Ferroelectric materials in rechargeable batteries

铁电性 电池(电) 纳米技术 材料科学 极化(电化学) 电化学 材料设计 电极 软件部署 偶极子 计算机科学 工程物理 合理设计 储能 再分配(选举) 多样性(控制论) 锂离子电池 焊剂(冶金) 表征(材料科学) 锂(药物) 锂电池 有机自由基电池
作者
Weizhong Liang,Yu You,Ziqin Liu,Kunyun Yan,Jialin Lin,Yongheng Wu,Qiwei Yu,Kun Zhao,Xiaowei Huang,C L Zhang,Jun Liu,Weifeng Wei
出处
期刊:Chemical Society Reviews [Royal Society of Chemistry]
卷期号:55 (9): 5491-5529
标识
DOI:10.1039/d6cs00069j
摘要

The pursuit of high-specific-energy rechargeable batteries is increasingly hindered by persistent electrode polarization, interfacial instability, and parasitic side reactions that conventional material designs struggle to address across diverse battery chemistries (such as lithium batteries and non-lithium batteries). These challenges call for materials capable of actively regulating electrochemical environments under realistic operating conditions. Ferroelectric materials, characterized by switchable spontaneous polarization, intrinsic dipolar asymmetry, and strong multi-field coupling, represent a fundamentally distinct class of functional materials for battery systems. Rather than relying solely on static chemical composition or structural reinforcement, ferroelectrics introduce dynamically build-in electric fields that reshape ion transport behavior, redistribute interfacial charge, and modify reaction energetics throughout the battery architecture. In this review, we first outline the historical development and fundamental physical principles of ferroelectric materials, establishing the theoretical basis for their functionality in electrochemical systems. We then examine how polarization-driven effects manifest differently when ferroelectrics are integrated into a variety of battery components. Within electrodes, polarization can influence ion flux and alleviate concentration gradients; at reactive metal/electrolyte interfaces, dipole-induced charge redistribution helps stabilize interfacial chemistry; and within solid or quasi-solid electrolytes, polarization-modified space-charge structures can alter transport kinetics and interfacial resistance. From the cross-system and cross-component perspectives, we summarize chemistry-specific and architecture-aware design principles for ferroelectric materials in practical battery environments. Finally, we identify key mechanistic bottlenecks and future research directions, outlining pathways toward the rational deployment of ferroelectric-enabled strategies for safe, durable, and high-energy-density rechargeable batteries.
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