Answers are grounded in this paper and cite their sources.
Given the increasing global energy demand and rapid advancement of low-carbon technologies, Li-O 2 batteries have attracted considerable attention owing to their exceptionally high theoretical energy density, offering great promise for advanced energy systems. However, the formation of harmful singlet oxygen ( 1 O 2 ) in both discharge and charge processes induces parasitic reactions that deteriorate round-trip efficiency and cycling stability. Herein, an anthracene-based covalent-organic framework (AntCOF) is introduced as a highly effective catalyst for the 1 O 2 reduction reaction (SORR) in Li-O 2 batteries. The conjugated porous framework selectively captures electrophilic 1 O 2 , enabling effective charge transfer from AntCOF to the empty π* orbital of 1 O 2 and promoting SORR in subsequent discharge processes. This mechanism suppresses 1 O 2 diffusion and mitigates associated side reactions, leading to reduced overpotentials and improved cycling performance when coupled with a RuO 2 catalyst. This work may enlighten further investigations into 1 O 2 -related chemistry across a broad range of oxygen-redox electrochemical systems.
No takes yet. Share an insight, caveat, or question.
Jiang et al. (2026) studied this question.
Synapse has enriched 10 related papers. Consider them for comparative context: