The rapid expansion of renewable energy sources such as solar and wind demands safe, low-cost, and durable stationary energy storage technologies. In this context, aqueous zinc-ion batteries (ZIBs) have emerged as attractive alternatives to lithium-ion systems because they combine the abundance and geopolitical accessibility of zinc with the intrinsic safety of water-based electrolytes. Nevertheless, conventional aqueous electrolytes still suffer from major limitations, including parasitic hydrogen evolution, zinc corrosion, interfacial instability, and structural degradation of cathodes during long-term cycling, particularly under low-rate operating conditions. To address these challenges, we developed a sustainable low-temperature transition mixture (LTTM) electrolyte based on ZnSO4·7H2O and glycerol in a 1:10 molar ratio. Both components are inexpensive and widely available, with glycerol representing an abundant by-product of biodiesel production. A detailed physicochemical investigation linked the thermal properties of the mixture with ionic transport characteristics and electrochemical stability. Despite reduced transport kinetics compared with conventional aqueous ZnSO4 solutions, the LTTM exhibited a significantly widened electrochemical stability window, enabling highly reversible Zn plating/stripping at low current density (0.05 mA cm-2). Morphological characterization confirmed uniform zinc deposition on carbon substrates, while proof-of-concept full-cell tests using a Zn anode and zinc hexacyanoferrate cathode demonstrated stable cycling, coulombic efficiencies above 90%, and a specific capacity of 50.6 mAh g-1, comparable to standard aqueous electrolytes.

Glycerol-based electrolyte for sustainable low-rate zinc-ion batteries

Daniele Motta;Claudia Barolo;Matteo Bonomo
2026-01-01

Abstract

The rapid expansion of renewable energy sources such as solar and wind demands safe, low-cost, and durable stationary energy storage technologies. In this context, aqueous zinc-ion batteries (ZIBs) have emerged as attractive alternatives to lithium-ion systems because they combine the abundance and geopolitical accessibility of zinc with the intrinsic safety of water-based electrolytes. Nevertheless, conventional aqueous electrolytes still suffer from major limitations, including parasitic hydrogen evolution, zinc corrosion, interfacial instability, and structural degradation of cathodes during long-term cycling, particularly under low-rate operating conditions. To address these challenges, we developed a sustainable low-temperature transition mixture (LTTM) electrolyte based on ZnSO4·7H2O and glycerol in a 1:10 molar ratio. Both components are inexpensive and widely available, with glycerol representing an abundant by-product of biodiesel production. A detailed physicochemical investigation linked the thermal properties of the mixture with ionic transport characteristics and electrochemical stability. Despite reduced transport kinetics compared with conventional aqueous ZnSO4 solutions, the LTTM exhibited a significantly widened electrochemical stability window, enabling highly reversible Zn plating/stripping at low current density (0.05 mA cm-2). Morphological characterization confirmed uniform zinc deposition on carbon substrates, while proof-of-concept full-cell tests using a Zn anode and zinc hexacyanoferrate cathode demonstrated stable cycling, coulombic efficiencies above 90%, and a specific capacity of 50.6 mAh g-1, comparable to standard aqueous electrolytes.
2026
GEI2026 - Giornate dell'elettrochimica italiane 2026
Milano
14/09/2026
-
-
-
Daniele Motta, Lucia Sorrill, Giorgia Zampardi, Claudia Barolo, Fabio La Mantia, Matteo Bonomo
File in questo prodotto:
File Dimensione Formato  
Motta_GEI2026.pdf

Accesso aperto

Tipo di file: MATERIALE NON BIBLIOGRAFICO
Dimensione 144.84 kB
Formato Adobe PDF
144.84 kB Adobe PDF Visualizza/Apri

I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.

Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2318/2164651
Citazioni
  • ???jsp.display-item.citation.pmc??? ND
  • Scopus ND
  • ???jsp.display-item.citation.isi??? ND
social impact