4.6 Article

Self-assembled, highly-lithiophilic and well-aligned biomass engineered MXene paper enables dendrite-free lithium metal anode in carbonate-based electrolyte

期刊

JOURNAL OF ENERGY CHEMISTRY
卷 69, 期 -, 页码 221-230

出版社

ELSEVIER
DOI: 10.1016/j.jechem.2022.01.024

关键词

MXene; Polysaccharide; Free dendrite; High lithiophilicity; Lithium metal anode

资金

  1. National Natural Science Foundation of China [51972198, 62133007]
  2. Taishan Scholars Program of Shandong Province [tsqn201812002, ts20190908, ts201511004]
  3. Natural Science Foundation of Shandong Province [ZR2020JQ19]
  4. Shenzhen Fundamental Research Program [JCYJ20190807093405503]

向作者/读者索取更多资源

A dendrite-free composite Li metal anode has been achieved using a flexible, freestanding, well-aligned, and highly-lithiophilic MXene paper. The MX@CS paper with a micro-crumpled surface effectively decreases the local current density, guides even Li plating, and suppresses dendritic Li growth. The surface-adsorbed chitosan enhances lithiophilicity and reduces Li nucleation overpotential. The dendrite-free Li morphology of the MX@CS-Li anode results in significantly improved cycling life and high Coulombic efficiency.
Lithium metal anode is the ideal candidate for high-energy-density rechargeable batteries. However, uncontrolled dendrite growth hampers its commercialization. Herein, a dendrite-free composite Li metal anode is realized by a flexible, freestanding, well-aligned and highly-lithiophilic MXene paper designed by a facile electrostatic self-assembly of the exfoliated MXene nanosheets and natural polysaccharidechitosan (MX@CS). The MX@CS paper gets a well-aligned layered-3D structure with a micro-crumpled surface that can effectively decrease the local current density, guide even Li plating and suppress dendritic Li growth. More importantly, surface-adsorbed chitosan endows enhanced lithiophilicity for MXene substrate and thus reduces the Li nucleation overpotential, which is confirmed by the density functional theory calculations. Abundant lithiophilic groups on MX@CS surface provide high concentration Li+ anchoring site promoting Li nucleation and laterally inducing uniform Li deposition, which effectively avoids the formation of dendritic Li. As a result, the MX@CS-Li anode with a dendrite-free Li morphology shows a significantly improved cycling life in commercial carbonate based electrolyte. When coupled with LiNi0.8Co0.1Mn0.1O2 cathode, the full cell exhibits a low capacity decay and steady ultrahigh Coulombic efficiency of 99.6% at a current density of 5C. These findings develop a new approach for designing high-performance metal-based rechargeable batteries. (c) 2022 Science Press and Dalian Institute of Chemical Physics, Chinese Academy of Sciences. Published by ELSEVIER B.V. and Science Press. All rights reserved.

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