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A Chemically Engineered Porous Copper Matrix with Cylindrical Core–Shell Skeleton as a Stable Host for Metallic Sodium Anodes
Author(s) -
Wang Chuanlong,
Wang Huan,
Matios Edward,
Hu Xiaofei,
Li Weiyang
Publication year - 2018
Publication title -
advanced functional materials
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 6.069
H-Index - 322
eISSN - 1616-3028
pISSN - 1616-301X
DOI - 10.1002/adfm.201802282
Subject(s) - materials science , anode , electrolyte , copper , electrochemistry , metal , chemical engineering , porosity , matrix (chemical analysis) , composite number , stripping (fiber) , dendrite (mathematics) , composite material , electrode , metallurgy , geometry , mathematics , chemistry , engineering
Abstract Sodium (Na) metal is the most promising alternative for lithium metal as anode for the next‐generation energy storage systems. However, its practical implementation is hindered by the huge volume change and severe Na metal dendrite growth during electrochemical stripping/plating. Herein, the use of a chemically engineered porous copper (Cu) matrix as a stable host for metallic Na anode is presented. By treating the commercial Cu foam through a facile and cost‐effective method, a composite matrix consists of cylindrical core–shell skeleton is achieved, facilitating uniform impregnation and confinement of Na within the matrix pores promoted by the chemical interaction between Na and the matrix. The unique matrix's surface characteristic can divert the Na deposition from the skeleton towards the Na reservoirs within the pores, suppressing the volume change and mossy/dendritic Na growth. A stable Na cycling behavior is demonstrated in carbonate electrolyte without any additives at a high capacity up to 3 mAh cm −2 with a current density up to 2 mA cm −2 . Moreover, electrochemical measurements of a full cell made of the Na composite matrix anode clearly reveal the superior performance at high rate (5C) over that using bare Na metal.