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用于稳定锂金属负极的介孔碳主体材料。

Mesoporous carbon host material for stable lithium metal anode.

作者信息

Jeong Jooyoung, Chun Jinyoung, Lim Won-Gwang, Kim Won Bae, Jo Changshin, Lee Jinwoo

机构信息

Department of Chemical and Biomolecular Engineering, Korea Advanced Institute of Science and Technology (KAIST), 291 Daehak-ro, Yuseong-gu, Daejeon 34141, Republic of Korea.

Korea Institute of Ceramic Engineering and Technology (KICET), 101 Soho-ro, Jinju 52851, Republic of Korea.

出版信息

Nanoscale. 2020 Jun 11;12(22):11818-11824. doi: 10.1039/d0nr02258f.

DOI:10.1039/d0nr02258f
PMID:32458877
Abstract

Lithium (Li) metal is a promising anode material for next-generation batteries because of its low standard reduction potential (-3.04 V vs. SHE) and high specific capacity (3860 mA h g-1). However, it is still challenging to directly use Li metal as anode material in commercial batteries because of unstable Li dendrite formation and accumulated solid-electrolyte interphase. Possible methods that can suppress the unwanted formation of Li dendrites are (i) by increasing the electrode surface area and (ii) formation of porosity for confining Li. Here, we tested microporous (<2 nm) carbon and mesoporous (2-50 nm) carbon as host materials for the Li metal anode to avoid their degradation during cycling of lithium metal batteries (LMBs). Mesoporous carbon was more effective than microporous carbon as a host material to confine the Li metal and the lifetime of mesoporous carbon was more than twice as long as those of the Cu foil and microporous carbon. After confirmed better anode performance of mesoporous carbon host material, we applied Li-plated mesoporous carbon as an anode in a lithium-sulfur battery (Li-S) full cell. This research work suggests that mesopores, in spite of their low specific surface area, are better than micropores in stabilizing the Li metal and that a mesoporous host material can be applied to Li metal anodes for use in next-generation battery applications.

摘要

锂(Li)金属因其低标准还原电位(相对于标准氢电极,为-3.04 V)和高比容量(3860 mA h g-1),是下一代电池极具前景的负极材料。然而,由于不稳定的锂枝晶形成和累积的固体电解质界面,在商业电池中直接使用锂金属作为负极材料仍然具有挑战性。能够抑制锂枝晶不必要形成的可能方法有:(i)增加电极表面积;(ii)形成用于限制锂的孔隙率。在此,我们测试了微孔(<2 nm)碳和介孔(2 - 50 nm)碳作为锂金属负极的主体材料,以避免它们在锂金属电池(LMBs)循环过程中发生降解。作为主体材料,介孔碳比微孔碳更有效地限制锂金属,且介孔碳的寿命比铜箔和微孔碳的寿命长两倍多。在确认介孔碳主体材料具有更好的负极性能后,我们将镀锂介孔碳用作锂硫电池(Li-S)全电池的负极。这项研究工作表明,尽管介孔的比表面积较低,但在稳定锂金属方面比微孔更好,并且介孔主体材料可应用于下一代电池应用的锂金属负极。

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