Lithium
(Li) metal is considered as a promising anode candidate
for high-energy-density batteries. However, the high reactivity of
Li metal leads to poor air stability, limiting its practical application.
Additionally, the interfacial instability, such as dendrite growth
and an unstable solid electrolyte interphase layer, further complicates
its utilization. Herein, a dense lithium fluoride (LiF)-rich interfacial
protective layer is constructed on the Li surface through a simple
reaction between Li and fluoroethylene carbonate (denoted as LiF@Li).
The LiF-rich interfacial protective layer consists of both organic
(ROCO2Li and C–F-containing species, which only
exist on the outer layer) and inorganic (LiF and Li2CO3, distribute throughout the layer) components with a thickness
of ∼120 nm. Specifically, chemically stable LiF and Li2CO3 play an important role in blocking air and
hence improve the air durability of LiF@Li anodes. Notably, LiF with
high Li+ diffusivity facilitates uniform Li+ deposition, while organic components with high flexibility relieve
volume change upon cycling, thereby enhancing the dendrite inhibition
capacity of LiF@Li. Consequently, LiF@Li exhibits remarkable stability
and excellent electrochemical performance in both symmetric cells
and LiFePO4 full cells. Moreover, LiF@Li maintains its
initial color and morphology even after air exposure for 30 min, and
the air-exposed LiF@Li anode still retains its superior electrochemical
performance, further establishing its outstanding air-defendable capability.
This work proposes a facile approach in constructing air-stable and
dendrite-free Li metal anodes toward reliable Li metal batteries.