High-energy lithium metal pouch cells with limited anode swelling and long stable cycles

Lithium metal anodes have attracted much attention as candidates for high-energy batteries, but there have been few reports of long cycling behaviour, and the degradation mechanism of realistic high-energy Li metal cells remains unclear. Here, we develop a prototypical 300 Wh kg −1 (1.0 Ah) pouch ce...

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Veröffentlicht in:Nature Energy 2019-07, Vol.4 (7), p.551-559
Hauptverfasser: Niu, Chaojiang, Lee, Hongkyung, Chen, Shuru, Li, Qiuyan, Du, Jason, Xu, Wu, Zhang, Ji-Guang, Whittingham, M. Stanley, Xiao, Jie, Liu, Jun
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Sprache:eng
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Zusammenfassung:Lithium metal anodes have attracted much attention as candidates for high-energy batteries, but there have been few reports of long cycling behaviour, and the degradation mechanism of realistic high-energy Li metal cells remains unclear. Here, we develop a prototypical 300 Wh kg −1 (1.0 Ah) pouch cell by integrating a Li metal anode, a LiNi 0.6 Mn 0.2 Co 0.2 O 2 cathode and a compatible electrolyte. Under small uniform external pressure, the cell undergoes 200 cycles with 86% capacity retention and 83% energy retention. In the initial 50 cycles, flat Li foil converts into large Li particles that are entangled in the solid-electrolyte interphase, which leads to rapid volume expansion of the anode (cell thickening of 48%). As cycling continues, the external pressure helps the Li anode maintain good contact between the Li particles, which ensures a conducting percolation pathway for both ions and electrons, and thus the electrochemical reactions continue to occur. Accordingly, the solid Li particles evolve into a porous structure, which manifests in substantially reduced cell swelling by 19% in the subsequent 150 cycles. Much has been said about the high-energy, long-lasting potential of Li metal batteries, and yet little has been demonstrated at the cell scale. Here, Jun Liu and colleagues demonstrate a Li metal pouch cell with a 300 Wh kg −1 energy density and a 200-cycle lifetime.
ISSN:2058-7546
2058-7546
DOI:10.1038/s41560-019-0390-6