Sacrificial Anode Research Articles

Insights Into Electrolyte Strategies for Suppressing Side Reactions Towards Aqueous Zinc‐Ion Batteries

AbstractAqueous zinc‐ion batteries (AZIBs) have gained significant attention as a promising technology for grid scale energy storage due to their high safety and low cost. Nevertheless, side reactions on the zinc anodes result in a decrease in effi‐ciency decay and capacity loss, hindering the wide‐spread application of AZIBs. Recently, great efforts have been con‐ducted to tackle these challenges, such as modifying the inter‐nal structure of zinc anodes, coating protection on the surface of zinc anodes, and optimizing the electrolytes. However, there is a lack of systematic summary on the design of side reac‐tions‐suppressed zinc anodes, especially through the optimi‐zation strategies of aqueous electrolytes. Herein, this review systematically summarizes the main mechanisms and influence factors of side reactions. Subsequently, we present the main modification strategies based on electrolyte engineering for alleviating side reactions, with a particular emphasis on poly‐mer electrolytes. Lastly, we shed light on the potential research directions and perspectives of aqueous electrolytes, which may promote the development of AZIBs.

Efficient phosphate and hydrogen recovery from sludge fermentation liquid by sacrificial iron anode in electro-fermentation system

Electro-fermentation (EF) has been extensively studied for recovering hydrogen and phosphorus from waste activated sludge (WAS), while was limited for the further application due to the low hydrogen yield and phosphorus recovery efficiency. This study proposed an efficient strategy for hydrogen and vivianite recovery from the simulated sludge fermentation liquid by sacrificial iron anode in EF. The optimum hydrogen productivity and the utilization efficiency of short chain fatty acids (SCFAs) reached 45.2 mmol/g COD and 77.6% at 5 d in pH 8. Phosphate removal efficiency achieved at 90.8% at 2 d and the high crystallinity and weight percentage of vivianite (84.8%) was obtained. The functional microbes, i.e., anaerobic fermentative bacteria, electrochemical active bacteria, homo-acetogens and iron-reducing bacteria were highly enriched and the inherent interaction between the microbial consortia and environmental variables was thoroughly explored. This work may provide a theoretical basis for energy/resource recovery from WAS in the further implementation.

Steering Interfacial Renovation with Highly Electronegative Cl Modulated Trinity Effect for Exceptional Durable Zinc Anode

AbstractThe poor anode/electrolyte interface triggered by abysmal dendritic growth and hydrogen evolution reactions (HER) hinders the development of aqueous zinc‐ion batteries (AZIBs). Here, a highly efficient electrolyte is formulated with sucralose (Sucral) additive to refresh solvated structure and steer interfacial renovation, for building highly electronegative Cl‐modulated trinity effect in the bulk‐interface between electrolyte and electrode. Experiment results and theoretical studies jointly reveal that Sucral with highly zincophilic and hydrophilic hydroxyl groups can remodel primary Zn2+ solvation shell and interrupt strong H‐bond network from H2O molecules, thus boosting fast de‐solvation and restricting undesirable HER. Simultaneously, three highly electronegative chlorides in the adsorbed Sucral possessing hydrophobic features can enable a H2O‐poor electric double‐layer (EDL), thus remodeling the Zn surface against corrosion. Additionally, it realizes preferential exposure of the Zn (002) plane for helping uniform interfacial deposition. The synergy of the above factors achieves a prolonged lifespan of 3000 h (1.0 mA cm−2, 1.0 mAh cm−2), much better than that with Sucrose (Suc) electrolyte. The Zn//V2O5 full cell at 5 A g−1 also maintains enhanced stability of 1500 cycles with 160 mAh g−1.

Alloying strategy to stabilize monocrystalline zinc anode under high utilization and working capacity

Zn(002) has been proven as a dendrite-free anode for Zn batteries. However, stable Zn plating/stripping behavior at an areal capacity exceeding 5 mAh cm−2 has remained unfulfilled so far. In this study, we show that the planar deposit on pure Zn (002) substrate is loosely stacked with high corrosion tendency by the aqueous electrolyte, the key obstacle to achieving considerable efficiency under high-capacity working conditions. To mitigate the side reactions, we introduce an alloying approach by combining monocrystalline Zn(002) with eutectic Al and Cu. The alloying strategy enhances the electrostatic interaction between deposits and substrate, favoring a dense-packed deposition morphology with improved corrosion resistant ability. Solid solution property of Al and Cu in Zn matrix also ensures the structure stability during repeated plating/stripping cycles. As a result, significant extension in cycle life of Zn alloy (002)-based symmetric cells even under 50 mA cm−2 and 25 mAh cm−2 and performance with high utilization also achieves a leading level without extra methods on surface protection. The modified Zn alloy (002) anode induces high anode utilization, paving the way for Zn batteries to meet the requirements of practical applications.

Achieving High Ionic Conductivity and Mechanical Strength by a Leather Gel Electrolyte for Flexible Zinc-Ion Batteries.

The continuous advancement in the field of flexible and wearable electronics has led to increased research interest in safe, low-cost, and flexible zinc-ion batteries, particularly with a focus on flexible electrolytes. In this study, we present a leather gel electrolyte (LGE) that offers robust mechanical properties and an excellent electrochemical performance. LGE exhibits an ionic conductivity of 1.36 × 10-2 S cm-1 and achieves a capacity of 303.7 mAh g-1 in flexible zinc-manganese dioxide batteries. Even after 1000 cycles, the capacity retention remains above 90%, demonstrating outstanding performance in protecting the zinc anode. Furthermore, such a flexible battery shows good resistance to damage due to the strong mechanical strength originating from leather. Notably, LGE utilizes green and sustainable leather as a raw material, making it a promising option for sustainable flexible devices.

A “two cooking with one fish” strategy for modulating both polyaniline cathode and zinc anode towards enhanced kinetics and cycling stability for aqueous zinc ion batteries

The adverse stability of both polyaniline (PANI) and Zn anode remains a challenge to the long−term cyclability and rate capability of aqueous Zn−PANI batteries. Herein, a “two–cooking with one fish” strategy is presented to modulate both PANI cathode and Zn anode, in which nanoscale graphene sheets in cathode can promote ordered growth of PANI array, being conducive to provide large electrochemical active area and efficient transport pathways and alleviate volume variation during repeated charging/discharging process. Meanwhile, the honeycomb–like structure of graphene sheets as protective layer can accelerate zinc ion transport kinetics and suppress side reactions and zinc dendrite growth. Consequently, the optimized G/Zn symmetric cell delivers a remarkable lifespan over 1000 h at 1 mA cm−2 with 1 mAh cm−2. Furthermore, the assembled PANI/G/CC||G/Zn battery could deliver a specific capacity of 265.8 mAh g−1 at 0.2 A g−1, excellent rate capability (145.5 mAh g−1 at 20 A g−1), a maximum energy density of 246.9 W h kg−1 and power density of 8675.9 W kg−1, and especially capacity retention of 91.1 % after 10000 cycles. Combining with additional merits of low cost, eco–friendliness, and safe operation, our design will shed light on resolving the issues on cyclability and rate capability of aqueous Zn−PANI batteries.

Using Silica Aerogel Layers for the Stabilization of Zn Metal Anodes in Zn‐Ion Batteries

AbstractAqueous zinc ion batteries have the advantages of low cost, high safety, high theoretical specific capacity. However, the charging and discharging process is usually accompanied by side reactions such as dendrite growth, hydrogenolysis, corrosion of electrodes, passivation, etc., which limits the development and application. In this work, the zinc anode is modified by constructing a silica aerogel layer with ultra‐high specific surface area and abundant polar functional groups (−OH, −COOH, −CH3), which not only provides abundant active sites for the uniform deposition of zinc ions, but also construct an artificial protective layer that acting as a desolvation layer and a zinc ion flux regulator. Consequently, the altered zinc anode exhibits an extremely durable zincophilic characteristic and a declining interfacial impedance. The constructed artificial layer can prevent side reactions and promote uniform zinc ion deposition to prevent the generation of zinc dendrites during the charge/discharge process. Results show that the symmetric cells composed of modified Zn anodes can be stably cycled for more than 1100 h at 0.5 mA cm−2 and 0.5 mAh cm−2, which is much higher than that of bare Zn. In addition, the life and capacity retention of the Zn/MnO2 full cells were also significantly improved.

Electric Double Layer Regulator Design through a Functional Group Assembly Strategy towards Long‐lasting Zinc Metal Batteries

Regulating the electric double layer (EDL) structure of the zinc metal anode by using electrolyte additives is an efficient way to suppress interface side reactions and facilitate uniform zinc deposition. Nevertheless, there are no reports investigating the proactive design of EDL‐regulating additives before the start of experiments. Herein, a functional group assembly strategy is proposed to design electrolyte additives for modulating the EDL, thereby realizing a long‐lasting zinc metal anode. Specifically, by screening ten common functional groups, N, N‐dimethyl‐1H‐imidazole‐1‐sulfonamide (IS) is designed by assembling an imidazole group, characterized by its high adsorption capability on the zinc anode, and a sulfone group, which exhibits strong binding with Zn2+ ions. Benefiting from the adsorption functionalization of the imidazole group, the IS molecules occupy the position of H2O in the inner Helmholtz layer of the EDL, forming a molecular protective layer to inhibit H2O‐induced side reactions. Meanwhile, the sulfone group in IS, acting as a binding site to Zn2+, promotes the de‐solvation of Zn2+ ions, facilitating compact zinc deposition. Consequently, the utilization of IS significantly extending the cycling stability of Zn||Zn and Zn||NaV3O8·1.5H2O full cell. This study offers an innovative approach to the design of EDL regulators for high‐performance zinc metal batteries.

Electric Double Layer Regulator Design through a Functional Group Assembly Strategy towards Long-lasting Zinc Metal Batteries.

Regulating the electric double layer (EDL) structure of the zinc metal anode by using electrolyte additives is an efficient way to suppress interface side reactions and facilitate uniform zinc deposition. Nevertheless, there are no reports investigating the proactive design of EDL-regulating additives before the start of experiments. Herein, a functional group assembly strategy is proposed to design electrolyte additives for modulating the EDL, thereby realizing a long-lasting zinc metal anode. Specifically, by screening ten common functional groups, N, N-dimethyl-1H-imidazole-1-sulfonamide (IS) is designed by assembling an imidazole group, characterized by its high adsorption capability on the zinc anode, and a sulfone group, which exhibits strong binding with Zn2+ ions. Benefiting from the adsorption functionalization of the imidazole group, the IS molecules occupy the position of H2O in the inner Helmholtz layer of the EDL, forming a molecular protective layer to inhibit H2O-induced side reactions. Meanwhile, the sulfone group in IS, acting as a binding site to Zn2+, promotes the de-solvation of Zn2+ ions, facilitating compact zinc deposition. Consequently, the utilization of IS significantly extending the cycling stability of Zn||Zn and Zn||NaV3O8·1.5H2O full cell. This study offers an innovative approach to the design of EDL regulators for high-performance zinc metal batteries.

Positively Charged Amino Acid-Modulated Interfacial Chemistry and Deposition Textures for Highly Reversible Zinc Anodes.

Interfacial active water molecule-induced parasitic reactions and stochastic Zn2+ transport-caused dendrite issue significantly impede the implementation of aqueous Zn-ion batteries. Herein, three positively charged amino acids, namely arginine, histidine, and lysine, were utilized as adsorption-type electrolyte additives to enhance the stability and reversibility of Zn anodes. Combined theoretical and experimental analyses verified that these amino acid cations can synergistically modulate the interfacial microenvironment and promote orientational Zn deposition. The adsorbed amino acid cations reconfigured the interfacial electric double layer structure, forming SO42-- and H2O-poor interfaces, thereby retarding hydrogen evolution and corrosion side reactions. Simultaneously, the preferential adsorption of the amino acid cations at specific facets induced crystallographic orientational Zn deposition along unterminated facets. Three deposition architectures, namely planar texture, subvertical alignment, and vertical erection, were obtained, all effectively inhibiting dendrite formation. Consequently, symmetric cells with the three amino acid cations exhibited high stripping/plating reversibility of over 2000 cycles at 5 mA cm-2. Moreover, MnO2-based full cells exhibited markedly improved stabilities compared with their additive-free counterparts.

Recent Advances in Catalyst Design and Performance Optimization of Nanostructured Cathode Materials in Zinc-Air Batteries.

This review focuses on the advanced design and optimization of nanostructured zinc-air batteries (ZABs), with the aim of boosting their energy storage and conversion capabilities. The findings show that ZABs favor porous nanostructures owing to their large surface area, and this enhances the battery capacity, catalytic activity, and life cycle. In addition, the nanomaterials improve the electrical conductivity, ion transport, and overall battery stability, which crucially reduces dendrite growth on the zinc anodes and improves cycle life and energy efficiency. To obtain a superior performance, the importance of controlling the operational conditions and using custom nanostructural designs, optimal electrode materials, and carefully adjusted electrolytes is highlighted. In conclusion, porous nanostructures and nanoscale materials significantly boost the energy density, longevity, and efficiency of Zn-air batteries. It is suggested that future research should focus on the fundamental design principles of these materials to further enhance the battery performance and drive sustainable energy solutions.

Identifying Current Collectors that Enable Light-Battery Interactions.

In recent years, there has been an increased focus on studying light-battery interactions in the context of operando optical studies and integrated photoelectrochemical energy harvesting. However, there has been little insight into identifying suitable "light-accepting" current collectors for this class of batteries. In this study, fluorine-doped tin oxide, indium-tin oxide, and silver nanowire-graphene films are analyzed along with carbon paper, carbon nanotube paper, and stainless-steel mesh as current collectors for optical batteries. They are categorized into two classes - transmissive and non-transmissive, based on the orientation of the light-electrode interaction. Various methods to prepare the electrode are highlighted, including drop casting and the fabrication of free-standing electrodes. The optical and electrical properties of these current collectors as well as their electrochemical stability are measured using linear sweep voltammetry against zinc and lithium anodes. Finally, the rate performance and long-term cycling stability of lithium manganese oxide (LiMn2O4) cathodes are measured against lithium anodes with these current collectors and their performance is compared. These results show which current collector to choose depends on the application and cell chemistry. These guidelines will assist in the design of future optical cells for in-situ measurements and photoelectrochemical energy storage.

Towards Reusable 3D-Printed Graphite Framework for Zinc Anode in Aqueous Zinc Battery

Aqueous zinc ion batteries (AZIBs) are an increasingly popular high-safety and eco-friendly energy storage solution. However, the development of high-performance zinc (Zn) anodes remains a formidable challenge, primarily due to dendrite formation and poor reversibility. To address these challenges, this study harnesses the potential of digital light process (DLP) 3D printing technology to fabricate reduced graphite oxide-based 3D gyroid structure (3DP-rGG) as zinc anode frameworks for aqueous zinc batteries. The 3D-printed structure effectively regulates local current density distribution, offering ample nucleation sites and free space for inducing uniform zinc deposition and accommodating diminutive zinc nodules. Consequently, the 3D-printed graphite framework demonstrates remarkable reversibility in zinc plating and stripping processes, resulting in commendable coulombic efficiency and low voltage hysteresis. The full battery with a 3D-printed anode structure, incorporating a polyaniline-intercalated vanadium oxide cathode (PVO), exhibits high specific capacity and superior long-term cycling stability. Remarkably, the robust 3DP-rGG structure can be reused over ten times without any discernible impact on its electrochemical performance, thereby underscoring the potential of this controllable and efficient fabrication of 3D graphite current collectors as a promising solution to develop reusable 3D frameworks for high-performance metal batteries.

High-performance zinc metal anode enabled by large-scale integration of superior ion transport layer

Aqueous zinc (Zn) metal battery is regarded as a promising candidate with low cost and high safety for energy storage systems at large scales. However, the destabilized Zn2+ transport at the reaction interface severely restricts the lifespan of zinc anode, and the strategies suitable for large-scale integration of the anode’s protection layer are required. Herein, an independent protective layer of Cu@CuO nanowire arrays is proposed to stabilize zinc anode with comprehensive regulation of Zn2+ transport. Through wet-chemical etching, the nanowire structure with a geometric area of 250 cm2 can be synthesized in one pot. From experimental analysis and simulation results, such a layer not only homogenizes the distribution of interfacial electric field, but also enhances Zn2+ transfer kinetics with improved ionic conductivity and increased transference number. Meanwhile, the activity of hydrogen evolution reaction (HER) is decreased due to the integration of this unique layer. As a result, the protected zinc anode can be stably operated at 2 mA cm−2/2 mAh cm−2, and the stable current density can further increase to 10 mA cm−2. Furthermore, the protective layer is featured with superior hydrophilicity, and can be feasibly utilized for large-area pouch cells, revealing the scalability and effectiveness in practical devices. This work proposes a facile protection strategy for zinc anode from the perspective of optimizing Zn2+ transport by large-scale integration of superior ion transport layer, showing great potential in high-performance zinc metal anode.

Polyoxometalate solution passivation enabling dendrite-free and high-performance zinc anodes in aqueous zinc-ion batteries

Zinc metal anodes in aqueous electrolytes commonly face challenges such as dendrite growth and undesirable side reactions, limiting their application in the field of aqueous zinc-ion batteries (AZIBs) for energy storage. Drawing inspiration from industrial practices involving molybdenum salt solutions for metal modification, a polyoxometalate solution was formulated as a passivation solution for zinc anodes (referred to as MO solution). The formed passivation layer, referred to as the MO layer, exhibited a uniform and protective nature with a thickness of approximately 10 μm. The experimental results demonstrated that this passivation layer effectively suppressed side reactions at the zinc anode interface, as evidenced by lower corrosion current density for MO-Zn anodes. Additionally, the newly plated Zn was uniformly deposited atop the MO layer, ensuring coating integrity and inhibiting dendrite growth. As a result, under more demanding conditions such as a larger current of 8 mA cm−2, the MO-Zn anode displayed an extended cycle life exceeding 420 h in a symmetric battery, with an overpotential as low as 98 mV. This performance significantly outperformed that of commercially available pure Zn foils (with a cycle life of 60 h and an overpotential of 192 mV). Notably, a self-made Na-doped V2O5 served as the cathode (referred to as NaVO), forming the MO-Zn//NaVO full battery. Even under high current test conditions of 2 A/g, the specific capacity of the MO-Zn//NaVO full battery remained substantial at 152.83 mAh/g after 1000 cycles. Furthermore, pouch batteries assembled with NaVO//MO-Zn successfully illuminated small bulbs. This study offers a viable optimization strategy for AZIB anodes and demonstrates the potential of using polyoxometalate solution for etching zinc anodes to inhibit dendrite growth and interfacial corrosion of zinc metal anodes.

Electrochemical hydrodefluorination of an aromatic trifluoromethyl group with ammonia as the hydrogen source

The aromatic difluoromethyl group (Ar-CF2H) is an emerging functional group found in pharmaceutical compounds. For synthesis, the hydrodefluorination of Ar-CF3 molecules is a straightforward approach in terms of atom economy and substrate scope. The reported hydrodefluorination reaction focused on the Ar-CF3 substrate bearing electron-withdrawing groups. In this report, we utilized electricity as the driving force for the hydrodefluorination of ArCF3, which involves electron-donating groups. By using ammonia as a traceless hydrogen and electron donor, the reaction could tolerate a variety of labile groups, including unprotected amine, pyrrole, furan, thioether, and silyl group, without sacrificial anodes in undivided cells. In this work, tBuOLi was found to be an essential additive for achieving good reactivity and chemoselectivity. Several Ar-CF2H pharmaceutical and intermediate products were synthesized via this approach.

Achieving highly reversible regulation of zinc deposition through ultrafast in situ construction of multifunctional zinc anode interfaces

The zinc anode surface suffers from severe zinc dendrite growth and side reactions, such as hydrogen evolution, significantly diminishing its reversibility and cycle life. In this study, we have introduced and successfully implemented, for the first time, the ultrafast in-situ construction of a periodic semi-spherical multifunctional interfacial layer composed of copper nanoparticles (Cu|Zn) on the zinc anode surface. By optimizing the distribution of the electric field and Zn2+ concentration, we effectively mitigate the “Tip effect”, achieving highly reversible control over zinc deposition, and the in-situ construction process takes only 3 min. Theoretical calculations and COMSOL simulations demonstrate that the Cu|Zn anode exhibits high binding energy, a uniform electric field, and Zn2+ concentration distribution. Experimental results reveal that the Cu|Zn anode achieves exceptional long-term cyclic stability, exceeding 3200 h at 1 mA cm−2 and remaining cyclically stable for over 2000 h at 5 mA cm−2. Furthermore, in a full cell with MnO2@MXene as the cathode material, the Cu|Zn anode delivers a capacity of 282.1 mA h g−1 after 1400 cycles at 2 A g−1. This study holds significance for the rational design of high-stability and reversible interface layers, promoting their practical application in aqueous zinc-ion batteries (AZBs).

Blocking the Passivation Reaction via Localized Acidification and Cation Selective Interface Towards Highly Stable Zinc Anode

The variations of pH triggers either the formation of zinc sulfate hydroxide (ZSH) or the hydrogen evolution reaction (HER), leading to unsatisfactory zinc anode efficiency. In order to establish a balanced approach that suppresses the HER while creating an acidic environment to eliminate ZSH formation, this study introduces an environmentally friendly chelating additive, tetrasodium iminodisuccinate (IDS), into the ZnSO4 electrolyte. This additive serves to generate a localized acidic environment and a cation-selective surface barrier. The preferentially adsorbed IDS anions create a water-poor interface and engage in synergistic regulation of cation and anion via electrostatic effects, promoting smooth Zn deposition and reducing by-product formation. Additionally, IDS can strongly interact with Zn2+ and adapt to pH variations, thereby providing a stable environment that mitigates side reactions. Unlike sacrificial additives, IDS demonstrates stability under test conditions, resulting in a truly reversible and stable electrolyte system. The implementation of this multifunctional additive results in a prolonged lifespan of metallic Zn, reaching 2548 hours, and a promoted coulombic efficiency of 99.5%. Furthermore, the improved stability of Zn anodes is observed in Zn//LiFePO4 cells, exhibiting the capacity retention of 97.0% over 800 cycles. This strategy opens up a new pathway for enhancing the stability and reversibility of Zn anodes.

Micro-cracking on the surface of zinc metal improves the cycle performance of aqueous zinc ion batteries

The notorious zinc dendrite is a severe constraint to the practical application of zinc-based batteries, as the metal tips growing vertically in two dimensions on the surface of the electrodes during cycling and loosely packed sharp edges may pierce through the diaphragm, posing a safety hazard. In this study, physical stress extrusion was used to generate micron- or submicron-sized cracks on zinc metal anodes, which significantly increased the specific surface area of the electrodes and mitigated the local current density of the electrodes. Zinc ion fluxes were significantly dispersed, producing a dense Zn2SO4(OH)6-xH2O (ZHS) layer, which differed distinctly from the by-products of the loose upright growth on the surface of Raw Zn (RZn). Additionally, three-dimensional structure of cracked zinc composition allows it to adjust the zinc volume variations during electroplating/stripping, and the abundance of nucleation sites significantly reduces the Zn polarization voltage, resulting in uniform Zn deposition. The average cycle life of the symmetric cell was >400 h at 1 mA cm−2 current density, and nearly 500 cycles at 5 mA cm−2 current density for the asymmetric cell, with an average Coulombic efficiency of 99.3 %. The activation energy substantially declined with the increase in Zn ion flux per unit time (29.615 KJ mol−1 vs. 44.041 KJ mol−1), demonstrating efficient desolvation kinetics. Furthermore, the Crack Zn || V2O5 full cell also exhibits outstanding self-discharge performance, with 85 % capacity retention in a 48 h resting charge/discharge testing, superior to the raw zinc foil anode (78.3 %). Herein, a method of creating microcrack configurations on the surface of zinc anodes using stress extrusion was presented, sparing the current density while optimizing the undesirable growth patterns of ZHS by-products.

A Temperature Self-Adaptive Electrolyte for Wide-Temperature Aqueous Zinc-Ion Batteries.

The advancement of aqueous zinc-ion batteries (AZIBs) is often hampered by the dendritic zinc growth and the parasitic side reactions between the zinc anode and the aqueous electrolyte, especially under extreme temperature conditions. This study unveils the performance decay mechanism of zinc anodes in harsh environments, characterized by "dead zinc" at low temperatures and aggravated hydrogen evolution and adverse by-products at elevated temperatures. To address these issues, a temperature self-adaptive electrolyte (TSAE), founded on the competitive coordination principle of co-solvent and anions, is introduced. This electrolyte exhibits a dynamic solvation capability, engendering an inorganic-rich solid electrolyte interface (SEI) at low temperatures while an organic alkyl ether- and alkyl carbonate-containing SEI at elevated temperatures. The self-adaptability of the electrolyte significantly enhances the performance of the zinc anode across a broad temperature range. A Zn//Zn symmetrical cell, based on the TSAE, showcases reversible plating/stripping exceeding 16,800 hours (>700 days) at room temperature under 1mA cm-2 and 1 mAh cm-2, setting a record of lifespan. Furthermore, the TSAE enables stable operation of the zinc full batteries across an ultra-wide temperature range of -35 to 75°C. This work illuminates a pathway for optimizing AZIBs under extreme temperatures by fine-tuning the interfacial chemistry. This article is protected by copyright. All rights reserved.