Catalytic Growth of Ionic Conductive Lithium Nitride Nanowire Array for Dendrite‐Free Lithium Metal Anode

Author:

Shen Chunli1,Meng Jiashen1,Yan Mengyu1,Liao Xiaobin1,Wang Hong1,Feng Wencong1,Yu Yongkun1,Zhou Cheng1,Gong Minjian1,Mai Liqiang1,Xu Xu123ORCID

Affiliation:

1. State Key Laboratory of Advanced Technology for Materials Synthesis and Processing School of Materials Science and Engineering Wuhan University of Technology Wuhan Hubei 430070 P. R. China

2. Hubei Longzhong Laboratory Wuhan University of Technology (Xiangyang Demonstration Zone) Xiangyang Hubei 441000 P. R. China

3. Hainan Institute Wuhan University of Technology Sanya 572000 P. R. China

Abstract

AbstractThe development of an artificial solid‐electrolyte interphase (SEI) has been recognized as the most efficient strategy to overcome the safety concerns associated with the lithium metal anode (LMA). Inorganic‐rich SEIs on the LMA are crucial for suppressing Li dendrites. Among the prevalent SEI inorganic compounds observed for LMA, lithium nitride (Li3N) is often found in the SEIs of high‐performance LMA. Herein, the Li3N nanowire array is successfully synthesized and the catalytic base‐growth mechanism is thoroughly investigated. The fast ionic conductor Li3N nanowires act as pillars to control the nucleation and growth of lithium metal along the vertical direction of the nanowire by bottom‐up self‐lubrication, which fundamentally prevents the dendrite growth. The Li3N is characterized by abundant lithiophilic nucleation sites, which effectively reduces the local current density, and facilitates homogeneous Li+ flux. Symmetric cells utilizing the Li3N@Li anode have demonstrated excellent stability, featuring uniform deposition without dendrite formation. Additionally, high‐capacity retentions of 98% at 0.5 C after 400 cycles and impressive high‐rate performance at 31.1 mA cm−2 have been realized in high‐loading Li3N@Li||LFP cells. The universal preparation of the Li3N nanowires with various precursors and substrates is further explored, which is expected to be applied in solid‐state batteries and hydrogen storage.

Funder

National Natural Science Foundation of China

National Key Research and Development Program of China

Natural Science Foundation of Hubei Province

Publisher

Wiley

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