过电位
双功能
法拉第效率
电池(电)
析氧
催化作用
阴极
材料科学
化学工程
聚合物
化学
电极
复合材料
有机化学
电化学
物理化学
量子力学
功率(物理)
物理
工程类
作者
Rajashekar Badam,Mayu Shibuya,Bharat Srimitra Mantripragada,Masaya Ohira,Lihang Zhou,Noriyoshi Matsumi
出处
期刊:Polymer Journal
[Springer Nature]
日期:2022-09-02
卷期号:54 (11): 1355-1366
被引量:8
标识
DOI:10.1038/s41428-022-00699-9
摘要
Among several strategies employed to reduce overpotential and achieve reliable reversibility with Li–O2 batteries, the use of atomically dispersed bifunctional carbon catalysts is very attractive. However, most of the methods used to prepare these bifunctional oxygen reduction reaction (ORR) and oxygen evolution reaction (OER) catalysts require high temperatures and exhibit low yields, and it is therefore difficult to predetermine the active sites qualitatively and quantitatively. Here, we propose the use of atomically dispersed metal centers coordinated to diimine moieties of conjugated polymers as bifunctional catalysts without further modification (pyrolysis or composite formation) for Li–O2 battery applications. Poly(bisiminoacenaphthenequinone) (BIAN) iron complex (BP-Fe) catalysts showed high OER activities, which enabled 100% coulombic efficiency for 160 galvanostatic charge discharge cycles with a capacity limit of 500 mAh/g at a current density of 250 mA/g. The overpotential corresponding to charging was as low as ~1.0 V and exhibited almost no change in discharge overpotential across 160 cycles. Additionally, it showed a commendable rate capability with only a 170 mV increase in charge overpotential when the charge‒discharge rate was increased from 100 to 500 mA/g. Conducting polymer support with atomically dispersed metal centers for oxygen reduction and evolution reaction catalysis is a promising strategy to enhance the cyclability of Li–O2 battery. We present a novel, reliable and highly efficient noble metal free polymer catalyst for Li air battery application. Novel cathode catalyst found to be very efficient for nearly 160 cycles with limiting the capacity to 500 mAh/g with relatively lower overpotential.
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