| Literature DB >> 26291218 |
Abstract
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 O2. 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.Entities:
Keywords: lithium peroxide-oxidation; lithium−oxygen (Li−O2) batteries; nucleation and growth; oxygen evolution reaction; potentiostatic intermittent titration technique (PITT)
Year: 2012 PMID: 26291218 DOI: 10.1021/jz3018368
Source DB: PubMed Journal: J Phys Chem Lett ISSN: 1948-7185 Impact factor: 6.475