In‐Plane Lithium Growth Enabled by Artificial Nitrate‐Rich Layer: Fast Deposition Kinetics and Desolvation/Adsorption Mechanism. Issue 28 (10th June 2020) - Wang, Xianshu
Abstract: An artificial lithium‐nitrate (LiNO3 )‐rich layer (LN‐RL) is developed to address dendritic lithium (Li) growth by a fusing–infusing strategy, in which LiNO3 is loaded into stainless steel mesh and a Li‐metal anode (LN‐RL@Li) is obtained by casting this LN‐RL onto Li foil. The LN‐RL enables fast Li deposition kinetics in carbonates and endows LN‐RL@Li with excellent cycleability. The underneath mechanism on the contribution of LN‐RL is uncovered by detailed characterizations combining with theoretical simulations. The LN‐RL promotes the desolvation and capacitive adsorption of Li ions and induces in‐plane Li growth along the edges of preplated Li with planar morphology. The improved cycleability of LN‐RL(@Li) is demonstrated by LiǁCu cell that presents a coulombic efficiency of 97.2% after 280 cycles and LiǁLi cell that proceeds over 1000 h at 0.5 mA cm −2 in carbonates. Additionally, the LiǁLiFePO4 cell shows a capacity retention of 58% after 400 cycles at 1 C (1 C = 170 mA g −1 ), compared to the 35% after 180 cycles for the control. This work presents not only a promising strategy for practical applications of Li‐metal batteries, but also a new understanding on the role of nitrate in Li plating/stripping kinetics. Abstract : Lithium‐nitrate (LiNO3 )‐rich layer (LN‐RL) that is constructed by molten LiNO3 infusing into stainless steel mesh skeleton can promote desolvation stage and capacitive adsorption of Li and induce in‐plane Li growth with smooth and even surface morphology. Therefore, LN‐RL(@Li) anode presents excellent cyclic stability and rate adaptability, evaluated by LiǁCu cells, LiǁLi symmetric cells, or LiǁLiFePO4 full cells.