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Free-Standing alpha-MoO3/Ti3C2 MXene Hybrid Electrode in Water-in-Salt Electrolytes
Journal article   Open access   Peer reviewed

Free-Standing alpha-MoO3/Ti3C2 MXene Hybrid Electrode in Water-in-Salt Electrolytes

Mohit Saraf, Christopher E. Shuck, Nazgol Norouzi, Kyle Matthews, Alex Inman, Teng Zhang, Ekaterina Pomerantseva and Yury Gogotsi
Energy & environmental materials (Hoboken, N.J.)
03 Jan 2023
url
https://doi.org/10.1002/eem2.12516View
Published, Version of Record (VoR)CC BY V4.0 Open

Abstract

Materials Science Materials Science, Multidisciplinary Science & Technology Technology
While transition-metal oxides such as alpha-MoO3 provide high capacity, their use is limited by modest electronic conductivity and electrochemical instability in aqueous electrolytes. Two-dimensional (2D) MXenes, offer metallic conductivity, but their capacitance is limited in aqueous electrolytes. Insertion of partially solvated cations into Ti3C2 MXene from lithium-based water-in-salt (WIS) electrolytes enables charge storage at positive potentials, allowing a wider potential window and higher capacitance. Herein, we demonstrate that alpha-MoO3/Ti3C2 hybrids combine the high capacity of alpha-MoO3 and conductivity of Ti3C2 in WIS (19.8 m LiCl) electrolyte in a wide 1.8 V voltage window. Cyclic voltammograms reveal multiple redox peaks from alpha-MoO3 in addition to the well-separated peaks of Ti3C2 in the hybrid electrode. This leads to a higher specific charge and a higher rate capability compared to a carbon and binder containing alpha-MoO3 electrode. These results demonstrate that the addition of MXene to less conductive oxides eliminates the need for conductive carbon additives and binders, leads to a larger amount of charge stored, and increases redox capacity at higher rates. In addition, MXene encapsulated alpha-MoO3 showed improved electrochemical stability, which was attributed to the suppressed dissolution of alpha-MoO3. The work suggests that oxide/MXene hybrids are promising for energy storage.

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Materials Science, Multidisciplinary
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