Laser-Induced Printing of Next Generation Silicon-Graphite Anodes for the Development of Advanced Lithium-Ion Batteries

Abstract

The expansion of renewable causing a rising demand for affordable and improved energy storage systems. Lithium-ion batteries (LIB) are one of the most promising technologies for this achievement, with further improvements to be made in terms of new materials and an advanced electrode architecture. As a new generation electrode material to be included in LIB, silicon is in the focus of the today’s investigations. Silicon offers one order of magnitude higher theoretical specific capacity (3579 mAh/g) compared to the state-of-the-art material graphite (372 mAh/g). However, during lithiation of silicon a volume expansion of up to 300 % takes place. Due to the huge volume expansion tremendous mechanical degradation of the anode occurs, resulting in a drop in capacity and a shorten lifetime.Laser induced forward transfer (LIFT) is applied in this study as printing technology to develop enhanced silicon-graphite electrode compositions and electrode architectures. LIFT was performed using a pulsed nanosecond UV-laser with a maximum power of 10 W and repetitions rate of up to 30 kHz. For the LIFT process of anodes, polyacrylic acid (PAA) is used as binder, in contrast to the polyvinylidene fluoride (PVDF) binder commonly used for LIFT assisted printing of electrodes. PAA is a more appropriate binder for silicon-containing anodes than PVDF. In addition, also a customized architecture using subtractive and additive laser process techniques is introduced for an increase in lifetime of batteries containing silicon-based electrodes. For this purpose, graphite electrodes were structured with an ultrashort pulse laser with pattern widths of 100 µm. Subsequently, silicon rich slurry was printed into the patterns to increase the areal capacity. The as-prepared electrodes have spatially separated graphite and silicon regions. The respective electrodes were electrochemically cycled in half-cells and charged at different C-rates up to 5C to investigate their lithiation capability. After the rate capability analysis, the cells were cycled at C/2 to investigate the long-term degradation. The cells with the printed electrodes were cycled for more than 450 cycles with a capacity fade of 5 %. At their end-of-life, the cells were analyzed post-mortem. Finally, full-cells were assembled with cathodes containing NMC 622 as the active cathode material. Subsequently to the cell priming a lifetime analysis was performed at a C-rate of C/2 and cycle stability as well as lithium loss during cycling were evaluated.