Liu Hengshuo, Sun Yongxin, Yang Yutian, Yang Jie, Zhang Dongdong, Chanajaree Rungroj, Wu Xiang, Zhang Xinyu, Qin Jiaqian, Cao Jin
School of Materials Science and Engineering, Shenyang University of Technology, Shenyang 110870, China.
Hubei Provincial Collaborative Innovation Center for New Energy Microgrid, College of Electrical Engineering & New Energy, China Three Gorges University, Yichang, Hubei 443002, China.
ACS Appl Mater Interfaces. 2024 Aug 28;16(34):44747-44755. doi: 10.1021/acsami.4c07645. Epub 2024 Aug 19.
The reconsideration of aqueous zinc-ion batteries (ZIBs) has been motivated by the attractive zinc metal, which stands out for its high theoretical capacity and cost efficiency. Nonetheless, detrimental side reactions triggered by the remarkable reactivity of HO molecules and rampant dendrite growth significantly compromise the stability of the zinc metal anode. Herein, a novel approach was proposed by leveraging the unique properties of acrylamide (AM) molecules to increase the driving force for nucleation and parasitic reactions. Combined with experimental data and theoretical simulations, it is demonstrated that the incorporation of AM additive can reconstruct the solvation shell around Zn and reduce the number of active HO molecules, thereby effectively reducing the HO molecule decomposition. Consequently, the Zn//Zn symmetric batteries with AM-containing ZnSO electrolytes can attain excellent long-term performances over 2000 h at 1 mA cm and nearly 500 h at 10 mA cm. The Zn//VO full batteries still display improved cycling performances and a high initial discharging capacity of 227 mA h g at 3 A g compared to the ZnSO electrolyte. This electrolyte optimization strategy offers new insights for achieving long-term ZIBs and advances the progress of ZIBs in energy storage.
水系锌离子电池(ZIBs)的重新受到关注,是因为具有吸引力的锌金属,它因其高理论容量和成本效益而脱颖而出。尽管如此,由HO分子的显著反应性引发的有害副反应和猖獗的枝晶生长,严重损害了锌金属阳极的稳定性。在此,通过利用丙烯酰胺(AM)分子的独特性质,提出了一种新方法,以增加成核驱动力和寄生反应。结合实验数据和理论模拟表明,加入AM添加剂可以重构Zn周围的溶剂化壳层,减少活性HO分子的数量,从而有效减少HO分子的分解。因此,含AM的ZnSO电解质的Zn//Zn对称电池在1 mA cm下可实现超过2000 h的优异长期性能,在10 mA cm下可实现近500 h的优异长期性能。与ZnSO电解质相比,Zn//VO全电池在3 A g下仍表现出改善的循环性能和227 mA h g的高初始放电容量。这种电解质优化策略为实现长期稳定的ZIBs提供了新的见解,并推动了ZIBs在储能领域的进展。