Liang Xiaoxiao, Zhang Binjie, Ahmad Niaz, Yu Xianzhe, Zeng Chaoyuan, Dong Qinxi, Yang Wen
School of Chemistry and Chemical Engineering, Key Laboratory of Ministry of Education for Advanced Materials in Tropical Island Resources, Collaborative Innovation Center of Ecological Civilization, Hainan University, No 58, Renmin Avenue, Haikou, 570228, China.
Key Laboratory of Cluster Science of Ministry of Education, Beijing Key Laboratory of Photoelectronic/Electrophotonic Conversion Materials, School of Chemistry, Chemical Engineering Beijing Institute of Technology, Beijing, 100081, P. R. China.
ChemSusChem. 2025 Feb 16;18(4):e202401768. doi: 10.1002/cssc.202401768. Epub 2024 Nov 10.
Silicon anodes have been considered one of the most promising candidates for Li-ion batteries due to their high theoretical specific capacity. However, the practical use of silicon anodes is impeded due to side reactions and volumetric change (from 300~400%) charge/discharge process. Binders played a crucial role in Li-ion batteries by effectively mitigating the stress resulting from the volumetric expansion in silicon-based anodes. Herein, we developed a mechanically stable polyimide binder PI-CF that introduced trifluoromethyl and hydroxyl groups for commercial microparticular silicon anodes. With a highest Young's modulus of ~921.1 MPa, the binder presented the maximum resilience during the charging and discharging of Micro-Si, integrating the morphology, and reducing the degree to which the electrode disrupted ion and electric pathways. Moreover, -OH and -CF groups of the binder could potentially interact with oxide layer at the surface of silicon through hydron bonds, and thereby results in a cross-linking network to improve interface stability during cycling. The as-prepared PI-CF binder with excellent intrinsic mechanical and electro-rich groups stabilizes the electrode structure and facilitates fast Li transportation. Consequently, micro-Si anode delivered initial specific capacity of 1838 mAh g (at 0.6 A g), and at high mass (Si loading = 0.78 mg cm) these was retained about 1219 mAh g after 330 cycles (only -0.061% capacity reduction per cycle).
由于具有高理论比容量,硅阳极被认为是锂离子电池最有前途的候选材料之一。然而,由于副反应和体积变化(300%至400%)的充放电过程,硅阳极的实际应用受到阻碍。粘结剂在锂离子电池中起着关键作用,它能有效减轻硅基阳极中体积膨胀产生的应力。在此,我们开发了一种机械稳定的聚酰亚胺粘结剂PI-CF,它为商用微颗粒硅阳极引入了三氟甲基和羟基。该粘结剂的最高杨氏模量约为921.1MPa,在微硅的充放电过程中表现出最大的回弹性,整合了形貌,并降低了电极破坏离子和电子传导路径的程度。此外,粘结剂的-OH和-CF基团可能通过氢键与硅表面的氧化层相互作用,从而形成交联网络,提高循环过程中的界面稳定性。所制备的具有优异固有机械性能和富电子基团的PI-CF粘结剂稳定了电极结构,促进了锂的快速传输。因此,微硅阳极在0.6A g时的初始比容量为1838mAh g,在高质量(硅负载量=0.78mg cm)下,330次循环后仍保持约1219mAh g(每循环容量仅降低0.061%)。