Article(id=1320090136092725633, tenantId=1146029695717560320, journalId=1263187385517883426, issueId=1320090116236882876, articleNumber=null, orderNo=null, doi=10.14062/j.issn.0454-5648.20240699, pmid=null, cstr=null, oa=null, hot=null, price=null, onlineType=0, articleFormat=0, articleType=null, articleTypeStr=null, receivedDate=1730649600000, receivedDateStr=2024-11-04, revisedDate=1734624000000, revisedDateStr=2024-12-20, acceptedDate=null, acceptedDateStr=null, onlineDate=1792663614533, onlineDateStr=2026-10-22, pubDate=1745078400000, pubDateStr=2025-04-20, doiRegisterDate=null, doiRegisterDateStr=null, onlineIssueDate=1792663614533, onlineIssueDateStr=2026-10-22, onlineJustAcceptDate=null, onlineJustAcceptDateStr=null, onlineFirstDate=null, onlineFirstDateStr=null, sourceXml=null, magXml=null, createTime=1792663614533, creator=13701087609, updateTime=1792663614533, updator=13701087609, issue=Issue{id=1320090116236882876, tenantId=1146029695717560320, journalId=1263187385517883426, year='2025', volume='53', issue='4', pageStart='733', pageEnd='1030', issueExtLink='null', onlineDate='null', pubDate='1745078400000', pubDateStr='2025-04-20', beforeIssueId=null, nextIssueId=null, price=null, status=1, issueComplete=1, articleOrder=1, issueType=-1, specialIssue=null, createTime=1792663609799, creator='13701087609', updateTime=1792663788359, updator='13701087609', preIssue=null, nextIssue=null, articleTotal=null, ext={EN=IssueExt(id=1320090865276670951, tenantId=1146029695717560320, journalId=1263187385517883426, issueId=1320090116236882876, language=EN, specialIssueTitle=, coverIllustrator=null, specialIssueEditor=, specialIssueAbout=), CN=IssueExt(id=1320090865276670952, tenantId=1146029695717560320, journalId=1263187385517883426, issueId=1320090116236882876, language=CN, specialIssueTitle=, coverIllustrator=null, specialIssueEditor=, specialIssueAbout=)}, issueFiles=null, downloadFileDto=null}, startPage=880, endPage=894, ext={EN=ArticleExt(id=1320090136306635138, articleId=1320090136092725633, tenantId=1146029695717560320, journalId=1263187385517883426, language=EN, title=Aluminum Metal Battery Anodes: Challenges and Progresses, columnId=1321897782982591319, journalTitle=Journal of the Chinese Ceramic Society, columnName=Special Issue on the 14th Inorganic and Non-metallic Materials Conference—Review, runingTitle=null, highlight=null, articleAbstract=

Rechargeable aluminum (Al) metal batteries (RAMBs) are considered as one of the most attractive alternatives to the existing battery technologies because of their low cost, high safety, high abundance of Al (the most earth-abundant metal element, over 3 700 times that of lithium), and the well-established Al industry. Furthermore, Al anode has a high theoretical gravimetric capacity of 2 981 mA·h·g−1 and the highest theoretical volumetric capacity of 8056 mA·h·cm−3, as well as a relatively low redox potential of−1.66 V versus the standard hydrogen electrode, thus enabling RAMBs to have a potentially high energy density. The importance of reversible Al plating and stripping is particularly pronounced for RAMBs. However, it is still non-trivial to achieve high Al plating/stripping reversibility and superior lifespan, regardless of whether in aqueous, ionic liquid (IL) or organic electrolytes. Therefore, the reversibility and development of Al anodes await a breakthrough in addressing significant challenges, i.e., passivation, corrosion, and dendritic growth. Unfortunately, there is still a lack of systematic discussions on the strategies for achieving highly reversible and long-life Al anodes.

This review discusses some challenges facing Al anodes in current electrolyte systems, analyzes failure mechanisms, and presents some advanced solutions. Specifically, in aqueous electrolytes, the passivation of Al by the formation of a thin yet dense Al2O3 layer on the Al surface hinders reversible stripping and plating. Moreover, the thermodynamic instability of Al in aqueous electrolytes induces and exacerbates the corrosion and hydrogen evolution side reactions during resting and cycling. To solve these problems, the structural optimization of Al anode and the development of high-performance modification layers can effectively alleviate side reactions and enhance cycling stability. Also, regulating electrolyte components and concentrations can facilitate the formation of a more efficient solid electrolyte interphase (SEI), thus preventing the performance degradation caused by hydrogen evolution and dendrite growth. Room-temperature ILs with high concentrations of AlCl3 salt can promote reversible Al plating and stripping under ambient conditions. However, their notorious corrosion nature causes continuous consumption of Al, and exacerbates the uneven nucleation and growth during deposition, thus resulting in Al dendrites. In addition to conventional strategies (i.e., anode structure modification, host design, and interfacial coating), Al alloying and control of preferential crystal orientation are proved as effective approaches to enhance the corrosion resistance of Al and reduce nucleation barriers. These approaches promote uniform deposition and mitigate dendrite growth. The incorporation of functional additives, such as leveling agents, into the electrolyte also offers an effective approach. These additives stabilize Al morphology and suppress corrosion. In the case of organic electrolytes, the high-volumetric-charge density and intense electron-withdrawing nature of Al3+ result in slow de-solvation kinetics and severe interface passivation, which represent major bottlenecks for Al anodes. To address these challenges, the introduction of chloride ions into organic electrolytes can enhance the reversibility of Al. Chloride ions partially disrupt the passivation layer and, more importantly, facilitate the formation of Al2Cl7- active anions, thereby improving the de-solvation kinetics of Al3+ in organic electrolytes.

Summary and Prospects

RAMBs are regarded as one of the most promising alternatives to the existing battery technologies for large-scale energy storage due to their low cost, high capacity, superior safety, and abundant availability of aluminum. However, RAMBs still encounter significant challenges, with the lack of highly reversible, long-lifetime Al anodes being a critical bottleneck. Although considerable progress has been made in this field, it remains in its early stages and requires further comprehensive investigation. A future research can focus on the following aspects, 1) Revealing the in-depth failure mechanisms and enhancing the stability of Al metal anodes. Whether through anode modification or electrolyte optimization, the underlying mechanisms must be thoroughly investigated, with particular attention to the failure processes and stability of the anode interface. In-situ characterization techniques are highly preferred to identify the fundamental causes of interface failure. Also, there is a need to refine some methods for evaluating anode stability and to establish standardized performance parameters and evaluation criteria. 2) Exploring high-performance, non-corrosive, and cost-effective RAMBs systems. The performance of RAMBs is highly depended on the properties of the electrolyte and its compatibility with Al anodes. To address the corrosion challenges posed by chloride-based ILs on both Al and other metallic parts, the design of non-corrosive electrolytes is essential for practical applications. However, employing such non-corrosive electrolytes necessitates overcoming an issue of natural Al2O3 passivation layer on Al anode. 3) Developing high-capacity and stable cathode materials. The extremely high charge density of Al3+ results in an intense Coulomb interaction with intercalation-type cathode materials, which slows down the intercalation/deintercalation kinetics of Al3+ and leads to an irreversible structural damage to the cathode. For conventional conversion-type cathodes, their intense bonding with Al3+ severely limits the reversibility of redox reactions. It is thus critical for advancing RAMBs to develop novel cathode materials that can efficiently utilize the three-electron-transfer mechanism of Al3+ and exhibit fast kinetics.

In this review, we emphasize the critical importance of the fundamental failure mechanisms of Al anodes and clarify Al3+ solvation and de-solvation behaviors and breakthroughs in the design of pivotal materials such as non-corrosive and high-performance electrolytes and high-capacity cathodes. This review provides valuable insights for the development of next-generation RAMBs and contributes to accelerating their practical application.

, authors=Qing HE1, 2, Bo ZHANG1, 2, Yiyuan LIU1, 2, Daliang HAN1, 2, Zhe WENG1, 2, Quanhong YANG1, 2, authorsList=Qing HE, Bo ZHANG, Yiyuan LIU, Daliang HAN, Zhe WENG, Quanhong YANG, authorCompany=null, correspAuthors=Daliang HAN, Zhe WENG, authorNote=

HE Qing (2001-), male, Master candidate; E-mail: ;

ZHANG Bo (1999-), male, Doctoral candidate.

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HAN Daliang (1990-), male, Associate Professor; E-mail: ;
WENG Zhe (1983-), male, Professor.
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铝金属电池因铝负极具有成本低、理论容量高、资源可及和氧化还原电位较负的优势,具有低成本、高安全和潜在高比能的优势,在大规模储能领域展现出广阔的应用前景。然而,铝离子极高的电荷密度和铝负极的高活性使得实现高可逆、长寿命的铝金属负极依然面临诸多瓶颈。本文系统回顾了铝金属电池的发展历程,总结并分析了不同电解液(水系、离子液体和有机)体系中铝金属负极所面临的挑战和改性策略。最后对高可逆、长寿命铝金属负极的构建和新型高性能可充电铝金属电池的未来研究方向进行了展望。

, authors=何清1, 2, 张渤1, 2, 刘艺媛1, 2, 韩大量1, 2, 翁哲1, 2, 杨全红1, 2, authorsList=何清, 张渤, 刘艺媛, 韩大量, 翁哲, 杨全红, authorCompany=null, correspAuthors=韩大量, 翁哲, authorNote=

何清(2001—),男,硕士研究生;

张渤(1999—),男,博士研究生。

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韩大量(1990—),男,副研究员;
翁哲(1983—),男,教授。
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铝金属电池负极:挑战及进展
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何清 1, 2 , 张渤 1, 2 , 刘艺媛 1, 2 , 韩大量 1, 2 , 翁哲 1, 2 , 杨全红 1, 2
硅酸盐学报 | 第14届无机非金属材料专题研讨会专题—综合评述 2025,53(4): 880-894
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硅酸盐学报 |第14届无机非金属材料专题研讨会专题—综合评述 2025 , 53 (4) : 880 -894
铝金属电池负极:挑战及进展
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何清1, 2 , 张渤1, 2 , 刘艺媛1, 2, 韩大量1, 2 , 翁哲1, 2 , 杨全红1, 2
作者信息
  • 1.天津市先进碳与电化学储能重点实验室,天津大学化工学院,天津 300350
  • 2.天津大学国家储能技术产教融合创新平台,天津 300350
通讯作者:
韩大量(1990—),男,副研究员;
翁哲(1983—),男,教授。
作者简介:

何清(2001—),男,硕士研究生;

张渤(1999—),男,博士研究生。

Aluminum Metal Battery Anodes: Challenges and Progresses
Qing HE1, 2 , Bo ZHANG1, 2 , Yiyuan LIU1, 2, Daliang HAN1, 2 , Zhe WENG1, 2 , Quanhong YANG1, 2
Affiliations
  • 1.Tianjin Key Laboratory of Advanced Carbon and Electrochemical Energy Storage, School of Chemical Engineering and Technology, Tianjin University, Tianjin 300350, China
  • 2.National Industry-Education Integration Platform of Energy Storage, Tianjin University, Tianjin 300350, China
  • Corresponding Author:
    HAN Daliang (1990-), male, Associate Professor; E-mail: ;
    WENG Zhe (1983-), male, Professor.

    HE Qing (2001-), male, Master candidate; E-mail: ;

    ZHANG Bo (1999-), male, Doctoral candidate.

出版时间: 2025-04-20 doi: 10.14062/j.issn.0454-5648.20240699
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铝金属电池因铝负极具有成本低、理论容量高、资源可及和氧化还原电位较负的优势,具有低成本、高安全和潜在高比能的优势,在大规模储能领域展现出广阔的应用前景。然而,铝离子极高的电荷密度和铝负极的高活性使得实现高可逆、长寿命的铝金属负极依然面临诸多瓶颈。本文系统回顾了铝金属电池的发展历程,总结并分析了不同电解液(水系、离子液体和有机)体系中铝金属负极所面临的挑战和改性策略。最后对高可逆、长寿命铝金属负极的构建和新型高性能可充电铝金属电池的未来研究方向进行了展望。

可充电铝金属电池  /  铝负极  /  钝化  /  腐蚀  /  枝晶

Rechargeable aluminum (Al) metal batteries (RAMBs) are considered as one of the most attractive alternatives to the existing battery technologies because of their low cost, high safety, high abundance of Al (the most earth-abundant metal element, over 3 700 times that of lithium), and the well-established Al industry. Furthermore, Al anode has a high theoretical gravimetric capacity of 2 981 mA·h·g−1 and the highest theoretical volumetric capacity of 8056 mA·h·cm−3, as well as a relatively low redox potential of−1.66 V versus the standard hydrogen electrode, thus enabling RAMBs to have a potentially high energy density. The importance of reversible Al plating and stripping is particularly pronounced for RAMBs. However, it is still non-trivial to achieve high Al plating/stripping reversibility and superior lifespan, regardless of whether in aqueous, ionic liquid (IL) or organic electrolytes. Therefore, the reversibility and development of Al anodes await a breakthrough in addressing significant challenges, i.e., passivation, corrosion, and dendritic growth. Unfortunately, there is still a lack of systematic discussions on the strategies for achieving highly reversible and long-life Al anodes.

This review discusses some challenges facing Al anodes in current electrolyte systems, analyzes failure mechanisms, and presents some advanced solutions. Specifically, in aqueous electrolytes, the passivation of Al by the formation of a thin yet dense Al2O3 layer on the Al surface hinders reversible stripping and plating. Moreover, the thermodynamic instability of Al in aqueous electrolytes induces and exacerbates the corrosion and hydrogen evolution side reactions during resting and cycling. To solve these problems, the structural optimization of Al anode and the development of high-performance modification layers can effectively alleviate side reactions and enhance cycling stability. Also, regulating electrolyte components and concentrations can facilitate the formation of a more efficient solid electrolyte interphase (SEI), thus preventing the performance degradation caused by hydrogen evolution and dendrite growth. Room-temperature ILs with high concentrations of AlCl3 salt can promote reversible Al plating and stripping under ambient conditions. However, their notorious corrosion nature causes continuous consumption of Al, and exacerbates the uneven nucleation and growth during deposition, thus resulting in Al dendrites. In addition to conventional strategies (i.e., anode structure modification, host design, and interfacial coating), Al alloying and control of preferential crystal orientation are proved as effective approaches to enhance the corrosion resistance of Al and reduce nucleation barriers. These approaches promote uniform deposition and mitigate dendrite growth. The incorporation of functional additives, such as leveling agents, into the electrolyte also offers an effective approach. These additives stabilize Al morphology and suppress corrosion. In the case of organic electrolytes, the high-volumetric-charge density and intense electron-withdrawing nature of Al3+ result in slow de-solvation kinetics and severe interface passivation, which represent major bottlenecks for Al anodes. To address these challenges, the introduction of chloride ions into organic electrolytes can enhance the reversibility of Al. Chloride ions partially disrupt the passivation layer and, more importantly, facilitate the formation of Al2Cl7- active anions, thereby improving the de-solvation kinetics of Al3+ in organic electrolytes.

Summary and Prospects

RAMBs are regarded as one of the most promising alternatives to the existing battery technologies for large-scale energy storage due to their low cost, high capacity, superior safety, and abundant availability of aluminum. However, RAMBs still encounter significant challenges, with the lack of highly reversible, long-lifetime Al anodes being a critical bottleneck. Although considerable progress has been made in this field, it remains in its early stages and requires further comprehensive investigation. A future research can focus on the following aspects, 1) Revealing the in-depth failure mechanisms and enhancing the stability of Al metal anodes. Whether through anode modification or electrolyte optimization, the underlying mechanisms must be thoroughly investigated, with particular attention to the failure processes and stability of the anode interface. In-situ characterization techniques are highly preferred to identify the fundamental causes of interface failure. Also, there is a need to refine some methods for evaluating anode stability and to establish standardized performance parameters and evaluation criteria. 2) Exploring high-performance, non-corrosive, and cost-effective RAMBs systems. The performance of RAMBs is highly depended on the properties of the electrolyte and its compatibility with Al anodes. To address the corrosion challenges posed by chloride-based ILs on both Al and other metallic parts, the design of non-corrosive electrolytes is essential for practical applications. However, employing such non-corrosive electrolytes necessitates overcoming an issue of natural Al2O3 passivation layer on Al anode. 3) Developing high-capacity and stable cathode materials. The extremely high charge density of Al3+ results in an intense Coulomb interaction with intercalation-type cathode materials, which slows down the intercalation/deintercalation kinetics of Al3+ and leads to an irreversible structural damage to the cathode. For conventional conversion-type cathodes, their intense bonding with Al3+ severely limits the reversibility of redox reactions. It is thus critical for advancing RAMBs to develop novel cathode materials that can efficiently utilize the three-electron-transfer mechanism of Al3+ and exhibit fast kinetics.

In this review, we emphasize the critical importance of the fundamental failure mechanisms of Al anodes and clarify Al3+ solvation and de-solvation behaviors and breakthroughs in the design of pivotal materials such as non-corrosive and high-performance electrolytes and high-capacity cathodes. This review provides valuable insights for the development of next-generation RAMBs and contributes to accelerating their practical application.

rechargeable aluminum metal battery  /  aluminum anode  /  passivation  /  corrosion  /  dendrite
何清, 张渤, 刘艺媛, 韩大量, 翁哲, 杨全红. 铝金属电池负极:挑战及进展. 硅酸盐学报, 2025 , 53 (4) : 880 -894 . DOI: 10.14062/j.issn.0454-5648.20240699
Qing HE, Bo ZHANG, Yiyuan LIU, Daliang HAN, Zhe WENG, Quanhong YANG. Aluminum Metal Battery Anodes: Challenges and Progresses[J]. Journal of the Chinese Ceramic Society, 2025 , 53 (4) : 880 -894 . DOI: 10.14062/j.issn.0454-5648.20240699
  • 国家自然科学基金(22479110; 22109116)
  • 国家重点研发计划(2022YFB2404500)
  • 天津市自然科学基金(23JCQNJC 01750)
  • 榆林中科洁净能源创新研究院能源革命科技专项项目(E411110705)
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doi: 10.14062/j.issn.0454-5648.20240699
  • 接收时间:2024-11-04
  • 首发时间:2026-10-22
  • 出版时间:2025-04-20
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  • 收稿日期:2024-11-04
  • 修回日期:2024-12-20
基金
国家自然科学基金(22479110; 22109116)
国家重点研发计划(2022YFB2404500)
天津市自然科学基金(23JCQNJC 01750)
榆林中科洁净能源创新研究院能源革命科技专项项目(E411110705)
作者信息
    1.天津市先进碳与电化学储能重点实验室,天津大学化工学院,天津 300350
    2.天津大学国家储能技术产教融合创新平台,天津 300350

通讯作者:

韩大量(1990—),男,副研究员;
翁哲(1983—),男,教授。
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