Abstract
Increasing the energy densities of Li-ion batteries necessitates operation of layered lithiated oxide cathodes at potentials exceeding 4 V vs Li/Li+. When continually exposed to such high potentials, these materials gradually deteriorate unless protected by sacrificial agents called electrolyte additives. During the formation cycles, these electrolyte additives decompose on the electrodes forming thin protective layers of insoluble products impeding further deleterious reactions. Some of these electrolyte additives spontaneously react when introduced into the electrolyte to yield specific surface-modifying products that alone protect the cathode; in other words, the nominal additive is the precursor and the secondary product is the protective agent. Guided by this insight, we used molecular engineering to obtain such surface-active secondary products in situ with 100% yield. Two of these electrolyte additives proved exceptional in that they delay both the impedance rise and capacity fade in the Li-ion cells. We demonstrate this protective action and scrutinize the activation of these additives in the electrolyte. By "taming" spontaneous reactions and regaining full control over the chemical structure, new avenues open to targeted synthesis of electrolyte additives extending the operation of high voltage Li-ion batteries.
| Original language | English |
|---|---|
| Pages (from-to) | 2459-2468 |
| Number of pages | 10 |
| Journal | Chemistry of Materials |
| Volume | 31 |
| Issue number | 7 |
| DOIs | |
| State | Published - Apr 9 2019 |
Funding
Support from the U.S. Department of Energy’s Vehicle Technologies Program (DOE-VTP), specifically from Peter Faguy and Dave Howell, is gratefully acknowledged. The electrodes and electrolytes used in this article are from Argonne’s Cell Analysis, Modeling and Prototyping (CAMP) Facility. Both facilities are supported within the core funding of the Applied Battery Research (ABR) for Transportation Program. TEM images were obtained at the Center for Nanoscale Materials at Argonne National Laboratory, which are supported by the U.S. Department of Energy, Office of Science, Office of Basic Energy Sciences, also under Contract No. DE-AC02-06CH11357. The submitted manuscript has been created by UChicago Argonne, LLC, Operator of Argonne National Laboratory (“Argonne”). Argonne, a U.S. Department of Energy Office of Science laboratory, is operated under Contract No. DE-AC02-06CH11357.