纳米笼
材料科学
钴
锂(药物)
化学工程
氧化还原
多孔性
阴极
碳纤维
动力学
电化学
无机化学
纳米技术
电极
催化作用
化学
物理化学
有机化学
复合数
复合材料
物理
医学
内分泌学
冶金
量子力学
工程类
作者
Huajin He,Ying‐Chih Liao,Wenhua Zuo,Guochang Li,Jiabao Gu,Yixiao Li,Zheng Hu,Yong Yang
出处
期刊:Small
[Wiley]
日期:2021-10-10
卷期号:17 (47)
被引量:4
标识
DOI:10.1002/smll.202103778
摘要
Abstract Reducing SF 6 (as gas cathode) in Li batteries is a promising concept for the double benefit of mildly converting greenhouse SF 6 and providing a high theoretical energy density of 3922 Wh kg −1 . However, the reduction process is hampered by its sluggish kinetics. Here, cobalt phthalocyanine (CoPc) molecules immobilized on porous carbon matrix are, for the first time, introduced to the LiSF 6 chemistry to deliver an enhanced energy density. It is revealed that the high redox potential of Co(II)Pc/[Co(I)Pc] − (≈2.85 V) facilitates the formation of Co(I)N 4 sites to catalyze the SF 6 electrochemical reduction. By using highly porous holey nitrogen‐doped carbon nanocages as carbon matrix, the LiSF 6 cells deliver a high discharge voltage of 2.82 V at 50 mA g C+CoPc −1 and an unprecedented areal capacity of 25 mAh cm −2 at 0.1 mA cm −2 , much superior to previous results. This work opens up new possibilities for high‐efficiency conversion of SF 6 in lithium batteries.
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