TY - JOUR
T1 - Hydrated eutectic electrolytes for high-performance Mg-ion batteries
AU - Zhu, Yunpei
AU - Guo, Xianrong
AU - Lei, Yongjiu
AU - Wang, Wenxi
AU - Emwas, Abdul-Hamid M.
AU - Yuan, Youyou
AU - He, Yao
AU - Alshareef, Husam N.
N1 - KAUST Repository Item: Exported on 2022-06-12
Acknowledgements: Research reported in this work was supported by King Abdullah University of Science Technology (KAUST).
PY - 2022
Y1 - 2022
N2 - Aqueous Mg-ion batteries are a promising electrochemical energy storage technology. However, Mg2+ ions interact strongly with electrolyte molecules and electrode materials, resulting in insufficient ionic conductivity and solid-state diffusion, and consequently limited cycling stability and rate capability. Herein, we design an aqueous Mg-ion battery chemistry involving a hydrated eutectic electrolyte, an organic molecule anode, and a copper hexacyanoferrate (CuHCF) cathode. This hydrated eutectic electrolyte features a three-dimensional percolating hydrogen bond network formed by water molecules, which facilitates fast Mg2+ transport in the electrolyte. Moreover, the suppression of water activity in the hydrated eutectic electrolyte can efficiently improve the cycling performance of the organic molecule anode by prohibiting the dissolution issue. After coupling with the open-framework CuHCF cathode, the resultant full battery delivers a wide operating voltage of 2.2 V, an energy density of 52.2 W h kg−1, and a decent low-temperature electrochemical performance. The electrolyte and electrode chemistries proposed in this work show an alternative way to develop low-cost, safe, and high-performance Mg battery technologies.
AB - Aqueous Mg-ion batteries are a promising electrochemical energy storage technology. However, Mg2+ ions interact strongly with electrolyte molecules and electrode materials, resulting in insufficient ionic conductivity and solid-state diffusion, and consequently limited cycling stability and rate capability. Herein, we design an aqueous Mg-ion battery chemistry involving a hydrated eutectic electrolyte, an organic molecule anode, and a copper hexacyanoferrate (CuHCF) cathode. This hydrated eutectic electrolyte features a three-dimensional percolating hydrogen bond network formed by water molecules, which facilitates fast Mg2+ transport in the electrolyte. Moreover, the suppression of water activity in the hydrated eutectic electrolyte can efficiently improve the cycling performance of the organic molecule anode by prohibiting the dissolution issue. After coupling with the open-framework CuHCF cathode, the resultant full battery delivers a wide operating voltage of 2.2 V, an energy density of 52.2 W h kg−1, and a decent low-temperature electrochemical performance. The electrolyte and electrode chemistries proposed in this work show an alternative way to develop low-cost, safe, and high-performance Mg battery technologies.
UR - http://hdl.handle.net/10754/675535
UR - http://xlink.rsc.org/?DOI=D1EE03691B
UR - http://www.scopus.com/inward/record.url?scp=85126061174&partnerID=8YFLogxK
U2 - 10.1039/d1ee03691b
DO - 10.1039/d1ee03691b
M3 - Article
SN - 1754-5706
VL - 15
SP - 1282
EP - 1292
JO - Energy & Environmental Science
JF - Energy & Environmental Science
IS - 3
ER -