Li Jian, Shen Xixun, Zhao Yanheng, Xu Qunjie
Shanghai Key Laboratory of Materials Protection and Advanced Materials in Electric Power, Shanghai Engineering Research Center of Heat-exchange System and Energy Saving, College of Environmental and Chemical Engineering, Shanghai University of Electric Power, Shanghai 200090, China.
Shanghai Institute of Pollution Control and Ecological Security, Shanghai 200092, China.
Dalton Trans. 2025 Apr 15;54(16):6576-6586. doi: 10.1039/d5dt00084j.
Aqueous zinc-ion batteries are regarded as having the potential for large-scale application owing to their low cost and inherent safety. However, due to the slow kinetics of cathode materials and the suboptimal microstructure, AZIBs often exhibit unsatisfactory stability during actual cycling. The rational design and development of cathode materials possessing high specific capacity and long-cycling stability hold significant importance for the progress of AZIBs. Here, carbon-nanosphere-composited zinc-ion-doped VO (SZVO@C) electrode materials were fabricated through a hydrothermal process with the assistance of sodium dodecyl sulfonate. Under the modulation of surfactants, the SZVO@C electrode exhibits a rose-like cluster structure composed of nanosheets, this confers a more extensive specific surface area, measuring 40.2 m g. Under a current density of 0.5 A g, the SZVO@C electrode exhibits an outstanding specific capacity of 360 mA h g. Moreover, it showcases exceptional cycling stability at 5 A g, retaining an impressive 98% of its capacity even after 2000 cycles. The SZVO@C electrode's remarkable cycling performance can be attributed to two key factors. First, it has an outstanding specific surface area. Second, there is a morphological alteration that occurs during the first charge. The tight bonding between the cathode material and conductive carbon improves electron transfer efficiency and effectively reduces charge transfer resistance. GITT tests show that the SZVO@C electrode has an excellent Zn diffusion coefficient of 1.3 × 10 to 1.52 × 10 cm s, which provides a strong guarantee for its excellent cycling performance. The XPS and XRD examinations unveil the storage mechanism of Zn. During the initial cycle, the SZVO@C electrode forms the new phase ZnVO·HO, and the pristine ZnVO engages in a subsequent reversible cycle along with the new phase. This research work clearly demonstrates that employing surfactants to regulate the microstructure of cathode materials and incorporating carbon materials constitute a potent strategy to enhance the performance.
水系锌离子电池因其低成本和内在安全性而被认为具有大规模应用的潜力。然而,由于正极材料动力学缓慢以及微观结构欠佳,水系锌离子电池在实际循环过程中常常表现出不尽人意的稳定性。合理设计和开发具有高比容量和长循环稳定性的正极材料对于水系锌离子电池的发展至关重要。在此,通过水热法并借助十二烷基磺酸钠制备了碳纳米球复合锌离子掺杂的VO(SZVO@C)电极材料。在表面活性剂的调控下,SZVO@C电极呈现出由纳米片组成的玫瑰状簇结构,这赋予了其更广泛的比表面积,为40.2 m g。在0.5 A g的电流密度下,SZVO@C电极展现出360 mA h g的出色比容量。此外,它在5 A g时表现出卓越的循环稳定性,即使在2000次循环后仍保留其容量的98%。SZVO@C电极出色的循环性能可归因于两个关键因素。首先,它具有出色的比表面积。其次,在首次充电过程中会发生形态变化。正极材料与导电碳之间的紧密结合提高了电子转移效率并有效降低了电荷转移电阻。GITT测试表明,SZVO@C电极具有1.3×10至1.52×10 cm s的优异锌扩散系数,这为其出色的循环性能提供了有力保障。XPS和XRD检测揭示了锌的存储机制。在初始循环期间,SZVO@C电极形成新相ZnVO·HO,原始的ZnVO与新相一起参与随后的可逆循环。这项研究工作清楚地表明,使用表面活性剂来调节正极材料的微观结构并引入碳材料是提高性能的有效策略。