High Cycling Stability Research Articles

Metal-Organic Framework for Aluminum based Energy Storage Devices: Utilizing Redox Additives for Significant Performance Enhancement.

There are various methods being tried to address the sluggish kinetics observed in Al-ion batteries (AIBs). They mostly deal with morphology tuning, but have led to limited improvement. A new approach is proposed to overcome this limitation. It focuses on the use of a redox additive modified electrolyte in combination with framework like materials, which have wider channels. The ordered microporous and interconnected framework of ZIF 67, with large surface area, effectively facilitates the diffusion of aluminum ions. Therefore, AIBs are able to exhibit a superior discharge capacity of 288 mAh g-1 at 0.2 A g-1 current density with robust cycling stability. The addition of potassium ferricyanide as a redox-active species in an aqueous solution of aluminum chloride (supporting electrolyte) leads to significant enhancement in the specific capacity with much higher cycling stability. Al-ion based BatCap devices can be assembled by using ZIF 67 as the cathode, ZIF 67 derived porous carbon as the anode, and a redox additive modified electrolyte. The BatCap device exhibits excellent energy density of 86 Wh kg-1 at a power density of 2 KW kg-1, which is higher than reported aqueous AIBs. The ex situ characterization clearly explains the unexplored mechanism of redox additives in AIBs.

Proton Self‐Limiting Effect of Solid Acids Boosts Electrochemical Performance of Zinc‐ion Batteries

AbstractAt present, aqueous rechargeable Zn–MnO2 batteries have attracted widespread attention as green potential application for renewable energy storage devices. MnO2 cathode has great potential for application, but its proton reaction results in side reactions of cathode, electrolyte consumption, and dramatic pH value changes, suffering from capacity degradation. To address the issues caused by proton deficit, a proton–limited domain strategy is proposed by integrating solid acids (Sulfonic acid type polystyrene–divinylbenzene, SATP) with proton exchange reactions into MnO2. SATP can act as a new proton source increasing the amount of H+ and reducing the generation of zinc hydroxide sulfate, by–product of proton at the cathode interface, via proton exchange reactions of ‐HSO3– group. As a result, Zn–MnO2/SATP battery delivered with excellent rate performance (218.4 mAh g–1 at 2 A g–1) and high cycling stability (the retained capacity of 115.8 mAh g–1 after 500 cycles at a current density of 1 A g–1. This work provides an innovative strategy for high performance aqueous Zn–MnO2 batteries.

Preparation and Capacitive Properties of Ni-Doped Zinc Cobaltate/Carbon Fiber Composite Porous Mesh Materials

Nickel-element-doped zinc cobaltate/carbon fiber composites (Ni-ZnCo2O4/CF) were prepared on carbon cloth (made of a combination of carbon fibers) conductive substrates using a simple ambient stirring method combined with heat treatment. Characterization tests of the materials revealed that the prepared products were porous Ni-ZnCo2O4/CF mesh structures. This porous network structure increases the surface area of the material and helps shorten the diffusion path of ions and electrons. The samples were analyzed using X-ray diffraction (XRD), scanning electron microscopy (SEM), and transmission electron microscopy (TEM) methods to investigate the effect of Ni elemental doping on the stability of the materials. The results show that there are no other impurity peaks and no other impurity elements in the Ni-ZnCo2O4/CF electrode material, which indicates that the sample purity is high. Meanwhile, the electrochemical properties of Ni-ZnCo2O4/CF electrode materials were studied. Under the condition of 15 A·g−1, the specific capacitance of Ni-ZnCo2O4/CF electrode material is 1470 F·g−1, and after 100 cycles, its specific capacity reaches 1456 F·g−1, which is 99.0% of the specific capacity of 1470 F·g−1, indicating that the electrode material has good stability. In addition, we assembled asymmetric supercapacitors (Ni-ZnCo2O4/CF//CNTs) with Ni-ZnCo2O4/CF as the positive material and carbon nanotubes (CNTs) as the negative material. In the cyclic stability experiment of Ni-ZnCo2O4/CF/CNTs devices, when the current density was 1 A·g−1, the specific capacitance was 182 F·g−1. After 10,000 cyclic charge–discharge tests, the specific capacity became 167 F·g−1, which was basically unchanged compared with the initial specific capacity, reaching 91.8%. It shows that it has higher charge–discharge performance and higher cycle stability.

Single-Crystal P2-Na0.67Mn0.67Ni0.33O2 Cathode Material with Improved Cycling Stability for Sodium-Ion Batteries.

Layered oxides constitute one of the most promising cathode materials classes for large-scale sodium-ion batteries because of their high specific capacity, scalable synthesis, and low cost. However, their practical use is limited by their low energy density, physicochemical instability, and poor cycling stability. Aiming to mitigate these shortcomings, in this work, we synthesized polycrystalline (PC) and single-crystal (SC) P2-type Na0.67-δMn0.67Ni0.33O2 (NMNO) cathode materials through a solid-state route and evaluated their physicochemical and electrochemical performance. The SC-NMNO cathode with a large mean primary particle size (D50) of 12.7 μm was found to exhibit high cycling stability leading to 47% higher capacity retention than PC-NMNO after 175 cycles at 1C rate in the potential window 4.2-1.5 V. This could be attributed to the effective mitigation of parasitic side reactions at the electrode-electrolyte interface and suppressed intergranular cracking induced by anisotropic volume changes. This is confirmed by the lower volume variation of SC-NMNO (ΔV ∼ 1.0%) compared to PC-NMNO (ΔV ∼ 1.4%) upon charging to 4.2 V. Additionally, the SC-NMNO cathode displayed slightly higher thermal stability compared to PC-NMNO. Both cathodes exhibited good chemical stability against air and water exposure, thus enabling material storage/handling in the ambient atmosphere as well as making them suitable for aqueous processing. In this regard, PC-NMNO was investigated with two low-cost aqueous binders, carboxymethyl cellulose, and sodium trimetaphosphate, which exhibited higher binding strength and displayed excellent electrochemical performance compared to PVDF, which could potentially lead to significant cost reduction in electrode manufacturing.

Magnetron Sputtered SnO₂ Layer Combined with NiCo−LDH Nanosheets for High‐Performance All‐Solid‐State Supercapacitors

AbstractNickel‐cobalt layered double hydroxide (NiCo−LDH) has attracted much attention because of its excellent electrochemical properties and regulability. And it is a potential pseudocapacitive electrode material, which is commonly used in supercapacitors and lithium‐ion batteries. Its application in the field of supercapacitors can improve the energy density, power density and cycle life of devices. However, NiCo−LDH still faces some challenges, such as poor electrical conductivity and the capacity attenuation caused by agglomeration of layered structures, which require further research and optimization. In this paper, SnO2 films were prepared on carbon cloth (CC) by magnetron sputtering method, and Ni−Co LDH nanosheets were grown by hydrothermal reaction to obtain NiCo−LDH@SnO2 composites. Due to the synergistic effect between NiCo−LDH and SnO2, NiCo−LDH@SnO2 composites exhibit high Cs and good cyclic stability. In addition, an all‐solid‐state flexible asymmetric supercapacitor (ASC) was assembled with activated carbon (AC) anodes, showing good specific capacitance(Cs) and energy density. And a high initial capacitance can still be retained after 10,000 cycles. This paper shows that NiCo−LDH@SnO2 shows excellent application potential in supercapacitors.

High-Efficiency Ag-Modified ZnO/g-C3N4 Photocatalyst with 1D-0D-2D Morphology for Methylene Blue Degradation

Photocatalysts with different molar ratios of Ag-modified ZnO to g-C3N4 were prepared through an electrostatic self-assembly method and characterized through techniques such as X-ray diffraction, Fourier transform infrared spectroscopy, and scanning electron microscopy. The resulting Ag-ZnO/g-C3N4 photocatalysts exhibited a unique 1D-0D-2D morphology and Z-type heterojunction. Moreover, g-C3N4 nanosheets with large layer spacing were prepared using acid treatment and thermal stripping methods. The Z-type heterostructure and localized surface plasmon resonance effect of Ag nanowires enabled high-speed electron transfer between the materials, while retaining large amounts of active substances, and broadened the light response range. Because of these features, the response current of the materials improved, and their impedance and photoluminescence reduced. Among the synthesized photocatalysts, 0.05Ag-ZnO/g-C3N4 (molar ratio of g-C3N4/ZnO: 0.05) exhibited the highest photocatalytic performance under UV–visible light. It degraded 98% of methylene blue in just 30 min, outperforming both g-C3N4 (21% degradation in 30 min) and Ag-ZnO (84% degradation in 30 min). In addition, 0.05Ag-ZnO/g-C3N4 demonstrated high cycling stability.

Biochar-Supported FeCo-MOF derivative catalyzes PDS-Mediated degradation of tetracycline

Bimetallic metal–organic framework (MOF) has gained wide attention in the field of advanced oxidative processes (AOPs), however, the agglomeration problem severely limits its active sites and its activation mechanism still needs to be further explored. This study developed the BC@CoFe composite material, utilizing biochar (BC) to support FeCo-MOF derivatives, effectively alleviating their agglomeration and structural collapse. The results of the BC@CoFe activated peroxydisulfate (PDS) system for the degradation of tetracycline (TC) revealed an excellent degradation efficiency up to 97.7 % in 2 h for TC solution (20 mg/L, degradation rate constants k = 7.066 mM-1min−1). Furthermore, the BC@CoFe/PDS system exhibits exceptionally high cyclic stability (73.23 % degradation efficiency after 12 h continuous degradation), a wide range of pH (3–11) and temperature tolerance (20-60℃), resistance to background ion interference (SO42-, H2PO4-, NO3– and HA), and reduced toxicity of the degradation products. X-ray photoelectron spectroscopy (XPS) and density functional theory (DFT) analyses show that the exceptional catalytic performance of BC@CoFe primarily stems from the synergistic effect between Fe(II)/Co(III) and Fe(III)/Co(II). Regarding the reactive active species involved in TC degradation, the contribution rates of 1O2, SO4•- and ·OH were measured and calculated to be 73.6 %, 14.9 %, and 11.5 %, respectively. Thus, the BC@CoFe/PDS system exhibits outstanding catalytic activity and has broad practical applications in water treatment.

Unveiling the potential of Na2FePO4F@PEG composite as cathode material for sodium-ion batteries

The economic and environmental advantages of Na2FePO4F fluorophosphate have positioned it as a highly promising cathode material for sodium-ion batteries (SIBs). This recognition stems from its demonstrated potential to address key challenges in energy storage systems, making it a subject of extensive research and studies.In this paper, the preparation of Na2FePO4F powder through a simplified, upscaling, and cost-effective approach that involves the direct use of phosphoric acid is described, aiming to evaluate its electrochemical performance. The obtained orthorhombic structure (S.G. Pbcn) is mixed with varying percentages of polyethylene glycol as a carbon source (15% and 20%) to generate large specific surfaces, improve electronic conductivity, and achieve an optimized carbon content for these materials. The 15% and 20% PEG-coated Na2FePO4F are evaluated at a 2 - 4 V voltage range at C/15 in Na-half cells using two electrolyte formulations: 5% FEC 1 M NaClO4:PC and 1 M NaPF6:PC. The NaPF6/FEC electrolyte exhibits better electrochemical characteristics and high cycling stability, especially in the case of the 15% PEG-coated material. These findings are also supported by the data from differential plots and rate capabilities, highlighting the potential of the coated material for applications in high-performance energy storage applications.

Graphene-Intercalated P4Se3@CNF Hybrid Electrode for Sustainable Energy Storage Solution: Enabling High Energy Density and Ultra-long Cyclic Stability

Non-metal-based compounds have emerged as promising electrodes in recent years to replace scarce and expensive transition-metals for energy storage applications. Herein, a simple electro-spinning technique followed by carbonization is used to create tetraphosphorus triselenide(P4Se3)nano-flakes encapsulated in carbon nanofiber (P4Se3@CNF) to obtain a binder-free, metal-free and flexible hybrid electrode with high electrical conductivity and cyclic stability. A remarkable capacitive performance (5.5-folds@P4Se3) of 810Fg-1/112.5mAhg-1@0.9Ag-1 has been obtained using P4Se3@CNF electrode with an excellent rate capability compared to pristine(P4Se3) which is further supported by theoretical calculations via intercalating graphene within bare P4Se3 flakes inducing partial charge redistribution in hetero-structure. A flexible pouch-type hybrid-supercapacitor followed by coin-cell has been manufactured offering exceptional energy-density without sacrificing power density and ultra-long durability over 35000 and 100000-cycles with capacitance-retention of 99.77% and 100%, respectively. It has been demonstrated that as-fabricated device has practical usefulness towards renewable energy harvesting and storage via integrating commercial solar cell module with supercapattery array that can enlighten the blue LED approximately for 31minutes, rotate the homemade windmill device, power Arduino and glow “INST” against 2minutes of charging. This work demonstrates a facile route towards the development of metal-free electrochemical renewable energy storage/transfer devices offering an inevitable adoption in industrial platforms.

Sandwich-like high-performance Ti3C2Tx MXene/NiCo2O4 nanosphere composites for asymmetric supercapacitor application

NiCo2O4 is a promising electrode material for supercapacitors due to its low cost, high theoretical specific capacitance and good cycling stability. However, NiCo2O4 has the disadvantages of poor electronic and ionic conductivities and easy agglomeration. Moreover, the irreversible structural damage caused by the NiCo2O4 volume expansions during charging and discharging limits its use in supercapacitors. Herein, we fabricated sandwich Ti3C2Tx MXene/NiCo2O4 composites via an electrostatic self-assembly method. The problem of easy agglomeration of the NiCo2O4 nanospheres was solved by intercalating Ti3C2Tx MXene layers with the NiCo2O4 nanospheres. Furthermore, the Ti3C2Tx MXene layer was also utilized as a protective layer to limit serious volume expansion and protect the structure of NiCo2O4 nanospheres from destruction. The results showed that the prepared Ti3C2Tx MXene/NiCo2O4 composite exhibited a high specific capacitance of 1025 F g−1 at a current density of 1 A g−1 and had an initial capacity of 81 % when the current density was increased to 10 A g−1. The Ti3C2Tx MXene/NiCo2O4 composite cathode and activated carbon anode were assembled in an asymmetric supercapacitor, which showed an energy density of 36.67 Wh kg−1 at 800 W kg−1 and a capacity retention of 88.2 % after 5000 cycles.

Metal oxide-based nanocomposites as advanced electrode materials for enhancing electrochemical performance of Supercapacitors: A comprehensive review

In recent years, the escalating use of nonrenewable fossil fuels has emerged as a significant threat to global sustainability, prompting the need for renewable, cost-effective, and eco-friendly energy storage solutions. Supercapacitors (SCs) are notable for their high power density (PD), cycle stability, and swift charge/discharge rates, although they fall short in energy density (ED) compared to traditional batteries. The performance of SCs is greatly influenced by the electrode materials used, highlighting the importance of material innovation in tackling the challenges posed by increasing fossil fuel consumption. Transition metal oxides (TMOs), known for their redox activity in energy storage, have been thoroughly investigated for their exceptional specific capacitance, which ranges from 100 to 2000F g−1, surpassing that of electrical double-layer capacitors (EDLCs). TMOs such as ruthenium oxide (RuO2), manganese oxide (MnO2), nickel oxide (NiO), cobalt oxide (Co3O4), tin oxide (SnO2), zinc oxide (ZnO), tungsten oxide (WO3), and vanadium pentoxide (V2O5) are widely researched for their high theoretical capacitance, affordability, and longevity. This review emphasizes the groundbreaking potential of metal oxide nanocomposites (NCs) formed by combining them with graphene, carbon nanotubes (CNTs), and polymers, leading to synergistic enhancements in electrical conductivity, surface area, and charge storage capacity. This thorough review not only presents an in-depth analysis of current research but also sheds light on potential future developments, contributing to the ongoing progress in the field of advanced electrode materials for energy storage.

Synthesis of natural oxygen-doped bamboo-derived hierarchical micro-mesoporous composite carbon materials using a green activation strategy

Utilizing biomass waste to synthesize hierarchical micro-mesoporous composite carbon materials for application in the field of supercapacitors realized green and sustainable energy development. This paper efficiently synthesized natural O-doped carbon materials using bamboo as biomass material by simple air pre-oxidation and secondary carbonization methods. Among them, KCl acted as a recyclable templating agent and flame retardant, facilitating the construction of mesoporous structures. The green activator CH3COOK promoted the generation of micropores. The combination of dual activation strategies (physical and chemical) contributed to the conversion of bamboo to hierarchical micro-mesoporous composite carbon materials. During pre-carbonization, air was used as a natural dopant which etched the carbon material and promoted the creation of oxygenated functional groups. The best carbon material exhibited an excellent electrochemical capacity of 321.65 F/g in 6 M KOH electrolyte. Furthermore, the symmetric supercapacitor exhibited high cycling stability (95.52 %) and outstanding power density. This work provided a new idea for preparing controllable biomass-derived carbon materials, while offering a reference for applying dual activation strategies in carbon material synthesis.

Poling‐induced enhancement of piezocatalytic performance of 0.96K0.5Na0.5NbO3‐0.04Bi0.5Na0.5ZrO3 ceramic blocks

AbstractCompared with powder particles, ceramic block piezocatalyst possesses the advantages of high cycle stability, decreasing secondary pollution, and easy recovery. Herein, with a simple strategy of the poling procedure, the piezocatalytic activity of 0.96K0.5Na0.5NbO3‐0.04Bi0.5Na0.5ZrO3 (abbreviated as 0.96KNN‐0.04BNZ) ceramic blocks can be considerably improved. A reaction rate constant k value of 14.70×10−3 min−1 in the poled sample can be obtained to degrade Rhodamine B, which is 3.44 times that of the unpoled one. Meanwhile, the poled sample also has good degradation effects against methylene blue and amino black 10B. The improvement of piezocatalytic activities originates from the reduction of crystal symmetry and the enhancement of electron‐hole pair separation, which accelerates the generation of charge carriers. This research displays a unique lead‐free bulk piezocatalyst and a convenient method for enhancing its piezocatalytic activity.

Pengaruh Konsentrasi Oksida Logam CuO Sebagai Superkapasitor Berbasis Karbon Aktif

Supercapacitors are promising energy storage devices in future energy technology. In this research, the primary and applied aspects of supercapacitors are developed. Various techniques have been developed specifically to estimate specific capacitances. Various attempts have been made in the literature to increase the specific capacitance value of the electrode materials. Electrode materials with unique structural and electrochemical properties, such as high capacity and cyclic stability, exhibit good supercapacitor performance. Many new electrode materials have been developed to play an essential role in capacitance behavior. This research focuses on the highly efficient application of nanostructured electrode materials such as nanoporous carbon and metal oxide CuO for supercapacitors. Nanopore carbon is made from coconut shell, which is synthesized using a simple heating method. Next, carbon nanopore and CuO nanoparticle composites were carried out with composition variations of 0.5,10,15, and 20% of the total weight. The results of cyclic voltammetry, electrochemical impedance spectroscopy, and charge-discharge tests, maximum results were obtained on a composition of 5% CuO nanoparticles with a capacitance of 280 F/gr and a conductivity of 1.14 X 10-2 S/cm. This result is due to an increase in the surface area between the pore surfaces, so more ions are trapped, causing the filling process to take place quickly.

A Chemical Sewing Enabled All‐In‐One Control Interface for Robust Zinc Metal Anodes

AbstractDeveloping artificial protective layers is an effective strategy to address the issue of dendrites for aqueous Zn‐metal batteries (ZMBS). However, drawbacks such as rough microscopic morphology, excessive thickness, and single functionality remain, limiting the attainment of a stable zinc anode. Herein, a novel multifunctional organic–inorganic hybrid artificial protective layer is produced by splicing inorganic fragments onto organic materials in situ using a chemical sewing. The protective layer is well‐compatible and also retains the function of organic and inorganic materials, which not only inhibits dendrite production but also alleviates Zn corrosion. The Si─OH bond of the zincophilic group enables planar Zn deposition while forming hydrogen bonds with water, suppressing water activity near the anode and reducing the hydrogen evolution reaction. As expected, the Zn||Zn symmetric cell with a protective layer provides high cycling stability of more than 1960 h at 1 mA cm−2, which is about 28 times higher than that of the symmetric cell assembled without the protective layer. More importantly, a Zn||V2O5 full cell with an ultra‐long lifetime has been achieved with an artificial protective layer. This work provides a potential viable path to achieve long‐lived ZMBS.

Novel sulfonated polyaniline/graphene oxide electrode with high cycling stability for all-solid-state flexible supercapacitors

Polyaniline (PANi) has high theoretical specific capacitance by storing energy through redox reactions and thus is widely used in supercapacitors. However, the skeleton of PANi expands and contracts during the process of ion inhalation and exfoliation, which leads to a decrease in electrochemical performance. To solve this problem, we graft the sulfonic acid group onto the PANi backbone via a borate ester bond, which serves as a proton reservoir to provide protons for PANi to undergo redox reactions and provide pseudocapacitance. SPANi is then polymerized in situ on graphene oxide (GO), and its comprehensive performance of the electrode is further enhanced by designing ordered structures and synergistic interactions. The SPANi5/GO5 composite that are created in-situ have a fantastic specific capacitance of 460.56 F g−1 at 1 A g−1 and maintained 85.19% of the primary capacitance after 10,000 cycles. The device is assembled with PAAM/H2SO4/GO as the gel electrolyte, which achieves a specific capacitance of 137.75 F g−1, and the capacitance is retains at 90.74% after 10,000 cycles. The supercapacitor exhibits a large energy density of 13.76 Wh kg−1 when the power density is 200.27 W kg−1. The present study presents a novel and efficient approach for the fabrication of high-performance supercapacitor electrodes.

Highly stable MXene/g-PPy@sulfonated cellulose composite electrodes for flexible supercapacitors

Traditional two-dimensional transition metal carbides/nitrides (MXene) have gained much academic concern due to their excellent physicochemical properties, but their susceptibility to self-stacking leads to poor cyclic stability. In this paper, an MXene-based electrode active material was successfully prepared. The generated modified PPy (g-PPy) increases the active site, increases the accessibility of ions, and can give full play to the pseudocapacitance. By the combination of modified PPy (g-PPy) nanoparticles with pseudocapacitive behavior polymerized in situ on sulfonated cellulose (SC) and MXene, not only the electrochemical performance was improved by exploiting the synergy between different electrode materials and different energy storage mechanisms, but also the MXene as a skeleton limited the volume expansion and contraction of PPy during charge/discharge cycles and the g-PPy and SC composites (g-PPy@SC) as a spacer supported the MXene layer, resulting in much higher cycle stability. Cycle stability of 98.4 % even after 10,000 cycle tests. In addition, a symmetric supercapacitor assembled from this electrode material maintains a stability of 84.4 % under 10,000 cycles at a low temperature of −40 °C. Therefore, this study provides a feasible method for the preparation of MXene-based electrodes with high cycling stability.

Zr0.1Fe0.9V1.1Mo0.9O7 as Cathode for Lithium-Ion Battery

Abstract With the development of lithium-ion batteries, high capacity and high cycle stability have been the two main goals being pursued. Recent studies have shown that ZrV2O7 does not perform well in energy storage due to its low electrical conductivity and poor cycling stability. Elemental doping has proven to be an effective strategy for improving electrochemical performance. In this paper, we prepared Zr0.1Fe0.9V1.1Mo0.9O7(ZFVMO) and Zr0.1Fe0.9V1.1Mo0.9O7@c (ZFVMO@c) materials using a simple solid-phase sintering method and a fast microwave sintering method. Double ionic heterovalent substitution of Zr4+/V5+ in ZrV2O7 using Fe3+/Mo6+, Fe3+/Mo6+ gives it near-zero thermal expansion characteristics and excellent conductive properties. In electrochemical tests, the first discharge capacities of ZFVMO and ZFVMO@C are 2261 mA h g−1 and 727 mA h g−1, respectively, and the batteries were finally stabilized for 475 and 500 cycles. Compared to ZrV2O7, the electrochemical properties of ZFVMO are greatly improved.

Nitrogen-Doped Graphene-Supported Nickel Nanoparticles Reveal Low Dehydrogenation Temperature and Long Cyclic Life of Magnesium Hydrides.

Magnesium hydride (MgH2) is a promising hydrogen storage candidate due to its large capacity; however, high dehydrogenation temperature and slow kinetic rates are the main bottlenecks. Herein, we proposed a strategy for designing nitrogen-doped graphene-supported Ni nanoparticles (NPs) (Ni@NC) to tackle these problems. The results showed that the MgH2 + 15 wt % Ni@NC nanocomposite reduced the on-set dehydrogenation temperature to 195 °C, which was 175 °C lower than pristine MgH2. In addition, MgH2 + 15 wt % Ni@NC achieved 1.7 and 6.5 wt % desorption capacities at 225 and 300 °C, respectively, while absorbing 5.5 wt % hydrogen at 100 °C. The MgH2 + 15 wt % Ni@NC nanocomposite showed high cyclic stability, achieving 98.0% capacity retention after 100 cycles at 270 °C with negligible loss in capacity. This remarkable hydrogen storage performance can be attributed to the homogeneous distribution of Ni NPs on N-doped graphene layers, in situ formed Mg2NiH2 NPs, and multiphasic regions, promoting the nucleation and growth process during hydrogenation/dehydrogenation, which stabilized and improved the cyclic stability. This strategy paves the way to developing high-performance MgH2 for large-scale applications.

Na+-Enriched Quinoid Polymer Layer with Fast Ion Transport for Dendrite-Free Sodium Metal Batteries with High Cyclic Stability

Na⁺-Enriched Quinoid Polymer Layer with Fast Ion Transport for Dendrite-Free Sodium Metal Batteries with High Cyclic Stability