电化学
阳极
电解质
溶解
锌
阴极
沉积(地质)
超级电容器
电流密度
化学工程
材料科学
储能
无机化学
阴极保护
氯化物
化学
电极
冶金
有机化学
功率(物理)
物理
物理化学
量子力学
工程类
古生物学
沉积物
生物
作者
Leandro Nicolás Bengoa,Rosa M. González-Gil,Pedro Gómez‐Romero
标识
DOI:10.1002/celc.202300517
摘要
Abstract As the interest in alternative Li‐based energy storage technologies increased during the last years, zinc emerged as a promising candidate. Despite several advantages over Li, Zn cycling stability is still a major issue. In this article, the use of near‐neutral electrolytes (non‐expensive 2 M ZnSO 4 ) with the addition of different additives (dimethylsulfoxide and tetratethylammonium chloride) is proposed as a solution. The Zn deposition/dissolution electrochemistry has been evaluated and the cycling stability was determined in Zn//Zn symmetric coin‐cells. Hybrid supercapacitors were also assembled and tested in a range of 0.2 V–1.8 V for 2000 cycles, using activated carbon electrodes as cathode and Zn foil as anode. The results show that dimethylsulfoxide strongly inhibits the Zn deposition process, evidenced by a decrease in the cathodic current density, as well as in the dissolution peak. DMSO affects the deposition mechanism, whereas tetratethylammonium chloride reduces the exchange current density, consistent with the adsorption of tetraethylammonium ions on the Zn surface. A synergy between both additives leading to further inhibition of Zn 2+ reduction is observed allowing cycling up to 250 hours for Zn//Zn devices. In addition, the performance of hybrid supercapacitors has also improved showing better capacity and extended cycle life.
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