法拉第效率
水溶液
电解质
材料科学
共晶体系
溶解
阳极
化学工程
储能
电池(电)
电化学
钠
无机化学
电极
合金
化学
有机化学
冶金
热力学
工程类
功率(物理)
物理
物理化学
作者
Tingting Liu,Han Wu,Xiaofan Du,Jinzhi Wang,Zheng Chen,Hao Wang,Jinran Sun,Jian-Jun Zhang,Jiaping Niu,Lishan Yao,Jingwen Zhao,Guanglei Cui
标识
DOI:10.1021/acsami.2c04893
摘要
Aqueous sodium batteries are one of the awaited technologies for large-scale energy storage, but remain poorly rechargeable because of the reactivity issues of water. Here, we present a hydrated eutectic electrolyte featuring a water-locked effect, which is exceptional in that the O-H bond of water is essentially strengthened via weak hydrogen bonding (relative to the original H2O-H2O hydrogen bonds) to low-donor-number anions and ligands. Even without interphase protection, both the anodic and cathodic water electrodecomposition reactions are delayed, extending the aqueous potential window to 3.4 V. Combined with the alleviated electrode dissolution, Na2MnFe(CN)6||NaTi2(PO4)3 batteries deliver a high energy density of ∼80 W h kg-1 at 0.5 C and undergo over 1000 cycles with a 74.5% capacity retention and a 99.4% Coulombic efficiency at 4.2 C. This work may offer a general guide to ultimately exploit the water's innate stability for realizing the promise of aqueous battery technologies.
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