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Direct observation of lithium metal dendrites with ceramic solid electrolyte
Maryam Golozar1,2, Andrea Paolella3, Hendrix Demers1
1Center of Excellence in Transportation Electrification and Energy Storage, Hydro-Québec, Varennes, QC, J0L 1N0, Canada.
Scientific Reports
|October 28, 2020
Summary
Lithium dendrite growth in batteries is suppressed by solid electrolytes like LLZO. In situ SEM revealed inhomogeneous lithium deposition and side reactions at the LLZO interface, hindering dendrite suppression.
Area of Science:
- Materials Science
- Electrochemistry
- Battery Technology
Background:
- Lithium metal anodes are prone to dendrite formation, risking battery short circuits.
- Solid electrolytes with high shear modulus are investigated to suppress dendrite growth.
- Lithium lanthanum zirconium oxide (LLZO) is a promising solid electrolyte due to its mechanical strength and stability.
Purpose of the Study:
- To investigate the interface behavior between lithium metal and LLZO during battery cycling under pressure.
- To understand the mechanisms of dendrite formation and LLZO degradation.
- To evaluate LLZO as an ionic conductive separator for lithium metal batteries.
Main Methods:
- In situ scanning electron microscopy (SEM) to observe real-time interface evolution.
- Cyclic testing of symmetrical Li-Li cells with LLZO.
- Energy dispersive spectroscopy (EDS) for elemental analysis of dendrites and LLZO cross-sections.
Main Results:
- SEM videos showed inhomogeneous lithium dissolution and deposition, leading to dendrite growth.
- EDS analysis confirmed Li, C, and O in dendrites.
- LLZO cross-sections revealed inhomogeneous distribution of La, Zr, and C after cycling, indicating lithium loss and side reactions.
Conclusions:
- LLZO's mechanical properties are advantageous, but electrochemical stabilization at the lithium metal interface requires improvement.
- Inhomogeneous lithium behavior and side reactions at the interface are key challenges for LLZO in lithium metal batteries.
- Further research is needed to enhance the electrochemical stability of the garnet-lithium metal interface.

