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Updated: Oct 29, 2026

Protocol of Electrochemical Test and Characterization of Aprotic Li-O2 Battery
Published on: July 12, 2016
Capture and reduction of singlet oxygen via an anthracene-based framework for stable Li-O2 batteries
Zhuoliang Jiang1,2, Zhao Zhao2, Liang Gao3
1Academy for Advanced Interdisciplinary Studies, Frontiers Science Center for New Organic Matter, State Key Laboratory of Advanced Chemical Power Sources, Key Laboratory of Advanced Energy Materials Chemistry (Ministry of Education), College of Chemistry, Nankai University, Tianjin 300071, China.
Abstract:
Given the increasing global energy demand and rapid advancement of low-carbon technologies, Li-O2 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 (1O2) 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 1O2 reduction reaction (SORR) in Li-O2 batteries. The conjugated porous framework selectively captures electrophilic 1O2, enabling effective charge transfer from AntCOF to the empty π* orbital of 1O2 and promoting SORR in subsequent discharge processes. This mechanism suppresses 1O2 diffusion and mitigates associated side reactions, leading to reduced overpotentials and improved cycling performance when coupled with a RuO2 catalyst. This work may enlighten further investigations into 1O2-related chemistry across a broad range of oxygen-redox electrochemical systems.
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