Du Jingwei, Zhang Jiaxu, Chu Xingyuan, Xu Hao, Zhao Yirong, Löffler Markus, Wang Gang, Li Dongqi, Guo Quanquan, Morag Ahiud, Du Jie, Zou Jianxin, Mikhailova Daria, Mazánek Vlastimil, Sofer Zdeněk, Feng Xinliang, Yu Minghao
Faculty of Chemistry and Food Chemistry & Center for Advancing Electronics Dresden (cfaed), Technische Universität Dresden, Dresden, 01062, Germany.
Physical Chemistry, Technische Universität Dresden, Zellescher Weg 19, Dresden, 01069, Germany.
Nat Commun. 2025 Apr 18;16(1):3707. doi: 10.1038/s41467-025-58859-3.
Aqueous zinc batteries are attractive for large-scale energy storage due to their inherent safety and sustainability. However, their widespread application has been constrained by limited energy density, underscoring a high demand of advanced cathodes with large capacity and high redox potential. Here, we report a reversible high-capacity six-electron-conversion Se cathode undergoing a ZnSe↔Se↔SeCl reaction, with Br/Br redox couple effectively stabilizes the Zn | |Se cell. This Se conversion, initiated in a ZnCl-based hydrogel electrolyte, presents rapid capacity decay (from 1937.3 to 394.1 mAh g after only 50 cycles at 0.5 A g) primarily due to the dissolution of SeCl and its subsequent migration to the Zn anode, resulting in dead Se passivation. To address this, we incorporate the Br/Br redox couple into the Zn | |Se cell by introducing bromide salt as an electrolyte additive. The generated Br species acts as a dead-Se revitalizer by reacting with Se passivation on the Zn anode and regenerating active Se for the cathode reaction. Consequently, the cycling stability of the Zn | |Se cell is improved, maintaining 1246.8 mAh g after 50 cycles. Moreover, the Zn | |Se cell exhibits a specific capacity of 2077.6 mAh g and specific energy of 404.2 Wh kg based on the overall cell reaction.
水系锌电池因其固有的安全性和可持续性而在大规模储能领域具有吸引力。然而,其广泛应用受到能量密度有限的限制,这凸显了对具有大容量和高氧化还原电位的先进阴极的高需求。在此,我们报道了一种可逆的高容量六电子转换硒阴极,其经历ZnSe↔Se↔SeCl反应,Br/Br氧化还原对有效地稳定了Zn || Se电池。这种硒转换在基于ZnCl的水凝胶电解质中引发,主要由于SeCl的溶解及其随后向锌阳极的迁移,导致死硒钝化,从而呈现出快速的容量衰减(在0.5 A g下仅50次循环后,从1937.3降至394.1 mAh g)。为了解决这个问题,我们通过引入溴化物盐作为电解质添加剂,将Br/Br氧化还原对引入Zn || Se电池中。生成的Br物种通过与锌阳极上的硒钝化反应并再生用于阴极反应的活性硒,起到死硒活化剂的作用。因此,Zn || Se电池的循环稳定性得到改善,在50次循环后保持1246.8 mAh g。此外,基于整个电池反应,Zn || Se电池表现出2077.6 mAh g的比容量和404.2 Wh kg的比能量。