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Considered as an imperative alternative to the commercial LiFePO

Sodium-ion batteries (SIBs) are considered a potential replacement for lithium-ion batteries in the area of low-cost large-scale energy storage. Due to its low operating voltage, high capacity, non-toxicity and low production cost, titanium dioxide is now among the anode materials under investigation and shows the most promise. However, its poor electrical conductivity is one of the main reasons limiting its large-scale application. Herein, we designed a ruthenium-doped anatase-type VTi2.6O7.2 ultrafine nanocrystal (Ru-VTO). As the anode of SIBs, Ru-VTO delivers a high specific capacity of 297 mAh g−1 at 50 mA g−1, a long cycle life of 2000 cycles and a high rate capability (104 mAh g−1 at 1000 mA g−1). The excellent performance may be related to the solid-solution interatomic interactions and the enhanced conductivity after ruthenium doping. These studies demonstrate the potential of Ru-VTO as an anode material for advanced SIBs.

The corrosion, parasitic reactions, and aggravated dendrite growth severely restrict development of aqueous Zn-ion batteries. Here, we report a novel strategy to break the hydrogen bond network between water molecules and construct the sulfolane-H2O deep eutectic solvents. This strategy cuts off the transfer of protons/hydroxides and inhibits the activity of H2O, as reflected in a much lower freezing point (-80 °C), a significantly larger electrochemical stable window (3 V), and suppressed evaporative water from electrolytes. Stable Zn plating/stripping for over 9600 h was obtained. Based on experimental characterizations and theoretical simulations, it has been proved that sulfolane can effectively regulate solvation shell and simultaneously build the multifunctional Zn-electrolyte interface. Moreover, the multi-layer homemade modular cell and 1.32 Ah pouch cell further confirm its prospect for practical application.

The problems with plastic materials and the good film-forming properties of polysaccharides motivated research in the development of polysaccharide-based films. In the last 5 years, there has been an explosion of publications on using green solvents, including ionic liquids (ILs), and deep eutectic solvents (DESs) as candidates to substitute the conventional solvents/plasticizers for preparations of desired polysaccharide-based films. This review summarizes related properties and recovery of ILs and DESs, a series of green preparation strategies (including pretreatment solvents/reaction media, ILs/DESs as components, extraction solvents of bioactive compounds added into films), and inherent properties of polysaccharide-based films with/without ILs and DESs. Major reported advantages of these new solvents are high dissolving capacity of certain ILs/DESs for polysaccharides (i.e., up to 30 wt% for cellulose) and better plasticizing ability than traditional plasticizers. In addition, they frequently display intrinsic antioxidant and antibacterial activities that facilitate ILs/DESs applications in the processing of polysaccharide-based films (especially active food packaging films). ILs/DESs in the film could also be further recycled by water or ethanol/methanol treatment followed by drying/evaporation. One particularly promising approach is to use bioactive cholinium-based ILs and DESs with good safety and plasticizing ability to improve the functional properties of prepared films. Whole extracts by ILs/DESs from various byproducts can also be directly used in films without separation/polishing of compounds from the extracting agents. Scaling-up, including costs and environmental footprint, as well as the safety and applications in real foods of polysaccharide-based film with ILs/DESs (extracts) deserves more studies.

No organism can avoid the process of aging, which is often accompanied by chronic disease. The process of biological aging is driven by a series of interrelated mechanisms through different signal pathways, including oxidative stress, inflammatory states, autophagy and others. In addition, the intestinal microbiota play a key role in regulating oxidative stress of microglia, maintaining homeostasis of microglia and alleviating age-related diseases. Tea polyphenols can effectively regulate the composition of the intestinal microbiota. In recent years, the potential anti-aging benefits of tea polyphenols have attracted increasing attention because they can inhibit neuroinflammation and prevent degenerative effects in the brain. The interaction between human neurological function and the gut microbiota suggests that intervention with tea polyphenols is a possible way to alleviate brain-aging. Studies have been undertaken into the possible mechanisms underpinning the preventative effect of tea polyphenols on brain-aging mediated by the intestinal microbiota. Tea polyphenols may be regarded as potential neuroprotective substances which can act with high efficiency and low toxicity.

Potassium-ion batteries (KIBs) are competitive alternatives to lithium-ion batteries (LIBs) due to the abundant K resources and high energy density. As an indispensable part of the battery, the electrolyte affects the battery capacity, rate capability, cycle life, and safety. Nevertheless, the researches on electrolytes and corresponding solid electrolyte interfaces (SEI) in KIB are still in its infancy and require further attention. In this review, recent progresses of various K+ containing electrolytes for KIBs are summarized comprehensively. Additionally, the effects of salts, solvents, additives, and concentrations on the properties of various electrolyte systems are discussed in detail. Thereafter, interface chemistry between electrode and electrolyte, as well as rational modification strategies for high-performance KIB are reviewed. Finally, the major challenges and the future perspectives are estimated for advanced KIB. This review will provide good directions for the development of high-performance KIB.

Metal–organic framework (MOF)-derived composites have gained wide attention due to their specific structures and enhanced performance. In this work, we prepared carbon nanotubes with Fe nanoparticles connected to two-dimensional (2D) hierarchical carbon network composites via a low-pressure gas–solid reaction strategy. Specifically, the three-dimensional (3D) networks derived from ZIF-8 exploited the carbon nanotubes with the function of charge modulation. Meanwhile, we utilized the interconnected 2D nanostructures to optimize impedance matching and facilitate multiple scattering, ultimately improving the overall microwave absorption performance. Furthermore, based on the well-designed structures, the composites prepared at 800 °C (Fe-N-C@CNTs-800) achieved the best reflection loss (RL) of −58.5 dB, thereby obtaining superior microwave absorption performance. Overall, this study provides a good groundwork for further investigation into the modification and dimension design of novel hierarchical microwave absorbers.

Potassium (K) metal batteries are identified as some of the most potential candidates for next-generation energy storage devices due to the abundant reserves, low redox potential and high theoretical capacity of K metal. However, the practical application of K metal batteries is severely hindered by the uncontrollable growth of K dendrites. Herein, a dendrite-free and high-performance K metal anode was obtained by constraining K metal on SnO2-modified commercial carbon cloth (K-CC@SnO2). In the K-CC@SnO2 structure, K metal wraps the SnO2 particles and forms a closely connected structure with the carbon cloth. CC@SnO2 not only shows excellent potassiophilicity, but also possesses high electronic conductivity and large void spaces, which can induce the homogeneous deposition of K metal and accommodate the large volume changes of K during the plating/stripping processes. Consequently, the as-constructed K-CC@SnO2 anodes exhibit low polarization and long cycling life with a dendrite-free morphology in symmetric cells with a carbonate-based electrolyte. In addition, a perylene-3,4,9,10-tetracarboxylic diimide (PTCDI)‖K-CC@SnO2 full cell shows excellent rate performance (112.5 mA h g−1 @ 5 A g−1) and ultralong cycling life (up to 10 000 cycles). A PTCDI‖K-CC@SnO2 pouch cell was successfully assembled and it delivers a long cycling life of 500 cycles with an energy density of 274 W h kg−1. These results indicate that a simple and effective strategy has been proposed for the development of K metal anodes with commercialization potential.

The development of high-performance cathode materials is the key to realize commercial applications of zinc-ion batteries (ZIBs). Vanadium-based materials have been used as cathode candidates for ZIBs due to their low cost and high capacity. However, the low conductivity, unstable layered structure and slow diffusion kinetics of Zn2+ are still the main problems for vanadium-based oxides. Herein, V10O24·nH2O with a large interlayer spacing and stable structure is successfully synthesized by inducing a VO2 phase transition through a simple refluxing process. As the ZIB cathode material, V10O24·nH2O demonstrates a high reversible capacity of 365.3 mA h g−1 at 0.2 A g−1, ultrahigh rate performance (127.2 mA h g−1 even at 80 A g−1), and long-term cycling stability (83.2% capacity retention over 3000 cycles at 5.0 A g−1). The excellent electrochemical performance is attributed to the synergistic effects of the ultrathin nanoribbon structures, oxygen vacancy and water molecules, which are favorable for enhancing the electron/ion transfer kinetics and maintaining structural stability of the V10O24·nH2O electrode in the whole cycling process. Furthermore, ex situ XRD and XPS analyses elucidate the Zn2+ storage mechanism of the V10O24·nH2O cathode.

Benefiting from loose assembly conditions, a high level of safety and environmentally friendly characteristics, rechargeable aqueous Zn-ion batteries (AZIBs) have attracted significant attention. The electrochemical kinetics and performance of the AZIBs are greatly affected by water in electrolytes or electrode materials. The corrosion and passivation of the Zn electrode caused by the inevitable solvation process of water molecules can lead to the growth of dendrites, thus resulting in a limited cycle life. Moreover, water in the electrode material, whether in the form of structural water or co-intercalated hydrated cations, can greatly affect the electrochemical behavior due to its small size, high polarity and hydrogen bonding. Unlike previous reports, this review focuses on the roles of water molecules during electrochemical processes in AZIBs. We comprehensively summarize the influencing mechanisms of water molecules during the energy storage process from the perspectives of the electrolyte, Zn anode, and cathode materials, and further include the basic theory, modification methods, and practical applications. The mystery concerning the water molecules and the electrochemical performance of AZIBs is revealed herein, and we also propose novel insights and actionable methods regarding the potential future directions in the design of high-performance AZIBs.

Calcium-based batteries have promising advantages over multivalent ion batteries. However, the fabrication of highly efficient calcium batteries is limited by the quality of available cathode materials, which motivates the exploration of electrodes that can enable reversible, stable Ca

Homologous recombination repair (HR) is an error-free DNA damage repair pathway to maintain genome stability and a basis of gene targeting using genome-editing tools. However, the mechanisms of HR in plants are still poorly understood. Through genetic screens for DNA damage response mutants (DDRM) in Arabidopsis, we find that a plant-specific ubiquitin E3 ligase DDRM1 is required for HR. DDRM1 contains an N-terminal BRCT (BRCA1 C-terminal) domain and a C-terminal RING (really interesting new gene) domain and is highly conserved in plants including mosses. The ddrm1 mutant is defective in HR and thus is hypersensitive to DNA-damaging reagents. Biochemical studies reveal that DDRM1 interacts with and ubiquitinates the transcription factor SOG1, a plant-specific master regulator of DNA damage responses. Interestingly, DDRM1-mediated ubiquitination promotes the stability of SOG1. Consistently, genetic data support that SOG1 functions downstream of DDRM1. Our study reveals that DDRM1-SOG1 is a plant-specific module for HR and highlights the importance of ubiquitination in HR.

Uneven distribution of electric fields at the electrolyte-anode interface and associated Zn dendrite growth is one of the most critical barriers that limit the life span of aqueous zinc-ion batteries. Herein, new-type Zn-A-O (A = Si, Ti) interface layers with thin and uniform thickness, porosity, and hydrophilicity properties are developed to realize homogeneous and smooth Zn plating. For ZnSiO

The low energy/power density of aqueous rechargeable batteries (ARBs) have limited their further development and application because of their voltage limitation of 1.23 V. Herein, K–Zn hybrid ARBs with a high discharge voltage of 1.937 V are reported for the first time. The selective ionic insertion/extraction mechanism into/from the zinc hexacyanoferrate (ZnHCF) cathode in the hybrid electrolyte was clearly revealed by in situ X-ray diffraction. The cathode material displays an outstanding rate capability of 300C and a high capacity of 78.7 mA h g−1. The constructed K–Zn hybrid ARBs exhibit an energy density of 67 W h kg−1, a high power density of 4.76 kW kg−1 and excellent rate performance with 67.6% capacity retention from 2C to 60C. These excellent performances contribute to the selected K+ insertion mechanism. These exciting results can offer an alternative path for the development of hybrid aqueous batteries for stable and high energy/power density energy storage techniques.

Aqueous potassium-ion batteries (AKIBs), utilizing fast diffusion kinetics of K+ and abundant electrode resources, are an emerging technology offering high power density and low cost. Many efforts have been made by far to enhance the electrochemical performances of AKIBs, and some encouraging milestones have been achieved. To provide a deep understanding of the progress, challenges, and opportunities of the emerging AKIBs, the recent advances in both cathode and anode materials, and electrolytes of the AKIB systems are comprehensively summarized and discussed. Additionally, the research efforts on the optimization of electrode material properties, the revealing of the reaction mechanism, the design of electrolytes, and the full cell fabrication for AKIBs are highlighted. Finally, insights into opportunities and future directions for achieving high-performance AKIBs and their applications are proposed. Agency for Science, Technology and Research (A*STAR) Ministry of Education (MOE) National Research Foundation (NRF) Submitted/Accepted version This work was supported by the National Natural Science Foundation of China (51832004, 21905218), the Key Research and Development Program of Hubei Province (2021BAA070), the Natural Science Foundation of Hubei Province (2019CFA001, 2020CFB519), the Sanya Science and Education Innovation Park of Wuhan University of Technology (2021KF0019, 2020KF0019), and the Fundamental Research Funds for the Central Universities (WUT: 2020IVB034, 2020IVA036). This work was supported by the Singapore Ministry of Education Academic Research Fund Tier 2 (MOE2019-T2-2-127 and MOE-T2EP50120-0002), A*STAR under AME IRG (A2083c0062), and the Singapore National Research Foundation Competitive Research Program (NRFCRP18-2017-02). This work was supported by A*STAR under its IAF-ICP Programme I2001E0067 and the Schaeffler Hub for Advanced Research at NTU. This work was also supported by NTU-PSL Joint Lab collaboration. X. Z. gratefully acknowledges financial support from the Chinese Scholarship Council.

The further demand for electric vehicles and smart grids prompts that the comprehensive function of lithium-ion batteries (LIBs) has been improved greatly. However, due to sluggish Li

Prussian blue analogues have attracted growing attention as the positive electrode materials in rechargeable potassium-ion batteries (KIBs) due to the intrinsic open frameworks and high theoretical...

Aqueous zinc-ion batteries (ZIBs) represent an attractive choice for stationary energy storage. Its widespread application relies on the development of novel, reliable cathode materials. Herein, we find NASICON structured Na3V2(PO4)3 manifests simultaneous Zn2+/Na+ intercalation/de-intercalation in a single component electrolyte (2.0 M Zn(CF3SO3)2). The Na3V2(PO4)3/rGO microspheres prepared by spray drying deliver a high specific capacity of 114 mAh g−1 with an average discharge platform of 1.23 V at 50 mA g−1. Impressively, a high capacity of 74 mAh g−1 can be obtained after 200 cycles at 500 mA g−1. These excellent electrochemical performances can be ascribed to the stable and open NASICON framework, fast ion diffusion, as well as continuous electron transport. This work sheds light on the development of secondary batteries with hybrid ion intercalation/de-intercalation behaviors using a single component electrolyte.

Meiosis is a fundamental process for sexual reproduction in most eukaryotes and the evolutionarily conserved recombinases RADiation sensitive51 (RAD51) and Disrupted Meiotic cDNA1 (DMC1) are essential for meiosis and thus fertility. The mitotic function of RAD51 is clear, but the meiotic function of RAD51 remains largely unknown. Here we show that RAD51 functions as an interacting protein to restrain the Structural Maintenance of Chromosomes5/6 (SMC5/6) complex from inhibiting DMC1. We unexpectedly found that loss of the SMC5/6 partially suppresses the rad51 knockout mutant in terms of sterility, pollen inviability, and meiotic chromosome fragmentation in a DMC1-dependent manner in Arabidopsis thaliana. Biochemical and cytological studies revealed that the DMC1 localization in meiotic chromosomes is inhibited by the SMC5/6 complex, which is attenuated by RAD51 through physical interactions. This study not only identified the long-sought-after function of RAD51 in meiosis but also discovered the inhibition of SMC5/6 on DMC1 as a control mechanism during meiotic recombination.

Aluminum-ion batteries have attracted great interest in the grid-scale energy storage field due to their good safety, low cost and the high abundance of Al. However, Al anodes suffer from severe dendrite growth, especially at high deposition rates. Here, we report a simple strategy for constructing a highly reversible, dendrite-free, Al-based anode through directly introducing a solid-solution-based metal coating to a Zn foil substrate. Compared with Cu foil substrates and bare Al, a Zn foil substrate shows a lower nucleation barrier of Al deposition due to the intrinsic, definite solubility between Al and Zn. During Al deposition, a thin, solid-solution alloy phase is first formed on the surface of the Zn foil substrate and then guides the parallel growth of flake-like Al on Zn substrate. The well-designed, Zn-coated Al (Zn@Al) anode can effectively inhibit dendrite growth and alleviate the corrosion of the Al anode. The fabricated Zn@Al–graphite battery exhibits a high specific capacity of 80 mAh·g−1 and an ultra-long lifespan over 10,000 cycles at a high current density of 20 A·g−1 in low-cost molten salt electrolyte. This work opens a new avenue for the development of stable Al anodes and can provide insights for other metal anode protection.

N-doped carbon-confined transition metal nanocatalysts display efficient oxygen reduction reaction (ORR) performance comparable to commercial Pt/C electrocatalysts because of their efficient charge transfer from metal atoms to active N sites. However, the sheathed active sites inside the electrocatalysts and relatively large-size confined metal particles greatly restrict their activity improvement. Here, we develop a facile and efficient "MOFs plus ZIFs" synthesis strategy to successfully construct ultrafine sub-5 nm Co nanodots confined into superficial N-doped carbon nanowires (Co@C@NC) via a well-designed synthesis process. The unique synthesis mechanism is based on low-pressure vapor superassembly of thin zeolitic imidazolate framework (ZIF) coatings on metal-organic framework substrates. During the successive pyrolysis, the preferential formation of the robust N-doped carbon shell from the ZIF-67 shell keeps the core morphology without shrinkage and limits the growth of Co nanodots. Benefiting from this architecture with accessible and rich active N sites on the surface, stable carbon confined architecture, and large surface area, the Co@C@NC exhibits excellent ORR performance, catching up to commercial Pt/C. Density functional theory demonstrates that the confined Co nanodots efficiently enhance the charge density of superficial active N sites by interfacial charge transfer, thus accelerating the ORR process.

Nickel sulfide (NiS2) is generally regarded as an appropriate anode for manufacturing new-type potassium-ion batteries (PIBs), while the development and application of NiS2 are hampered by poor intrinsic electrical conductivity and huge volumetric change during potassiation/de-potassiation. Herein, we construct self-adaptive NiS2 nanoparticles confined to a three-dimensional graphene oxide (NiS2/3DGO) electrode via in situ sulfurization and self-assembly processes. The as-obtained NiS2/3DGO exhibits high reversible capacity (391 mA h g−1) and outstanding rate behavior (stable cycling at 1000 mA g−1) for PIBs. Furthermore, in situ X-ray diffractometry and ex situ Raman test results elucidate partially reversible transformation from the cubic NiS2 phase to the KxNiS2 intermediate, followed by generating a Ni0 and K2S4 product. This phenomenon is caused by the conversion reaction mechanism of NiS2 nanocrystals along with an amorphous phase transition during the initial cycle. Such understandings may shed new light on the application of metal sulfides and give directions to design novel electrodes with desirable structural stability and lifespan.

The highly dynamic nature of grid-scale energy systems necessitates fast kinetics in energy storage and conversion systems. Rechargeable aqueous batteries are a promising energy-storage solution for renewable-energy grids as the ionic diffusivity in aqueous electrolytes can be up to 1-2 orders of magnitude higher than in organic systems, in addition to being highly safe and low cost. Recent research in this regard has focussed on developing suitable electrode materials for fast ionic storage in aqueous electrolytes. In this review, breakthroughs in the field of fast ionic storage in aqueous battery materials, and one-/two-/three-dimensional (1D/2D/3D) and over-3D-tunnel materials are summarized, and tunnels in over-3D materials are not oriented in any direction in particular. Various materials with different tunnel sizes have been developed to be suitable for the different ionic radii of Li+ , Na+ , K+ , H+ , NH4+ , and Zn2+ , which show significant differences in the reaction kinetics of ionic storage. New topochemical paths for ion insertion/extraction, which provide superfast ionic storage, are also discussed. This article is protected by copyright. All rights reserved.

Realizing stable cycling performance with high areal capacity is a great challenge for metal-ion battery anodes. Achieveing high areal capacity generally requires the electrode in a high active loading with increased electrode thickness, which is not beneficial to the cycling stability. In this work, novel nanosheet-assembled compact CaV4O9 microflowers are firstly synthesized through a facile method, which exhibit both high areal capacity and stable cycling performance at high mass loadings. The compact microflower structure leads to an increased tap density of the electrode materials, benefiting to reduce the anode thickness at high mass loadings. Meanwhile, the assembled nanosheets maintain the nano-effects of the active materials for favorable electrochemical reactions. These merits together with the intrinsic superior electrochemical properties of CaV4O9, result in the outstanding electrochemical performance. When used as Li-ion battery anodes, a high areal capcity of ~2.5 mAh cm−2 at a high mass loading of 4.4 mg cm−2 is obtained, and a stable cycling over 400 cycles with the areal capacity over 1.5 mAh cm−2 is demonstrated. Besides, the superior electrochemical performance at high mass loadings is also observed for Na storage. These achievements may pave the way for constructing applicable high-capacity and stable anode materials in metal-ion batteries.

Iron sulfide is an attractive anode material for lithium-ion batteries (LIBs) due to its high specific capacity, environmental benignity, and abundant resources. However, its application is hindered by poor cyclability and rate performance, caused by a large volume variation and low conductivity. Herein, iron sulfide porous nanowires confined in an N-doped carbon matrix (FeS@N-C nanowires) are fabricated through a simple amine-assisted solvothermal reaction and subsequent calcination strategy. The as-obtained FeS@N-C nanowires, as an LIB anode, exhibit ultrahigh reversible capacity, superior rate capability, and long-term cycling performance. In particular, a high specific capacity of 1,061 mAh·g−1 can be achieved at 1 A·g−1 after 500 cycles. Most impressively, it exhibits a high specific capacity of 433 mAh·g−1 even at 5 A·g−1. The superior electrochemical performance is ascribed to the synergistic effect of the porous nanowire structure and the conductive N-doped carbon matrix. These results demonstrate that the synergistic strategy of combining porous nanowires with an N-doped carbon matrix holds great potential for energy storage.

Symmetric sodium-ion batteries (SIBs) are considered as promising candidates for large-scale energy storage owing to the simplified manufacture and wide abundance of sodium resources. However, most symmetric SIBs suffer from suppressed energy density. Here, a superior congeneric Na4V2(PO4)3 anode is synthesized via electrochemical preintercalation, and a high energy density symmetric SIB (Na3V2(PO4)3 as a cathode and Na4V2(PO4)3 as an anode) based on the deepened redox couple of V4+/V2+ is built for the first time. When measured in half cell, both electrodes show stabilized electrochemical performance (over 3000 cycles). The symmetric SIBs exhibit an output voltage of 3.0 V and a cell-level energy density of 138 W h kg–1. Furthermore, the sodium storage mechanism under the expanded measurement range of 0.01–3.9 V is disclosed through an in situ X-ray diffraction technique.

Constructing novel heterostructures has great potential in tuning the physical/chemical properties of functional materials for electronics, catalysis, as well as energy conversion and storage. In this work, heterostructured Bi2S3-Bi2O3 nanosheets (BS-BO) have been prepared through an easy water-bath approach. The formation of such unique BS-BO heterostructures was achieved through a controllable thioacetamide-directed surfactant-assisted reaction process. Bi2O3 sheets and Bi2S3 sheets can be also prepared through simply modifying the synthetic recipe. When employed as the sodium-ion battery anode material, the resultant BS-BO displays a reversible capacity of ∼630 mA h g-1 at 100 mA g-1. In addition, the BS-BO demonstrates improved rate capability and enhanced cycle stability compared to its Bi2O3 sheets and Bi2S3 sheets counterparts. The improved electrochemical performance can be ascribed to the built-in electric field in the BS-BO heterostructure, which effectively facilitates the charge transport. This work would shed light on the construction of novel heterostructures for high-performance sodium-ion batteries and other energy-related devices.

Rechargeable aqueous zinc-ion batteries are highly desirable for grid-scale applications due to their low cost and high safety; however, the poor cycling stability hinders their widespread application. Herein, a highly durable zinc-ion battery system with a Na2V6O16·1.63H2O nanowire cathode and an aqueous Zn(CF3SO3)2 electrolyte has been developed. The Na2V6O16·1.63H2O nanowires deliver a high specific capacity of 352 mAh g–1 at 50 mA g–1 and exhibit a capacity retention of 90% over 6000 cycles at 5000 mA g–1, which represents the best cycling performance compared with all previous reports. In contrast, the NaV3O8 nanowires maintain only 17% of the initial capacity after 4000 cycles at 5000 mA g–1. A single-nanowire-based zinc-ion battery is assembled, which reveals the intrinsic Zn2+ storage mechanism at nanoscale. The remarkable electrochemical performance especially the long-term cycling stability makes Na2V6O16·1.63H2O a promising cathode for a low-cost and safe aqueous zinc-ion battery.