z-logo
Premium
Long‐Life Zn Anode Enabled by Low Volume Concentration of a Benign Electrolyte Additive
Author(s) -
Shang Yuan,
Kumar Priyank,
Musso Tiziana,
Mittal Uttam,
Du Qijun,
Liang Xiao,
Kundu Dipan
Publication year - 2022
Publication title -
advanced functional materials
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 6.069
H-Index - 322
eISSN - 1616-3028
pISSN - 1616-301X
DOI - 10.1002/adfm.202200606
Subject(s) - electrolyte , anode , materials science , battery (electricity) , chemical engineering , volume fraction , aqueous solution , electrode , organic chemistry , chemistry , composite material , thermodynamics , power (physics) , physics , engineering
Inexpensive and energy‐dense Zn metal anodes is key to the promise of aqueous Zn‐ion batteries, which are heralded as an exciting battery chemistry for renewable and stationary storage. Yet, Zn deposition instability under demanding cycling conditions leads to rapid dendritic cell failure, and the hydrogen evolution reaction aggravates the issue. Electrolyte additives are a scalable solution to address the problem, but a high volume fraction is typically required for a noticeable effect. Here, a benign alcohol molecule propylene glycol is presented as an electrolyte additive that enables remarkably stable Zn anode cycling of over 1000 h at a practical 2 mA–2 mA h cm −2 at a low volume concentration when the reference cell shorts only after 30 h. The dramatic performance improvement at the low additive concentration is attributed to the effective morphology regulation and inhibition of hydrogen evolution, as revealed by spectroscopic and microscopic investigations. Ab initio molecular dynamics simulations reveal unprecedented atomistic insights behind the concentration‐dependent effectivity of propylene glycol as an electrolyte additive. Excellent full cell cycling with two different positive host materials, even with high loading, highlights the potential for practical development.

This content is not available in your region!

Continue researching here.

Having issues? You can contact us here