and promoting the generation of cathodic atomic hydrogen (H*). Under optimal conditions, the degradation rate of tigecycline (TGC) reached as high as 90.1 % ± 2.4 % within 60 min. The anode-generated OH and HClO, along with the cathode-generated H, further promoted the degradation of TGC through co-catalysis. The degradation pathways were analyzed using density-functional theory (DFT) calculations and liquid chromatography-mass spectrometry (LC-MS) techniques. Moreover, toxicity analysis of the degradation products was carried out to ensure the safety of the treated wastewater discharge. A reflux continuous effluent reactor was also designed to achieve high degradation efficiency and low energy consumption after stable operation, laying the foundation for industrial applications. This technology provides new ideas for the design of green, efficient, stable, and low-consumption electrocatalytic reactors and contributes to a sustainable future environment.

Phase Engineering-Mediated D-Band Center of Ru Sites Promote the Hydrogen Evolution Reaction Under Universal pH Condition.

The rational design of pH-universal electrocatalyst with high-efficiency, low-cost and large current output suitable for industrial hydrogen evolution reaction (HER) is crucial for hydrogen production via water splitting. Herein, phase engineering of ruthenium (Ru) electrocatalyst comprised of metastable unconventional face-centered cubic (fcc) and conventional hexagonal close-packed (hcp) crystalline phase supported on nitrogen-doped carbon matrix (fcc/hcp-Ru/NC) is successfully synthesized through a facile pyrolysis approach. Fascinatingly, the fcc/hcp-Ru/NC displayed excellent electrocatalytic HER performance under a universal pH range. To deliver a current density of 10 mA cm-2, the fcc/hcp-Ru/NC required overpotentials of 16.8, 23.8 and 22.3 mV in 1 M KOH, 0.5 M H2SO4 and 1 M phosphate buffered solution (PBS), respectively. Even to drive an industrial-level current density of 500 and 1000 mA cm-2, the corresponding overpotentials are 189.8 and 284 mV in alkaline, 202 and 287 mV in acidic media, respectively. Experimental and theoretical calculation result unveiled that the charge migration from fcc-Ru to hcp-Ru induced by work function discrepancy within fcc/hcp-Ru/NC regulate the d-band center of Ru sites, which facilitated the water adsorption and dissociation, thus boosting the electrocatalytic HER performance. The present work paves the way for construction of novel and efficient electrocatalysts for energy conversion and storage.

Reinforced interfacial coupling effect of NiO/Ni2P by Fe doping for boosting water splitting.

Nickel-based catalysts are suitable for water splitting to generate hydrogen. However, the low conductivity and weak stability have always been urgent issues to be addressed in nickel-based catalysts. Fe-doped nickel oxide/nickel phosphide (Fe-NiO/Ni2P) was prepared as a bifunctional electrocatalyst by doping metal and constructing heterogeneous interface. The introduction of Fe contributed to the reinforced interfacial coupling effect of NiO/Ni2P to promote charge transfer and accelerate reaction kinetics. The heterojunction regulated the interfacial charge density between NiO and Ni2P to improve the electronic environment of Ni2+ and enhance conductivity. The O-Fe-P bond at the heterogeneous interface induced the directional transfer of electrons and ensured the structure stability. The synergistic effect of Fe doping and heterogeneous interface increased the adsorption energy of *O and coordinated the adsorption energy of *H, advancing the catalytic performance. Fe-NiO/Ni2P exhibited the overpotential of 242 mV and 141 mV at 10 mA cm-2 for oxygen and hydrogen evolution, respectively.

Platinum/Platinum Sulfide on Sulfur-Doped Carbon Nanosheets with Multiple Interfaces toward High Hydrogen Evolution Activity.

Platinum (Pt)-based materials are among the most competitive electrocatalysts for the hydrogen evolution reaction (HER) due to suitable hydrogen adsorption energy. Due to the rarity of Pt, it is desirable to develop cost-effective Pt-based electrocatalysts with low Pt loading. Herein, Pt/PtS electrocatalysts on S-doped carbon nanofilms (PPS/C) have been successfully fabricated through a precursor reduction route with a complex of Pt and 1-dodecanethiol (1-DDT) as the precursor. The PPS/C achieved at 400 °C (PPS/C-400) exhibits excellent HER performances with an ultralow overpotential of 41.3 mV, a low Tafel slope of 43.1 mV dec-1 at a current density of 10 mA cm-2, and a long-term stability of 10 h, superior to many recently reported Pt-based HER electrocatalysts. More importantly, PPS/C-400 shows a high mass-specific activity of 0.362 A mgPt-1 at 30 mV, which is 1.88 times of that of commercial 20% Pt/C (0.193 A mgPt-1). The introduction of sulfur leads to the formation of PtS, which not only reduces the content of Pt but also realizes the interface regulation of Pt/PtS, as well as the doping of carbon. Both regulations make the resulting catalyst have abundant active centers and rapid electron transfer/transport, which is conducive to balancing the adsorption and resolution of intermediate products, and finally achieving great mass-specific activity and stability. The research work may provide ideas for designing effective Pt-based multi-interface electrocatalysts.

In Situ Construction of Bimetallic Selenides Heterogeneous Interface on Oxidation-Stable Ti3C2Tx MXene Toward Lithium Storage with Ultrafast Charge Transfer Kinetics.

Ti3C2Tx (MXene) is widely acknowledged as an excellent substrate for constructing heterogeneous structures with transition metal chalcogenides (TMCs) for boosting the electrochemical performance of lithium-ion storage. However, conventional synthesis strategies inevitably lead to poor electrochemical charge transfer due to Ti3C2Tx-derived TiO2 at the heterogeneous interface between Ti3C2Tx and TMCs. Here, an innovative in situ selenization strategy is proposed to replace the originally generated TiO2 on Ti3C2Tx with metallic TiSe2 interphase, clearing the bottleneck of slow charge transfer barrier caused by MXene oxidation. The construction of bimetallic selenide formed by CoSe2 and TiSe2 generates intrinsic electric fields to guide the fast ion diffusion kinetics in a heterogeneous interface. Additionally, the CoSe2/TiSe2/Ti3C2Tx heterogeneous structure with enhanced structural stability and improved rate performance is confirmed by both experiments and theoretical calculations. The engineered heterogeneous structure exhibits an ultra-high pseudocapacitance contribution (73.1% at 0.1 mV s-1), rendering it well-suited to offset the kinetics differences between double-layer materials. The assembled lithium-ion capacitor based on CoSe2/TiSe2/Ti3C2Tx possesses a high energy density and an ultralong life span (89.5% after 10 000 times at 2 A g-1). This devised strategy provides a feasible solution for utilizing the performance advantages of MXene substrates in lithium storage with ultrafast charge transfer kinetics.

Atomic-engineered gradient tunable solid-state metamaterials.

Metamaterial has been captivated a popular notion, offering photonic functionalities beyond the capabilities of natural materials. Its desirable functionality primarily relies on well-controlled conditions such as structural resonance, dispersion, geometry, filling fraction, external actuation, etc. However, its fundamental building blocks-meta-atoms-still rely on naturally occurring substances. Here, we propose and validate the concept of gradient and reversible atomic-engineered metamaterials (GRAM), which represents a platform for continuously tunable solid metaphotonics by atomic manipulation. GRAM consists of an atomic heterogenous interface of amorphous host and noble metals at the bottom, and the top interface was designed to facilitate the reversible movement of foreign atoms. Continuous and reversible changes in GRAM's refractive index and atomic structures are observed in the presence of a thermal field. We achieve multiple optical states of GRAM at varying temperature and time and demonstrate GRAM-based tunable nanophotonic devices in the visible spectrum. Further, high-efficiency and programmable laser raster-scanning patterns can be locally controlled by adjusting power and speed, without any mask-assisted or complex nanofabrication. Our approach casts a distinct, multilevel, and reversible postfabrication recipe to modify a solid material's properties at the atomic scale, opening avenues for optical materials engineering, information storage, display, and encryption, as well as advanced thermal optics and photonics.

Ultraflexible Ultrathin 3D/1D Hierarchical Interpenetrating Ni-MOF/CNT Buckypaper Composites: Microstructures and Microwave Absorption Properties.

Metal-organic frameworks (MOFs) have attracted attention due to their designable structures. However, recently reported MOF microwave-absorbing materials (MAMs) are dominated by powders. It remains a challenge to design MOF/carbon nanotube (CNT) composite structures that combine the mechanical properties of self-supporting flexibility with excellent microwave absorption. This work involves the hydrothermal approach to grow Ni-MOF of different microstructures in situ on the CNT monofilament by adjusting the molar ratio of nickel ions to organic ligands. Subsequently, an ultraflexible self-supporting Ni-MOF/CNT buckypaper (BP) is obtained by directional gas pressure filtration technology. The BP porous skeleton and the Ni-MOF with a unique porous structure provide effective impedance matching. The CNTs contribute to the conduction loss, the cross-scale heterogeneous interface generated by Ni-MOF/CNT BP provides rich interfacial polarization loss, and the porous structure complicates the microwave propagation path. All factors work together to give Ni-MOF/CNT BP an excellent microwave absorption capacity. The minimum reflection losses of Ni-MOF/CNT BPs decorated with granular-, hollow porous prism-, and porous prism-shaped Ni-MOFs reach -50.8, -57.8, and -43.3 dB, respectively. The corresponding effective absorption bandwidths are 4.5, 6.3, and 4.8 GHz, respectively. Furthermore, BPs show remarkable flexibility as they can be wound hundreds of times around a glass rod with a diameter of 4 mm without structural damage. This work presents a new concept for creating ultraflexible self-supported MOF-based MAMs with hierarchical interpenetrating porous structures, with potential application advantages in the field of flexible electronics.

Nitrate Chemodenitrification by Iron Sulfides to Ammonium under Mild Conditions and Transformation Mechanism.

Autotrophic denitrification utilizing iron sulfides as electron donors has been well studied, but the occurrence and mechanism of abiotic nitrate (NO3-) chemodenitrification by iron sulfides have not yet been thoroughly investigated. In this study, NO3- chemodenitrification by three types of iron sulfides (FeS, FeS2, and pyrrhotite) at pH 6.37 and ambient temperature of 30 °C was investigated. FeS chemically reduced NO3- to ammonium (NH4+), with a high reduction efficiency of 97.5% and NH4+ formation selectivity of 82.6%, but FeS2 and pyrrhotite did not reduce NO3- abiotically. Electrochemical Tafel characterization confirmed that the electron release rate from FeS was higher than that from FeS2 and pyrrhotite. Quenching experiments and density functional theory calculations further elucidated the heterogeneous chemodenitrification mechanism of NO3- by FeS. Fe(II) on the FeS surface was the primary site for NO3- reduction. FeS possessing sulfur vacancies can selectively adsorb oxygen atoms from NO3- and water molecules and promote water dissociation to form adsorbed hydrogen, thereby forming NH4+. Collectively, these findings suggest that the NO3- chemodenitrification by iron sulfides cannot be ignored, which has great implications for the nitrogen, sulfur, and iron cycles in soil and water ecosystems.

Observing and Modeling the Wear Process of Heterogeneous Interface.

Understanding and controlling the wear process of heterogeneous interfaces between soft and hard phases is crucial for designing and fabricating materials, such as improving the wear resistance of particle reinforced metal matrix composites and the accuracy and efficiency of chemical mechanical polishing. However, the wear process can be hardly observed, as interfaces are buried under the surface. Here, we proposed a nanowear test method by combining focused ion beam cutting to expose interfaces, atomic force microscopy to rub against interfaces, and scanning electron microscope to characterize the interface damage. Using this method, three typical wear forms had been observed in Al/SiC composite, i.e., merely matrix wear, particle fracture, and particle pullout. A theoretical model was proposed that revealed that the increasing interfacial friction would induce particle fracture or pullout, depending on the particle edge angle and tip edge angle. This work sheds light on wear control in composites and nanofabrication.

Heterogeneous engineering and carbon confinement strategy to synergistically boost the sodium storage performance of transition metal selenides.

Transition metal selenides (TMSs) stand out as a promising anode material for sodium-ion batteries (SIBs) owing to their natural resources and exceptional sodium storage capacity. Despite these advantages, their practical application faces challenges, such as poor electronic conductivity, sluggish reaction kinetics and severe agglomeration during electrochemical reactions, hindering their effective utilization. Herein, the dual-carbon-confined CoSe2/FeSe2@NC@C nanocubes with heterogeneous structure are synthesized using ZIF-67 as the template by ion exchange, resorcin-formaldehyde (RF) coating, and subsequent in situ carbonization and selenidation. The N-doped porous carbon promotes rapid electrolyte penetration and minimizes the agglomeration of active materials during charging and discharging, while the RF-derived carbon framework reduces the cycling stress and keeps the integrity of the material structure. More importantly, the built-in electric field at the heterogeneous boundary layer drives electron redistribution, optimizing the electronic structure and enhancing the reaction kinetics of the anode material. Based on this, the nanocubes of CoSe2/FeSe2@NC@C exhibits superb sodium storage performance, delivering a high discharge capacity of 512.6 mA h g-1 at 0.5 A g-1 after 150 cycles and giving a discharge capacity of 298.2 mA h g-1 at 10 A g-1 with a CE close to 100.0 % even after 1000 cycles. This study proposes a viable method to synthesize advanced anodes for SIBs by a synergy effect of heterogeneous interfacial engineering and a carbon confinement strategy.

Construction of heterogeneous interfaces for water activation and dissociation to synergistically boost overall water splitting.

Construction of heterogeneous interfaces with dual active components to synergistically promote both hydrogen evolution reaction (HER) and oxygen evolution reaction (OER) is an effective strategy for facilitating electrochemical water splitting, but the appropriate active component regulation via simple synthesis procedures is still challenging. Herein, the Co and Co2Mo3O8 active components are screened to construct effective heterogeneous interfaces and successfully integrated on Ni foam by thermal reduction of cobalt molybdate precursor. And this bifunctional electrode (Co/Co2Mo3O8/NF) required overpotentials of only 164 and 360 mV to drive the 100 mA cm-2 for HER and OER in alkaline media, respectively. Theoretical calculations showed that the electron transfer occurred from Co to Co2Mo3O8 at the interface, then the formed interfacial cobalt atoms with deficient electron were beneficial for water activation, and reduced energy barrier of water dissociation under the synergistic effect of Co2Mo3O8. Notably, the alkaline electrolyzer based on symmetric Co/Co2Mo3O8/NF electrodes generated 100 mA cm-2 at a voltage of only 1.75 V, surpassing commercially available precious-metal Pt/RuO2-based catalysts.

Multilevel Heterogeneous Interfaces Enhanced Polarization Loss of 3D-Printed Graphene/NiCoO2/Selenides Aerogels for Boosting Electromagnetic Energy Dissipation.

Heterointerface engineering is an attractive approach to modulating electromagnetic (EM) parameters and EM wave absorption performance. However, the weak interfacial interactions and poor impedance matching would lead to unsatisfactory EM absorption performance due to the limitation of the construction materials and design strategies. Herein, multilevel heterointerface engineering is proposed by in situ growing nanosheet-like NiCoO2 and selenides with abundant interface structures on 3D-printed graphene aerogel (GA) skeletons, which strengthens the interfacial effect and improves the dielectric polarization loss. Benefiting from the features of substantially enhanced polarization loss and optimized impedance matching, the graphene/S-NiCoO2/selenides (G/S-NCO/Se) have achieved brilliant EM wave absorption performance with a strong reflection loss (RL) value of -60.7 dB and a broad effective absorption bandwidth (EAB) of 8 GHz, which is about six times greater than that of the graphene aerogel (-9.8 dB). Moreover, it is further confirmed by charge density differences and off-axis electron holography that a large amount of polarized charge accumulates at the interface, leading to significant polarization relaxation behaviors. This work provides a deep understanding of the effect of a multilevel heterogeneous interface on dielectric polarization loss, which injects a fresh and infinite vitality for designing high-efficiency EM wave absorbers.

Ultrasmall Ru nanoparticles-decorated nickel/nickel oxide three phase heterojunctions to boost alkaline hydrogen evolution.

The rational design and optimization of heterogeneous interface for low loading noble metal HER eletrocatalysts to facilitate the upscaling of alkaline water/seawater electrolysis is highly challenging. Herein, we present a facile deep corrosion strategy induced by NaBH4 to precisely construct an ultrasmall Ru nanoparticle-decorated Ni/NiO hybrid (r-Ru-Ni/NiO) with highly dispersed triple-phase heterostructures. Remarkably, it exhibits superior activity with only 53 mV and 70 mV at 100 mA cm-2 for hydrogen evolution reaction (HER) in alkaline water and seawater, respectively, surpassing the performance of Pt/C (109.7 mV, 100 mA cm-2, 1 M KOH). It is attributed to collaborative optimization of electroactive interfaces between well-distributed ultrasmall Ru nanoparticles and Ni/NiO hybrid. Moreover, the assembled r-Ru-Ni/NiO system just require 2.03 V at 1000 mA cm-2 in anion exchange membrane (AEM) electrolyzer, outperforming a RuO2/NF || Pt/C system, while exhibiting outstanding stability at high current densities. This study offers a logical design for accurate construction of interfacial engineering, showing promise for large-scale hydrogen production via electrochemical water splitting.

Island-Like Heterogeneous Interface Generating Tandem Toroidal Built-In Electric Field for Efficient Potassium Ions Diffusion.

For large-size potassium accommodation, heterostructure usually suffers severe delamination and exfoliation at the interfaces due to different volume expansion of two-phase during charge/discharge process, resulting in the deconstruction of heterostructures and shortened lifespan of batteries. Here, an innovative strategy is proposed through constructing a microscopic heterostructure system containing copper quantum dots (Cu QDs) highly dispersed in the triphenyl-substituted triazine graphdiyne (TPTG) substrates (TPTG@CuQDs) to solve this problem. The copper quantum dots are uniformly anchored on TPTG substrates, generating a myriad of island-like heterogeneous structures, together with tandem toroidal built-in electric field (BIEF) between every micro heterointerface. The island-like heterostructure endows both benefits of exposed contact interface and robust architecture. Generated tandem toroidal BIEF provides efficient transport pathways with lower energy barriers, reducing the diffusion resistance and facilitating the reaction kinetics of potassium ions. When used as anode, the TPTG@CuQDs exhibit highly reversible capacity and low-capacity degradation (≈0.01% over 5560 cycles at 1 A g-1). Moreover, the TPTG@CuQDs-based full cell delivers an outstanding reversible capacity of ≈110 mAh g-1 over 800 cycles at 1 A g-1. This quantum-scale heterointerface construction strategy offers a new approach toward stable heterostructure design for the application of metal ion batteries.

Zeolitic Imidazolate Framework-Derived Co3S4@NiFe-LDH Core-Shell Heterostructure as Efficient Bifunctional Electrocatalyst for Water Splitting.

The development of stable and efficient bifunctional electrocatalysts is of utmost importance for overall water splitting. This study introduces Co3S4@NiFe-LDH core-shell heterostructure prepared via an electrodeposition of ultrathin NiFe-LDH nanosheet on zeolitic imidazolium framework-derived Co3S4 nanosheet arrays. The bifunctional Co3S4@NiFe-LDH/NF exhibits impressive catalytic performance and long-term stability for both the OER and HER with low overpotentials of 100 mA cm-2 at 235 mV and 10 mA cm-2 at 95 mV in 1 M KOH, respectively. The assembled cell with Co3S4@NiFe-LDH/NF as both cathode and anode shows voltages of 1.595 and 1.666 V at current densities of 10 and 20 mA cm-2, respectively, as well as ultralong stability over 500 h. DFT calculations expose a robust electron interaction at the heterogeneous interface of the Co3S4@NiFe-LDH/NF core-shell structure. This interaction promotes electron transfer from NiFe-LDH to Co3S4 and reduces the energy barriers for OER intermediates, thereby enhancing electrocatalytic activity. This research contributes novel insights toward the promising materials for electrochemical water splitting through the construction of heterojunction interfaces.

Joule-Heating-Driven Synthesis of a Honeycomb-Like Porous Carbon Nanofiber/High Entropy Alloy Composite as an Ultralightweight Electromagnetic Wave Absorber.

High entropy alloys (HEA) have garnered significant attention in electromagnetic wave (EMW) absorption due to their efficient synergism among multiple components and tunable electronic structures. However, their high density and limited chemical stability hinder their progress as lightweight absorbers. Incorporating HEA with carbon offers a promising solution, but synthesizing stable HEA/carbon composite faces challenges due to the propensity for phase separation during conventional heat treatments. Moreover, EMW absorption mechanisms in HEAs may be different from established empirical models due to their high-entropy effect. This underscores the urgent need to synthesize stable and lightweight HEA/carbon absorbers and uncover their intrinsic absorption mechanisms. Herein, we successfully integrated a quinary FeCoNiCuMn HEA into a honeycomb-like porous carbon nanofiber (HCNF) using electrostatic spinning and the Joule-heating method. Leveraging the inherent lattice distortion effects and honeycomb structure, the HCNF/HEA composite demonstrates outstanding EMW absorption properties at an ultralow filler loading of 2 wt %. It achieves a minimum reflection loss of -65.8 dB and boasts a maximum absorption bandwidth of up to 7.68 GHz. This study not only showcases the effectiveness of combining HCNF with HEA, but also underscores the potential of Joule-heating synthesis for developing lightweight HEA-based absorbers.