TY - JOUR
T1 - Inhibiting interfacial side reactions via constructing a hydrophilic separator toward durable and fast Zn storage
AU - Shen, Jiasen
AU - Zhang, Kai
AU - Yu, Caiyan
AU - Li, Shijia
AU - Huang, Ren
AU - Sun, Caiyun
AU - Chen, Bingbing
AU - Yang, Hui Ying
AU - Yan, Dong
AU - Bai, Ying
N1 - Publisher Copyright:
© 2025
PY - 2025/5
Y1 - 2025/5
N2 - Aqueous Zn-ion batteries have garnered considerable attention ascribed to the cost-effectiveness, high safety and environmental sustainability. However, the cycling life is severely restricted primarily due to H2O-induced side reactions. Herein, the interfacial side reactions are significantly restrained via fixing H2O molecules within a smartly designed hydrophilic separator. Consequently, the durable and fast Zn storage performance is not only remarkably achieved, but the effects of hydrophilic separator on inhibiting interfacial side reactions are also comprehensively revealed. First, the interfacial H2O molecules can be anchored in the designed hydrophilic separator through a hydrogen bonding between hydroxyl groups and H2O molecules, effectively decreasing the moisture content at the electrode-electrolyte interfaces, thereby significantly inhibiting interfacial side reactions. Second, desolvation process of hydrated Zn ions is prominently enhanced when passing through the hydrophilic separator, in favor of boosting kinetics performances. As a result, the as-designed hydrophilic separator enables symmetric cells with a long lifespan (2000 h at 10 mA cm−2), as well as full cells with fast-charging (183.2 mAh g−1 at 20 A g−1) and stable-cycling capabilities (81.26 % retention after 5000 cycles). This study illustrates how hydroxyl groups inhibit interfacial side reactions and provides insights for developing other advanced separators in aqueous batteries.
AB - Aqueous Zn-ion batteries have garnered considerable attention ascribed to the cost-effectiveness, high safety and environmental sustainability. However, the cycling life is severely restricted primarily due to H2O-induced side reactions. Herein, the interfacial side reactions are significantly restrained via fixing H2O molecules within a smartly designed hydrophilic separator. Consequently, the durable and fast Zn storage performance is not only remarkably achieved, but the effects of hydrophilic separator on inhibiting interfacial side reactions are also comprehensively revealed. First, the interfacial H2O molecules can be anchored in the designed hydrophilic separator through a hydrogen bonding between hydroxyl groups and H2O molecules, effectively decreasing the moisture content at the electrode-electrolyte interfaces, thereby significantly inhibiting interfacial side reactions. Second, desolvation process of hydrated Zn ions is prominently enhanced when passing through the hydrophilic separator, in favor of boosting kinetics performances. As a result, the as-designed hydrophilic separator enables symmetric cells with a long lifespan (2000 h at 10 mA cm−2), as well as full cells with fast-charging (183.2 mAh g−1 at 20 A g−1) and stable-cycling capabilities (81.26 % retention after 5000 cycles). This study illustrates how hydroxyl groups inhibit interfacial side reactions and provides insights for developing other advanced separators in aqueous batteries.
KW - Aqueous Zn-ion battery
KW - Hydrophilic separator
KW - Hydroxyl group
KW - Interfacial side reaction
UR - http://www.scopus.com/inward/record.url?scp=105003993909&partnerID=8YFLogxK
U2 - 10.1016/j.ensm.2025.104292
DO - 10.1016/j.ensm.2025.104292
M3 - 文章
AN - SCOPUS:105003993909
SN - 2405-8297
VL - 78
JO - Energy Storage Materials
JF - Energy Storage Materials
M1 - 104292
ER -