4.8 Article

In Situ Visualizing the Interfacial Failure Mechanism and Modification Promotion of LAGP Solid Electrolyte toward Li Metal Anode

期刊

ADVANCED ENERGY MATERIALS
卷 12, 期 41, 页码 -

出版社

WILEY-V C H VERLAG GMBH
DOI: 10.1002/aenm.202202250

关键词

failure mechanism; in situ observations; interface modifications; NASICON; solid-state batteries; solid-state electrolytes

资金

  1. National Key Research and Development Program of China [2021YFB3800300]
  2. National Natural Science Foundation of China [52072138]
  3. Australian Research Council (ARC) [DP180102297]

向作者/读者索取更多资源

Understanding the failure process of solid-state electrolyte (SSE) and providing potential solutions are crucial for the development of solid-state batteries (SSBs). In this study, the dynamic failure process of SSE is observed using in-situ electrochemical SEM, revealing the main origins of continuously generated side-reaction layer and stress-induced cracks. By introducing C3N4 as a modification layer, the interfacial side-reaction is restrained and Li+ flux becomes well-distributed, preventing stress-induced mechanical failure in SSE.
In-depth understanding the failure process of solid-state electrolyte (SSE) and providing potential solutions are crucial for the development of solid-state batteries (SSBs). Typical techniques are powerful to investigate the chemical/electrochemical degradation of SSE. While, mechanical failure, which would undoubtedly affect battery performance, is difficult to detect by normal techniques and lack effective characterizations. Herein, via in situ electrochemical SEM, the dynamic failure process of SSE is observed, revealing the continuously generated side-reaction layer and the stress-induced cracks are the main origins. C3N4 (CN) is introduced as the modification layer for Li and SSE. Via in situ scanning electron microscope, Li growth is regulated by CN from dendrite-like to particulate-like growth. The properties of electronic transportation and ionic migration in CN are quantitatively measured, and CN promotion mechanism is revealed. Thanks to CN layer, the interfacial side-reaction is restrained, simultaneously, Li+ flux becomes well-distributed for dense Li deposition, preventing stress-induced mechanical failure in SSE. Li symmetrical batteries with CN can endure the maximum current density up to 2.0 mA cm(-2) and stably cycle for 3000 h at 300 mu A cm(-2). This work suggests a promising method to circumvent SSE degradation against Li and open opportunities for future SSBs.

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