Asenbauer Jakob, Kuenzel Matthias, Eisenmann Tobias, Birrozzi Adele, Chang Jeng-Kuei, Passerini Stefano, Bresser Dominic
Helmholtz Institute Ulm (HIU), Helmholtzstrasse 11, 89081 Ulm, Germany.
Karlsruhe Institute of Technology (KIT), P.O. Box 3640, 76021 Karlsruhe, Germany.
J Phys Chem Lett. 2020 Oct 1;11(19):8238-8245. doi: 10.1021/acs.jpclett.0c02198. Epub 2020 Sep 16.
High-capacity lithium-ion anodes such as alloying-, conversion-, and conversion/alloying-type materials are subjected to extensive volume variation upon lithiation/delithiation. However, a careful examination of these processes at the particle and electrode level as well as the impact of the kind of lithium-ion uptake mechanism is still missing. Herein, we investigated the volume variation upon lithiation/delithiation for a series of conversion/alloying materials with a varying relative contribution of the alloying and conversion reaction, i.e., carbon-coated ZnFeO, ZnFeO, and SnFeO by dilatometry and scanning electron microscopy of the electrode cross section. While the theoretical estimation at the particle level indicates a rather large volume expansion of 113% (ZnFeO) and more, the true volume variation on the electrode level reveals very limited changes of only around 11% (ZnFeO). Combining the experimental findings with some theoretical considerations highlights the (to a certain extent unexpected) impact of the initial electrode porosity.