电解质
溶剂化
催化作用
法拉第效率
阳极
相间
材料科学
化学工程
电极
化学物理
工作(物理)
电池(电)
纳米技术
选择性催化还原
离子
晶界
静电学
分子
催化循环
作者
Shuibin Tu,Ming Chen,Long Qian,Yukun Lei,Shaojian Zhang,Chao Ye,Clotilde S. Cucinotta,Shi-Zhang Qiao
标识
DOI:10.1038/s41560-026-02074-x
摘要
Abstract Anion-rich interfacial solvation structures (ISS) are critical for stable fast charging of anodes. Here we propose interfacial anion-reduction catalysis as a new paradigm, in which catalytic centres regulate the ISS to direct solid electrolyte interphase formation. Using S vacancies as prototypical catalytic sites, we demonstrate that electrostatic potential wells induced by these centres attract bis(fluorosulfonyl)imide (FSI − ) to the interface and form contact ion pairs during charging, creating FSI − -rich ISS in commercial electrolytes. This catalytically regulated ISS promotes preferential FSI − reduction and ultrafine LiF grain formation, generating a compact LiF-rich solid electrolyte interphase with rapid Li + transport pathways. Si-based anode with catalytic interface demonstrates stable cycling with an average coulombic efficiency of ~99.94%. Pouch cells achieve ~91.4% and ~85.3% charge in 10 min and 6 min, respectively, while providing ~240.4 Wh kg −1 under 6 min charging. This work establishes catalytic regulation of ISS as a promising strategy for fast battery charging.
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