Lithium (Li) metal is the most promising anode material for Li-metal batteries due to its high theoretical capacity (3,860 mAh g-1) and low electrochemical potential (-3.04 V vs. the standard hydrogen electrode). However, many of previously studies for Li-metal batteries utilized a relatively thick ~ 50 μm Li metal foils, which lowers overall energy densities of the cells. Therefore, there have been growing research to reduce the thickness of the Li-metal anode to improve the energy density of batteries. Typical anode current collector of a copper foil show low affinity of Li metals with great initial deposition overpotentials when Li-metals are eletrodeposited. Such lithiophobicity accelerate the problems of Li dendritic growth with reduction in cycle life, which has been critical problems in practical applications of pristine Cu current collectors for Li-metal batteries. Therefore, various types of surface modification methods have been reported so far, such as coatings of carbon materials such as GO or metal-based materials such as Ag, Au. However, only carbon or metal modifications have been suffering from the relatively low lithiophilicity of the carbons and pulverizations of metals during cyclings by alloying and dealloying with Li-metals, respectively. Carbon and metal hybrid composites were also studied to mitigate these problems, but there still large rooms for further improvements showing unstable cycle performances at high C-rates.Herein, we report the fabrication of lithiophilic graphene oxide (GO) and silver nanowire (AgNW) nanocomposite anodes by Layer-by-Layer (LbL) assembly methods for uniform Li depositions. GO provides a fast Li ion movement channel with high ionic conductivity, and AgNW shows low nucleation overpotential behavior due to the formation of an alloy with Li. Therefore, we alternately stack these two materials using the LbL assembly method to induce a synergistic effect of their advantages. The resulting GO and AgNW nanocomposite films show uniformly deposited morphology after Li depositions and low nucleation overpotential compared to copper foils when pre-deposited at capacity of 4 mAh cm-2. The symmetric cells with the GO-AgNW composite electrodes with 4 mAh cm-2 of Li pre-depositions show stable behavior for 400 cycles with an overpotential of 10 mV at 1 mA cm-2 and 1 mAh cm-2. In addition, the full cells using LFP cathode materials operate more than 400 cycles at 1 C-rate and 200 cycles even at high 3 C-rate, showing longer cycle life and capacity retention than copper foil. These LbL self-assembled anodes provides a facile route to prepare lithiophillic anode coatings that can be advantageous for the preparations of high energy density Li-metal batteries.
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