4.6 Article

Insights on the work function of the current collector surface in anode-free lithium metal batteries

Journal

JOURNAL OF MATERIALS CHEMISTRY A
Volume 10, Issue 39, Pages 20984-20992

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/d2ta04078f

Keywords

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Funding

  1. LG energy solution-KAIST Frontier Research Laboratory
  2. Individual Research Program through the National Research Foundation of Korea (NRF) of Korea - Ministry of Science, ICT [2020R1A2C2101968]
  3. Technology Development Program to Solve Climate Changes through the NRF - Ministry of Science, ICT [2018M1A2A2063807]
  4. National Research Foundation of Korea [2018M1A2A2063807, 2020R1A2C2101968] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)

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This study explores the role of the work function of metallic current collectors in anode-free lithium metal batteries (LMBs). It was found that higher index surface facets lead to lower work functions and higher surface energies. A lower work function favors binding with lithium, but it also leads to electrolyte decomposition and the formation of a thick solid electrolyte interphase layer. Increasing the work function can reduce the irreversible capacity and capacity fade rate of anode-free LMBs.
Lithiophilicity has been a major factor in the design of current collectors for anode-free lithium metal batteries (LMBs). However, another design factor, work function, has not been considered in spite of its critical role in electron transfer at the current collector. Herein, we explore the role of the work function of the metallic current collector using two model Cu current collectors with different major surface facets of (111) and (310). According to DFT calculations, a higher index surface facet leads to a lower work function and a higher surface energy. Electrochemical analysis revealed that the Cu current collector with low work function favorably binds with Li, however, it is prone to decompose the liquid electrolyte and form a thick solid electrolyte interphase layer due to a lowered energy barrier for electron transfer. Although the two opposite effects vary depending on operating conditions, the irreversible capacity at the first cycle and the early capacity fade rate, which are the most critical issues for anode-free LMBs, are diminished by increasing the work function. This work provides a fresh perspective on the design of current collectors for advanced anode-free LMBs.

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