β-FeOOH decorated highly porous carbon aerogels composite as a cathode material for rechargeable Li-O2 batteries

被引:16
|
作者
Chen, Wei [1 ]
Lai, Yanqing [1 ]
Zhang, Zhian [1 ]
Gan, Yongqing [1 ]
Jiang, Shaofeng [1 ]
Li, Jie [1 ]
机构
[1] Cent South Univ, Sch Met & Environm, Changsha 410083, Hunan, Peoples R China
关键词
LITHIUM-AIR BATTERIES; EFFICIENT BIFUNCTIONAL CATALYST; ELECTROCHEMICAL PROPERTIES; HIGH-CAPACITY; ALPHA-MNO2; NANORODS; O-2; ELECTRODE; IN-SITU; PERFORMANCE; ELECTROCATALYST; NANOPARTICLES;
D O I
10.1039/c4ta06879c
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
A composite of beta-FeOOH-carbon aerogels (FCAs) was designed and prepared via a simple hydrothermal method. The samples were characterized by X-ray diffraction, field emission scanning electron microscopy and N-2 adsorption/desorption measurements. It is found that the composite possesses a large pore volume and, especially, has a high proportion of mesopores. The material was studied as an O-2 electrode for non-aqueous lithium-O-2 batteries and the electrochemical performance of the electrode was evaluated by using galvanostatic discharge-charge processes and cyclic voltammetry (CV). The FCAs electrode exhibits excellent performance and delivers a discharge capacity of up to similar to 10 230 mA h g(carbon+catalyst)(-1) at 0.1 mA cm(-2) and a high C-rate performance with a discharge capacity of similar to 6110 mA h g(carbon+catalyst)(-1) at 0.2 mA cm(-2) and similar to 4270 mA h g(carbon+catalyst)(-1) at 0.5 mA cm(-2), it also exhibits a stable discharge voltage plateau at 2.75 V and a charge voltage plateau of similar to 3.75 V, and shows a good cycle performance. The excellent electrochemical performance of the FCAs is attributed to the synergistic effect of the good catalytic activity of beta-FeOOH and the high porosity of the carbon aerogels. These results demonstrate that the carbon aerogels are suitable for the skeleton material to load the catalyst and the FCAs can be an outstanding material for the cathode of Li-O-2 batteries.
引用
收藏
页码:6447 / 6454
页数:8
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