Du Wenjia, Zhang Zhenyu, Iacoviello Francesco, Zhou Shangwei, Owen Rhodri E, Jervis Rhodri, Brett Dan J L, Shearing Paul R
Electrochemical Innovation Lab, Department of Chemical Engineering, University College London, London WC1E 7JE, U.K.
The Faraday Institution, Quad One, Harwell Science and Innovation Campus, Didcot OX11 0RA, U.K.
ACS Appl Mater Interfaces. 2023 Mar 9;15(11):14196-205. doi: 10.1021/acsami.2c19895.
The zinc-ion battery is one of the promising candidates for next-generation energy storage devices beyond lithium technology due to the earth's abundance of Zn materials and their high volumetric energy density (5855 mA h cm). To date, the formation of Zn dendrites during charge-discharge cycling still hinders the practical application of zinc-ion batteries. It is, therefore, crucial to understand the formation mechanism of the zinc dendritic structure before effectively suppressing its growth. Here, the application of operando digital optical microscopy and in situ lab-based X-ray computed tomography (X-ray CT) is demonstrated to probe and quantify the morphologies of zinc electrodeposition/dissolution under multiple galvanostatic plating/stripping conditions in symmetric Zn||Zn cells. With the combined microscopy approaches, we directly observed the dynamic nucleation and subsequent growth of Zn deposits, the heterogeneous transportation of charged clusters/particles, and the evolution of 'dead' Zn particles via partial dissolution. Zn electrodeposition at the early stage is mainly attributed to activation, while the subsequent dendrite growth is driven by diffusion. The high current not only facilitates the formation of sharp dendrites with a larger mean curvature at their tips but also leads to dendritic tip splitting and the creation of a hyper-branching morphology. This approach offers a direct opportunity to characterize dendrite formation in batteries with a metal anode in the laboratory.
由于地球上锌材料储量丰富且具有高体积能量密度(5855 mA h cm),锌离子电池是超越锂技术的下一代储能设备的有前景的候选者之一。迄今为止,充放电循环过程中锌枝晶的形成仍然阻碍着锌离子电池的实际应用。因此,在有效抑制锌枝晶生长之前,了解其形成机制至关重要。在此,展示了操作数显光学显微镜和基于实验室的原位X射线计算机断层扫描(X射线CT)的应用,以探测和量化对称Zn||Zn电池中多种恒电流电镀/剥离条件下锌电沉积/溶解的形态。通过组合显微镜方法,我们直接观察到锌沉积物的动态成核和随后的生长、带电簇/颗粒的非均匀传输以及“死”锌颗粒通过部分溶解的演变。早期的锌电沉积主要归因于活化,而随后的枝晶生长由扩散驱动。高电流不仅促进了尖端具有更大平均曲率的尖锐枝晶的形成,还导致枝晶尖端分裂并形成超分支形态。这种方法为在实验室中表征具有金属阳极的电池中的枝晶形成提供了直接机会。