The electrolyte filling process of battery cells is one of the time-critical bottlenecks in cell production. Wetting is of particular importance here, since only completely wetted electrode sections are working. In order to accelerate and facilitate this process, the authors of this study developed a method to significantly increase the wettability of graphite-based anodes by a laser surface modification using low energy nanosecond laser pulses. The anode surface microstructure was evaluated by means of white-light interferometry and scanning electron microscopy. The assessment of wettability was done by drop test and capillary rise test of the liquid electrolyte. The results show that there is a predominantly selective ablation process for laser energy inputs below 2 J/m by which the graphite active material remains unaffected and the binder material is decomposed. The observed increase in surface roughness correlates with the increasing wettability. Investigations using Raman spectroscopy showed that laser treatment leads to a damage on the crystalline structure of the graphite particle surface. However, treating an entire anode including 6 wt% binder and conductive carbon black has shown that the overall amorphous content of the anodes surface can be reduced by 32% through treating the surface with a laser energy of 1.29 J/m. Up to that point, which is the resulting parameter range for the selective process, it is possible to ablate the amorphous binder and carbon black phase coevally exposing graphite particles while keeping their crystalline structure. Exceeding that range, ablation of the whole anode composite dominates and amorphization of the graphite surface occurs. The electrode’s capacity was tested on half-cells in coin cell format. For the whole laser parameter range investigated, the anodes capacity matches the mass loss caused by laser ablation. No additional capacity loss was observed due to amorphization of the exterior graphite particle’s surface.
Perforation of lithium-ion battery electrodes has recently become an increasing interest in science and industry. Perforated electrodes have shown improved electrochemical properties compared to conventional, nonperforated electrodes. It has been demonstrated that through perforation, the fast-charging capability and the lifetime of these batteries can be significantly improved. The electrodes for lithium-ion batteries consist of a copper foil onto which the electrode material is applied as a porous layer. This layer is mainly composed of active material particles, which are bound together by a binder phase. Here, synthetic graphite was used as an active material. Up to now, it has been shown that an advantageous and precise perforation geometry can be produced by ultrashort laser pulse ablation. Since the ablation volumes during perforation of the porous electrode material with ultrashort laser pulses are unusually high compared to solids, this work investigates the parameter dependency on the ablation mechanisms in detail. For this purpose, in particular, single-pulse ablation was investigated with respect to the ablation thresholds at different pulse durations. The pulse durations were varied over a large range from 400 fs to 20 ps. By varying the number of pulses per perforation up to 50 and the single-pulse energy up to 45 μJ, it could be shown that a homogeneous ablation down to the conductor foil through the 63 μm thick active material layer can be achieved.
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