4.8 Article

Surface Functionalization of Silicon, HOPG, and Graphite Electrodes: Toward an Artificial Solid Electrolyte Interface

期刊

ACS APPLIED MATERIALS & INTERFACES
卷 10, 期 28, 页码 24172-24180

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acsami.8b04877

关键词

solid electrolyte interface; lithium-ion battery; X-ray photoelectron spectroscopy; time-of-flight secondary ion mass spectrometry; thiol-yne click chemistry; diazonium salt

资金

  1. German Research Foundation (DFG) [SFB 1176]
  2. Karlsruhe Nano Micro Facility (KNMF)
  3. Helmholtz research infrastructure at Karlsruhe Institute of Technology (KIT)

向作者/读者索取更多资源

Electrografting of diazonium salts containing a protected alkyne moiety was used for the first functionalization of silicon and highly ordered pyrolytic graphite model surfaces. After deprotection with tetrabutylammonium fluoride, further layers were added by the thiol-yne click chemistry. The composition of each layer was characterized via X-ray photoelectron spectroscopy and time-of-flight secondary ion mass spectrometry. The same approach was then used to functionalize graphite powder electrodes, which are classically used as negative electrode in lithium-ion batteries. The effect of the coating on the formation of the solid electrolyte layer was investigated electrochemically by cyclovoltammetry and galvanostatic measurements. The modified graphite electrodes showed different reduction peaks in the first cycle, indicating reduced and altered decomposition processes of the components. Most importantly, the electrochemical investigations show a remarkable reduction of irreversible capacity loss of the battery.

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