TY - JOUR
T1 - Metal Aluminum-Free Configuration Toward High-Performance Aqueous Aluminum Ion Battery
AU - Wang, Huaizhi
AU - Gao, Yaning
AU - Li, Yu
AU - Yang, Haoyi
AU - Liu, Wenhao
AU - Long, Bo
AU - Wu, Feng
AU - Bai, Ying
AU - Wu, Chuan
N1 - Publisher Copyright:
Copyright © 2024 Huaizhi Wang et al.
PY - 2024/1
Y1 - 2024/1
N2 - Rechargeable aluminum batteries hold great promise for high energy density and low-cost energy storage applications but are stalled by severe electrochemical side reactions (e.g., dendrite, passivation, and corrosion) at aluminum (Al) metal anode. Here, we design an aluminum ion battery with an Al-free configuration to circumvent the problems caused by the above side reactions. The feasibility of AlxMnO2·nH2O cathode in aluminum ion batteries is revealed in conjunction with TiO2 anodes by using the optimal 5 M Al(OTF)3 electrolyte. The as-assembled aluminum ion battery enables high initial discharge capacity of 370.4 mAh g–1 at 30 mA g–1, favorable stability with low irreversible capacity loss, and enhanced safety. Further, the mechanism is intensively elucidated by multiple characterization results, indicative of the Al3+ ions (de)intercalation redox chemistry. Revealed by empirical analyses, the capacity contribution of high-voltage plateau, corresponding to the disproportionation reaction of Mn3+ in an AlxMnO2·nH2O battery system, tends to increase with the increasing electrolyte concentration. Our findings may provide fresh impetus to the rational design of aluminum ion batteries with excellent electrochemical properties.
AB - Rechargeable aluminum batteries hold great promise for high energy density and low-cost energy storage applications but are stalled by severe electrochemical side reactions (e.g., dendrite, passivation, and corrosion) at aluminum (Al) metal anode. Here, we design an aluminum ion battery with an Al-free configuration to circumvent the problems caused by the above side reactions. The feasibility of AlxMnO2·nH2O cathode in aluminum ion batteries is revealed in conjunction with TiO2 anodes by using the optimal 5 M Al(OTF)3 electrolyte. The as-assembled aluminum ion battery enables high initial discharge capacity of 370.4 mAh g–1 at 30 mA g–1, favorable stability with low irreversible capacity loss, and enhanced safety. Further, the mechanism is intensively elucidated by multiple characterization results, indicative of the Al3+ ions (de)intercalation redox chemistry. Revealed by empirical analyses, the capacity contribution of high-voltage plateau, corresponding to the disproportionation reaction of Mn3+ in an AlxMnO2·nH2O battery system, tends to increase with the increasing electrolyte concentration. Our findings may provide fresh impetus to the rational design of aluminum ion batteries with excellent electrochemical properties.
UR - http://www.scopus.com/inward/record.url?scp=85206806749&partnerID=8YFLogxK
U2 - 10.34133/energymatadv.0117
DO - 10.34133/energymatadv.0117
M3 - Article
AN - SCOPUS:85206806749
SN - 2692-7640
VL - 5
JO - Energy Material Advances
JF - Energy Material Advances
M1 - 0117
ER -