Probing the Reaction Kinetics of the Charge Reactions of Nonaqueous Li-O2 Batteries

被引:319
作者
Lu, Yi-Chun [1 ,2 ,3 ]
Shao-Horn, Yang [1 ,2 ,3 ]
机构
[1] MIT, Dept Mech Engn, Cambridge, MA 02139 USA
[2] MIT, Dept Mat Sci & Engn, Cambridge, MA 02139 USA
[3] MIT, Electrochem Energy Lab, Cambridge, MA 02139 USA
来源
JOURNAL OF PHYSICAL CHEMISTRY LETTERS | 2013年 / 4卷 / 01期
关键词
SILVER THIOSULFATE COMPLEXES; INITIAL-STAGES; ELECTROCRYSTALLIZATION; CATALYSTS; ELECTRODES; DISCHARGE;
D O I
10.1021/jz3018368
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
Understanding the reaction mechanism of nonaqueous oxygen reduction reaction (ORR) and oxygen evolution reaction (OER) is key to increase the low round-trip efficiency and power capability of rechargeable Li-air batteries. Here we show that the ORR kinetics are much faster than OER kinetics and OER occurs in two distinct stages upon Li-air battery charging. The first OER stage occurs at low overpotentials (<400 mV) with a slopping voltage profile, whose kinetics are relatively insensitive to charge rates and catalysts. This OER stage could be attributed to the delithiation of the outer part of Li2O2 forming lithium-deficient Li2-xO2,which is chemically disproportionate to evolve O-2. The second stage takes place at high overpotentials (400-1200 mV), whose kinetics are sensitive to discharge/charge rates and catalysts, which can be attributed to the oxidation of bulk Li2O2 particles. Our study provides insights into bridging current two schools of thought on the OER mechanism.
引用
收藏
页码:93 / 99
页数:7
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