4.8 Article

Low-Cost Regulating Lithium Deposition Behaviors by Transition Metal Oxide Coating on Separator

期刊

ADVANCED FUNCTIONAL MATERIALS
卷 31, 期 16, 页码 -

出版社

WILEY-V C H VERLAG GMBH
DOI: 10.1002/adfm.202007255

关键词

layer‐ by‐ layer Li deposition; lithium metal batteries; self‐ healing interface; sustained release; transition metal oxide

资金

  1. National Natural Science Foundation of China [21973008, 21434003, 21875016]

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A strategy involving transition metal oxides (TMOs) particles coated porous polypropylene (PP) separator has been developed to regulate lithium deposition behaviors, improving Coulombic efficiency and inhibiting lithium dendrites formation. This approach allows for the formation of an artificial solid electrolyte interface (SEI) passivating layer, leading to a significant increase in cycling performance of lithium batteries.
The application of lithium metal anode, despite being of the highest capacity, is hindered by low Coulombic efficiency (CE) and serious lithium dendrites formation. A strategy of transition metal oxides (TMOs) particles coated porous polypropylene (PP) separator is developed to regulate lithium deposition behaviors through in situ forming artificial solid electrolyte interface (SEI) passivating layers. By virtue of quite low solubilities of TMOs in the electrolyte, the concentration of TMOs in the electrolyte can be maintained at a constant and the dissolved TMOs can be reduced to produce Li2O and Mn particles, which not only function as lithium nucleating seeds but are also involved in the formation of the SEI layer. The sustainably existed trace of TMOs ensures the artificial SEI layer can be re-healed once damaged by the volume expansion of lithium. With the help of one typical TMO of MnO coating on PP, an interesting dendrite-free dual layer Li deposition is observed, which significantly improves the CE of Li||Cu cells and cycling life of Li||Li cells. Using MnO coated PP, ultra-thin lithium films are deposited on copper foils with an in situ constructed SEI passivating layer, which exhibits a much improved cycling performance in liquid ether electrolyte and even better performance in gel polymer electrolyte.

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