TY - JOUR
T1 - A Bifunctional Imidazolyl Iodide Mediator of Electrolyte Boosts Cathode Kinetics and Anode Stability Towards Low Overpotential and Long-Life Li-O2 Batteries
AU - Liu, Jing
AU - Li, Yuejiao
AU - Ding, Yajun
AU - Wu, Lisha
AU - Qin, Jieqiong
AU - Chen, Tongle
AU - Meng, Caixia
AU - Zhou, Feng
AU - Ma, Xiangkun
AU - Wu, Zhong Shuai
N1 - Publisher Copyright:
© 2024 Wiley-VCH GmbH.
PY - 2025/3/3
Y1 - 2025/3/3
N2 - The addition of a redox mediator as soluble catalyst into electrolyte can effectively overcome the bottlenecks of poor energy efficiency and limited cyclability for Li-O2 batteries caused by passivation of insulating discharge products and unfavorable byproducts. Herein we report a novel soluble catalyst of bifunctional imidazolyl iodide salt additive, 1,3-dimethylimidazolium iodide (DMII), to successfully construct highly efficient and durable Li-O2 batteries. The anion I− can effectively promote the charge transport of Li2O2 and accelerate the redox kinetics of oxygen reduction/oxygen evolution reactions on the cathode side, thereby significantly decreasing the charge/discharge overpotential. Simultaneously, the cation DMI+ forms an ultrathin stably solid-electrolyte interphase film on Li metal, greatly inhibiting the shuttle effect of I− and improving the stability of anode. Using this DMII additive, our Li-O2 batteries achieve an extremely low voltage of 0.52 V and ultra-long cycling stability over 960 h. Notably, up to 95.8 % of the Li2O2 yield further proves the reversible generation/decomposition of Li2O2 without the occurrence of side reactions. Both experimental and theoretical results disclose that DMII enables Li+ easily solvated, testifying the dominance of the solution-induced reaction mechanism. This work provides the possibility to design the soluble catalysts towards high-performance Li-O2 batteries.
AB - The addition of a redox mediator as soluble catalyst into electrolyte can effectively overcome the bottlenecks of poor energy efficiency and limited cyclability for Li-O2 batteries caused by passivation of insulating discharge products and unfavorable byproducts. Herein we report a novel soluble catalyst of bifunctional imidazolyl iodide salt additive, 1,3-dimethylimidazolium iodide (DMII), to successfully construct highly efficient and durable Li-O2 batteries. The anion I− can effectively promote the charge transport of Li2O2 and accelerate the redox kinetics of oxygen reduction/oxygen evolution reactions on the cathode side, thereby significantly decreasing the charge/discharge overpotential. Simultaneously, the cation DMI+ forms an ultrathin stably solid-electrolyte interphase film on Li metal, greatly inhibiting the shuttle effect of I− and improving the stability of anode. Using this DMII additive, our Li-O2 batteries achieve an extremely low voltage of 0.52 V and ultra-long cycling stability over 960 h. Notably, up to 95.8 % of the Li2O2 yield further proves the reversible generation/decomposition of Li2O2 without the occurrence of side reactions. Both experimental and theoretical results disclose that DMII enables Li+ easily solvated, testifying the dominance of the solution-induced reaction mechanism. This work provides the possibility to design the soluble catalysts towards high-performance Li-O2 batteries.
KW - 1,3-dimethylimidazole iodide
KW - long-life Li-O batteries
KW - low overpotential
KW - redox mediators
KW - solution mechanism
UR - http://www.scopus.com/inward/record.url?scp=85214803773&partnerID=8YFLogxK
U2 - 10.1002/anie.202421107
DO - 10.1002/anie.202421107
M3 - Article
AN - SCOPUS:85214803773
SN - 1433-7851
VL - 64
JO - Angewandte Chemie - International Edition
JF - Angewandte Chemie - International Edition
IS - 10
M1 - e202421107
ER -