Jagodziński Karol, Boaretto Nicola, Casado Nerea, Martínez-Ibañez María
Centre for Cooperative Research on Alternative Energies (CIC energiGUNE), Basque Research and Technology Alliance (BRTA), 01510 Vitoria-Gasteiz, Spain.
University of the Basque Country (EHU/UPV), Paseo Manuel Lardizabal, 3, 20018 Donostia, Gipuzkoa, Spain.
ACS Appl Polym Mater. 2025 Feb 28;7(5):2973-2985. doi: 10.1021/acsapm.4c03625. eCollection 2025 Mar 14.
The development of high-energy-density lithium-ion batteries (LIBs) is essential for the advancement of electric vehicles and portable electronics. Silicon-rich anodes, with their exceptional theoretical capacity, hold promise for revolutionizing energy storage. However, challenges such as volumetric expansion during cycling hinder their practical use. Ionically conductive binders have been shown to enhance the mechanical stability and cyclability of silicon-based electrodes. Herein, water-soluble binders for silicon anodes were prepared by functionalization of poly(ethylene--maleic anhydride) (PEaMAn) with ion-conducting polyether side chains and hydrolyzation of maleic anhydride at different ratios. Six binders were synthesized and characterized, and their electrochemical performance was evaluated in half-cells. Our results indicate that polyether-functionalized binders significantly reduced the slurry viscosity and thus enhanced electrodes' processability, compared to that of the fully hydrolyzed poly(ethylene--maleic acid) (PEaMAc) binder. However, they also led to poor adhesion to the current collector, faster impedance increase, and capacity decay during cycling as compared to PEaMAc. On the contrary, electrodes with the fully hydrolyzed PEaMAc binder showed strong adhesion to the current collector and superior electrochemical performance, with an initial Coulombic efficiency of 71.3% and delithiation capacities of 2230 mAh g at C/10 and 1190 mAh g at 1C. Moreover, PEaMAc demonstrated significantly better rate performance compared to that of the conventional LiPAA binder, highlighting its potential as a highly effective binder for silicon anodes in lithium-ion batteries.
高能量密度锂离子电池(LIBs)的发展对于电动汽车和便携式电子产品的进步至关重要。富含硅的阳极具有出色的理论容量,有望彻底改变能量存储方式。然而,诸如循环过程中的体积膨胀等挑战阻碍了它们的实际应用。离子导电粘合剂已被证明可以增强硅基电极的机械稳定性和循环性能。在此,通过用离子导电聚醚侧链对聚(乙烯-马来酸酐)(PEaMAn)进行功能化以及在不同比例下对马来酸酐进行水解,制备了用于硅阳极的水溶性粘合剂。合成并表征了六种粘合剂,并在半电池中评估了它们的电化学性能。我们的结果表明,与完全水解的聚(乙烯-马来酸)(PEaMAc)粘合剂相比,聚醚功能化粘合剂显著降低了浆料粘度,从而提高了电极的可加工性。然而,与PEaMAc相比,它们还导致对集流体的粘附性差、阻抗增加更快以及循环过程中的容量衰减。相反,具有完全水解的PEaMAc粘合剂的电极对集流体表现出很强的粘附性和优异的电化学性能,初始库仑效率为71.3%,在C/10时的脱锂容量为2230 mAh/g,在1C时为1190 mAh/g。此外,与传统的LiPAA粘合剂相比,PEaMAc表现出明显更好的倍率性能,突出了其作为锂离子电池中硅阳极高效粘合剂的潜力。