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A Self-Healing Amalgam Interface in Metal Batteries
Authors:Ye Fan  Tao Tao  Yuxuan Gao  Chao Deng  Baozhi Yu  Ying
Affiliation:1. School of Materials and Energy, Guangdong University of Technology, Guangzhou, 510006 P. R. China;2. Institute for Frontier Materials, Deakin University, 75 Pigdons Road, Waurn Ponds, Victoria, 3216 Australia
Abstract:Poor cyclability and safety concerns caused by the uncontrollable dendrite growth and large interfacial resistance severely restrict the practical applications of metal batteries. Herein, a facile, universal strategy to fabricate ceramic and glass phase compatible, and self-healing metal anodes is proposed. Various amalgam-metal anodes (Li, Na, Zn, Al, and Mg) show a long cycle life in symmetric cells. It has been found that liquid Li amalgam shows a complete wetting with the surface of lanthanum lithium titanate electrolyte and a glass-phase solid-state electrolyte. The interfacial compatibility between the lithium metal anode and solid-state electrolyte is dramatically improved by using an in situ regenerated amalgam interface with high electron/ion dual-conductivity, obviously decreasing the anode/electrolyte interfacial impedance. The lithium-amalgam interface between the metal anode and electrolyte undergoes a reversible isothermal phase transition between solid and liquid during the cycling process at room temperature, resulting in a self-healing surface of metal anodes.
Keywords:amalgam  metal batteries  solid-state electrolytes
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