Ap-phenylenediamine oligomer-mediated Li–O2battery with an extremely low charge potential of 3.1 V

التفاصيل البيبلوغرافية
العنوان: Ap-phenylenediamine oligomer-mediated Li–O2battery with an extremely low charge potential of 3.1 V
المؤلفون: Xiangfeng Liu, Deqing Li, Zhonghua Wu, Zhongjun Chen, Bozhen Chen, Junkai Wang
المصدر: Journal of Materials Chemistry A. 8:22754-22762
بيانات النشر: Royal Society of Chemistry (RSC), 2020.
سنة النشر: 2020
مصطلحات موضوعية: Battery (electricity), Renewable Energy, Sustainability and the Environment, Oxygen evolution, chemistry.chemical_element, 02 engineering and technology, General Chemistry, Electrolyte, Overpotential, 010402 general chemistry, 021001 nanoscience & nanotechnology, Electrochemistry, 01 natural sciences, Redox, 0104 chemical sciences, chemistry.chemical_compound, chemistry, Chemical engineering, General Materials Science, Lithium, 0210 nano-technology, Lithium peroxide
الوصف: High overpotential is one of the disadvantages of lithium–air batteries, which can cause electrolyte decomposition to damage the electrochemical performance of the battery. Redox mediators (RMs) have been extensively investigated for reducing the overpotential of Li–O2 batteries. However, most RMs have a limited effect on overpotential reduction and can only reach about 3.5 V. Herein, we report the use of a p-phenylenediamine oligomer (pPO) as an effective dual-functional RM to significantly reduce the charge potential to 3.1 V and to enhance the discharge capacity and rate capability. During the discharge process, pPO containing a benzoquinone group, is first reduced to pPOo−, which adsorbs lithium ions and oxygen, and promotes the formation of lithium peroxide. During charging, pPO containing active N sites is preferentially oxidized to pPON+, which combines with lithium peroxide and promotes its decomposition. Similarly, we synthesized two other oligomers (mPO and oPO) that do not affect the overpotential due to differences in the molecular structure. Furthermore, pPO can also promote surface passivation of the lithium anode by forming a protective layer that allows facile cycling of the cells directly in air. The special molecular structure and functional groups determine the interaction between the RM and products. This study offers insights into designing bifunctional RMs to improve both the oxygen reduction and the oxygen evolution reaction activities in Li–O2 batteries.
تدمد: 2050-7496
2050-7488
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::2ac57bdada6fa49df70d65080d602686
https://doi.org/10.1039/d0ta09627j
حقوق: CLOSED
رقم الأكسشن: edsair.doi...........2ac57bdada6fa49df70d65080d602686
قاعدة البيانات: OpenAIRE