These are preliminary reports that have not been peer-reviewed. They should not be regarded as conclusive, guide clinical practice/health-related behavior, or be reported in news media as established information. For more information, please see our FAQs.
manuscript.pdf (1.21 MB)

The Role of Interface in Stabilizing Reaction Intermediates for Hydrogen Evolution in Aprotic Li-Ion Battery Electrolyte

submitted on 09.06.2019 and posted on 11.06.2019 by Ivano E. Castelli, Dusan Strmcnik, Milena Zorko, Thomas Østergaard, Pedro Farinazzo Bergamo Dias Martins, Pietro Papa Lopes, Byron K. Antonopoulos, Filippo Maglia, Nenad M. Markovic, Jan Rossmeisl
p { margin-bottom: 0.1in; direction: ltr; color: rgb(0, 0, 10); line-height: 120%; text-align: left; }p.western { font-size: 12pt; }p.cjk { font-size: 12pt; }a:link { color: rgb(5, 99, 193); }

By combining idealized experiments with realistic quantum mechanical simulations of the interface, we investigate electro-reduction reactions of HF and water impurities on the single crystal (111) facets of Au, Pt, Ir and Cu in an organic aprotic electrolyte, 1M LiPF6 in EC/EMC 3:7w (LP57), which are common reactions happening during the formation of the SEI on graphite. In our previous work, we have established that the LiF formation, accompanied with H2 evolution, is caused by a reduction of HF impurities and requires the presence of Li at the interface, which catalyzes the HF dissociation. In the present paper, we find that the measured potential of the electrochemical response for these reduction reactions correlates with the work function of the electrode surfaces and that the work function determines the potential for Li+ adsorption. The reaction path is investigated further by electrochemical simulations suggesting that the overpotential of the reaction is related to stabilizing the active structure of the interface having Li+ adsorbed. The Li+ is needed to facilitate the dissociation of HF which is the source of proton. Further experiments on the other proton sources, water and methanesulfonic acid, show that if the hydrogen evolution involves negatively charged intermediates, F- or HO-, a cation at the interface can stabilize them and facilitate the reaction kinetics. When the proton source is already significantly dissociated (in the case of a strong acid), there is no negatively charged intermediate and thus the hydrogen evolution can proceed at much lower overpotentials. This reveals a situation where the overpotential for electrocatalysis is related to stabilizing the active structure of the interface, facilitating the reaction rather than providing the reaction energy. This has implications for the SEI layer formation in Li-ion batteries and for reduction reactions in alkaline environment as well as for design principles for better electrodes.


Email Address of Submitting Author


Technical University of Denmark



ORCID For Submitting Author


Declaration of Conflict of Interest

No conflict of interest