Ren Kaixin, Li Min, Wang Qinghong, Liu Baohua, Sun Chuang, Yuan Boyu, Lai Chao, Jiao Lifang, Wang Chao
School of Chemistry and Materials Science, Jiangsu Normal University, Xuzhou, 221116, Jiangsu, People's Republic of China.
Jiangsu Key Laboratory of Advanced Laser Materials and Devices, School of, Physics and Electronic Engineering, Jiangsu Normal University, Xuzhou, 221116, Jiangsu, People's Republic of China.
Nanomicro Lett. 2024 Feb 15;16(1):117. doi: 10.1007/s40820-023-01310-3.
Zinc ion batteries are considered as potential energy storage devices due to their advantages of low-cost, high-safety, and high theoretical capacity. However, dendrite growth and chemical corrosion occurring on Zn anode limit their commercialization. These problems can be tackled through the optimization of the electrolyte. However, the screening of electrolyte additives using normal electrochemical methods is time-consuming and labor-intensive. Herein, a fast and simple method based on the digital holography is developed. It can realize the in situ monitoring of electrode/electrolyte interface and provide direct information concerning ion concentration evolution of the diffusion layer. It is effective and time-saving in estimating the homogeneity of the deposition layer and predicting the tendency of dendrite growth, thus able to value the applicability of electrolyte additives. The feasibility of this method is further validated by the forecast and evaluation of thioacetamide additive. Based on systematic characterization, it is proved that the introduction of thioacetamide can not only regulate the interficial ion flux to induce dendrite-free Zn deposition, but also construct adsorption molecule layers to inhibit side reactions of Zn anode. Being easy to operate, capable of in situ observation, and able to endure harsh conditions, digital holography method will be a promising approach for the interfacial investigation of other battery systems.
锌离子电池因其低成本、高安全性和高理论容量的优点而被视为潜在的储能设备。然而,锌阳极上发生的枝晶生长和化学腐蚀限制了它们的商业化。这些问题可以通过优化电解质来解决。然而,使用常规电化学方法筛选电解质添加剂既耗时又费力。在此,开发了一种基于数字全息术的快速简便方法。它可以实现电极/电解质界面的原位监测,并提供有关扩散层离子浓度演变的直接信息。在估计沉积层的均匀性和预测枝晶生长趋势方面既有效又省时,从而能够评估电解质添加剂的适用性。通过对硫代乙酰胺添加剂的预测和评估进一步验证了该方法的可行性。基于系统表征,证明硫代乙酰胺的引入不仅可以调节界面离子通量以诱导无枝晶锌沉积,还可以构建吸附分子层以抑制锌阳极的副反应。数字全息术方法操作简便,能够进行原位观察,并且能够承受苛刻条件,将成为用于其他电池系统界面研究的一种有前途的方法。