Samantha T Hung, Yuchun Wang, Ziman Cai, Chongzhen Wang, Zirui Shao, Juanjuan Sun, Haoran Li, Jinding Liang, Lu Bai, Erxiao Wu, Ulderico Ulissi, Xiaolin Yan, Fangyun Chen, Falin Zhu, Junhao He, Xiaonan Luo, Na Liu, Hansen Wang, Chuying Ouyang
Understanding and suppressing gas evolution is critical to enabling high-energy-density lithium metal batteries (LMBs). Yet, comprehensive investigations in ether-based systems remain limited. Here we quantify gas generation in ether-based LMBs and elucidate the underlying mechanisms. We link CO and CO2 production to the cathode, and CH4 evolution to the anode. Notably, CO and CO2 are consumed at the Li anode to form Li-containing species such as Li2CO3. Although CH4 ultimately dominates the gaseous products, its evolution during cycling is delayed until a distinct onset point. We show that in a high-concentration ether electrolyte, anode activation improves Li deposition morphology and suppresses interfacial reactions, extending the number of cycles to gas onset and cell failure by an order of magnitude. Achieving these gains without altering the electrolyte enables the reconsideration of seemingly impractical electrolytes, highlighting a practical strategy to enhance the safety and performance of commercial LMBs.