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Enhancing electrochemical intermediate solvation through electrolyte anion selection to increase nonaqueous Li-O2 battery capacity.
Burke, Colin M; Pande, Vikram; Khetan, Abhishek; Viswanathan, Venkatasubramanian; McCloskey, Bryan D.
Afiliación
  • Burke CM; Department of Chemical and Biomolecular Engineering, University of California, Berkeley, CA 94720; Environmental Energy Technologies Division, Lawrence Berkeley National Laboratory, Berkeley, CA 94720;
  • Pande V; Department of Mechanical Engineering, Carnegie Mellon University, Pittsburgh, PA 15213;
  • Khetan A; Institute for Combustion Technology, Rheinisch-Westfälische Technische Hochschule Aachen, 52056 Aachen, Germany.
  • Viswanathan V; Department of Mechanical Engineering, Carnegie Mellon University, Pittsburgh, PA 15213; venkvis@cmu.edu bmcclosk@berkeley.edu.
  • McCloskey BD; Department of Chemical and Biomolecular Engineering, University of California, Berkeley, CA 94720; Environmental Energy Technologies Division, Lawrence Berkeley National Laboratory, Berkeley, CA 94720; venkvis@cmu.edu bmcclosk@berkeley.edu.
Proc Natl Acad Sci U S A ; 112(30): 9293-8, 2015 Jul 28.
Article en En | MEDLINE | ID: mdl-26170330
ABSTRACT
Among the "beyond Li-ion" battery chemistries, nonaqueous Li-O2 batteries have the highest theoretical specific energy and, as a result, have attracted significant research attention over the past decade. A critical scientific challenge facing nonaqueous Li-O2 batteries is the electronically insulating nature of the primary discharge product, lithium peroxide, which passivates the battery cathode as it is formed, leading to low ultimate cell capacities. Recently, strategies to enhance solubility to circumvent this issue have been reported, but rely upon electrolyte formulations that further decrease the overall electrochemical stability of the system, thereby deleteriously affecting battery rechargeability. In this study, we report that a significant enhancement (greater than fourfold) in Li-O2 cell capacity is possible by appropriately selecting the salt anion in the electrolyte solution. Using (7)Li NMR and modeling, we confirm that this improvement is a result of enhanced Li(+) stability in solution, which, in turn, induces solubility of the intermediate to Li2O2 formation. Using this strategy, the challenging task of identifying an electrolyte solvent that possesses the anticorrelated properties of high intermediate solubility and solvent stability is alleviated, potentially providing a pathway to develop an electrolyte that affords both high capacity and rechargeability. We believe the model and strategy presented here will be generally useful to enhance Coulombic efficiency in many electrochemical systems (e.g., Li-S batteries) where improving intermediate stability in solution could induce desired mechanisms of product formation.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Idioma: En Revista: Proc Natl Acad Sci U S A Año: 2015 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Idioma: En Revista: Proc Natl Acad Sci U S A Año: 2015 Tipo del documento: Article