The solid electrolyte interphase (SEI) dictates the stability and cycling performance of highly reactive battery electrodes. Characterization of the thin, dynamic, and environmentally sensitive nature of the SEI presents a formidable challenge, which calls for the use of microscopic, time-resolved methods. Herein, we employ scanning electrochemical microscopy (SECM) to directly probe the heterogeneous surface electronic conductivity during SEI formation and degradation. Complementary electrochemical quartz crystal microbalance (EQCM) and X-ray photoelectron spectroscopy (XPS) provide comprehensive analysis of the dynamic size and compositional evolution of the complex interfacial microstructure. We have found that stable anode passivation occurs at potentials of 0.5 V vs Li/Li, even in cases where anion decomposition and interphase formation occur above 1.0 V. We investigated the bidirectional relationship between the SEI and lithium plating-stripping, finding that plating-stripping ruptures the SEI. The current efficiency of this reaction is correlated to the anodic stability of the SEI, highlighting the interdependent relationship between the two. We anticipate this work will provide critical insights on the rational design of stable and effective SEI layers for safe, fast-charging, and long-lifetime lithium metal batteries.
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http://dx.doi.org/10.1021/acsami.3c08485 | DOI Listing |
Angew Chem Int Ed Engl
January 2025
Harbin Institute of Technology, School of Chemistry and Chemical Engineering, No. 92, West Dazhi Street, 150001, Harbin, CHINA.
Commercial hard carbon (HC) anode suffers from unexpected interphase chemistry rooted in the parasitic reactions between surface oxygen-functional groups and ester-based electrolytes. Herein, an innovative strategy is proposed to regulate interphase chemistry by tailoring targeted functional groups on the HC surface, where highly active undesirable oxygen-functional groups are skillfully converted into a Si-O-Si molecular layer favorable for anchoring anions. Then, an inorganic/organic hybrid solid electrolyte interphase with low interfacial charge transfer resistance and enhanced cycling durability is constructed successfully.
View Article and Find Full Text PDFAngew Chem Int Ed Engl
January 2025
Sun Yat-Sen University, School of Material Science and Engineering, Nr.135 Xingang Xi Road, 510275, Guangzhou, CHINA.
Degradable features are highly desirable to advance next-generation organic mixed ionic-electronic conductors (OMIECs) for transient bioinspired artificial intelligence devices.It is highly challenging that OMIECs exhibit excellent mixed ionic-electronic behavior and show degradability simultaneously.Specially,in OMIECs,doping is often a tradeoff between structural disorder and charge carrier mobilities.
View Article and Find Full Text PDFChem Sci
January 2025
School of Chemistry and Chemical Engineering, Anhui University of Technology Ma'anshan 243032 Anhui China
Organic compounds present promising options for sustainable zinc battery electrodes. Nevertheless, the electrochemical properties of current organic electrodes still lag behind those of their inorganic counterparts. In this study, nitro groups were incorporated into pyrene-4, 5, 9, 10-tetraone (PTO), resulting in an elevated discharge voltage due to their strong electron-withdrawing capabilities.
View Article and Find Full Text PDFAngew Chem Int Ed Engl
January 2025
Beihang University, 37 Xue Yuan Road, Hai Dian District, 100191, Beijing, CHINA.
Sodium-ion batteries (SIBs), endowed with relatively small Stokes radius and low desolvation energy for Na+, are reckoned as a promising candidate for fast-charging endeavors. However, the C-rate charging capability of practical energy-dense sodium-ion pouch cells is currently limited to ≤1C, due to the high propensity for detrimental metallic Na plating on the hard carbon (HC) anode at elevated rates. Here, an ampere-hour-level sodium-ion pouch cell capable of 3C charging is successfully developed via phosphorus (P)-sulfur (S) interphase chemistry.
View Article and Find Full Text PDFJ Colloid Interface Sci
January 2025
Key Laboratory of Low-Carbon and Green Agriculture Chemistry in Universities of Shandong, College of Chemistry and Material Science, Shandong Agricultural University, Tai'an, Shandong 271018, China. Electronic address:
Meliorating the behavior deposition of lithium polysulfides (LiPS) is crucial for enhancing the electrochemical performance of sulfur cathodes, which could be implemented by the precise modulation on the catalytic host. Herein, heterostructure engineering is employed to tune up the catalytic capability of CeVO, by introducing CeO through a simple adjustment in the addition sequence of reactants. The formed CeVO/CeO heterostructure has been demonstrated to exhibit appropriate interaction strength with LiPS for accelerating the catalytic conversion process, as well as an engineered surface for inducing three dimensional (3D) LiS deposition, thereby endowing the corresponding sulfur cathodes with excellent electrochemical performance under harsh conditions.
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