电解质
阳极
锂(药物)
氧化还原
阴极
化学
无机化学
化学工程
离子液体
极化(电化学)
材料科学
电池(电)
电极
物理化学
热力学
有机化学
医学
功率(物理)
物理
工程类
内分泌学
催化作用
作者
Alireza Ahmadiparidari,Shadi Fuladi,L. Majidi,Samuel Plunkett,Erik Sarnello,Hamed Gholivand,Zahra Hemmat,Sina Rastegar,Saurabh N. Misal,Nallely Jimenez,Paul C. Redfern,Jianguo Wen,Tao Li,Anh T. Ngo,Fatemeh Khalili‐Araghi,Larry A. Curtiss,Amin Salehi‐Khojin
标识
DOI:10.1016/j.jpowsour.2021.229506
摘要
Li–O2 batteries have recently emerged to meet nowadays elevated electric energy demands. Redox mediators (RMs) for solution-inducing decomposition of discharge products are one approach to increase energy efficiency and reduce high overpotentials in these batteries. However, multiple obstacles hinder their usage such as redox shuttling, capacity fading, electrolyte degradation, etc. Herein, we present a new chemistry based on a combination of LiNO3, TEGDME and an ionic liquid that enables LiI (1 M) to lower the charge potential (3.5V) with a long cycle life of 270 cycles. 0.1 M LiI increases the cyclability up to 500 with a slightly increased charge potential (~4V) for a fixed capacity of 1000 mAh/g. Up to 100 cycles, this battery system retained ~95% Li2O2 capacity with a ~0.8 V charge-discharge polarization gap. The addition of LiNO3 to the electrolyte provides a protective solid electrolyte interface (SEI) on anode that works in synergy with the LiI RM. Moreover, we found that this electrolyte blend results in domain formation of ionic and neutral species enhancing the discharge and charge processes. Finally, DFT calculations provide a better understanding of the role of the anode SEI layer and the Li2O2 decomposition promoted by the LiI during charge on the cathode.
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