溶剂化
材料科学
电化学
电解质
电池(电)
阳极
阴极
有机自由基电池
原电池
氯化亚砜
电化学动力学
锂(药物)
动力学
无机化学
化学工程
氯化物
电极
有机化学
功率(物理)
化学
离子
物理化学
冶金
工程类
热力学
物理
量子力学
细胞
生物化学
内分泌学
医学
作者
Qiuchen Xu,Shitao Geng,Bin Yuan,Meng Liao,Lei Ye,Xiaoju Zhao,Yan Wang,Xiao Zhang,Shuo Wang,Zongtao Qu,Moonsik Han,Zhibin Yang,Yue Gao,Bingjie Wang,Yongfeng Zhou,Huisheng Peng,Hao Sun
标识
DOI:10.1002/adfm.202210343
摘要
Abstract Lithium/thionyl chloride (Li/SOCl 2 ) primary batteries are appealing power solutions because of their remarkable electrochemical performances. However, their mass applications are hindered by the challenges in sustainability, cost and safety concerns owing to the employed Li chemistry. Here, magnesium (Mg) chemistry is shown as a promising alternative through synergistic optimization of electrolyte solvation and electrode reaction kinetics. The first Mg/SOCl 2 primary battery yields surprisingly high specific capacities up to ≈14 000 mAh g −1 at a decent discharge voltage of ≈1.67 V, which outperforms the state‐of‐the‐art Mg‐based primary batteries. In addition, it retains almost 100% of the original capacity after 20‐day reservation. The impressive battery performances are originated from the stabilized MgCl 2 formation on high‐surface‐area carbon cathode and suppressed Mg anode corrosion via the Mg‐induced solvation effect. Mg/SOCl 2 primary batteries are promising candidates for low‐cost and recyclable power supplies, and they thus open new avenues for the development of sustainable battery chemistries.
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