Stability Of Materials Research Articles

Six element high-entropy Prussian blue analogue cathode enabling high cycle stability for sodium-ion batteries

Prussian blue analogues (PBA) are promising cathode materials for sodium-ion batteries. However, the cycle life of PBA is limited due to its structure instability during cycling. Here, we successfully introduce six transition metals into N coordination site to increase the configurational entropy, significantly improving the structure stability and cycle life of PBA cathode materials. Electrochemical characterization methods are used to compare the behavior of hexa-, penta-, quadr-, and tri-metal PBA, exhibiting the characteristic of performance increasing with entropy. Time-resolved in situ X-ray diffraction confirms the “quasi-zero-strain” structure of H-PBA during desodiation/sodiation process. X-ray absorption spectroscopy and density functional theory calculations reveal that Mn, Fe, Co and Cu contribute the high capacity of H-PBA, while Ni and Zn stabilize the structure. The strategy will inspire new ideas in designing long life cathode materials with high capacity for sodium-ion batteries.

Edge‑nitrogen/sulfur co-doping boost high potassium ion storage of carbon nanosheet anode materials

Potassium-ion batteries (PIBs) have garnered considerable attention as a potential alternative to lithium-ion batteries. However, the larger radius of K+ poses challenges, including slow kinetic processes and significant volume changes, which adversely affect the rate performance and cycling stability of electrode materials. Herein, N, S co-doped carbon nanosheets (xNS-HC) are synthesized as anode materials of PIBs by carbonization of citric acid and CH₄N₂S precursors in LiCl/KCl molten salts. Of these, 5NS-HC possesses a high N content of 20.19 at.% with 90.90 % of edge N-species and a S content of 2.53 at.%. The 5NS-HC material exhibits a high specific K+ storage capacity of 368.2 mAh g−1 at 0.1 A g−1, superior rate capability (106.1 mAh g−1 at 10 A g−1), and long-term cycling stability (205.8 mAh g−1 after 2800 cycles at 1 A g−1). In-depth analysis via in-situ XPS and DFT calculations reveals that the active sites doped with edge-N/S exhibit a profound affinity towards K+, thus contributing to the outstanding electrochemical K+ storage performance observed in 5NS-HC. The full cell of K0.4Mn0.9Li0.1O2·0.33H2O||5NS-HC exhibits a high specific capacity of 141.2 mAh g−1, supporting a high energy density of 147.1 Wh kg−1. These compelling results illustrate that edge-N/S co-doping can significantly enhance the K+ storage of carbon anode materials.

On the origin of superior stability of coherent nanoparticles under ion irradiation

Recently, a new anti-irradiation mechanism relying on reversible disorder-ordering transition of coherent nanoparticles was discovered, which significantly improves the microstructural stability and void swelling resistance of metallic materials. However, the factors that govern the outstanding stability and superb radiation tolerance are still not clear. Here, two kinds of FeCrAl alloys were designed, each strengthened by a different type of coherent phase: L21-ordered Fe2AlV and B2-ordered Ni (Al, Fe). It was observed that the two alloys exhibited disparate responses to high-dose ion irradiations at elevated temperatures. The L21-Fe2AlV precipitates were found to be completely dissolved after 50 dpa of ion irradiation at 500–600 °C, whereas the B2-NiAl precipitates remained stability even after 200 dpa irradiation. This research challenges the conventional wisdom that the stability of nanoparticles is governed by the balance between radiation-enhanced coarsening and radiation dissolution. Instead, it demonstrates the re-nucleation and subsequent interface-controlled solute reshuffling processes govern the stability of coherent chemically-ordered nanoparticles under radiation at high temperatures. We demonstrate that the low interfacial energy, which is related to both the simply chemically-ordered lattice structure and low lattice misfit interface, is crucial for enabling such short-range elemental reshuffling process to repeatedly form nanoprecipitates that cannot be suppressed by radiation.

Effect of carbonation curing on the characterization and properties of steel slag-based cementitious materials

Steel slag (SS)-based cementitious materials usually exhibit poor bulk stability, poor early activity and low mechanical strength, which greatly limits the consumption of SS in construction materials. Carbonation curing can not only control volume expansion but also improve the mechanical properties and durability of SS-based cementitious materials. First, the physicochemical properties of the SS were summarized. Then, the reaction mechanism of carbonation curing was analyzed. Next, the mineral composition, microstructure, morphology and CO2 uptake of the SS-based materials during carbonation curing were discussed, and the effects of carbonation curing on the mechanical properties, volume stability and durability of the SS-based materials were investigated. Finally, some suggestions for the application of carbonation curing in SS-based materials were given. The development and application of carbonation curing in SS-based materials can achieve the large-scale utilization of SS in cementitious materials and the effective reduction of CO2 emissions.

Novel Preparation and Characterization of Zinc Ricinoleate Through Alkali Catalysis

The enhanced thermal and chemical stability of Zinc oxide-based materials make them excellent candidates for the removal of odor-producing pollutants and compounds. The zinc salt of ricinoleic acid, commonly known as zinc ricinoleate, is viewed as the top performer. This article describes an innovative two-step synthesis of zinc ricinoleate, where the first step consists of the preparation of an intermediate compound, methyl ricinoleate, which is synthesized via transesterification of castor oil with methanol and catalyzed by sodium hydroxide. The second step comprises the preparation of zinc ricinoleate through the saponification of methyl ricinoleate in the presence of zinc oxide particles. XRD, FTIR, and NMR spectroscopies confirmed the synthesis of methyl ricinoleate and zinc ricinoleate. HR-SEM and AFM images showed the formation of larger particles, while the thermal stability of the materials was confirmed by TGA.

The effect of whitening toothpastes on the surface properties and color stability of different ceramic materials

ObjectivesThis study aimed to evaluate the effect of whitening toothpastes on the surface roughness and colour change of CAD-CAM materials.Materials and methodsA total of 96 samples (2 × 10 × 12 mm3) were prepared from Cerasmart (CS) and Celtra Duo blocks. Celtra Duo samples were divided into two groups. One group was fired with glaze paste (CDG) and the other was not treated (CD). All groups were then divided into 4 subgroups (n = 8). The groups were brushed with conventional (Colgate™ Max Fresh), silica (Opalescence™), charcoal (Curaprox™ Black in White) and blue covarine (Signal™ White Now) toothpastes for 30,000 brushing cycles. The initial and final surface roughness values were measured with contact profilometer and a dental spectrophotometer used for obtaining colour values. One sample from each brushed group was analyzed using a scanning electron microscope. Data was analyzed with Kruskal-Wallis and Mann-Whitney tests (p = 0.05).ResultsThe surface roughness of CS samples brushed with Opalescence™ and Curaprox™ was significantly higher than CD and CDG. Surface roughness change values of CS samples brushed with Curaprox™ were significantly higher than the CD and CDG. Curaprox™ brushed samples showed significant difference in colour change values for all materials.ConclusionsBrushing increases the surface roughness of CAD-CAM ceramic materials. The roughness of resin-based materials is higher than zirconia-reinforced lithium silicates. Silica-contained toothpastes may cause discoloration of nanoceramic and zirconia-reinforced glass ceramic restorations.Clinical relevanceIt should be clinically considered that whitening toothpastes may cause roughness in ceramic materials and change the desired color.

X-Type Ligands Effect on the Operational Stability of Heavy-Metal-Free Quantum Dot Light-Emitting Diodes.

ZnSeTe quantum dots (QDs) offer an efficient avenue for realizing heavy-metal-free light-emitting diodes (LEDs) that meet the Rec.2100 blue standard. Synthetic core-shell engineering has enabled big advances in the external quantum efficiency (EQE) of ZnSeTe QD-LEDs. However, the mechanisms behind the degradation of the operational stability of ZnSeTe QD-LEDs remain relatively unexplored. In this study, we explore the impact of ligand density and composition on both material and device stability. We developed a solid-film ligand exchange utilizing an inorganic X-type ligand (zinc chloride), revealing that the substitution of inorganic ligands for organic counterparts significantly influences the stability of both materials and devices.

A Bandgap‐Tuned Tetragonal Perovskite as Zero‐Strain Anode for Potassium‐Ion Batteries

AbstractPIBs are emerging as a promising energy storage system due to high abundance of potassium resources and theoretical energy density, however, progress of PIBs is severely hindered by structural instability and poor cycling of anode material during continual insertion and extraction of larger‐sized K+. Hence, developing anode material with structural stability and stable cycling remains a great challenge. Herein, band gap‐tuned Mo‐doped and carbon‐coated lead titanate (CMPTO) with zero‐strain K+ storage is presented as ultra‐stable PIBs anode. Mo doping introduces narrowed band gap and optimized crystal lattice for enhanced intrinsic electron and ion transfer. Demonstrated by in situ XRD characterizations, the crystal structure stays stable with unchanged peak positions, fully revealing zero‐strain characteristic of CMPTO anode during potassium storage for stable cyclic capability. Ultimately, CMPTO anode achieved ultra‐stable cycling performance of 7000 cycles at 500 mA g−1 with high capacity retention of 90 % and considerable specific capacity of 130.9 mAh g−1 after 600 cycles at 100 mA g−1; with relatively large density, CMPTO realized eminent volumetric capacity of 1111.09 mAh cm−3 and ultra‐long cycling life of 10000 cycles at 7041 mA cm−3. This work introduces a promisingly new route into developing anode materials with ultra‐stable performance for PIBs.

Improved Charge‐Transfer Doping in Crystalline Polymer for Efficient and Stable Perovskite Solar Cells

AbstractPerovskite solar cells (PSCs) have significant potential for next‐generation photovoltaic technology applications. However, the instability of hole transport layers (HTLs) becomes the major obstacle to long‐term operational devices, which are affected by the intrinsic thermal instability and loose structure of hole transport materials, as well as the hygroscopicity and migration of dopants. Here, poly(3‐hexylthiophene‐2,5‐diyl) (P3HT) is used as a model crystalline polymer to thoroughly investigate effective p‐type doping strategies and the underlying mechanism. According to Hard–Soft‐Acid–Base theory, the soft base P3HT is more likely to form a stable Lewis acid–base adduct with the reactive soft acid radical, resulting in a strong charge‐transfer interaction, thereby enhancing conductivity and regulating the energy band of the HTL. Meanwhile, the radical cation salt can promote pre‐nucleation to optimize the crystallization orientation of P3HT. The resulting PSCs exhibited the efficiency of 25.16%, which is the highest efficiency reported so far based on doped P3HT. In addition, the resulting devices demonstrated excellent stability, maintaining 96.5%, 96%, and 91% of their initial efficiency after aging under continuous illumination for 2028 h, at 85 °C for 1080 h, and at maximum power point (MPP) tracking under continuous 1 Sun illumination at 85 °C for 528 h, respectively.

Insight into performance and lifetime of ecofriendly pollution barriers in landfill for emergency: A thermogravimetric analysis for novel polymer materials

The novel polymer barrier wall is an in-situ remediation technology designed to effectively control the migration of pollution and prevent the diffusion of pollutants by blocking, sealing, or altering the direction of groundwater flow. With its advantages of rapid chemical reaction (achieving 95 % strength within 15 min) and portable equipment suitable for narrow and rugged emergency sites, this innovative polymer barrier demonstrates promising prospects for practical application. Hence, ensuring the long-term durability of new materials under corrosive and high-temperature leachate conditions is crucial. In this study, a comprehensive investigation was conducted on the corrosion and thermal aging performance of novel polymer materials. Firstly, the mechanical tensile properties of the polymer materials were examined after immersion in leachates, aiming to elucidate the degradation mechanism underlying these properties. Subsequently, thermogravimetric (TG) analysis was performed on the polymer materials immersed in various leachates. And the thermal stability and oxidation stability of novel materials were investigated using a thermogravimetric analyzer coupled with a Fourier transform infrared spectrometer (TG-FTIR). Based on the results obtained from thermal analysis, the service life of polymer materials under different pollutants was ultimately predicted utilizing the Arrhenius model. The findings indicate that the novel polymer materials exhibit commendable durability and pose little risk of causing secondary pollution.

Fiber-Reinforced Flexible Self-Healing Strain Sensor with Failure-Improving Sensitivity Recovery.

In this work, we address the inherent limitations of porous, flexible, fibrous, and self-healing strain sensors. Specifically, we tackle issues such as the fatigue failure of carbon-fibrous materials and the long-term flow and low mechanical stability of self-healing materials. We achieve this by combining self-healing carbon/PBS blends with fibrous materials, creating a fiber-reinforced self-healing composite. The self-healing carbon/PBS blends provide strain sensitivity and the ability to recover after fatigue and impact failure, while the fibers prevent the long-term flow of material and the scattering of pieces during impact and fatigue failure within the elastic deformation regime, enabling shape recovery. We fabricated composite wearable strain sensors with a viscoelastic functional layer composed of two continuous phases: (i) a self-healing polymer-carbon blend and (ii) long electrospun fibers of commercial polyurethane. This setup also eliminates the other drawbacks of bulk materials, such as nonlinearity of volt-ampere characteristics, irreversibility of deformation, and a low working factor, and allows improvement of the working factor after failure and healing. Most importantly, we discovered that hindered self-healing, like in the case of the MWCNT/PBS system, enables improvement of sensor sensitivity after large strains and failure, which is due to partial failure of the network formed by conductive particles.

Facilitating Ion Storage and Transport Pathways by In Situ Constructing 1D Carbon Nanotube Electric Bridges between 2D MXene Interlayers.

Multiple van der Waals (vdW) gaps invoke abundant opportunities for contriving artificial architectures and tailoring desired properties via the intercalation route beyond the reach of conventional concepts. Intriguingly, the electrochemical intercalation strategy can precisely and reversibly tune the intercalation stage of charged functional species. This study presents a valid structural editing protocol facilitated by electrochemical intercalation to engineer MXene interlayers, ultimately incorporating in situ constructed carbon nanotube (CNT) electric bridges for enhanced ion storage and transport pathways. The method allows for the precise modulation of electrochemical forces to tailor materials for specific applications. Deep intercalation and in situ growth processes establish robust anchoring sites and connectivity hubs between MXenes and CNTs, ensuring structural homogeneity and stability in advanced electrode materials. The results demonstrate the effectiveness of electrochemistry-mediated interlayer nanoengineering in MXenes, offering a versatile approach to design vdW heterostructures with tailored functionalities for energy storage and conversion applications. This work highlights the potential of electrochemical modulation in advancing materials engineering strategies for next-generation energy storage technologies.

High-Entropy Layered Oxide Cathode Materials with Moderated Interlayer Spacing and Enhanced Kinetics for Sodium-Ion Batteries.

Sodium-ion batteries (SIBs) with low cost and environmentally friendly features have recently attracted significant attention for renewable energy storage. Sodium layer oxides stand out as a type of promising cathode material for SIBs owing to their high capacity, good rate performance, and high compatibility for manufacturing. However, the poor cycling stability of layer oxide cathodes due to structure distortion greatly impacts their practical applications. Herein, a high entropy doped Cu, Fe, and Mn-based layered oxide (HE-CFMO), Na0.95Li0.05Mg0.05Cu0.20Fe0.22Mn0.35Ti0.13O2 for high-performance SIBs, is designed. The HE-CFMO cathode possesses high-entropy transition metal (TM) layers with a homogeneous stress distribution, providing a moderated interlayer spacing to maintain the structure stability and enhance Na+ ion diffusion. In addition, Li doping in TM layers increases the Mn valence state, which effectively suppresses John-Teller effect, thus stabilizing the layered structure during cycling. Furthermore, the use of nontoxic and low-cost raw materials benefits future commercialization and reduces the risk of environmental pollution. As a result, the HE-CFMO cathode exhibits a super cycling performance with a 95% capacity retention after 300 cycles. This work provides a promising strategy to improve the structure stability and reaction kinetics of cathode materials for SIBs.

Rapid and controllable microwave synthesis of nickel cobalt sulfide electrodes for high-performance asymmetric supercapacitors

The efficient and controllable synthesis method of high-performance energy storage electrode materials is crucial for advancing the development of energy storage technologies. Herein, by leveraging microwave heating technology in the sulfidation of nickel cobalt MOF, we effectively enhanced the efficiency of the synthesis process. Notably, sulfidation time emerged as a pivotal factor in tuning the crystalline phase structure and conductive properties of the material, leading to the successful development of NCS2 electrode material with a unique structure through optimized sulfidation conditions. Electrochemical performance tests of the NCS2 material revealed exceptional results; it exhibited a specific capacity of 1311 Fg[Formula: see text] at a current density of 1 Ag[Formula: see text] and retained 73.4% of its initial capacity when the current density increased to 10 Ag[Formula: see text], demonstrating outstanding rate performance. The composite NCS2//AC supercapacitor exhibits an energy density of 24.2 Whkg[Formula: see text] at power density of 800 Wkg[Formula: see text], even though after 1000 consecutive charge-discharge cycles, the capacity retention rate remained high at 77.1%, validating the exceptional stability and reliability of the NCS2 material during cycling. This work employs microwave sulfidation for the rapid and controlled synthesis of nickel cobalt sulfides, providing a green and efficient synthetic strategy for metal sulfide active materials.

Effect of Multivitamins on the Color Stability of Dental Materials Used in Pediatric Dentistry: An In Vitro Study

The longevity and acceptance of aesthetic dental materials are directly proportional to color stability. The aim of this study was to analyze the relationship between the use of multivitamins and the color stability of dental restorative materials. A total of 45 discs of nanohybrid composite, 45 of Reinforced Glass Ionomer (RGI), and 45 of Giomer were prepared. Subsequently, the samples were randomly divided into three solution groups (n = 15): Group 1—Sambucol Pediatric Syrup, Group 2—Hidropolivital Baby Drops, and Group 3—artificial saliva, which is preparation for patients with xerostomia. For 28 days, the specimens were immersed in 10 mL of each multivitamin for two minutes every 24 h. Color measurements were repeated on days 7, 14, 21, and 28. Statistical analysis was performed using the Jamovi software version 2.2.5, employing the Shapiro–Wilk test for normality and the Kruskal–Wallis test for non-parametric data. When comparing materials, statistically significant differences (p < 0.001) were observed between RGI and Giomer, and RGI and composite, but not between Giomer and composite (p = 0.716). The highest change was observed in RGI–Hidropolivital ΔE00 = 3.27 (2.38–4.59) and the least in composite–Sambucol ΔE00 = 0.72 (0.30–1.18). In conclusion, the exposure time and the multivitamin influence the color change of restorative materials.

Gel polymer electrolytes containing SiO2 spheres with tuned sizes to increase rechargeability of quasi-solid-state Zn-air batteries

Rechargeable zinc–air batteries (RZABs) with high energy densities and low costs have attracted tremendous interest for meeting the ever-growing demand for flexible and portable applications. In these batteries, the quasi-solid/solid-state electrolyte plays a critical role in the battery performance, such as the cycling performance rate and power output. In this study, porous poly (vinyl alcohol) (PVA) and poly (acrylic acid) (PAA) composite gel polymer electrolytes (GPEs) were modified by incorporating SiO2 as a water retainer. For this reason, SiO2 spheres of different sizes were synthesized by varying the temperature (5, 20, 60, and 80 °C) and reaction time (2, 6, 18, and 24 h). According to the SEM micrographs, the average size ranged from 107 to 710 nm depending on the conditions. The porous PVA/PAA–SiO2 GPEs obtained by selecting three SiO2 sizes (107, 425, and 630 nm) exhibited higher water retention capability than the unmodified GPE. Among them, the GPE with SiO2–630 nm displayed the highest battery performance (1.46 V, 85 mWcm−2 @ 0.8 V). This was achieved using CoMn2O4 spinel as a bifunctional electrocatalyst, with a catalyst loading of 2 mg cm−2. The quasi-solid-state RZAB displayed twice the rechargeability of the RZAB assembled with Pt/C+IrO2/C (120 vs. 62 cycles). According to post-mortem tests, this can be related to the improved water retention, the decrease in the size of the formed Zn dendrites, and the stability of the bifunctional material. Thus, fine-tuning of the electrocatalyst/electrolyte interface strongly affects the rechargeability.

Instability analysis of Li-ion battery electrode particles induced by chemomechanical growth using incremental deformation theory

Volumetric swelling due to lithiation into active battery materials is a well-known phenomenon. A chemo-mechanical framework can suitably explain the deformations of the electrode and the generation of diffusion-induced stresses (DIS). Various experimental works have shown that the effects of DIS further cause the active material to lose its structural stability. However, relatively few frameworks exist that can investigate such phenomena in a comprehensive manner. These are mainly based on the Euler–Bernoulli beam theory and the von-Karman plate theory. In the present work we present a generalized three-dimensional instability framework incorporating the theory of incremental deformation. We use this theory on a widely used chemo-mechanical framework. Notably, similar existing instability investigations on negative electrode materials are based only on incompressible material behaviour. As opposed to it, in this work we have considered a compressible material. Also, we account for the spatial and temporal nature of growth, which is a significant departure from the existing instability frameworks. Therefore, this current work brings the investigation of structural instability of electrode material closer to physical reality. In our study, we use the compound matrix method to find the critical lithiation parameter. Then we consider three sets of problems, each with a particular combination of boundary conditions applied on the inner and outer cylindrical surfaces of hollow cylindrical anode particles. These are free-free, fixed-free, and free-fixed, where each combination represents a particular type of interaction between an electrode particle and its surroundings. Most importantly, we find that the free-free and fixed-free conditions show only a pure axial and mixed mode of instability, and do not show the pure circumferential mode. The free-fixed conditions, however, shows all three modes of instability. Additionally, the presence of mode crossover makes the instability pattern of such electrode particles significant.

Exploring the Possibilities of Using Recovered Collagen for Contaminants Removal—A Sustainable Approach for Wastewater Treatment

Collagen is a non-toxic polymer that is generated as a residual product by several industries (e.g., leather manufacturing, meat and fish processing). It has been reported to be resistant to bacteria and have excellent retention capacity. However, the recovered collagen does not meet the requirements to be used for pharmaceutical and medical purposes. Due to the scarcity of water resources now affecting all continents, water pollution is a major concern. Another major field that could integrate the collagen generated as a by-product is wastewater treatment. Applications of collagen-based materials in wastewater treatment have been discussed in detail, and comparisons with already frequently used materials have been made. Over the last years, collagen-based materials have been tested for removal of both organic (e.g., pharmaceutical substances, dyes) and inorganic compounds (e.g., heavy metals, noble metals, uranium). They have also been tested for the manufacture of oil-water separation materials; therefore, they could be used for the separation of emulsified oily wastewater. Because they have been analysed for a wide range of substances, collagen-based materials could be good candidates for removing contaminants from wastewater streams that have seasonal variations in composition and concentration. The use of recovered collagen in wastewater treatment makes the method eco-friendly and cost efficient. This paper also discusses some of the challenges related to wastewater treatment: material stability, reuse and disposal. The results showed that collagen-based materials are renewable and reusable without significant loss of initial properties. In the sorption processes, the incorporation of experiments with real wastewater has demonstrated that there is a significant competition among the substances present in the sample.

Inherent Water Competition Effect-Enabled Colloidal Electrode for Ultra-stable Aqueous Zn-I Batteries.

Electrode material stability is crucial for the development of next-generation ultralong-lifetime batteries. However, current solid- and liquid-state electrode materials face challenges such as rigid atomic structure collapse and uncontrolled species migration, respectively, which contradict the theoretical requirements for ultralong operation lifetimes. Herein, we present a design concept for a soft colloid polyvinylpyrrolidone iodine (PVP-I) electrode, leveraging the inherent water molecule competition effect between (SO4)2- from the electrolyte and PVP-I from the cathode in an aqueous Zn||PVP-I battery. Electrochemical demonstrations measured under various simulated and practical (integrated with photovoltaic solar panel) conditions highlight the potential for an ultralong battery lifetime. The PVP-I colloid exhibits a dynamic response to the electric field during battery operation. More importantly, the water competition effect between (SO4)2- from the electrolyte and water-soluble polymer cathode materials establishes a new electrolyte/cathode interfacial design platform for advancing ultralong-lifetime aqueous batteries.

NASICON-structured Na3Ti0.8V1.2(PO4)3/C as a high-performance cathode for aqueous sodium-zinc hybrid batteries

Phosphate cathode materials have a stable and open backbone structure and are expected to be one of the ideal cathode materials for aqueous zinc ion batteries (ZIBs). In this work, a new compound Na3Ti0.8V1.2(PO4)3 is synthesised by sol-gel method and used as a cathode material for ZIBs. The battery delivered a reversible and stable capacity of 120.1 mA h g−1 over 100 cycles at 0.5 C. Impressively, the battery demonstrated exceptional cycling performance and outstanding rate performance, maintaining a capacity retention of 95.6 % after 1000 cycles at 5.0 C. It is demonstrated that the dissolution of V in water is effectively inhibited by partial Ti ion occupancy at the V site, which accelerates the ion diffusion rate and greatly improves the electrochemical performance. In this work, the charging and discharging process of NASICON structured Na3Ti0.8V1.2(PO4)3 cathode was investigated to show the mechanism of Na+ and Zn2+ co-doping. This discovery offers a novel phosphate cathode material for ZIBs, as well as a fresh approach to enhancing the specific capacity and stability of phosphate cathode materials.