Electrocatalytic Activity Studies of Select Metal Surfaces and Implications in Li-Air Batteries
Name
Shao-Horn_Electrocatalytic activity.pdf
Size
972.26 KB
Format
Adobe PDF
Checksum (MD5)
52ef29b4dd0c061f5f4fb857d0916ad7
Author(s) • • • •
Gasteiger, Hubert A.
Crumlin, Ethan J.
McGuire, Robert
Shao-Horn, Yang
Lu, Yi-chun
Date Issued
July 2010
Journal
Journal of The Electrochemical Society
Publisher
The Electrochemical Society
Citation
Lu, Yi-Chun, Hubert A. Gasteiger, Ethan Crumlin, Robert McGuire, and Yang Shao-Horn. Electrocatalytic Activity Studies of Select Metal Surfaces and Implications in Li-Air Batteries. Journal of The Electrochemical Society 157, no. 9 (2010): A1016. © 2010 ECS - The Electrochemical Society
Version
Final published version
Abstract
Rechargeable lithium-air batteries have the potential to provide ≈3 times higher specific energy of fully packaged batteries than conventional lithium rechargeable batteries. However, very little is known about the oxygen reduction reaction (ORR) and oxygen evolution in the presence of lithium ions in aprotic electrolytes, which hinders the improvement of low round-trip efficiencies of current lithium-air batteries. We report the intrinsic ORR activity on glassy carbon (GC) as well as polycrystalline Au and Pt electrodes, where Au is the most active with an activity trend of Au > GC > Pt . Rotating disk electrode (RDE) measurements were used to obtain the kinetic current of the ORR and the reaction order with respect to oxygen partial pressure in 1 M LiClO[subscript 4] propylene carbonate:1,2-dimethoxyethane (1:2 v/v). In addition, air electrodes with Vulcan carbon or Au or Pt nanoparticles supported on Vulcan were examined in Li–O[subscript 2] single cells, where the observed discharge cell voltages follow the catalytic trend established by RDE measurements. The ORR mechanism and the rate-determining steps were discussed and contrasted with the ORR activity trend in acid and alkaline solutions.
MIT Department
Massachusetts Institute of Technology. Department of Chemistry
Massachusetts Institute of Technology. Department of Materials Science and Engineering
Massachusetts Institute of Technology. Department of Mechanical Engineering
Massachusetts Institute of Technology. Electrochemical Energy Laboratory
Terms of Use
Article is made available in accordance with the publisher's policy and may be subject to US copyright law. Please refer to the publisher's site for terms of use.
Persistent DSpace Link
DOI of Published Version
https://doi.org/10.1149/1.3462981