TY - JOUR
T1 - High-rate aqueous magnesium ion battery enabled by Li/Mg hybrid superconcentrated electrolyte
AU - Yang, Tian
AU - Ma, Fengming
AU - Zhang, Xinqun
AU - Yang, Ya'nan
AU - Lv, Jinsheng
AU - Jin, Zifeng
AU - Wang, Liru
AU - Gao, Huimin
AU - Wang, Xiaolin
AU - Chen, Nan
N1 - Publisher Copyright:
© 2024 Elsevier B.V.
PY - 2024/7/1
Y1 - 2024/7/1
N2 - Rechargeable aqueous magnesium ion batteries (AMIBs) are considered a promising energy storage system due to the relatively high energy density, excellent rate performance and reversibility, and absence of dendrite formation during cycling. However, the high surface charge density of Mg2+ ions results in slow diffusion kinetics, and high voltage leads to excessive electrolyte decomposition at the electrode/aqueous electrolyte interface, thereby limiting the development of high-energy–density MIBs. In this work, we extend the electrochemical stability window of the aqueous electrolyte to 2.1 V by using a hybrid ion superconcentrated electrolyte at concentrations not achievable with Mg2+ electrolytes alone. The AMIB with a water-in-salt (WIS) electrolyte delivers discharge capacities of up to 200.6 and 84.4 mAh g−1, and energy densities of 170.1 and 68.1 Wh Kg−1 at 0.5 and 20 A g−1, respectively, representing excellent rate performance, while retaining 85 % of the specific capacity after 2000 cycles. Additionally, we explore the corresponding electrochemical reaction mechanism, revealing the synergistic effect of Mg2+ and Li+ ions in the charge/discharge process, which supports the excellent electrochemical performance of AMIB.
AB - Rechargeable aqueous magnesium ion batteries (AMIBs) are considered a promising energy storage system due to the relatively high energy density, excellent rate performance and reversibility, and absence of dendrite formation during cycling. However, the high surface charge density of Mg2+ ions results in slow diffusion kinetics, and high voltage leads to excessive electrolyte decomposition at the electrode/aqueous electrolyte interface, thereby limiting the development of high-energy–density MIBs. In this work, we extend the electrochemical stability window of the aqueous electrolyte to 2.1 V by using a hybrid ion superconcentrated electrolyte at concentrations not achievable with Mg2+ electrolytes alone. The AMIB with a water-in-salt (WIS) electrolyte delivers discharge capacities of up to 200.6 and 84.4 mAh g−1, and energy densities of 170.1 and 68.1 Wh Kg−1 at 0.5 and 20 A g−1, respectively, representing excellent rate performance, while retaining 85 % of the specific capacity after 2000 cycles. Additionally, we explore the corresponding electrochemical reaction mechanism, revealing the synergistic effect of Mg2+ and Li+ ions in the charge/discharge process, which supports the excellent electrochemical performance of AMIB.
KW - Aqueous Magnesium ion hybrid batteries
KW - Binding energy
KW - High energy density
KW - Superconcentrated electrolyte
UR - http://www.scopus.com/inward/record.url?scp=85189704732&partnerID=8YFLogxK
U2 - 10.1016/j.apsusc.2024.159995
DO - 10.1016/j.apsusc.2024.159995
M3 - Article
AN - SCOPUS:85189704732
SN - 0169-4332
VL - 660
JO - Applied Surface Science
JF - Applied Surface Science
M1 - 159995
ER -