Concurrent electrode–electrolyte interfaces engineering via nano-Si3N4 additive for high-rate, high-voltage lithium metal batteries
Energy Environ. Sci., 2025, Advance ArticleDOI: 10.1039/D4EE03862B, Paper Open Access   This article is licensed under a Creative Commons Attribution 3.0 Unported Licence.Jinuk Kim, Dong Gyu Lee, Ju Hyun Lee, Saehun Kim, Cheol-Young Park, Jiyoon Lee, Hyeokjin Kwon, Hannah Cho, Jungyoon Lee, Donghyeok Son, Hee-Tak Kim, Nam-Soon Choi, Tae Kyung Lee, Jinwoo LeeThe nano-Si3N4 additive enables the concurrent engineering of electrode–electrolyte interfaces. It promotes the formation of a bilayer, inorganic-rich SEI via its involvement in SEI formation and Li+ solvation, and a uniform CEI by scavenging HF.To cite this article before page numbers are assigned, use the DOI form of citation above.The content of this RSS Feed (c) The Royal Society of Chemistry
Energy Environ. Sci., 2025, Advance Article
DOI: 10.1039/D4EE03862B, Paper
DOI: 10.1039/D4EE03862B, Paper
Open Access
This article is licensed under a Creative Commons Attribution 3.0 Unported Licence.Jinuk Kim, Dong Gyu Lee, Ju Hyun Lee, Saehun Kim, Cheol-Young Park, Jiyoon Lee, Hyeokjin Kwon, Hannah Cho, Jungyoon Lee, Donghyeok Son, Hee-Tak Kim, Nam-Soon Choi, Tae Kyung Lee, Jinwoo Lee
The nano-Si3N4 additive enables the concurrent engineering of electrode–electrolyte interfaces. It promotes the formation of a bilayer, inorganic-rich SEI via its involvement in SEI formation and Li+ solvation, and a uniform CEI by scavenging HF.
To cite this article before page numbers are assigned, use the DOI form of citation above.
The content of this RSS Feed (c) The Royal Society of Chemistry
The nano-Si3N4 additive enables the concurrent engineering of electrode–electrolyte interfaces. It promotes the formation of a bilayer, inorganic-rich SEI via its involvement in SEI formation and Li+ solvation, and a uniform CEI by scavenging HF.
To cite this article before page numbers are assigned, use the DOI form of citation above.
The content of this RSS Feed (c) The Royal Society of Chemistry
