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A cost-effective water-in-salt electrolyte enables highly stable operation of a 2.15-V aqueous lithium-ion battery

  • Meital Turgeman
  • , Vered Wineman-Fisher
  • , Fyodor Malchik
  • , Arka Saha
  • , Gil Bergman
  • , Bar Gavriel
  • , Tirupathi Rao Penki
  • , Amey Nimkar
  • , Valeriia Baranauskaite
  • , Hagit Aviv
  • , Mikhael D. Levi
  • , Malachi Noked
  • , Dan Thomas Major
  • , Netanel Shpigel
  • , Doron Aurbach

نتاج البحث: نشر في مجلةمقالةمراجعة النظراء

42 اقتباسات (Scopus)

ملخص

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.

اللغة الأصليةالإنجليزيّة
رقم المقال100688
دوريةCell Reports Physical Science
مستوى الصوت3
رقم الإصدار1
المعرِّفات الرقمية للأشياء
حالة النشرنُشِر - 19 يناير 2022
منشور خارجيًانعم

بصمة

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