Sacrificial Anode Research Articles

Nanofluid channels mitigated Zn2+ concentration polarization prolonged over 30 times lifespan for reversible zinc anodes

Despite interfacial engineering protects zinc anode from electrolyte corrosion, the suppressed kinetics process on the anode surface/interface circumscribes their cyclic stability, especially dendritic growth induced by ion concentration gradients. Here, the zinophilic nanofluid channels (ZNC) protective layer on zinc surface are designed for the rapid Zn2+ transport kinetic in the reversible cycling process. The ZNC demonstrates high separation pressure between ions and the channel surface due to the capillary effect, allowing Zn2+ to quickly migrate along the channel wall (Zn2+ transference numbers up to 0.72). Therefore, the unique channel modules alleviate concentration polarization from rapid Zn2+ consumption and maintain uniform deposition of Zn ions. Consequently, The ZNC protective layer anode exhibits significantly improved cycle life by more than 30 times (over 4000 h at 1 mA cm−2) that of bare Zn. The full battery exhibits stable cycling performance with excellent capacity retention (∼100%) after 5000 cycles. Our work provides innovative insights into the role of nanofluids in improving the stability of zinc anodes, offering enlightening perspectives for long-cycle life zinc-based batteries.

Effects of alloying elements on the corrosion behavior and discharge performance of Al-Zn-Mg-In-Ti-Sn sacrificial anode

Effects of alloying elements on the corrosion behavior and discharge performance of Al-Zn-Mg-In-Ti-Sn sacrificial anode

Enhancing corrosion resistance of Al alloy sheets with potential gradient by arc-sprayed Zn coatings

To improve the corrosion resistance and wide the application of Al alloy sheet in the engineering production, a corrosion potential gradient along the thickness of the Al alloy sheet was fabricated using the sprayed Zn layer. The process of arc spraying was employed to obtain the Zn coating with optimizing the parameters. Electrochemical testing was conducted on the surface of Al alloy sprayed with Zn layers at different depths. As the depth in the thickness direction increases, the content of Zn alloy elements gradually decreases and the potential gradually increases. This exhibits a gradual decrease in corrosion tendency. The results of electrochemical impedance spectra (EIS) revealed the existence of pitting corrosion on the surface of the Al alloy. This even extended to the underlying substrate material. In contrast, the Zn coating, when exposed to a corrosive environment, demonstrated the beneficial cathodic effect as a sacrificial anode and the protective function of a passivating film, thus mitigating corrosion. The gradual increase in charge transfer resistance in the impedance spectrum suggested that the corrosion resistance of the sample is increasingly improved. Therefore, it exhibited remarkable resistance to corrosion. Additionally, the SEM surface morphology and XRD pattern were utilized to further explain the corrosion mechanism of the arc-sprayed Zn coating. The Zn coating can provide sacrificial protection to the Al layer due to its higher negative potential and localized corrosion reactivity. This is attributed to the micro-galvanic couples formed between the Zn and Al layer, thus increasing the corrosion resistance of the sheets.

Chemical and electrochemical repair methods for the anchorage regions of grouted, post-tensioned concrete systems

Grouted, post-tensioned concrete systems are commonly used for constructing bridges with an intended corrosion-free service life of 100+ years. However, the use of inadequate grout materials and improper grouting techniques have caused voids at the anchorage regions – resulting in premature corrosion (say, within one or two decades) of strands. In addition, re-grouting the voids with repair grout has aggravated the corrosion of strands at the interface between the base grout (usually carbonated) and repair grout due to the differences in their chemical properties – raising concerns and leading to reluctance in re-grouting the voids in tendons. This work focused on developing non-invasive chemical (re-alkalization) and electrochemical (galvanic cathodic protection) methods to repair the anchorages of grouted, post-tensioned concrete systems. Immersion experiments were conducted to assess the efficiency of alkaline solutions in re-alkalizing the carbonated grouts. It was found that 1M Ca(OH)2 solution can restore the pH of the carbonated grouts in about a day. Moreover, the electrochemical impedance spectroscopy studies indicated that 1M Ca(OH)2 solution can re-passivate the embedded strands within a week. It can be sometimes challenging to achieve complete re-alkalization and re-grouting of voids; hence, a redundant electrochemical system that could work from outside the anchorage was found necessary. Therefore, experiments were conducted to evaluate the viability of galvanic anodes in protecting the anchorages. It was found that a thin layer of grout surrounding the strand would be sufficient to provide ionic conductivity for the galvanic anode (connected to the strand-end outside the anchorage) to protect the strand portions inside the anchorage. Based on the study, recommendations for the repair of the anchorage regions using chemical and electrochemical methods are presented.

Breath inspired multifunctional low-cost inorganic colloidal electrolyte for stable zinc metal anode

The practical application of aqueous zinc-ion batteries (AZIBs) is primarily constrained by issues such as corrosion, zinc dendrite formation, and the hydrogen evolution reaction occurring at the zinc metal anode. To overcome these challenges, strategies for optimizing the electrolyte are crucial for enhancing the stability of the zinc anode. Inspired by the role of hemoglobin in blood cells, which facilitates oxygen transport during human respiration, an innovative inorganic colloidal electrolyte has been developed: calcium silicate-ZnSO4 (denoted as CS-ZSO). This electrolyte operates in weak acidic environment and releases calcium ions, which participate in homotopic substitution with zinc ions, while the solvation environment of hydrated zinc ions in the electrolyte is regulated. The reduced energy barrier for the transfer of zinc ions and the energy barrier for the desolvation of hydrated ions imply faster ion transfer kinetics and accelerated desolvation processes, thus favoring the mass transfer process. Furthermore, the silicate colloidal particles act as lubricants, improving the transfer of zinc ions. Together, these factors contribute to the more uniform concentration of zinc ions at the electrode/electrolyte interface, effectively inhibiting zinc dendrite formation and reducing by-product accumulation. The Zn//CS-ZSO//Zn symmetric cell demonstrates stable operation for over 5000 h at 1 mA cm−2, representing 29-fold improvement compared to the Zn//ZSO//Zn symmetric cell, which lasts only 170 h. Additionally, the Zn//CS-ZSO//Cu asymmetric cell shows stable average Coulombic efficiency (CE) exceeding 99.6% over 2400 cycles, significantly surpassing the performance of the ZSO electrolyte. This modification strategy for electrolytes not only addresses key limitations associated with zinc anodes but also provides valuable insights into stabilizing anodes for the advancement of high-performance aqueous zinc-ion energy storage systems.

Bifunctional electrolyte additive enabling long cycle life of vanadium-based cathode aqueous zinc ion batteries

Aqueous zinc ion batteries have received extensive attention due to their many advantages, but they still face problems such as dendrite growth and interface reaction of Zn anode and collapse of vanadium-based cathode structure. Here, a bifunctional electrolyte additive Methionine (MET) is proposed, which exhibits a unique role in inducing uniform deposition of zinc anode and inhibiting the failure of vanadium-based cathode materials. MET affects the solvated structure of the electrolyte to inhibit water activity and reduce HER and other related parasitic reactions. At the same time, it regulates the flux of Zn2+, improves the deposition kinetics of Zn2+ on the zinc anode side, and induces the preferential growth of the Zn (1 0 1) crystal plane to promote ordered Zn deposition. In particular, MET can in-situ generate a CEI containing such as ZnF2 on the surface of the vanadium-based cathode to inhibit the failure of the vanadium-based cathode, while adjusting the surface electronic state and Zn2+ diffusion behavior, and reducing the structural damage of the vanadium-based cathode caused by the Zn2+ intercalation process by inducing a strengthened surface pseudocapacitive reaction. Compared with the bare electrolyte, the capacity retention rate of the K2V8O21||Zn full-cell with OTF-M50 electrolyte increased from 10.2 % to 99.8 % after 800 cycles at a low current density of 1 A/g. Therefore, MET exhibits considerable application prospects as a bifunctional additive that can improve the stability of vanadium-based cathode and promote the stable deposition of zinc anode.

Regulating the Zn electrode/electrolyte interface with lactose additive for high performance Zn anode

The practical utilization of rechargeable aqueous zinc metal batteries (AZMBs) has been constrained by the formation of zinc dendrites and other associated issues. This article introduces lactose, a compound rich in hydroxyl groups, as an electrolyte additive into the aqueous solution of the electrolyte with the objective of suppressing the harmful growth of zinc dendrites. The lactose additive, with its strong zincophilicity, robust intermolecular hydrogen bonding, and a large number of exposed high electronegativity hydroxyl groups, enables lactose to effectively modulate the electrode/electrolyte interface in a dynamic manner, thereby achieving the stability and reversibility of the zinc anode. The findings presented in this work demonstrate the uniform deposition and stripping of zinc in a 2 M ZnSO4 electrolyte with the addition of lactose, thereby enhancing the cycling performance of Zn||Zn batteries. The alteration of the zinc ion environment on the surface of the zinc electrode, in conjunction with the dynamic modulation of the Gouy-Chapman-Stern (GCS) layer by lactose, increases the nucleation overpotential, thereby facilitating to a uniform deposition morphology in lieu of the formation of large-scale dendrites. Furthermore, the formation of hydrogen bonds serves to prevent the occurrence of side reactions. These factors act in concert to enhance the electrochemical performance of AZMBs. The addition of lactose to the electrolyte has resulted in a significant enhancement in the Coulombic efficiency of the card-type Zn||Cu asymmetric battery, reaching 99.7 %. The biodegradability of lactose and the sustainability of its source make this research conducive to the development of environmentally friendly battery electrolyte additives.

Achieving the dendrite-free zinc anode by constructing a Sn-C interfacial layer with zincophilic and conductive network

Under the basic national policy of sustainable green development, high-performance and low-cost energy storage devices are urgently needed for intermittent generation of clean energy and storage of electrical energy. Zn metal with high capacity, abundant reserves and excellent plasticity, but the inevitable side reactions (hydrogen precipitation and corrosion, etc.) of the Zn metal anode itself have severely limited the development of aqueous Zn ion batteries (AZIBs) in the market. In this study, an artificial protective layer of polymer-derived carbon material combined with Sn is prepared to inhibit hydrogen precipitation and corrosion and prolong the lifetime of AZIBs. With these advantages, the Zn@Sn@N doped carbon (Zn@CNS) symmetric cell could achieve a stable cycle life of 1000 h at 2 mA cm-2 and low overpotential. The excellent stripping life of over 400 h is achieved in half-cells assembled with Cu foils. Furthermore, the α-MnO2//Zn@CNS full battery shows superior stability in rate capability and long-term capacity retention compared to the α-MnO2//Zn battery, indicating that the CNS coating provides excellent performance and practical value.

Separator functionalization realizing stable zinc anode through microporous metal-organic framework with special functional group

Aqueous zinc ion batteries (AZIBs) have been regarded as one of the most promising energy storage systems because of their security, high specific capacity and abundant zinc resources, etc. Despite the promising prospects of AZIBs, their practical application is still plagued by dendrite and side reactions on zinc surface. In this paper, glass fiber separators were modified by in-situ loading metal-organic framework MIL-125 (M-125) and its -NH2-functionalized material (NM-125). The designed separator pore structure was successfully adjusted and endowed with -NH2 functional groups, which can ultimately dramatically enhance the electrochemical performance of AZIBs under practical operation conditions. The functionalized NM-125 with smaller pore size and particle size enables NM-125-GF to prevent the transport of macromolecular anions in the electrolyte, guiding and promoting zinc ions to undergo an orderly migration. In addition, -NH2 of NM-125 can adsorb Zn2+ and detach them from the solvated structure, inhibiting the generation of anode-side reactions and optimizing battery performance. Notably, Zn||MnO2 full cell assembled with -NH2 functionalized separator also shows a high initial discharge specific capacity (160.2 mAh g-1) with a high capacity retention of ∼99.8% even after 700 cycles. The rational design of the functionalized separator provides a useful guideline for optimizing high-performance AZIBs.

Toward Continuous Electrochemical Synthesis of Ferrate

AbstractFerrate (Fe(VI)) is of great interest in energy storage solutions, organic synthesis, and wastewater treatment due to its decent oxidation potential and non‐toxic end‐product formation, making it a green oxidizer. The electrochemical generation of ferrate in NaOH at current densities of j ≥ 100 mA cm−2 is presented using low‐cost sacrificial iron anodes, mild steel, and spheroidal graphite cast iron (ductile iron). Under optimized reaction parameters with 40 wt.% (14 m) NaOH and a ZrO2‐based diaphragm, spheroidal graphite cast iron shows no signs of passivation in 5 h experiments even at j = 150 mA cm−2. The results are used in a novel electrolysis cell with a combined geometric anode surface area of 230 cm2, incorporated in a mini‐plant suitable for continuous synthesis. This setup produces a peak ferrate concentration of 10.1 g L−1 (84 mm) after 5 h in 1.6 L anolyte volume, resulting in a total ferrate mass of 16.2 g. Optimal electrolysis temperatures are between 35 and 50 °C. The highest current efficiency is 63.0%, and the lowest specific energy consumption is 9.2 kWh kg−1 ferrate. The presented work is an essential step toward the continuous electrochemical synthesis of ferrate using sacrificial anodes under basic conditions.

Multidentate Chelating Ligands Enable High-Performance Zinc-Bromine Flow Batteries.

Zinc bromine flow battery (ZBFB) is a promising battery technology for stationary energy storage. However, challenges specific to zinc anodes must be resolved, including zinc dendritic growth, hydrogen evolution reaction, and the occurrence of "dead zinc". Traditional additives suppress side reactions and zinc dendrite formation by altering the solvation structure of Zn2+ and adsorbing onto the zinc surface through only a limited number of zincophilic sites, resulting in weak adsorption on zinc metal and potential inability to simultaneously optimize the solvation structure of zinc ions. Obviously, increasing the number of potential zincophilic sites in the additive can significantly enhance the interaction with zinc. Herein, we propose a strong chelate, ethylenediamine tetramethylene phosphonic acid (EDTMPA) as the additive, which boasts six potent zincophilic sites, not only promotes the formation of the water-deficient inner Helmholtz plane but also plays a crucial role in restructuring the solvation environment of Zn2+. As a result, the zinc symmetric flow battery with EDTMPA exhibited exceptional coulombic efficiency of 99.4% over 800 cycles, surpassing the previous studies by a significant margin. Furthermore, the assembled ZBFB has showcased a dendrite-free and enduring cycling over 400 cycles at 80 mA cm-2.

Multidentate Chelating Ligands Enable High‐Performance Zinc‐Bromine Flow Batteries

Zinc bromine flow battery (ZBFB) is a promising battery technology for stationary energy storage. However, challenges specific to zinc anodes must be resolved, including zinc dendritic growth, hydrogen evolution reaction, and the occurrence of "dead zinc". Traditional additives suppress side reactions and zinc dendrite formation by altering the solvation structure of Zn2+ and adsorbing onto the zinc surface through only a limited number of zincophilic sites, resulting in weak adsorption on zinc metal and potential inability to simultaneously optimize the solvation structure of zinc ions. Obviously, increasing the number of potential zincophilic sites in the additive can significantly enhance the interaction with zinc. Herein, we propose a strong chelate, ethylenediamine tetramethylene phosphonic acid (EDTMPA) as the additive, which boasts six potent zincophilic sites, not only promotes the formation of the water‐deficient inner Helmholtz plane but also plays a crucial role in restructuring the solvation environment of Zn2+. As a result, the zinc symmetric flow battery with EDTMPA exhibited exceptional coulombic efficiency of 99.4% over 800 cycles, surpassing the previous studies by a significant margin. Furthermore, the assembled ZBFB has showcased a dendrite‐free and enduring cycling over 400 cycles at 80 mA cm−2.

Phase Engineering of ZnSe by Small Molecules as a High-Performance Protective Layer for Zn Anode.

The practical application of aqueous zinc ion batteries is still hampered by the side reactions and dendrite growth on Zn anode. Herein, the phase engineering of ZnSe coating layer by incorporating small molecules is developed to enhance the performance of Zn anode. The unique electronic structure of ZnSe⋅0.5N2H4 promises strong adsorption for Zn atoms and enhanced ability to inhibit hydrogen evolution, thereby promoting uniform Zn deposition and preventing by-product and dendrite growth. Meanwhile, fast Zn2+ transfer and deposition kinetics are also demonstrated by ZnSe⋅0.5N2H4. As a result, the ZnSe⋅0.5N2H4@Zn symmetric cell achieves long-term cycling stability up to 1900 h and 300 h at high current densities of 5 mA cm-2 and 20 mA cm-2, respectively. The assembled ZnSe⋅0.5N2H4@Zn||NH4V4O10 full cell presents outstanding cycling stability and rate capability. This work highlights the key role of crystal phase control of protective layer for high-performance zinc anode.

Poly(3, 4-Ethylenedioxythiophene) as Promising Energy Storage Materials in Zinc-Ion Batteries.

Benefiting from the advantages of high conductivity and good electrochemical stability, the conjugated conducting polymer poly (3, 4-ethylenedioxythiophene) is a promising energy storage material in zinc-ion batteries. Zinc-ion batteries have the advantages of high safety, environmental friendliness, and low cost, but suffer from unstable cathode material structure, poor electrical conductivity, and uncontrollable dendritic growth of zinc anodes. PEDOT, with its fast electrochemical response and wide potential window, is expected to make up for the shortcomings and enhance capacity and cycle life of zinc-ion batteries. Herein, in this review different polymerization methods of poly (3, 4-ethylenedioxythiophene) as well as their structure and properties are summarized; the progress in doping strategies related to the increasing conductivity and dispersivity of poly (3, 4-ethylenedioxythiophene) materials is discussed; specific applications of poly (3, 4-ethylenedioxythiophene)-based materials in anode, cathode, electrolyte, and binder of zinc-ion batteries are explored; and the representative advancements for improving the electrochemical performance of poly (3, 4-ethylenedioxythiophene) in zinc-ion batteries are emphasized. Finally, the current challenges of poly (3, 4-ethylenedioxythiophene) as promising materials in zinc-ion batteries and an insight into their future research directions are pointed out.

Turning crisis into opportunity: Intrinsically polarised low concentration eutectic electrolytes enable highly reversible zinc anodes

Low-concentration electrolytes (LCEs) hold great promise for sustainable energy storage due to their low viscosity, excellent wettability, and cost-effectiveness. However, their intrinsic polarization issues often lead to side reactions and dendrite growth, hindering their broader application. Herein, we present an approach to convert the negative effects of intrinsic polarization in LCEs into advantages, overcoming these challenges. The experimental and theoretical analyses demonstrate that acetate-adsorbed zinc anodes can harness the intrinsic polarization of LCEs to direct the electrocrystallization process on their surfaces. This promotes the preferential orientation of Zn(002) plane with high stability, resulting in symmetric batteries loaded with low-concentration eutectic electrolytes (LCEE) that maintain surprisingly low voltage polarization during the dendrite-free growth of up to 3150 h. In addition, by forming an organic-inorganic composite film enriched with N and Cl, LCEE achieves rapid migration of Zn2+. This allows Zn//PANI full batteries with LCEE to demonstrate superior capacity and cycling stability compared to other Zn-based batteries with LCEs. This study not only achieves a divergent design in LCEs but also provides clear guidance for future electrolyte development.

Soft-hard zwitterionic additives for aqueous halide flow batteries.

Aqueous redox flow batteries with halide-based catholytes (where the halogen atom (X) is Br or I) are promising for sustainable grid energy storage. However, the formation of polyhalides during electrochemical charging and the associated phase separation into X2 limits the operable state of charge (SoC), results in vaporization and self-discharge inefficiencies, and spurs complete device failure1-3. Here we introduce soft-hard zwitterionic trappers (SH-ZITs) as complexing agents composed of a polyhalide-complexing 'soft' cationic motif and a water-soluble 'hard' anionic motif to enable homogeneous halide cycling. More than 300 structures were designed and 13 were characterized, showcasing the ability to complex polyhalides in homogeneous aqueous solution, to deter cation-exchange membrane crossover and to alter the electrochemical electrode mechanism. In flow battery cycling at a standard catholyte SoC of 66.6 per cent (stoichiometrically X3-), an average coulombic efficiency of more than 99.9 per cent at 40 milliamperes per square centimetre with no apparent decay was observed after more than 1,000 cycles over 2 months, with stability at elevated temperatures also demonstrated. Interestingly, SH-ZITs enable homogeneous cycling of the halide catholyte up to 90 per cent SoC at 2 moles per litre (47.7 ampere-hours per litre) for bromide, revealing previously unknown polyhalide regimes to be studied. Ultimately, SH-ZIT enables ultrahigh catholyte capacity utilization up to over 120 ampere-hours per litre at 80 per cent SoC with homogeneous cycling as well as the ability to pair with a zinc anode in a hybrid flow battery.

Stabilizing zinc anodes by a solvation sheath modification with toluenesulfonate additive

As an advanced electrochemical energy storage device, aqueous zinc-ion batteries offer high theoretical capacity and energy density, employing water-based electrolytes to reduce fire and explosion risks. However, zinc tends to form dendrites during charge-discharge processes, leading to reduced electrode surface area and shortened cycling lifespan. In this study, we propose the use of a commonly used and cost-effective additive, sodium p-toluenesulfonate (OTM), to stabilize zinc anodes. Experimental and theoretical simulations demonstrate that OTM can enter the solvation sheath of Zn2+, reduce the activity of nearby H2O molecules, facilitate uniform Zn2+ deposition, and suppress zinc dendrite formation. Therefore, Zn//Zn symmetric batteries utilizing ZnSO4 (ZSO) electrolytes containing OTM achieved outstanding long-term performance exceeding 1700 h at 1 mA cm−2, significantly surpassing those employing ZSO electrolytes. Additionally, Zn//VO2 full batteries with OTM additives exhibited enhanced cycling stability and an initial discharge capacity of 180 mAh g−1 at 3 A g−1, demonstrating its superior application potential.

Harnessing biological insights: Integrating proton regulation, pH buffer and zincophility for highly stable Zn anode

Zinc anodes are severely threatened by hydrogen evolution, dendrite growth and by-products. Inspired by the mechanisms of L-carnosine (L-car) in maintaining intracellular pH stability and fostering mucosal repair in biological systems, this study innovatively proposed a comprehensive strategy integrating proton regulation, pH buffer and zincophility by introducing L-car as an electrolyte additive to achieve remarkable stability of zinc anode. Experimental validations and theoretical calculations demonstrate that the abundant N and O sites in L-car can form robust hydrogen bonds with protons, effectively impeding interfacial proton transport and substantially mitigating HER. Moreover, dual pH buffering sites of L-car facilitate dynamic modulation of proton concentration, stabilizing the pH of electrolyte, and suppressing Zn corrosion/passivation/by-product. Concurrently, the robust chelation between L-car and Zn2+ orchestrates uniform zinc ion deposition. This synergistic trifecta of L-car endows Zn ion batteries with an extraordinary cycling stability, extending to an ultralong duration of 5500 h. Furthermore, the Zn//MnO2 full battery, demonstrates remarkable stability, retaining a specific capacity of 106.1 mAh/g with 79.2 % retention after 1000 cycles at 3 A/g. This study pioneers the interdisciplinary application of L-car in electrolyte modification, presenting a novel paradigm for stabilizing zinc anodes.

Organic Electrolyte Additives for Aqueous Zinc Ion Batteries:Progress and Outlook.

Aqueous zinc ion batteries (AZIBs) are considered one of the most prospective new-generation electrochemical energy storage devices with the advantages of high specific capacity, good safety, and high economic efficiency. Nevertheless, the enduring problems of low Coulombic efficiency (CE) and inadequate cycling stability of zinc anodes, originating from dendrites, hydrogen precipitation and passivation, are closely tied to their thermodynamic instability in aqueous electrolytes, which significantly shortens the cycle life of the battery. Electrolyte additives can solve the above difficulties and are important for the advancement of affordable and reliable AZIBs. Organic electrolyte additives have attracted widespread attention due to their unique properties, however, there is a lack of systematic discussion on the performance and mechanism of action of organic electrolyte additives. In this review, a comprehensive overview of the application of organic electrolyte additives in AZIBs is presented. The role of organic electrolyte additives in stabilizing zinc anodes is described and evaluated. Finally, further potential directions and prospects for improving and directing organic electrolyte additives for AZIBs are presented.

Transforming Zinc-Ion Batteries with DTPA-Na: A Synergistic SEI and CEI Engineering Approach for Exceptional Cycling Stability and Self-Discharge Inhibition.

Aqueous zinc-ion batteries (ZIBs) hold immense potential for large-scale energy storage, but their practical implementation faces significant challenges related to the zinc anode, including dendrite formation, corrosion, and hydrogen evolution. This study addresses these challenges by introducing diethylenetriamine pentaacetate sodium salt (DTPA-Na) as a novel electrolyte additive. DTPA-Na exhibits a unique dual functionality, enabling the formation of a robust, multi-layered solid electrolyte interphase (SEI) on the zinc anode and a stable cathode electrolyte interphase (CEI) on the MnOOH cathode. The engineered SEI effectively suppresses interfacial side reactions, facilitates uniform zinc deposition, and mitigates dendrite growth, while the CEI inhibits MnOOH dissolution and detrimental cathode side reactions. This synergistic SEI/CEI engineering approach significantly enhances ZIB performance, achieving remarkable cycling stability and self-discharge inhibition, as evidenced by the extended lifespan of Zn||Zn symmetrical cells (4400 hours at 0.5 mA/cm2) and the exceptional capacity retention of Zn||MnOOH full cells after prolonged rest (98.61 % after 720 hours).