In Situ Derived Mixed Ion/Electron Conducting Layer on Top of a Functional Separator for High‐Performance, Dendrite‐Free Rechargeable Lithium‐Metal Batteries

Author:

Yan Min1,Wang Chen‐Yang1,Fan Min2,Zhang Yuying23,Xin Sen23ORCID,Yue Junpei2,Zeng Xian‐Xiang2,Liang Jia‐Yan2,Song Yue‐Xian2,Yin Ya‐Xia23,Wen Rui23,Liu Zhitian1,Wan Li‐Jun23,Guo Yu‐Guo23ORCID

Affiliation:

1. Hubei Key Laboratory of Plasma Chemistry and Advanced Materials Hubei Engineering Technology Research Center of Optoelectronic and New Energy Materials School of Materials Science and Engineering Wuhan Institute of Technology Wuhan 430205 P. R. China

2. CAS Key Laboratory of Molecular Nanostructure and Nanotechnology CAS Research/Education Center for Excellence in Molecular Sciences Beijing National Laboratory for Molecular Sciences (BNLMS) Institute of Chemistry Chinese Academy of Sciences (CAS) Beijing 100190 P. R. China

3. University of Chinese Academy of Sciences Beijing 100049 P. R. China

Abstract

AbstractRechargeable lithium‐metal batteries (RLBs), which employ the Li‐metal anode to acquire notably boosted specific energy at cell level, represent the “Holy Grail” for “beyond Li‐ion” electrochemical energy storage technology. Currently, the practical use of RLBs is impeded by poor cycling and safety performance, which are derived from high chemical reactivity of metallic Li and uncontrollable formation and propagation of metal dendrites during repeated Li plating/stripping. In this study, a new strategy is demonstrated to stabilize the anode electrochemistry of RLBs by applying a Mg3N2‐decorated functional separator onto the Li‐metal surface. An in situ conversion‐alloying reaction occurring at Li‐separator interface assists formation of a mixed ion/electron conducting layer that consists mainly of Li3N and Li‐Mg solid‐solution. The inorganic interlayer effectively suppresses parasitic reactions at Li‐electrolyte interface while simultaneously homogenizes Li+/e flux across the interface and therefore, contributes to dendrite‐free operation of Li‐metal anode. A Li||LiNi0.6Co0.2Mn0.2O2 battery based on the functional separator delivers a reversible capacity of 129 mAh g‐1 after 600 cycles at 0.5 C, which corresponds to a capacity retention of 75.9%. The preparation of functional separator is scalable and adaptive to battery manufacture, which brings new opportunities to realize high‐energy RLBs with long cycle life and improved safety.

Funder

National Natural Science Foundation of China

Natural Science Foundation of Hubei Province

Wuhan University of Technology

Natural Science Foundation of Beijing Municipality

Publisher

Wiley

Subject

Electrochemistry,Condensed Matter Physics,Biomaterials,Electronic, Optical and Magnetic Materials

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