TY - JOUR
T1 - Solid Electrolyte Interface Regulated by Solvent-in-Water Electrolyte Enables High-Voltage and Stable Aqueous Mg-MnO2 Batteries
AU - Xu, Yan
AU - Liu, Zaichun
AU - Zheng, Xinhua
AU - Li, Ke
AU - Wang, Mingming
AU - Yu, Wei
AU - Hu, Hanlin
AU - Chen, Wei
N1 - Publisher Copyright:
© 2022 Wiley-VCH GmbH.
PY - 2022/6/9
Y1 - 2022/6/9
N2 - Mg batteries utilizing divalent Mg2+ as charge carriers have been attracting significant attention for energy storage owing to their uniqueness in terms of low cost, high safety, and high energy density. However, the short cycling life arising from the accumulation of a passivation layer on the Mg anode prohibits their further development. Here, a new strategy to suppress the accumulation of the passivation layer is presented, thus stabilizing the Mg anode by constructing a robust interfacial layer using organic solvent-in-water electrolytes. The organic solvents decompose on the Mg anode to form a MgO, polyether Mg enriched organic-inorganic hybrid interfacial layer, preventing free water attack to the Mg anode. In addition, the organic solvent forms an H-bond with H2O to suppress the water activity and therefore protecting the Mg anode. As an illustration to benefits of the solvent-in-water electrolytes, a Mg-MnO2 battery that is coupled by a MnO2 cathode in Mn2+/MnO2 chemistry with the Mg anode is developed. The Mg-MnO2 battery exhibits a well-maintained discharge plateau at ≈2.5 V and a discharging capacity of ≈500 mAh g−1 over 1000 cycles. This result highlights the feasibility to stabilize the Mg anode by interface engineering through the solvent-in-water electrolyte design.
AB - Mg batteries utilizing divalent Mg2+ as charge carriers have been attracting significant attention for energy storage owing to their uniqueness in terms of low cost, high safety, and high energy density. However, the short cycling life arising from the accumulation of a passivation layer on the Mg anode prohibits their further development. Here, a new strategy to suppress the accumulation of the passivation layer is presented, thus stabilizing the Mg anode by constructing a robust interfacial layer using organic solvent-in-water electrolytes. The organic solvents decompose on the Mg anode to form a MgO, polyether Mg enriched organic-inorganic hybrid interfacial layer, preventing free water attack to the Mg anode. In addition, the organic solvent forms an H-bond with H2O to suppress the water activity and therefore protecting the Mg anode. As an illustration to benefits of the solvent-in-water electrolytes, a Mg-MnO2 battery that is coupled by a MnO2 cathode in Mn2+/MnO2 chemistry with the Mg anode is developed. The Mg-MnO2 battery exhibits a well-maintained discharge plateau at ≈2.5 V and a discharging capacity of ≈500 mAh g−1 over 1000 cycles. This result highlights the feasibility to stabilize the Mg anode by interface engineering through the solvent-in-water electrolyte design.
KW - Mg anodes
KW - Mg-MnO batteries
KW - MnO cathodes
KW - solid electrolyte interfaces
KW - solvent-in-water electrolytes
UR - http://www.scopus.com/inward/record.url?scp=85127266322&partnerID=8YFLogxK
U2 - 10.1002/aenm.202103352
DO - 10.1002/aenm.202103352
M3 - 文章
AN - SCOPUS:85127266322
SN - 1614-6832
VL - 12
JO - Advanced Energy Materials
JF - Advanced Energy Materials
IS - 22
M1 - 2103352
ER -