Fast charging promotes Li dendrite formation and its growth on graphite anodes, which affects cell performance in Li-ion batteries (LIBs). This work reports the formation of a robust SEI layer by introducing a KPF inorganic additive into the electrolyte. An optimal concentration of 0.001 M KPF effectively inhibits the growth of Li dendrites at 2C charging rates, compared with a commercial electrolyte. Electrolytes containing a KPF additive are shown here to deliver dual effects to mitigate the growth of dendrites. A thin LiF-rich SEI layer is formed on graphite, which blocks the electron leakage pathways. Additionally, K resides at defect sites (such as particle boundaries) due to its faster diffusion rate and blocks the incoming Li and restricts the growth of Li dendrites. The electrolyte with optimum concentration of KPF, i.e., 0.001 M, effectively directs Li transport through the thin, durable, and low resistance LiF-rich SEI layer. This has implications for fast charging through optimization of the electrode/electrolyte interphase by controlling additive concentrations.
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http://dx.doi.org/10.1021/acsami.2c11175 | DOI Listing |
ACS Appl Mater Interfaces
January 2025
School of Material Science and Engineering, Jiangsu Collaborative Innovation Center for Photovoltaic Science and Engineering, Jiangsu Province Cultivation Base for State Key Laboratory of Photovoltaic Science and Technology, Changzhou University, Changzhou 213164, China.
Lithium (Li) metal's extremely high specific energy and low potential make it critical for high-performance batteries. However, uncontrolled dendrite growth and an unstable solid-electrolyte interphase (SEI) during repeated cycling still seriously hinder its practical application in Li metal batteries. Herein, we demonstrate a facile and effective approach to fabricate a flexible and robust hybrid SEI layer using two kinds of organo-polysulfides with different sulfur chain lengths [bis(3-(triethoxysilyl)propyl)disulfide (Si-O-2S) and bis(3-(triethoxysilyl)propyl)tetrasulfide (Si-O-4S)] as the additives in the electrolyte.
View Article and Find Full Text PDFChemSusChem
January 2025
Harbin University of Science and Technology, School of Electrical and Electronic Engineering, CHINA.
In the pursuit of high-energy-density lithium metal batteries (LMBs), the development of stable solid electrolyte interphase (SEI) is critical to address issues such as lithium dendrite growth and low Coulombic efficiency. Herein, we propose a facile strategy for the in-situ fabrication of a LiCl-rich artificial SEI layer on Li surfaces through reaction of MoCl5 with Li (Li@MoCl5). The resulting artificial SEI significantly enhances the uniformity of Li deposition, effectively suppresses dendrite formation, and improves electrochemical performance.
View Article and Find Full Text PDFAcc Chem Res
January 2025
Helmholtz Institute Ulm (HIU) Electrochemical Energy Storage, Helmholtzstrasse 11, 89081 Ulm, Germany.
ConspectusLithium-ion batteries (LIBs) based on graphite anodes are a widely used state-of-the-art battery technology, but their energy density is approaching theoretical limits, prompting interest in lithium-metal batteries (LMBs) that can achieve higher energy density. In addition, the limited availability of lithium reserves raises supply concerns; therefore, research on postlithium metal batteries is underway. A major issue with these metal anodes, including lithium, is dendritic formation and insufficient reversibility, which leads to safety risks due to short circuits and the use of flammable electrolytes.
View Article and Find Full Text PDFJ Colloid Interface Sci
April 2025
College of Physics, Qingdao University, Qingdao 266071, China. Electronic address:
Polyacrylonitrile (PAN)-based composite solid electrolytes (CSEs) hold great promise in the practical deployment of solid lithium batteries (SLBs) owing to their high voltage stability but suffer from poor stability against Li-metal. Herein, a poly(1,3-dioxolane) (PDOL)-graphitic CN (g-CN, i.e.
View Article and Find Full Text PDFSmall
January 2025
State Key Laboratory of Advanced Technology for Materials Synthesis and Processing, Wuhan University of Technology, Wuhan, 430070, China.
The development of aqueous zinc metal batteries (AZMBs) is hampered by dendrites and side reactions induced by reactive HO. In this study, a hydrated eutectic electrolyte with restrictive water consisting of zinc trifluoromethanesulfonate (Zn(OTf)), 1,3-propanediol (PDO), and water is developed to improve the stability of the anode/electrolyte interface in AZMBs via the formation of a water-deficient interface. Additionally, PDO participates in the Zn solvation structure and inhibits the movement of water molecules.
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