Electrostatic Regulation of Na+ Coordination Chemistry for High-Performance All-Solid-State Sodium Batteries

作者：Penghui Song, Suli Chen, Junhong Guo, Junchen Wu, Qiongqiong Lu, Haijiao Xie, Qingsong Wang, Tianxi Liu · 发表于：Nano-Micro Letters · 年份：2025 · DOI：10.1007/s40820-025-01910-1 · 被引用次数：17 · 研究领域：Advanced Battery Materials and Technologies、Advancements in Battery Materials、Thermal Expansion and Ionic Conductivity

Abstract Ion migration capability and interfacial chemistry of solid polymer electrolytes (SPEs) in all-solid-state sodium metal batteries (ASSMBs) are closely related to the Na + coordination environment. Herein, an electrostatic engineering strategy is proposed to regulate the Na + coordinated structure by employing a fluorinated metal–organic framework as an electron-rich model. Theoretical and experimental results revealed that the abundant electron-rich F sites can accelerate the disassociation of Na-salt through electrostatic attraction to release free Na + , while forcing anions into a Na + coordination structure though electrostatic repulsion to weaken the Na + coordination with polymer, thus promoting rapid Na + transport. The optimized anion-rich weak solvation structure fosters a stable inorganic-dominated solid–electrolyte interphase, significantly enhancing the interfacial stability toward Na anode. Consequently, the Na/Na symmetric cell delivered stable Na plating/stripping over 2500 h at 0.1 mA cm −2 . Impressively, the assembled ASSMBs demonstrated stable performance of over 2000 cycles even under high rate of 2 C with capacity retention nearly 100%, surpassing most reported ASSMBs using various solid-state electrolytes. This work provides a new avenue for regulating the Na + coordination structure of SPEs by exploration of electrostatic effect engineering to achieve high-performance all-solid-state alkali metal batteries. Graphical Abstract