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Cubic hollow-structured NiCo-LDH was synthesized using a solvothermal method. Subsequently, clay-like Ti3C2Tx MXenes were electrostatically self-assembled with NiCo layered double hydroxides (NiCo-LDH) to form composites featuring three-dimensional porous heterostructures. The composites were characterized using SEM, TEM, XRD, XPS, and FT-IR spectroscopy. Ti3C2Tx MXenes exhibit excellent electrical conductivity and hydrophilicity, providing abundant binding sites for NiCo-LDH, thereby promoting an increase in ion diffusion channels. The formation of three-dimensional porous heterostructural composites enhances charge transport, significantly improving sensor sensitivity and response speed. Consequently, the sensor demonstrates excellent electrochemical detection capability for quercetin (Qu), with a detection range of 0.1-20 µM and a detection limit of 23 nM. Additionally, it has been applied to the detection of Qu in natural plants such as onion, golden cypress, and chrysanthemum. The recovery ranged from 97.6 to 102.28%.

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Layered double hydroxide (LDH)-carbon composites effectively mitigate the inherent issues of agglomeration and poor conductivity in LDH. However, the weak binding energy and insufficient charge transfer capability between LDH and carbon substrate significantly compromise the active substance loading, cyclic stability and practical capacity of the composites. Herein, N/O co-doping porous carbon nanofibers (NOPCNFs) are first prepared by blending diminutive zinc imidazolate framework-8 nanoparticles with polyacrylonitrile for electrospinning, and then densely packed NiCo LDH nanosheets are homogeneously anchored on NOPCNFs to form NiCo LDH@NOPCNFs heterostructure via a hydrothermal method. The experimental findings and density functional theory calculation results indicate that N/O atoms exhibit robust binding forces with metal atoms through enhanced electrostatic adsorption and p-d covalent hybridization, which facilitates the nucleation and development of NiCo LDH on carbon nanofibers. Meanwhile, these heteroatoms also serve as the bridge for electron transfer from NiCo LDH to NOPCNF, leading to a strong interfacial electric field, thus accelerating charge transfer behaviors. Benefitting from the synergistic interaction between NiCo LDH and NOPCNF, the obtained NiCo LDH@NOPCNFs demonstrate an elevated mass loading of active substance (55 wt%), an impressive specific capacitance of 1340 F/g at 1 A/g (based on the mass of NiCo LDH, 2463 F/g), and good cyclic durability for 5000 cycles. Moreover, an all-solid-state asymmetric supercapacitor using NOPCNFs and NiCo LDH@NOPCNFs shows promising practical application prospects. This work gives insights into the important influence of heteroatom doping in carbon, and provides a feasible approach for the efficient integration of electroactive and carbon material.

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The accumulation of small doses of hydrogen peroxide (H2O2) into food can cause many diseases in the human body, and it is urgent to develop efficient detection methods of H2O2. Herein, the hierarchical structure composite of NiCo-LDH nanosheets crosslinked NiMoO4 nanorods was grown in situ on carbon cloth (NiMoO4 NRs@NiCo-LDH NSs/CC) by micro-plasma assisted hydrothermal method. Thanks to the synergistic effect of three metals and (NiMoO4 NRs@NiCo-LDH NSs/CC) provided by nanorods/nanosheets hierarchical structure, NiMoO4 NRs@NiCo-LDH NSs/CC exposes more active sites and achieves rapid electron transfer. The H2O2 electrochemical sensor was constructed as the working electrode with a linear range of 1 µmol L-1 to 9.0 mmol L-1 and detection limit of 112 nmol L-1. In addition, the sensor has been successfully applied to the detection of H2O2 in food samples, the recovery rate is 95.2%-106.62%, RSD < 4.89%.

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Nickel cobaltate/NiCo-layered double hydroxides (NiCo2O4/NiCo-LDH) as energy storage materials offer considerable potential for various applications. However, many of current methods for synthesizing NiCo2O4/NiCo-LDH suffer from long synthesis times, complex preparation process, and high temperatures and high pressures. In this study, we present a green, simple, and efficient approach known as assisted liquid-phase plasma electrolysis, which realizes the rapid fabrication of ultra-fine NiCo2O4/NiCo-LDH nanoparticle-decorated electrospun carbon nanofibers (NiCo2O4/NiCo-LDH/CNFs) composites. Ultra-fine NiCo2O4/NiCo-LDH nanoparticles (<70 nm) are uniformly deposited on the CNF surface. The CNFs are intertwined to form a highly conductive three-dimensional mesh structure, which synergizes the NiCo2O4/NiCo-LDH nanoparticles with a high specific capacitance in favor of ion/electron transport efficiency. In addition, the cooperative effect between the two phases of NiCo2O4 and NiCo-LDH further improves the electrochemical properties. The NiCo2O4/NiCo-LDH/CNFs composites exhibit a high specific capacitance of 1534.7 F/g at 1 A/g and a capacitance retention of 93.9 % after 5000 cycles. An assembled asymmetric supercapacitor using activated carbon and NiCo2O4/NiCo-LDH/CNFs composites achieves an energy density of 33.8 Wh/kg at a power density of 400 W/kg and a capacitance retention of 93.0 % after 5000 cycles. Notably, two series-connected NiCo2O4/NiCo-LDH/CNFs ASC supercapacitors can light up an LED bulb, which maintains a certain brightness even after 50 min. Hence, this work provides a new and efficient route for synthesizing carbon-based NiCo2O4/NiCo-LDH composites for use as advanced energy storage materials.

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Currently, new clean energy storage technology must be effective, affordable, and ecologically friendly so as to meet the diverse and sustainable needs of the energy supply. In this work, NiCo-LDH containing intercalated EG was successfully prepared within 210 s using an ultrafast microwave radiation technique. Subsequently, a series of characterization and systematic electrochemical tests were conducted to analyze the composition, structure, and energy storage mechanism of the NiCo-LDH material. The Ni:Co ratio of 5:5 results in the highest capacitance value of 2156 F/g at 1 A/g and an outstanding rate performance of 86.8% capacity retention rate at 10 A/g. The results demonstrated that the unique porous structure of NiCo-LDH and large layer spacing were conducive to more electrochemical reactions. Additionally, an electrochemical test was carried out on the NiCo-LDH as a hybrid supercapacitor electrode material, with NiCo-LDH-5:5 serving as the positive electrode and activated carbon as the negative electrode, the asymmetric supercapacitor can achieve a maximum energy density of 82.5 Wh kg-1 and power density of 8000 W kg-1. The NiCo-LDH-5:5//AC hybrid supercapacitors own 81.5% cycle stability and 100% coulombic efficiency after 6000 cycles at 10 A/g.

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The oxygen evolution reaction (OER) performance of NiCo LDH electrocatalysts can be improved through fluorine doping. The roles of Ni and Co active sites in such catalysts remain ambiguous and controversial. In addressing the issue, this study draws upon the molecular orbital theory and proposes the active center competitive mechanism between Ni and Co. The doped F-atoms can directly impact the valence state of metal atoms or exert an indirect influence through the dehydrogenation, thereby modulating the active center. As the F-atoms are progressively aggregate, the eg orbitals of Ni and Co transition from e2 g to e1 g, and subsequently to e0 g. The corresponding valence state elevates from +2 to +3, and then to +4, signifying an initial increase followed by a subsequent decrease in the electrocatalytic performance. Furthermore, a series of F-NiCo LDH catalysts are synthesized to verify the eg orbital occupancy analysis, and the catalytic OER overpotentials are 303, 243, 240, and 246 mV at the current density of 10 mA cm-2, respectively, which coincides well with the theoretical prediction. This investigation not only provides novel mechanistic insights into the transition and competition of Ni and Co in F-NiCo LDH catalysts but also establishes a foundation for the design of high-performance catalysts.

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Formaldehyde is susceptible to illegal addition to foodstuffs to extend their shelf life due to its antimicrobial, preservative and bleaching properties. In this study, a self-supporting "nanosheet on nanosheet" arrays electrocatalyst with core-shell heterostructure was prepared in situ by coupling NiCo layer double hydroxide with 2D ZIF derived Co-nitrogen-doped porous carbon on carbon cloth (Co-N/C@NiCo-LDH NSAs/CC). Co-N/C nanosheet arrays act as a scaffold core with good electrical conductivity, providing more NiCo-LDH nucleation sites to avoid NiCo-LDH agglomeration, thus having fast mass/charge transfer performance. While the NiCo-LDH nanosheet arrays shell with high specific surface area provide more active sites for electrochemical reactions. As an electrocatalytic sensing electrode, Co-N/C@NiCo-LDH NSAs/CC has a wide linear range of 1 µM to 13 mM for formaldehyde detection, and the detection limit is 82 nM. Besides, the sensor has been applied to the detection of formaldehyde in food samples with satisfactory results.

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Rechargeable zinc-air batteries (ZABs) have garnered attention as a viable choice for large-scale energy storage due to their advantageous characteristics, such as high energy density and cost-effectiveness. Strategies aimed at improving the kinetics of the oxygen evolution reaction (OER) through advanced electrocatalytic materials or structural designs can significantly enhance the efficiency and longevity of ZABs. In this study, we introduce a three-dimensional (3D) leaf-vein system heterojunction architecture. In this structure, NiCoO2 nanowire arrays form the central vein, surrounded by an outer leaf composed of NiCo layered double hydroxide (LDH) nanosheets. All these components are integrated onto a substrate made of Ni foam. Notably, when tested in an alkaline environment, the NiCoO2@NiCo LDH exhibited an overpotential of 272 mV at a current density of 10 mA cm-2, and extended durability evaluations over 12 h underscored its robustness at 99.76 %. The rechargeable ZABs achieved a peak power density of 149 mW cm-2. Furthermore, the NiCoO2@NiCo LDH demonstrated stability by maintaining high round-trip efficiencies throughout more than 680 cycles (equivalent to 340 h) under galvanostatic charge-discharge cycling at 5 mA cm-2. The leaf-vein system heterojunction significantly increased the active sites of the catalysts, facilitating charge transport, improving electronic conductivity, and enhancing overall stability.

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Reaction kinetics can be improved by the enhanced electrical contact between different components growing symbiotically. But so far, due to the necessity for material synthesis conditions match, the component structures of cooperative growth are similar, and the materials are of the same type. The collaborative growth of high-reaction kinetics composite homogeneous core-shell heterostructure between various materials is innovatively proposed with different structures in one step. The NiCo-LDH and PPy successfully symbiotically grow on activated carbon fiber fabric in one step. The open channel structure of the NiCo-LDH nanosheets is preserved while PPy effectively wrapped around the NiCo-LDH. The well-defined nanostructure with abundant active sites and convenient ion diffusion paths is favorable for electrolyte entry into the entire nanoarrays. In addition, owing to the enhanced electronic interaction between different components through XPS analysis, the NiCo-LDH@PPy electrode shows outstanding reaction kinetics and structural stability. The as-synthesized NiCo-LDH@PPy exhibited excellent super-capacitive storage capabilities, robust capacitive activity, and good rate survival. Furthermore, an asymmetric supercapacitor (ASC) device made of NiCo-LDH@PPy and activated carbon (AC) is able to maintain a long cycle life while achieving high power and energy densities.

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Defect engineering through modification of their surface linkage is found to be an effective pathway to escalate the solar energy conversion efficiency of metal-organic frameworks (MOFs). Herein, defect engineering using controlled decarboxylation on the NH2-UiO-66 surface and integration of ultrathin NiCo-LDH nanosheets synergizes the hydrogen evolution reaction (HER) under a broad visible light regime. Diversified analytical methods including positron annihilation lifetime spectroscopy were employed to investigate the role of Zr3+-rich defects by analyzing the annihilation characteristics of positrons in NH2-UiO-66, which provides a deep insight into the effects of structural defects on the electronic properties. The progressively tuned photophysical properties of the NiCo-LDH@NH2-UiO-66-D-heterostructured nanocatalyst led to an impressive rate of HER (∼2458 µmol h-1 g-1), with an apparent quantum yield of ∼6.02%. The ultrathin NiCo-LDH nanosheet structure was found to be highly favored toward electrostatic self-assembly in the heterostructure for efficient charge separation. Coordination of Zr3+ on the surface of the NiCo-LDH nanosheet support through NH2-UiO-66 was confirmed by X-ray absorption spectroscopy and electron paramagnetic resonance spectroscopy techniques. Femtosecond transient absorption spectroscopy studies unveiled a photoexcited charge migration process from MOF to NiCo-LDH which favorably occurred on a picosecond time scale to boost the catalytic activity of the composite system. Furthermore, the experimental finding and HER activity are validated by density functional theory studies and evaluation of the free energy pathway which reveals the strong hydrogen binding over the surface and infers the anchoring effect of the ultrathin layered double hydroxide (LDH) in the vicinity of the Zr cluster with a strong host-guest interaction. This work provided a novel insight into efficient photocatalysis via defect engineering at the linker modulation in MOFs.

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Layered double hydroxides (LDHs) have come to the foreground recently, considering their unique layered structure and short ion channels when they act as electrode materials for supercapacitors (SCs). However, due to their poor rate and cycle performance, they are not highly sought after in the market. Therefore, a flower-like hierarchical NiCo-LDH@C nanostructure with flake NiCo-LDH anchored on the carbon skeleton has emerged here, which is constructed by calcination and hydrothermal reaction and applying flake ZIF-67 as a precursor. In this structure, NiCo-LDH grows outward with abundant and homogeneously distributed Co nanoparticles on Co@C as nucleation sites, forming a hierarchical structure that is combined tightly with the carbon skeleton. The flower-like hierarchical nanostructures formed by the composite of metal-organic frameworks (MOFs) and LDHs have successfully enhanced the cycle and rate performance of LDH materials on the strength of strong structural stability, large specific surface area, and unique cooperative effect. The NiCo-LDH@C electrode displays superb electrochemical performance, with a specific capacitance of 2210.6 F g-1 at 1 A g-1 and 88.8% capacitance retention at 10 A g-1. Furthermore, the asymmetric supercapacitor (ASC) constructed with NiCo-LDH@C//RGO reveals a remarkable energy density of 45.02 W h kg-1 with a power density of 799.96 W kg-1. This project aims to propose a novel avenue to exploit NiCo-LDH electrode materials and provide theory and methodological guidance for deriving complex structures from MOF derivatives.

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It is necessary to efficient detection hydrazine in food. Exploring highly sensitive, low-cost and fast response electrochemical hydrazine sensing methods has been a challenge in this field. In this paper, a conformal transformation method is used to prepare rose flower-like NiCo-LDH derivating from the bimetallic NiCo-MOFs, and the N2H4 sensing platform with a large electrocatalytic area, high conductivity and good stability was constructed. Based on the synergy between Ni and Co and the remarkable catalytic activity of the rough 3D flower-like structure, the N2H4 sensor has a linear response in the concentration range of 0.001-1 mmol/L and 1-7 mmol/L, with a sensitivity of 5342 µA L mmol-1 cm-2 and 2965 µA L mmol-1 cm-2 (S/N = 3), respectively, and low limit of detection of 0.043 µmol/L. This study opens a new door for the successful application of electrochemical sensors to detect N2H4 in real food samples.

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RESUMEN

Two-step water electrolysis has been proposed to tackle the ticklish H2/O2 mixture problems in conventional alkaline water electrolysis recently. However, low buffering capacity of pure nickel hydroxide electrode as redox mediator limited practical application of two-step water electrolysis system. A high-capacity redox mediator (RM) is urgently needed to permit consecutive operation of two-step cycles and high-efficiency hydrogen evolution. Consequently, a high mass-loading cobalt-doped nickel hydroxide/active carbon cloth (NiCo-LDH/ACC) RM is synthesized via a facile electrochemical method. The proper Co doping can apparently enhance the conductivity and simultaneously remain the high-capacity of the electrode. Density functional theory results further confirms more negative values in redox potential of NiCo-LDH/ACC than Ni(OH)2/ACC on account of the charge redistribution induced by Co doping, which can prevent the parasitic O2 evolution on RM electrode during decoupled H2 evolution step. As a result, the NiCo-LDH/ACC combined the superiorities of high-capacity Ni(OH)2/ACC and high-conductivity Co(OH)2/ACC, and the NiCo-LDH/ACC with 4:1 ratio of Ni to Co presented a large specific capacitance of 33.52F/cm2 for reversible charge-discharge and high buffering capacity with two-step H2/O2 evolution duration of 1740 s at 10 mA/cm2. The necessary input voltage (2.00 V) of the whole water electrolysis was broken into two smaller ones, 1.41 and 0.38 V, for H2 and O2 production, respectively. NiCo-LDH/ACC provided a favorable electrode material for the practical application of two-step water electrolysis system.

RESUMEN

Nickel-cobalt bimetallic layered double hydroxides (NiCo LDHs) are potential electrocatalysts with high performance and stability for overall water-splitting. However, its weak conductivity limits its practical applications. Herein, a simple hydrothermal in-situ conversion strategy is employed for constructing the novel heterogeneous electrocatalyst of Ni3S2/Co9S8 embedded poor crystallinity (Pc) NiCo LDH nanosheet arrays grown on the Ni foam (Pc-NiCo LDH/ Ni3S2/Co9S8), which can improve the conductivity via regulating the crystallinity. The crystallinity of NiCo LDH is well regulated by adjusting the amount of sulfur source, and the construction of Ni3S2/Co9S8 heterostructure exposes more active sites, improves the electrical conductivity, enhances the electronic interaction between NiCo LDH and Ni3S2/Co9S8, and significantly promotes the kinetics of water splitting. The optimized Pc-NiCo LDH/Ni3S2/Co9S8 hierarchical structure as both the anode and cathode exhibit the overall water splitting performance with the cell voltage of only 1.744 V to achieve the current density of 50 mA cm-2 in the alkaline media and shows the competitive H2 and O2 production rate of 6.4 and 3.1 µL s-1, respectively, suggesting its potential practical applications. This work provides a novel idea for the design of multiphase composite electrocatalysts applied in water splitting.

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The employment of electromagnetic (EM) absorbers integrating elaborate architecture, enhanced microwave absorption and multifunctional features remains a formidable challenge in practical applications including military stealth and incoming 5G electronic information era. Herein, a novel microwave absorber has been fabricated by in-situ growing carbon nanotubes (CNTs) on the prismatic nickel-cobalt (NiCo) clusters derived from Ni-Co layered double hydroxides (NiCo-LDH) via catalytic carbonization of ethyl acetate. The NiCo/CNTs composites with highly porous texture could provide sufficient open space to balance the impedance and introduce magnetic loss mechanism. Accordingly, the absorbers achieved remarkable EM absorption performance with a minimum reflection loss of -46.2 dB at 1.5 mm and broad bandwidth of 5.8 GHz owing to synergistic magnetic-dielectric effects and distinct structural merits. The NiCo/CNTs absorber manifests superior radar wave attenuation by the radar cross section simulation and density functional theory (DFT) was also performed to elucidate the potential mechanisms of the heterostructure formation and performance enhancement in the NiCo/CNTs composites. This work is expected to provide new insights or inspirations to modulate EM properties by rationally designing heterostructure for the elimination of severe EM pollution.

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Faraday-type electrode materials and devices for electrochemical capacitors have been widely investigated. However, their applications are severely limited by the preparation method and cost of electrode materials. In this work, high-performance electrochemical capacitors were successfully assembled using Fe2O3-decorated reduced graphene oxide (rGO) nanocomposites and NiCo-Layered Double Hydroxides (LDH) as the anode and cathode, respectively. An easy and efficient approach (the modified precipitation method) for the large-scale fabrication was used to prepare Fe2O3 and NiCo-LDH, supported by rGO sheets, respectively. The anode material, Fe2O3-rGO, exhibited an excellent specific capacitance (Csp) of 1073 F g-1 at a current density of 1 A g-1 and a retention rate of 92 % at 10 A g-1, while the NiCo-LDH-rGO cathode material provided a Csp of 1850 F g-1 at 1 A g-1 and maintained 84 % at 10 A g-1. The effective combination of these electrodes for the NiCo-LDH-rGO//Fe2O3-rGO electrochemical capacitors resulted in an excellent energy density of 108 Wh/kg at a power density of 884 W/kg, with remarkable cycling stability (80 % after 1000 cycles at 10 A g-1). We believe that this work, including the proposed method and electrode materials, will advance the further development and commercialization of electrochemical capacitors.

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The research on the structure of advanced electrode materials is significant in the field of supercapacitors. Herein, for the first time, we propose a novel 3D/3D composite structure by a multi-step process, in which 3D hollow NiCo LDH nanocages are immobilized on 3D sea urchin-like CoO microspheres. Results show that the 3D CoO acts as an efficient and stable channel for ion diffusion, while the hollow NiCo LDH provides abundant redox-active sites. The calculated results based on density function theory (DFT) show that the CoO@NiCo LDH heterostructure has an enhanced density of states (DOS) near the Fermi level and strong adsorption capacity for OH-, indicating its excellent electrical conductivity and electrochemical reaction kinetics. As a result, the CoO@NiCo LDH electrode has an areal specific capacity of 4.71C cm-2 at a current density of 3 mA cm-2 (440.19C g-1 at 0.28 A g-1) and can still maintain 88.76 % of the initial capacitance after 5000 cycles. In addition, the assembled hybrid supercapacitor has an energy density of 5.59 mWh cm-3 at 39.54 mW cm-3.

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One of the key factors to improve electrochemical properties is to find exceptional electrode materials. In this work, the nickel-cobalt layered double hydroxide (CNT@CoS/NiCo-LDH) with the structure of a hollow nanocage was prepared by etching CNT@CoS with zeolitic imidazolate framework-67 (ZIF-67) as a template. The results show that the addition of nickel has a great influence on the structure, morphology and chemical properties of materials. The prepared material CNT@CoS/NiCo-LDH-100 (C@CS/NCL-100) inherited the rhombic dodecahedral shape of ZIF-67 well and the CNTs were evenly interspersed among the rhombic dodecahedrons. The presence of CNTs improved the conductivity and surface area of the samples. The C@CS/NCL-100 demonstrates a high specific capacitance of 2794.6 F·g-1 at 1 A·g-1. Furthermore, as an assemble device, the device of C@CS/NCL-100 as a positive electrode exhibits a relatively high-energy density of 35.64 Wh·kg-1 at a power density of 750 W·kg-1 Further, even at the high-power density of 3750 W·kg-1, the energy density can still retain 26.38 Wh·kg-1. Hence, the superior performance of C@CS/NCL-100 can be ascribed to the synergy among CNTs, CoS and NiCo LDH, as well as the excellent three-dimensional structure obtained by used ZIF-67 as a template.

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Well-defined polyhedral ZIF-67 metal-organic frameworks (MOFs) are usually synthesized using methanol as solvent. In this work, methanol is replaced with deionized water as a solvent to synthesize ZIF-67 MOFs with unique nanoflake morphology. The ZIF-67 nanoflakes are synthesized directly byin situmethod on reduced graphene oxide (rGO) to obtain ZIF-67/rGO-xprecursors which are further transformed into NiCo-layered double hydroxide nanocomposites (NiCo-LDH/rGO-x,x = 10, 30, 50 and 90 mg of rGO). The NiCo-LDH/rGO-xnanostructured composites are found to be excellent materials for battery type supercapacitor (supercapattery) applications. Among these samples, the NiCo-LDH/rGO-30 composite gives maximum specific capacity of 829 C g-1(1658 F g-1) at a current density of 1 A g-1and high rate capability. The as fabricated 2-electrode symmetric Swagelok deviceNiCo-LDH/rGO-30NiCo-LDH/rGO-30delivered a high energy density of 49.2 Wh kg-1and a power density of 4511 W kg-1, and enabled us to glow red, blue and white LED bulbs using three coin cells. The device can show good capacity retention even after 3000 continuous charge-discharge cycles. The NiCo-LDH/rGO-30 composite,in situderived from ZIF-67 MOF in combination with optimal amount of rGO, is an excellent material to deliver both high energy density and high power density in supercapattery devices.

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Aqueous alkaline rechargeable nickel-zinc (Ni-Zn) batteries possess great potential for large-scale energy storage systems because of their high output voltage, cheap cost, and intrinsic safety. However, the practical applicability of Ni-Zn batteries has been limited by traditional Ni-based cathodes with low capacity and poor cycle stability. Rational design of electrode structure and composition is highly desired but still significantly challenging. Herein, uniform self-supported hierarchical heterostructure composites interacting NiCo-layered double hydroxide with 1D nickel sulfides heteronanowire rooted on Ni foam (NF\Ni3 S2 /NiS@NiCo-LDH) are successfully developed by a hydrothermal sulfurization-electrodeposition process. The self-supported 3D hierarchical heterostructured composites nanoarray provides abundant reactive sites, rapid ion diffusion channels, and fast electron transfer routes, as well as strong structural stability. More significantly, the strong interfacial charge transfer between Ni3 S2 /NiS heteronanowire and NiCo-LDH effectively modifies the electronic structure of the composites and thereby improving the reaction kinetics. Consequently, the NF\Ni3 S2 /NiS@NiCo-LDH electrode presents a superior capacity of 434.5 mAh g-1 (1.73 mAh cm-2 ) at 3 mA cm-2 . In addition, the fabricated NF\Ni3 S2 /NiS@NiCo-LDH//Zn battery can offer a maximal energy density and power density as large as 556.3 Wh kg-1 and 26.3 kW kg-1 , respectively, as well as an exceptional cycling performance.