Journal article

Electrochemical Lithiation/Delithiation of ZnO in 3D-Structured Electrodes: Elucidating the Mechanism and the Solid Electrolyte Interphase Formation


Authors listKreissl, Julian J. A.; Petit, Jan; Oppermann, Raika; Cop, Pascal; Gerber, Tobias; Joos, Martin; Abert, Michael; Tuebke, Jens; Miyazaki, Kohei; Abe, Takeshi; Schroeder, Daniel

Publication year2021

Pages35625-35638

JournalACS Applied Materials & Interfaces

Volume number13

Issue number30

ISSN1944-8244

eISSN1944-8252

DOI Linkhttps://doi.org/10.1021/acsami.1c06135

PublisherAmerican Chemical Society


Abstract
Conversion/alloy active materials, such as ZnO, are one of the most promising candidates to replace graphite anodes in lithium-ion batteries. Besides a high specific capacity (q(ZnO) = 987 mAh g(-1)), ZnO offers a high lithium-ion diffusion and fast reaction kinetics, leading to a high-rate capability, which is required for the intended fast charging of battery electric vehicles. However, lithium-ion storage in ZnO is accompanied by the formation of lithium-rich solid electrolyte interphase (SEI) layers, immense volume expansion, and a large voltage hysteresis. Nonetheless, ZnO is appealing as an anode material for lithium-ion batteries and is investigated intensively. Surprisingly, the conclusions reported on the reaction mechanism are contradictory and the formation and composition of the SEI are addressed in only a few works. In this work, we investigate lithiation, delithiation, and SEI formation with ZnO in ether-based electrolytes for the first time reported in the literature. The combination of operando and ex situ experiments (cyclic voltammetry, X-ray photoelectron spectroscopy, X-ray diffraction, coupled gas chromatography and mass spectrometry, differential electrochemical mass spectrometry, and scanning electron microscopy) clarifies the misunderstanding of the reaction mechanism. We evidence that the conversion and alloy reaction take place simultaneously inside the bulk of the electrode. Furthermore, we show that a two-layered SEI is formed on the surface. The SEI is decomposed reversibly upon cycling. In the end, we address the issue of the volume expansion and associated capacity fading by incorporating ZnO into a mesoporous carbon network. This approach reduces the capacity fading and yields cells with a specific capacity of above 500 mAh g(-1) after 150 cycles.



Citation Styles

Harvard Citation styleKreissl, J., Petit, J., Oppermann, R., Cop, P., Gerber, T., Joos, M., et al. (2021) Electrochemical Lithiation/Delithiation of ZnO in 3D-Structured Electrodes: Elucidating the Mechanism and the Solid Electrolyte Interphase Formation, ACS Applied Materials & Interfaces, 13(30), pp. 35625-35638. https://doi.org/10.1021/acsami.1c06135

APA Citation styleKreissl, J., Petit, J., Oppermann, R., Cop, P., Gerber, T., Joos, M., Abert, M., Tuebke, J., Miyazaki, K., Abe, T., & Schroeder, D. (2021). Electrochemical Lithiation/Delithiation of ZnO in 3D-Structured Electrodes: Elucidating the Mechanism and the Solid Electrolyte Interphase Formation. ACS Applied Materials & Interfaces. 13(30), 35625-35638. https://doi.org/10.1021/acsami.1c06135



Keywords


ANODE MATERIALSether-based electrolyteHIGH-PERFORMANCEmetal oxideNANOROD ARRAYSNEGATIVE ELECTRODESreaction mechanismSODIUM-ION BATTERIESSPUTTERING YIELDSZINC-OXIDE NANOPARTICLES

Last updated on 2025-02-04 at 00:22