Quantifying and Suppressing Proton Intercalation to Enable High-Voltage Zn-Ion Batteries

Published

November 4, 2021

Author(s)

Fei Wang, Lauren E. Blanc, Qin Li, Antonio Faraone, Xiao Ji, Huaiyu H. Chen-Mayer, Rick L. Paul, Joseph Dura, Enyuan Hu, Kang Xu, Linda F. Nazar, Chunsheng Wang

Abstract

We explore the Zn-ion intercalation mechanisms/interfacial dynamics of VPO₄F and quantify the water dynamics in water-in-salt (WISE) and hybrid aqueous-non aqueous electrolytes (HANEs). We demonstrate that H⁺ intercalation dominates electrochemical activity during discharge of oxide-based cathode materials in aqueous media due to the hydroxylated nature of the interface. Such H⁺ electrochemistry diminishes low-rate and/or long-term electrochemical performance and inhibits implementation for practical applications. Quantifications of the water dynamic in various electrolytes are demonstrated for the first time. Detailed investigations of water dynamic in various WISE and HANEs systems allowed for the design of an electrolyte that enables increased aqueous anodic stability and suppresses water/proton activity during discharge. Tuning Zn²⁺/H⁺ intercalation kinetics enables both a high voltage (1.9 V) and long-lasting aqueous zinc-ion battery: Zn|Zn(OTf)₂·nH₂O-PC|Zn_xVPO₄F.

Citation

Advanced Energy Materials

Volume

11

Issue

41

Pub Type

Journals

Citation

Wang, F. , Blanc, L. , Li, Q. , Faraone, A. , Ji, X. , Chen-Mayer, H. , Paul, R. , Dura, J. , Hu, E. , Xu, K. , Nazar, L. and Wang, C. (2021), Quantifying and Suppressing Proton Intercalation to Enable High-Voltage Zn-Ion Batteries, Advanced Energy Materials (Accessed April 25, 2024)