Spontaneous colloidal metal network formation driven by molten salt electrolysis.

The molten salt-based direct reduction process for reactive solid metal outperforms traditional pyrometallurgical methods in energy efficiency. However, the simplity and rapidity of this process require a deeper understanding of the interfacial morphology in the vicinity of liquid metal deposited at the cathode. For the first time, here we report the time change of electrode surface on the sub-millisecond/micrometre scale in molten LiCl-CaCl at 823 K.