Liu Chaozheng, Xu Wangwang, Zhang Lei, Zhang Daotong, Xu Weina, Liao Xiaobin, Chen Weimin, Cao Yizhong, Li Mei-Chun, Mei Changtong, Zhao Kangning
Co-Innovation Center of Efficient Processing and Utilization of Forest Resources, College of Materials Science and Engineering, Nanjing Forestry University, Nanjing, 210000, China.
Mechanical & Industrial Engineering Department, Louisiana State University, Baton Rouge, LA-70803, USA.
Angew Chem Int Ed Engl. 2024 Feb 26;63(9):e202318063. doi: 10.1002/anie.202318063. Epub 2024 Jan 23.
The aqueous zinc-ion battery is promising as grid scale energy storage device, but hindered by the instable electrode/electrolyte interface. Herein, we report the lean-water ionic liquid electrolyte for aqueous zinc metal batteries. The lean-water ionic liquid electrolyte creates the hydrophobic tri-layer interface assembled by first two layers of hydrophobic OTF and EMIM and third layer of loosely attached water, beyond the classical Gouy-Chapman-Stern theory based electrochemical double layer. By taking advantage of the hydrophobic tri-layer interface, the lean-water ionic liquid electrolyte enables a wide electrochemical working window (2.93 V) with relatively high zinc ion conductivity (17.3 mS/cm). Furthermore, the anion crowding interface facilitates the OTF decomposition chemistry to create the mechanically graded solid electrolyte interface layer to simultaneously suppress the dendrite formation and maintain the mechanical stability. In this way, the lean-water based ionic liquid electrolyte realizes the ultralong cyclability of over 10000 cycles at 20 A/g and at practical condition of N/P ratio of 1.5, the cumulated areal capacity reach 1.8 Ah/cm , which outperforms the state-of-the-art zinc metal battery performance. Our work highlights the importance of the stable electrode/electrolyte interface stability, which would be practical for building high energy grid scale zinc-ion battery.
水系锌离子电池作为一种用于电网规模储能的装置具有广阔前景,但却受到不稳定的电极/电解质界面的阻碍。在此,我们报道了一种用于水系锌金属电池的贫水离子液体电解质。这种贫水离子液体电解质形成了由前两层疏水性的OTF和EMIM以及第三层松散附着的水组装而成的疏水三层界面,超越了基于经典 Gouy-Chapman-Stern理论的电化学双层。通过利用疏水三层界面,贫水离子液体电解质实现了较宽的电化学工作窗口(2.93 V)以及相对较高的锌离子电导率(17.3 mS/cm)。此外,阴离子聚集界面促进了OTF分解反应,从而形成机械梯度固体电解质界面层,以同时抑制枝晶形成并保持机械稳定性。通过这种方式,基于贫水的离子液体电解质在20 A/g的电流密度下实现了超过10000次循环的超长循环稳定性,并且在N/P比为1.5的实际条件下,累积面积容量达到1.8 Ah/cm²,这超过了目前最先进的锌金属电池性能。我们的工作突出了稳定的电极/电解质界面稳定性的重要性,这对于构建高能量电网规模的锌离子电池具有实际意义。