The DOI matches its Crossref record; 2 of the 2 references it cites were found in a registry or an index.
Predicting Solvent Stability in Aprotic Electrolyte Li–Air Batteries: Nucleophilic Substitution by the Superoxide Anion Radical (O2•–)
Abstract
There is increasing evidence that cyclic and linear carbonates, commonly used solvents in Li ion battery electrolytes, are unstable in the presence of superoxide and thus are not suitable for use in rechargeable Li-air batteries employing aprotic electrolytes. A detailed understanding of related decomposition mechanisms provides an important basis for the selection and design of stable electrolyte materials. In this article, we use density functional theory calculations with a Poisson-Boltzmann continuum solvent model to investigate the reactivity of several classes of aprotic solvents in nucleophilic substitution reactions with superoxide. We find that nucleophilic attack by O(2)(•-) at the O-alkyl carbon is a common mechanism of decomposition of organic carbonates, sulfonates, aliphatic carboxylic esters, lactones, phosphinates, phosphonates, phosphates, and sulfones. In contrast, nucleophilic reactions of O(2)(•-) with phenol esters of carboxylic acids and O-alkyl fluorinated aliphatic lactones proceed via attack at the carbonyl carbon. Chemical functionalities stable against nucleophilic substitution by superoxide include N-alkyl substituted amides, lactams, nitriles, and ethers. The results establish that solvent reactivity is strongly related to the basicity of the organic anion displaced in the reaction with superoxide. Theoretical calculations are complemented by cyclic voltammetry to study the electrochemical reversibility of the O(2)/O(2)(•-) couple containing tetrabutylammonium salt and GCMS measurements to monitor solvent stability in the presence of KO(2)(•) and a Li salt. These experimental methods provide efficient means for qualitatively screening solvent stability in Li-air batteries. A clear correlation between the computational and experimental results is established. The combination of theoretical and experimental techniques provides a powerful means for identifying and designing stable solvents for rechargeable Li-air batteries.
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Cites
Lee, C., Yang, W., & Parr, R. G. (1988) · Physical Review B · doi:10.1103/physrevb.37.785 · Cited by 100,874
Reaction of superoxide with alkyl halides and tosylates
San Filippo, J., Chern, C.-I., & Valentine, J. S. (1975) · The Journal of Organic Chemistry · doi:10.1021/jo00899a048 · Cited by 105
Cited by
Electrolytes and Interphases in Li-Ion Batteries and Beyond
Xu, K. (2014) · Chemical Reviews · doi:10.1021/cr500003w · Cited by 5,566
Electrochemical in situ investigations of SEI and dendrite formation on the lithium metal anode
Bieker, G., Winter, M., & Bieker, P. (2015) · Physical Chemistry Chemical Physics · doi:10.1039/c4cp05865h · Cited by 777
Materials Design for Rechargeable Metal-Air Batteries
Wang, H.-F., & Xu, Q. (2019) · Matter · doi:10.1016/j.matt.2019.05.008 · Cited by 580
From lithium to sodium: Cell chemistry of room temperature sodium–air and sodium–sulfur batteries
Adelhelm, P., Hartmann, P., Bender, C. L., Busche, M., Eufinger, C., & Janek, J. (2015) · Beilstein Journal of Nanotechnology · doi:10.3762/bjnano.6.105 · Cited by 478
Critical Challenges in Rechargeable Aprotic Li–O2 Batteries
Feng, N., He, P., & Zhou, H. (2016) · Advanced Energy Materials · doi:10.1002/aenm.201502303 · Cited by 423
Metadata
- Authors
- Bryantsev, V. S., Giordani, V., Walker, W., Blanco, M., Zecevic, S., Sasaki, K., Uddin, J., Addison, D., & Chase, G. V.
- Venue
- The Journal of Physical Chemistry A
- Publisher
- American Chemical Society (ACS)
- Published
- 2011-10-18
- Volume
- 115
- Issue
- 44
- Pages
- 12399-12409
- ISSN
- 1089-5639 (ISSN-L)
- 1520-5215
- OpenAlex
- W2314331081
- Cited by
- 355
- References
- 2
- FWCI
- 22.28
- Type
- journal article
- Language
- en
- Open access
- closed
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