4.8 Article

Built-in superionic conductive phases enabling dendrite-free, long lifespan and high specific capacity composite lithium for stable solid-state lithium batteries

Journal

ENERGY & ENVIRONMENTAL SCIENCE
Volume 16, Issue 3, Pages 1049-1061

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/d2ee03709b

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A composite lithium anode (CLA) was designed and prepared to solve the obstacles of huge interfacial resistance and growth of detrimental Li dendrites in solid-state lithium metal batteries (SSLMBs). The CLA significantly improved the intrinsic ionic diffusion capability of the lithium anode and simultaneously enhanced the wettability of the anode towards solid-state electrolyte, resulting in a robust and high ionic conductive solid-state interface. The SSLMB with the CLA achieved excellent cycling performance and high-rate capability, demonstrating its potential for high-performance solid-state Li metal batteries.
Solid-state lithium metal batteries (SSLMBs) are considered as one of the most promising energy storage systems because of their high-energy density and intrinsic good safety. However, the practical application of SSLMBs is hindered by the huge interfacial resistance and growth of detrimental Li dendrites. To solve these obstacles, a composite lithium anode (CLA) with built-in well-dispersed ionic conductive Li3N and LiNxOy species is specially designed and prepared, which on one hand greatly promote the intrinsic ionic diffusion capability of the bulk lithium anode, and on the other hand simultaneously improve the wettability of the anode towards solid-state electrolyte (SSE), construct a robust and high ionic conductive solid-state interface and effectively enhance the chemical contact of Li/SSE as demonstrated by density functional theory (DFT) calculations. A top-level area specific capacity (1.5 mA h cm(-2), 0.5 mA cm(-2)) and ultra-high critical current density (1.4 mA cm(-2)) are achieved for all-solid-state symmetric cells at room temperature. The full SSLMB coupling with the CLA and commercial LiFePO4 (LFP) cathode achieves excellent cycling performance as long as 500 cycles with a capacity retention of 80.0% and high-rate capability of 2.0 C. Even under high voltage (4.3 V) conditions, the solid-state full cell matched with LiNi0.8Co0.1Mn0.1O2 (NCM811) could stably be cycled more than 115 times with a retention of 80.0%. The findings provide a new composite anode strategy for high-performance solid-state Li metal batteries.

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