Communication: The influence of CO2 poisoning on overvoltages and discharge capacity in non-aqueous Li-Air batteries
Author(s) -
Yedilfana Setarge Mekonnen,
Kristian B. Knudsen,
Jón Steinar Garðarsson Mýrdal,
Reza Younesi,
Jonathan Højberg,
Johan Hjelm,
Poul Norby,
Tejs Vegge
Publication year - 2014
Publication title -
the journal of chemical physics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.071
H-Index - 357
eISSN - 1089-7690
pISSN - 0021-9606
DOI - 10.1063/1.4869212
Subject(s) - nucleation , adsorption , aqueous solution , cathode , density functional theory , chemical physics , overvoltage , materials science , chemistry , chemical engineering , computational chemistry , thermodynamics , physics , power (physics) , organic chemistry , engineering
The effects of Li2CO3 like species originating from reactions between CO2 and Li2O2 at the cathode of non-aqueous Li-air batteries were studied by density functional theory (DFT) and galvanostatic charge-discharge measurements. Adsorption energies of CO2 at various nucleation sites on a stepped (11̅00) Li2O2 surface were determined and even a low concentration of CO2 effectively blocks the step nucleation site and alters the Li2O2 shape due to Li2CO3 formation. Nudged elastic band calculations show that once CO2 is adsorbed on a step valley site, it is effectively unable to diffuse and impacts the Li2O2 growth mechanism, capacity, and overvoltages. The charging processes are strongly influenced by CO2 contamination, and exhibit increased overvoltages and increased capacity, as a result of poisoning of nucleation sites: this effect is predicted from DFT calculations and observed experimentally already at 1% CO2. Large capacity losses and overvoltages are seen at higher CO2 concentrations.
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