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Anode-Free Li-Metal Battery Based on Sustainable Sulfolane Electrolyte: Performance–Anode Structure Correlation 基于可持续亚砜电解质的无阳极锂金属电池:性能-阳极结构相关性
IF 4.7 4区 材料科学
Batteries & Supercaps Pub Date : 2026-03-26 DOI: 10.1002/batt.202500943
Michael Witt, Ivan Genov, Sebastian Mai, Alexader Tesfaye, Svetlozar Ivanov
{"title":"Anode-Free Li-Metal Battery Based on Sustainable Sulfolane Electrolyte: Performance–Anode Structure Correlation","authors":"Michael Witt,&nbsp;Ivan Genov,&nbsp;Sebastian Mai,&nbsp;Alexader Tesfaye,&nbsp;Svetlozar Ivanov","doi":"10.1002/batt.202500943","DOIUrl":"10.1002/batt.202500943","url":null,"abstract":"<p>Anode-free concept can fully utilize the unmatched theoretical specific energy of lithium-metal battery. However, the low stability of the anode interface, including both the morphology of Li metal and the solid electrolyte interphase (SEI), hinders the practical battery implementation and creates safety concerns. In this work, sulfolane-based localized high-concentration electrolyte (LHCE) is applied as a sustainable and applicable electrolyte for anode-free Li-metal batteries (AFLMBs). The effects of important factors, including type of anode current collector, electrolyte properties, and cycling conditions, are explored in terms of clarifying their impact on the structural and functional properties of LFP‖Cu cells. Flammability tests indicate that the electrolyte is nonflammable by direct ignition under the applied conditions, which is highly beneficial for the safety and sustainability of the AFLMB. The performance of SL-based LHCE is tested for Li plating–stripping reaction on Cu-engineered substrates, where the microporous Cu substrates display major improvement, which can be attributed to their enlarged active surface area and open and highly interconnected porous structure. The influence of the key operation parameters, state of charge, depth of discharge, and current density is explored, and useful correlations of these factors with the anode structural properties and battery cycling stability are established.</p>","PeriodicalId":132,"journal":{"name":"Batteries & Supercaps","volume":"9 3","pages":""},"PeriodicalIF":4.7,"publicationDate":"2026-03-26","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://chemistry-europe.onlinelibrary.wiley.com/doi/epdf/10.1002/batt.202500943","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"147585107","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Interfacial Evaluation in ZnO-Coated NaxMn0.5Fe0.5O2 Cathodes and Hard Carbon Anodes Induced by Sodium Azide: Operando EIS and Structural Insights 叠氮化钠诱导zno - NaxMn0.5Fe0.5O2阴极和硬碳阳极的界面评价:Operando EIS和结构见解
IF 4.7 4区 材料科学
Batteries & Supercaps Pub Date : 2026-03-25 Epub Date: 2025-11-19 DOI: 10.1002/batt.202500680
Rawdah Whba, Ebru Doğan, Özgür Duygulu, Abdullah K. Alanazi, Muhammad Arshad, Radostina Stoyanova, Violeta Koleva, Mehmet Nurullah Ates, Serdar Altin
{"title":"Interfacial Evaluation in ZnO-Coated NaxMn0.5Fe0.5O2 Cathodes and Hard Carbon Anodes Induced by Sodium Azide: Operando EIS and Structural Insights","authors":"Rawdah Whba,&nbsp;Ebru Doğan,&nbsp;Özgür Duygulu,&nbsp;Abdullah K. Alanazi,&nbsp;Muhammad Arshad,&nbsp;Radostina Stoyanova,&nbsp;Violeta Koleva,&nbsp;Mehmet Nurullah Ates,&nbsp;Serdar Altin","doi":"10.1002/batt.202500680","DOIUrl":"10.1002/batt.202500680","url":null,"abstract":"<p>This article explores the synthesis and electrochemical properties of Na<sub><i>x</i></sub>Mn<sub>0.5</sub>Fe<sub>0.5</sub>O<sub>2</sub> powders, prepared via a conventional solid-state reaction. Subsequently, the powders are functionalized with a ZnO protective coating through a wet-chemical approach employing zinc acetate in ethanol. Structural characterization confirmed that the ZnO layer maintained the P2-type (<i>P6</i><sub>3</sub><i>/mmc</i>) structure, while energy-dispersive X-ray spectrometry mapping verified the successful coating. Electrochemical analyses, including electrochemical impedance spectroscopy (EIS) and cyclic voltammetry, revealed that although the redox reaction mechanism remained unchanged, the charge–transfer resistance (<i>R</i><sub>ct</sub>) depended on the coating thickness. ZnO-coated NMFO electrodes exhibited initial discharge capacities of 159.3, 153.6, and 124.8 mAh g<sup>−</sup><sup>1</sup> with respective capacity retentions of 48.9%, 41.9%, and 52.0% after 100 cycles for ZnO contents of 0.2, 0.4, and 0.6 wt.%. The galvanostatic intermittent titration technique results indicated that the diffusion coefficients varied with the coating conditions. Operando EIS from 1.5 to 4.3 V showed stable bulk resistance (<i>R</i><sub>b</sub>) but voltage-dependent variations in solid electrolyte interface resistance (<i>R</i><sub>SEI</sub>) and <i>R</i><sub>ct</sub>. Additionally, sodium azide is used to presodiate the hard carbon (HC) anode to enhance the full-cell performance. The ZnO-coated cathode paired with NaN<sub>3</sub> presodiated HC delivered a capacity of over 120 mAh g<sup>−</sup><sup>1</sup> at C/10. Ex situ analysis after 500 cycles confirmed structural stability, demonstrating that ZnO coating and NaN<sub>3</sub> presodiation collectively improve sodium-ion battery performance.</p>","PeriodicalId":132,"journal":{"name":"Batteries & Supercaps","volume":"9 3","pages":""},"PeriodicalIF":4.7,"publicationDate":"2026-03-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"147567615","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Determination of the Entropic Heat Coefficient of Lithium-Ion Batteries Based on a Continuous Measurement Method 基于连续测量法的锂离子电池熵热系数测定
IF 4.7 4区 材料科学
Batteries & Supercaps Pub Date : 2026-03-25 Epub Date: 2025-11-21 DOI: 10.1002/batt.202500468
Anne Heß, Thomas Wetzel, Philipp Seegert
{"title":"Determination of the Entropic Heat Coefficient of Lithium-Ion Batteries Based on a Continuous Measurement Method","authors":"Anne Heß,&nbsp;Thomas Wetzel,&nbsp;Philipp Seegert","doi":"10.1002/batt.202500468","DOIUrl":"10.1002/batt.202500468","url":null,"abstract":"<p>A comprehensive understanding of thermal battery behavior and, consequently, the design of efficient thermal management systems are crucial for optimal performance, a high safety level, and the prolonged lifetime of batteries in automotive applications. In this context, knowledge of the heat release within the battery is a key parameter. In this work, a methodology is investigated for determining the reversible heat release based on continuous quasi-open-circuit-voltage (qOCV) measurements, which is not yet fully established in the literature. Three key factors influencing the evaluation of the entropic heat coefficient are presented and it is discussed in detail how these should be taken into account for the first time. The entropic coefficients derived from the continuous approach are compared with values obtained from potentiometric measurements of the same pouch cell and show a high level of accuracy for the continuous qOCV method. The standard battery cycler is used, with a measuring uncertainty of 1 mV, yields results that are in very good agreement with the broad spectrum of literature values, obtained using different methodologies and uncertainties. The validity and robustness of the approach are further demonstrated by applying the continuous method to data from a different automotive prismatic cell with a significantly different testing procedure.</p>","PeriodicalId":132,"journal":{"name":"Batteries & Supercaps","volume":"9 3","pages":""},"PeriodicalIF":4.7,"publicationDate":"2026-03-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://chemistry-europe.onlinelibrary.wiley.com/doi/epdf/10.1002/batt.202500468","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"147567891","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Advancing Polybenzimidazole Membrane by Knitting Soft Poly(vinyl imidazolium) for Vanadium Redox Flow Batteries 编织软聚(乙烯基咪唑)制备钒氧化还原液流电池用聚苯并咪唑膜
IF 4.7 4区 材料科学
Batteries & Supercaps Pub Date : 2026-03-25 Epub Date: 2025-11-23 DOI: 10.1002/batt.202500714
Prashant Upadhyay, Jeet Sharma, Vaibhav Kulshrestha
{"title":"Advancing Polybenzimidazole Membrane by Knitting Soft Poly(vinyl imidazolium) for Vanadium Redox Flow Batteries","authors":"Prashant Upadhyay,&nbsp;Jeet Sharma,&nbsp;Vaibhav Kulshrestha","doi":"10.1002/batt.202500714","DOIUrl":"10.1002/batt.202500714","url":null,"abstract":"<p>Polybenzimidazole (PBI)-based membranes are well known for their potential in electrochemical applications. However, these membranes often have poor conductivity. The modification of <i>N</i>-alkylation of benzimidazole unit improves the conductivity of membranes, which are mostly found in alkaline water electrolysis and fuel cells. Only a few membranes are incorporated in vanadium redox flow battery (VRFB). Herein, a new class of polyimidazolium-knitted PBI-based membranes are synthesized via de novo approach using 3,3′-diaminobenzidine and 4,4′-biphenyldicarboxylic acid with infused grafting of halato-telechelic poly(vinyl imidazolium) (PVIm) for VRFB. As evidenced, the PVIm-grafted membranes show increase in the electrochemical properties. OPBI-VIm-<i>x</i> demonstrates improved water uptake attributes and bulk ion conductivities compared to Nafion-212 (N-212). Further, OPBI-VIm-<i>x</i> membranes are assessed based on several key parameters like vanadium crossover, ion selectivity, and vanadium single-cell setup. Among them, OPBI-VIm-1.25 achieves lowest vanadium permeability and highest ion selectivity with maximum single-cell performance (Coulombic efficiency ≈98%, voltage efficiency ≈71%, and energy efficiency ≈70%) with stable cycling up to 300 cycles. As evidence, a promising strategy to address limitations of traditional OPBI involves the functional tethering of stable poly-cationic moieties, which enhance hydrophilicity while preserving the inherent thermal and chemical stability of pristine PBI membranes.</p>","PeriodicalId":132,"journal":{"name":"Batteries & Supercaps","volume":"9 3","pages":""},"PeriodicalIF":4.7,"publicationDate":"2026-03-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"147568262","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Sustainable Synthesis of Structurally Robust LiNi1/3Mn1/3Co1/3O2 Cathodes with Enhanced Electrochemical Performance for Lithium-Ion Batteries 结构坚固的LiNi1/3Mn1/3Co1/3O2阴极的可持续合成及增强锂离子电池电化学性能
IF 4.7 4区 材料科学
Batteries & Supercaps Pub Date : 2026-03-25 Epub Date: 2025-12-17 DOI: 10.1002/batt.202500641
Thirumalaisamy Kiruthika, Chunghyeon Choi, Devaraj Lakshmi, Suryaprabha Thirumalaisamy, Ki Ro Yoon, Pachagounder Sakthivel, Byungil Hwang, Paneerselvam Christopher Selvin
{"title":"Sustainable Synthesis of Structurally Robust LiNi1/3Mn1/3Co1/3O2 Cathodes with Enhanced Electrochemical Performance for Lithium-Ion Batteries","authors":"Thirumalaisamy Kiruthika,&nbsp;Chunghyeon Choi,&nbsp;Devaraj Lakshmi,&nbsp;Suryaprabha Thirumalaisamy,&nbsp;Ki Ro Yoon,&nbsp;Pachagounder Sakthivel,&nbsp;Byungil Hwang,&nbsp;Paneerselvam Christopher Selvin","doi":"10.1002/batt.202500641","DOIUrl":"10.1002/batt.202500641","url":null,"abstract":"<p>This study reports on the green synthesis of high-performance LiNi<sub>1/3</sub>Mn<sub>1/3</sub>Co<sub>1/3</sub>O<sub>2</sub> (NMC111) cathode materials using <i>Actinidia deliciosa</i> (kiwi) extract as a natural chelating and reducing agent. The electrochemical and structural performance of the green-synthesized NMC (GS-NMC) is systematically compared with NMCs prepared using sol–gel and solid-state methods. Structural and surface analyses show that GS-NMC possesses a highly ordered layered structure with minimal cation mixing, improved crystallinity, and increased surface area. Electron microscopy and Brunauer–Emmett–Teller analyses confirm a refined nanoscale morphology with well-developed porosity. The X-ray photoelectron spectroscopy results indicate reduced surface impurities and an optimal distribution of transition-metal oxides. Electrochemical testing in a three-electrode aqueous LiOH system demonstrates that GS-NMC achieves enhanced surface redox activity, low interfacial resistance, and stable pseudocapacitive behavior (≈120 mAh g<sup>−1</sup> within a ±1.0 V window) over 1000 cycles. In comparison, sol–gel and solid-state samples exhibit higher polarization and faster capacity fading. Although tested under aqueous half-cell conditions, the results show that green synthesis offers a promising route to produce structurally robust and electrochemically responsive NMC materials. The findings also highlight the promise of biogenic synthesis as a sustainable alternative to traditional methods and as a versatile platform for designing high-performing cathode materials for next-generation lithium-ion batteries.</p>","PeriodicalId":132,"journal":{"name":"Batteries & Supercaps","volume":"9 3","pages":""},"PeriodicalIF":4.7,"publicationDate":"2026-03-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"147566371","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Aromatic Diester Anolytes for Nonaqueous Redox Flow Batteries 非水氧化还原液流电池用芳香二酯阳极液
IF 4.7 4区 材料科学
Batteries & Supercaps Pub Date : 2026-03-25 Epub Date: 2025-11-24 DOI: 10.1002/batt.202500478
Nicolas Daub, Dimitar Georgiev, René A. J. Janssen
{"title":"Aromatic Diester Anolytes for Nonaqueous Redox Flow Batteries","authors":"Nicolas Daub,&nbsp;Dimitar Georgiev,&nbsp;René A. J. Janssen","doi":"10.1002/batt.202500478","DOIUrl":"https://doi.org/10.1002/batt.202500478","url":null,"abstract":"<p>Nonaqueous redox flow batteries require highly-soluble and easy-to-synthesize organic redox-active molecules that offer deep reduction or high oxidation potentials and that are stable in each state of charge. Herein, aromatic diesters for use as anolytes are investigated. Dimethyl terephthalate exhibits two single-electron reductions. Compared to its radical anion, the dianion is unstable. Introducing 1,1′-biphenyl and 2,2′-bipyridyl aromatic units, stabilizes the diesters in their doubly-reduced state via extension of the <i>π</i>-conjugation and less deep reduction potentials. Solubility is enhanced by using oligo(ethylene glycol) esters. The most promising anolyte that emerges from this work, bis(2-(2-ethoxyethoxy)ethyl) [2,2′-bipyridine]−5,5′-dicarboxylate, is used in combination with 2,5-di-tert-butyl-1,4-bis(2-methoxyethoxy)benzene as a catholyte in redox flow cell batteries. The mixed system flow battery has a nominal battery voltage of 2.82 V and a capacity retention of 99.5% per cycle for 260 cycles.</p>","PeriodicalId":132,"journal":{"name":"Batteries & Supercaps","volume":"9 3","pages":""},"PeriodicalIF":4.7,"publicationDate":"2026-03-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://chemistry-europe.onlinelibrary.wiley.com/doi/epdf/10.1002/batt.202500478","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"147568962","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Interfacial Mo(VI)/Mo(IV) Redox-Mediated Ultrafast Charge Storage in MXene/Carbon Nanotube Hybrid Electrodes in Acidic Media 酸性介质中MXene/碳纳米管杂化电极界面Mo(VI)/Mo(IV)氧化还原介导的超快电荷存储
IF 4.7 4区 材料科学
Batteries & Supercaps Pub Date : 2026-03-25 Epub Date: 2025-11-19 DOI: 10.1002/batt.202500640
M. Arunkumar, S. Rajasekar, K. Nasrin, A. Sivashanmugam, M. Sathish
{"title":"Interfacial Mo(VI)/Mo(IV) Redox-Mediated Ultrafast Charge Storage in MXene/Carbon Nanotube Hybrid Electrodes in Acidic Media","authors":"M. Arunkumar,&nbsp;S. Rajasekar,&nbsp;K. Nasrin,&nbsp;A. Sivashanmugam,&nbsp;M. Sathish","doi":"10.1002/batt.202500640","DOIUrl":"10.1002/batt.202500640","url":null,"abstract":"<p>Enhancing the energy density of supercapacitors while maintaining high power output is critical for sustainable energy storage applications. Herein, the fabrication of an MXene/carbon nanotube (MXene/CNT) composite electrode via a one-step ultrasonication process, coupled with a redox-additive electrolyte to improve electrochemical performance,being is reported. The incorporation of sodium molybdate (Na<sub>2</sub>MoO<sub>4</sub>) into a sulfuric acid (H<sub>2</sub>SO<sub>4</sub>) electrolyte significantly enhances faradaic charge storage, extends the electrochemical window, and improves charge transfer kinetics. The resulting system exhibits a specific capacitance of 152 F g<sup>−</sup><sup>1</sup> at 3 A g<sup>−</sup><sup>1</sup>, a substantial increase compared to 47 F g<sup>−</sup><sup>1</sup> at the same current density in H<sub>2</sub>SO<sub>4</sub>. Moreover, the energy density of the MXene/CNT composite electrode in the sodium molybdate redox additive reaches 41 Wh kg<sup>−</sup><sup>1</sup>, nearly doubling that of the conventional H<sub>2</sub>SO<sub>4</sub> electrolyte, with the power density being almost the same in both cases. This enhancement is attributed to the redox interactions between MoO<sub>4</sub><sup>2−</sup> ions and H<sup>+</sup> ions, which facilitate efficient charge storage. These findings highlight the potential of redox-active electrolytes in advancing next-generation sustainable supercapacitors for high-performance energy storage.</p>","PeriodicalId":132,"journal":{"name":"Batteries & Supercaps","volume":"9 3","pages":""},"PeriodicalIF":4.7,"publicationDate":"2026-03-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"147567614","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
A Perspective: Accelerating Electrochemical Energy Storage for a Reliable, Affordable, Resilient, and Secure Electric Grid 展望:为可靠、经济、有弹性和安全的电网加速电化学储能
IF 4.7 4区 材料科学
Batteries & Supercaps Pub Date : 2026-03-23 DOI: 10.1002/batt.202500746
Xiaolin Li, David M. Reed, Won-Gwang Lim, Vilayanur V. Viswanathan, Fredrick Omenya, Marcos Lucero, Guosheng Li, Gabriel Nambafu, Matthew Fayette, Alasdair Crawford, Aaron Hollas, Henry H. Han, Mark Weller, Jung Hui Kim, Bhuvaneswari M. Sivakumar, Wei Wang, Ruozhu Feng, Qian Huang, Daiwon Choi, Edwin C. Thomsen, Nimat Shamim, Vijay Murugesan, Jie Bao, Ajay S. Karakoti, Matt Paiss, Jaime T. Kolln, Vincent Sprenkle, Kevin P. Schneider
{"title":"A Perspective: Accelerating Electrochemical Energy Storage for a Reliable, Affordable, Resilient, and Secure Electric Grid","authors":"Xiaolin Li,&nbsp;David M. Reed,&nbsp;Won-Gwang Lim,&nbsp;Vilayanur V. Viswanathan,&nbsp;Fredrick Omenya,&nbsp;Marcos Lucero,&nbsp;Guosheng Li,&nbsp;Gabriel Nambafu,&nbsp;Matthew Fayette,&nbsp;Alasdair Crawford,&nbsp;Aaron Hollas,&nbsp;Henry H. Han,&nbsp;Mark Weller,&nbsp;Jung Hui Kim,&nbsp;Bhuvaneswari M. Sivakumar,&nbsp;Wei Wang,&nbsp;Ruozhu Feng,&nbsp;Qian Huang,&nbsp;Daiwon Choi,&nbsp;Edwin C. Thomsen,&nbsp;Nimat Shamim,&nbsp;Vijay Murugesan,&nbsp;Jie Bao,&nbsp;Ajay S. Karakoti,&nbsp;Matt Paiss,&nbsp;Jaime T. Kolln,&nbsp;Vincent Sprenkle,&nbsp;Kevin P. Schneider","doi":"10.1002/batt.202500746","DOIUrl":"10.1002/batt.202500746","url":null,"abstract":"<p>A reliable, affordable, resilient, and secure power grid is the foundation of modern society. Energy storage shapes bidirectional electricity flow and hence provides solutions for a future-ready grid. This article highlights the importance of energy storage, particularly electrochemical energy storage in balancing supply and demand and creating new infrastructure planning options from deferral to rapid expansion. Emerging and innovative electrochemical energy storage technologies at the Pacific Northwest National Laboratory are summarized. Perspectives of future research are also provided with a focus on superior cost and performance characteristics, unlocking tremendous opportunities for a wide range of key stakeholders including utilities and growing industrial facilities like artificial intelligence centers.</p>","PeriodicalId":132,"journal":{"name":"Batteries & Supercaps","volume":"9 3","pages":""},"PeriodicalIF":4.7,"publicationDate":"2026-03-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://chemistry-europe.onlinelibrary.wiley.com/doi/epdf/10.1002/batt.202500746","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"147568150","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Mitigating Mg Anode Passivation in Aqueous Rechargeable Batteries: Insights Into Interfacial Engineering and Electrolyte Design 减轻Mg阳极钝化在水溶液可充电电池:洞察到界面工程和电解质设计
IF 4.7 4区 材料科学
Batteries & Supercaps Pub Date : 2026-03-20 DOI: 10.1002/batt.202500957
Shuxin Zhang, Ruotong Ren, Yanna NuLi
{"title":"Mitigating Mg Anode Passivation in Aqueous Rechargeable Batteries: Insights Into Interfacial Engineering and Electrolyte Design","authors":"Shuxin Zhang,&nbsp;Ruotong Ren,&nbsp;Yanna NuLi","doi":"10.1002/batt.202500957","DOIUrl":"https://doi.org/10.1002/batt.202500957","url":null,"abstract":"<p>Aqueous rechargeable magnesium batteries (ARMBs) have attracted increasing attention as promising candidates for next-generation energy storage systems. However, the practical application of Mg metal anodes in aqueous electrolytes is fundamentally hindered by their spontaneous passivation upon contact with H<sub>2</sub>O, resulting in the formation of electrically insulating MgO/Mg(OH)<sub>2</sub>. This passivation layer severely increases interfacial resistance and blocks reversible Mg<sup>2+</sup> transport, leading to rapid performance degradation and premature anode failure. Consequently, conventional Mg anodes are generally regarded as incompatible with aqueous systems. In this review, recent progress toward enabling reversible Mg electrochemistry in aqueous environments is systematically summarized, with a particular focus on the synergistic design of anode materials and electrolyte systems. Key strategies, including artificial interfacial engineering, <i>in situ</i> alloy formation, and multidimensional electrolyte design (high-concentration, eutectic, gel/solid-state, and hybrid aqueous-organic electrolytes), are critically discussed from both mechanistic and practical perspectives. By establishing correlations between interfacial chemistry, solvation structure, and electrochemical behavior, this review aims to clarify the fundamental challenges associated with Mg anode passivation and highlight viable pathways toward stable and reversible Mg metal anodes in aqueous media. The insights provided herein are expected to guide the rational design of high-performance, safe, and sustainable ARMBs.</p>","PeriodicalId":132,"journal":{"name":"Batteries & Supercaps","volume":"9 3","pages":""},"PeriodicalIF":4.7,"publicationDate":"2026-03-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"147567581","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Mitigating Mg Anode Passivation in Aqueous Rechargeable Batteries: Insights Into Interfacial Engineering and Electrolyte Design 减轻Mg阳极钝化在水溶液可充电电池:洞察到界面工程和电解质设计
IF 4.7 4区 材料科学
Batteries & Supercaps Pub Date : 2026-03-20 DOI: 10.1002/batt.202500957
Shuxin Zhang, Ruotong Ren, Yanna NuLi
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