“…One routine way is to promote in situ formation of a stable SEI layer by optimizing the electrolytes, including sacrificial additives, highly concentrated electrolytes, and fluorinated electrolytes . Nevertheless, the so-formed SEI continuously grows by constantly consuming the electrolyte solvents, salt anions, or sacrificial additives in the electrolyte, making it difficult to modulate the composition and structure of the SEI. − Accordingly, the improvement in cycling stability by using a large excess of electrolyte inevitably compromises the energy density of batteries. Another approach is to replace the electrolyte-derived SEI by ex-situ formed artificial SEI layers such as inorganic materials (for example, Li 3 PO 4 , LiF, Li 2 S), organic polymers (for example, polyrotaxane- co -poly(acrylic acid) (PR–PAA), P(St-MaI), polydimethylsiloxane, and copolymer of poly(ethylene glycol) methyl ether methacrylate and 2-[3-(6-methyl-4-oxo-1,4-dihydropyrimidin-2-yl)ureido]ethyl methacrylate), and organic–inorganic composites. − However, ionic insulation or poor ionic conductivity would definitely retard the Li + transfer across the interface, resulting in increased polarization and dendrite growth .…”