4.8 Article

Gradient nano-recipes to guide lithium deposition in a tunable reservoir for anode-free batteries

期刊

ENERGY STORAGE MATERIALS
卷 45, 期 -, 页码 40-47

出版社

ELSEVIER
DOI: 10.1016/j.ensm.2021.11.037

关键词

Anode-free lithium batteries; Solid electrolyte interface; Concentration gradient; Electron paramagnetic resonance; cryo-TEM

资金

  1. Basic Research Project of the Science and Technology Innovation Commission of Shenzhen [JCYJ20200109141640095]
  2. Shenzhen Key Laboratory of Interfacial Science and Engineering of Materials [ZDSYS20200421111401738]
  3. Guangdong-Hong Kong-Macao Joint Laboratory [2019B121205001]
  4. National Natural Science Foundation of China [21875097]

向作者/读者索取更多资源

This study proposes a method of in-situ growing a gradient solid electrolyte interface (SEI) layer on a pre-designed micro-hole grid (MHG) Cu reservoir in anode-free batteries (AFBs). The method improves the stability of the electrode interface and reduces surface stress, resulting in higher areal capacity and cycling performance.
Anode-free batteries (AFBs) have the potential of ultra-high energy density, but lithium dendrite has largely hindered their practical applications. In this work, an in-situ grown gradient solid electrolyte interface (SEI) layer on pre-designed micro-hole-grid (MHG) Cu reservoir is proposed to guide uniform lithium deposition and propagation, by which the electrode interface is stabilized and the surface stress is considerably decreased endowing the AFBs with outstanding areal capacity and cycling performance. The gradient SEI is confirmed by cryogenictransmission electron microscopy (Cryo-TEM) and XPS to be composed of (1) an elastic organic top layer to hinder non-Li species migration and withstand volume fluctuation, and (2) a lithophilic LiCl-rich bottom layer to render the rapid lithium supply. Operando electron paramagnetic resonance (EPR) shows a dynamic Li deposition, unambiguously demonstrating a dendrites-free behavior. As a result, the full cells of a gradient SEI modified Cu reservoir paired with a LiFePO4 cathode exhibit high capacity of 95 mAh g(-1) and Coulombic efficiency (CE) of 99.5% after 100 cycles, much better than the control cells with planar current collectors (1.6 mAh g(-1), 2.6%). These findings are enlightening in engineering better interphases for high energy and safe rechargeable lithium metal batteries.

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