Enhancing redox stability of lithium-oxygen batteries via introducing an oxygen pre-coordinated vanadyl phthalocyanine catalyst

被引:0
|
作者
Kim, Boran [1 ]
Kweon, Hyunji [2 ,3 ,4 ]
Lim, Yeji [1 ]
Park, Hyunyoung [2 ,3 ,4 ]
Kim, Jongsoon [2 ,3 ,4 ]
Ryu, Won-Hee [1 ]
机构
[1] Sookmyung Womens Univ, Dept Chem & Biol Engn, 100 Cheongpa Ro 47 Gil, Seoul 04310, South Korea
[2] Sungkyunkwan Univ, Dept Energy Sci, 2066 Seobu Ro, Suwon 16419, South Korea
[3] Sungkyunkwan Univ, SKKU Inst Energy Sci & Technol SIEST, 2066 Seobu Ro, Suwon 16419, South Korea
[4] Sungkyunkwan Univ, KIST SKKU Carbon Neutral Res Ctr, Suwon 16419, South Korea
基金
新加坡国家研究基金会;
关键词
LI-O-2; MEDIATORS; SPECTRA;
D O I
10.1039/d4ta07071b
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Since various metal phthalocyanines (MPcs) possesses the properties of transferring electrons and spontaneously binding with oxygen species, their application as catalysts in Li-O2 batteries (LOBs) can stabilize the highly active superoxide radical (O2-) to suppress side reactions, leading to enhanced electrochemical performance. MPcs have usually considered common binding behavior directly with empty metal center. However, no attempt has been made to employ MPcs with pre-coordination of the oxygen group on the metal center, which can result in unexpected catalytic behavior. In this work, we demonstrate that a novel oxygen-pre-coordinated MPc catalyst, vanadyl phthalocyanine (VOPc), can facilitate the formation and decomposition of Li-containing discharge products, such as LixO2, during charging/discharging in LOBs. This results in enhanced electrochemical performance, including decreased polarization and stable cycling-performance. Moreover, redox mediation and reaction pathways in the oxygen-pre-coordinated VOPc-applied LOB are confirmed through combined studies using first-principles calculations and various experiments, clearly supporting that the effective catalytic effect of oxygen-pre-coordinated VOPc affords the outstanding electrochemical properties of the LOB.
引用
收藏
页码:8466 / 8473
页数:8
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