Ferroelectric interface for efficient sodium metal cycling in anode-free solid-state batteries

被引:2
|
作者
Sun, Chen [1 ]
Li, Yang [1 ]
Sun, Zheng [1 ]
Yuan, Xuanyi [2 ]
Jin, Haibo [1 ]
Zhao, Yongjie [1 ]
机构
[1] Beijing Inst Technol, Sch Mat Sci & Engn, Beijing Key Lab Construct Tailorable Adv Funct Mat, Beijing 100081, Peoples R China
[2] Renmin Univ China, Dept Phys, Beijing Key Lab Optoelect Funct Mat & Micronano De, Beijing 100872, Peoples R China
基金
中国国家自然科学基金;
关键词
Anode-free solid-state batteries; Ferroelectric composite substrate; Built-in electric field; NASICON electrolyte; LITHIUM; ELECTROLYTE; GROWTH;
D O I
10.1016/j.mattod.2024.09.018
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
Anode-free solid-state batteries (AFSSBs) are considered one of the promising solutions for achieving high energy density and safety of electrochemical energy storage systems. However, owing to mechanochemical contact losses and metallic dendrite growth caused by the degradation at the current collector (CC)/electrolyte interface, the feasibility of AFSSBs is critically limited, especially upon the involvement of rigid ceramic electrolytes. Here, a new strategy is reported for NASICONstructure Na3Zr2Si2PO12 (NZSP) electrolyte-based AFSSBs by introducing a resilient ferroelectric composite substrate coated onto Al CC, eventually achieving efficient and stable operation. Compared with the bare Al foil, the ferroelectric composite substrate not only renders an intimate CC/electrolyte interface compatibility, but also dynamically regulates the distribution and migration of Na+ flux at the CC/electrolyte interface through the built-in electric field stem from ferroelectric BaTiO3, guiding homogeneous and dense sodium metal deposition. Stable plating/stripping cycling can be achieved even at a high current density of 1.2mA cm-2 with the Coulombic efficiency of (99.7 %). Significantly, the NZSP-based AFSSB integrated with the ferroelectric composite substrate and mainstream sodium ion cathodes demonstrates stable cycling and excellent capacity retention.
引用
收藏
页码:395 / 405
页数:11
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