阴极
材料科学
电化学
电解质
电池(电)
镁
电极
分析化学(期刊)
化学工程
冶金
化学
色谱法
工程类
物理化学
功率(物理)
物理
量子力学
作者
Jiaxi Zhang,Hui Liu,Jiefeng Huang,Ying Liu,Hongjie Fang,Qian Zhang,Xuehua He,Juemin Song,Zheng Li,Xiaochang Xu,Kun Yu
标识
DOI:10.1149/1945-7111/ac694b
摘要
A binder-free AgCl@Ag (SPL-A) cathode was prepared via a facile one-step synthesis by the in situ growth of AgCl active material on the surface of Ag foil substrate. Compared with the AgCl cathode (SPL-B) prepared by the traditional smelting-rolling method, the coarse-grained particulates of AgCl in AgCl@Ag cathode facilitated the permeation of the electrolyte. In addition, it exhibited a preferred growth orientation of the (111), (222), and (311) crystal planes to reduce the charge transfer resistance. The electrochemical behaviors of the optimized SPL-A-24 cathode (prepared with reaction time of 24 h) and the SPL-B cathode were also compared. The galvanostatic discharge results showed that SPL-A-24 cathode had a more positive electrode potential than SPL-B cathode (−0.06 V vs −0.19 V at 50 mA cm −2 ). Moreover, SPL-A cathode exhibited a stable discharge process that SPL-B cathode could not achieve at 100 mA cm −2 and 250 mA cm −2 . The magnesium seawater-activated battery assembled with SPL-A-24 cathode displayed a shorter time to reach the voltage plateau (0.2 s), a higher maximum discharge voltage (1.69 V), a larger specific power (255.5 mWh g −1 ), and higher specific capacity (167.7 mAh g −1 ) at the discharge current density of 50 mA cm −2 .
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