TY - JOUR
T1 - A cost-effective water-in-salt electrolyte enables highly stable operation of a 2.15-V aqueous lithium-ion battery
AU - Turgeman, Meital
AU - Wineman-Fisher, Vered
AU - Malchik, Fyodor
AU - Saha, Arka
AU - Bergman, Gil
AU - Gavriel, Bar
AU - Penki, Tirupathi Rao
AU - Nimkar, Amey
AU - Baranauskaite, Valeriia
AU - Aviv, Hagit
AU - Levi, Mikhael D.
AU - Noked, Malachi
AU - Major, Dan Thomas
AU - Shpigel, Netanel
AU - Aurbach, Doron
N1 - Publisher Copyright:
© 2021 The Author(s)
PY - 2022/1/19
Y1 - 2022/1/19
N2 - Extensive efforts are currently underway to develop safe and cost-effective electrolytes for large-scale energy storage. In this regard, water-based electrolytes may be an attractive option, but their narrow electrochemical stability window hinders their realization. Although highly concentrated fluorinated electrolytes have been shown to be highly effective in suppression of water splitting, enabling significant widening of the applied potential range, they utilize expensive salts (e.g., lithium bis(trifluoromethane sulfonyl) imide [LiTFSI] or lithium trifluoromethane sulfonate [LiOTf]); hence, they cannot be considered for practical applications. Here, we demonstrate a cost-effective aqueous electrolyte solution combining 14 M LiCl and 4 M CsCl that allows stable operation of a 2.15-V battery comprising a TiO2 anode and LiMn2O4 cathode. Addition of CsCl to the electrolyte plays a double role in system stabilization: the added chloride anions interact with the free water molecules, whereas the chaotropic cesium cations adsorb at the electrified interface, preventing hydrogen formation.
AB - Extensive efforts are currently underway to develop safe and cost-effective electrolytes for large-scale energy storage. In this regard, water-based electrolytes may be an attractive option, but their narrow electrochemical stability window hinders their realization. Although highly concentrated fluorinated electrolytes have been shown to be highly effective in suppression of water splitting, enabling significant widening of the applied potential range, they utilize expensive salts (e.g., lithium bis(trifluoromethane sulfonyl) imide [LiTFSI] or lithium trifluoromethane sulfonate [LiOTf]); hence, they cannot be considered for practical applications. Here, we demonstrate a cost-effective aqueous electrolyte solution combining 14 M LiCl and 4 M CsCl that allows stable operation of a 2.15-V battery comprising a TiO2 anode and LiMn2O4 cathode. Addition of CsCl to the electrolyte plays a double role in system stabilization: the added chloride anions interact with the free water molecules, whereas the chaotropic cesium cations adsorb at the electrified interface, preventing hydrogen formation.
KW - LiCl electrolyte
KW - LiMnO
KW - TiO
KW - aqueous batteries
KW - aqueous electrolytes
KW - hydrogen evolution
UR - http://www.scopus.com/inward/record.url?scp=85122917280&partnerID=8YFLogxK
U2 - 10.1016/j.xcrp.2021.100688
DO - 10.1016/j.xcrp.2021.100688
M3 - ???researchoutput.researchoutputtypes.contributiontojournal.article???
AN - SCOPUS:85122917280
SN - 2666-3864
VL - 3
JO - Cell Reports Physical Science
JF - Cell Reports Physical Science
IS - 1
M1 - 100688
ER -