TY - JOUR
T1 - Synergistic Li-Na co-alloying for high-capacity, long-life, dual-alkali ion batteries
AU - Ahad, Syed Abdul
AU - Owen, Christopher
AU - Patil, Niraj Nitish
AU - Adegoke, Temilade Esther
AU - Downing, Clive
AU - Ryan, Kevin M.
AU - Singh, Shalini
AU - Morris, Andrew J.
AU - Geaney, Hugh
N1 - Publisher Copyright:
© 2025 The Authors
PY - 2025/12/1
Y1 - 2025/12/1
N2 - High-capacity, alloying-mode sodium-ion battery (NIB) anode materials remain elusive, mostly due to poor Na ion diffusivity within attractive candidates such as Ge and Si. Herein, for the first time, increased cation activity is unlocked in a Ge nanowire active material, through the use of a dual ion Li/Na electrolyte. In comparison to low specific capacity (297 mAh g−1) in the Na-only electrolyte, the dual electrolyte enabled a 2x capacity increase (605 mAh g−1) via a dual-cation alloying mechanism which has never been reported before. Electrochemical data and material characterization demonstrates that the mechanism follows an amorphous path, with the formation of amorphous Na-rich and Li-rich Ge phases during electrochemical alloying reactions. Complex stoichiometries of Li-Na-Ge ternary phases were validated using ab-initio random structure searching (AIRSS) computational technique. This dual-cation mechanism led to exceptional specific capacity (80 % capacity retention after 1000 cycles at 1 mA cm−2), with demonstrated full-cell compatibility using a sustainable FeS2 cathode.
AB - High-capacity, alloying-mode sodium-ion battery (NIB) anode materials remain elusive, mostly due to poor Na ion diffusivity within attractive candidates such as Ge and Si. Herein, for the first time, increased cation activity is unlocked in a Ge nanowire active material, through the use of a dual ion Li/Na electrolyte. In comparison to low specific capacity (297 mAh g−1) in the Na-only electrolyte, the dual electrolyte enabled a 2x capacity increase (605 mAh g−1) via a dual-cation alloying mechanism which has never been reported before. Electrochemical data and material characterization demonstrates that the mechanism follows an amorphous path, with the formation of amorphous Na-rich and Li-rich Ge phases during electrochemical alloying reactions. Complex stoichiometries of Li-Na-Ge ternary phases were validated using ab-initio random structure searching (AIRSS) computational technique. This dual-cation mechanism led to exceptional specific capacity (80 % capacity retention after 1000 cycles at 1 mA cm−2), with demonstrated full-cell compatibility using a sustainable FeS2 cathode.
UR - http://dx.doi.org/10.1016/j.nanoen.2025.111443
U2 - 10.1016/j.nanoen.2025.111443
DO - 10.1016/j.nanoen.2025.111443
M3 - Article
SN - 2211-2855
VL - 145
JO - Nano Energy
JF - Nano Energy
M1 - 111443
ER -