The development of nonaqueous Li–oxygen batteries, which relies on the reversible reaction of Li + O2 to give lithium peroxide (Li2O2), is challenged by several factors, not the least being the high charging voltage that results when carbon is typically employed as the cathode host. We report here on the remarkably low 3.2 V potential for Li2O2 oxidation on a passivated nanostructured metallic carbide (Mo2C), carbon-free cathode host. Furthermore, online mass spectrometry coupled with X-ray photoelectron spectroscopy unequivocally demonstrates that lithium peroxide is simultaneously oxidized together with the LixMoO3-passivated conductive interface formed on the carbide, owing to their close redox potentials. We found that the process rejuvenates the surface on each cycle upon electrochemical charge by releasing LixMoO3 into the electrolyte, explaining the low charging potential.
Kundu, Dipan, et al. "Nanostructured metal carbides for aprotic Li-O<sub>2</sub> batteries. New insights into interfacial reactions and cathode stability." Journal of Physical Chemistry Letters, vol. 6, no. 12, May. 2015. https://doi.org/10.1021/acs.jpclett.5b00721
Kundu, Dipan, Black, Robert, Adams, Brian, Harrison, Katharine, Zavadil, Kevin R., & Nazar, Linda F. (2015). Nanostructured metal carbides for aprotic Li-O<sub>2</sub> batteries. New insights into interfacial reactions and cathode stability. Journal of Physical Chemistry Letters, 6(12). https://doi.org/10.1021/acs.jpclett.5b00721
Kundu, Dipan, Black, Robert, Adams, Brian, et al., "Nanostructured metal carbides for aprotic Li-O<sub>2</sub> batteries. New insights into interfacial reactions and cathode stability," Journal of Physical Chemistry Letters 6, no. 12 (2015), https://doi.org/10.1021/acs.jpclett.5b00721
@article{osti_1235282,
author = {Kundu, Dipan and Black, Robert and Adams, Brian and Harrison, Katharine and Zavadil, Kevin R. and Nazar, Linda F.},
title = {Nanostructured metal carbides for aprotic Li-O<sub>2</sub> batteries. New insights into interfacial reactions and cathode stability},
annote = {The development of nonaqueous Li–oxygen batteries, which relies on the reversible reaction of Li + O2 to give lithium peroxide (Li2O2), is challenged by several factors, not the least being the high charging voltage that results when carbon is typically employed as the cathode host. We report here on the remarkably low 3.2 V potential for Li2O2 oxidation on a passivated nanostructured metallic carbide (Mo2C), carbon-free cathode host. Furthermore, online mass spectrometry coupled with X-ray photoelectron spectroscopy unequivocally demonstrates that lithium peroxide is simultaneously oxidized together with the LixMoO3-passivated conductive interface formed on the carbide, owing to their close redox potentials. We found that the process rejuvenates the surface on each cycle upon electrochemical charge by releasing LixMoO3 into the electrolyte, explaining the low charging potential.},
doi = {10.1021/acs.jpclett.5b00721},
url = {https://www.osti.gov/biblio/1235282},
journal = {Journal of Physical Chemistry Letters},
issn = {ISSN 1948-7185},
number = {12},
volume = {6},
place = {United States},
publisher = {American Chemical Society},
year = {2015},
month = {05}}