Yi-Tong Zhang , Jin-Xin Xue , Rui Wang , Si-Xin Jia , Jian-Jun Zhou , Lin Li
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引用次数: 0
Abstract
Silicon (Si) is a promising substitute for graphite anode due to the high theoretical specific capacity (4200 mAh g−1). However, too large volume change exists during the lithiation/delithiation process. Composite anode, prepared by mixing Si with graphite, can realize higher specific capacity than graphite and much better cycle performance than Si anode. However, the capacity decay caused by pulverization of Si particles is still a great challenge. Here, a cross-linkable binder rich in nitrile, carboxyl and hydroxyl groups is designed for composite silicon-graphite (Si-C) anode. The nitrile and hydroxyl groups can be in situ cross-linked in the batteries through Ritter reaction. The cross-linked binder has excellent resilience and good adhesion to the active materials and current collector. The cycle performance of the cell with cross-linked binder is much better than the counterpart. Scanning electron microscopy results of the cycled Si-C anode show that the cross-linked binder can suppress the volume expansion and pulverization. Moreover, the investigation with X-ray photoelectronic spectrum and density function theory calculation demonstrate that the decomposition of ester solvent and LiPF6 on Si anode has been mitigated and more stable SEI film is formed on the Si-C anode. Our strategy of in situ cross-linking binder in the batteries has provided a feasible way for designing the next generation of silicon-based anodes with higher specific capacity and longer cycling life.
硅(Si)具有很高的理论比容量(4200 mAh g-1),因此很有希望成为石墨负极的替代品。然而,在石化/脱硅过程中体积变化太大。通过将硅与石墨混合制备的复合负极可以实现比石墨更高的比容量,循环性能也比硅负极好得多。然而,硅颗粒粉化导致的容量衰减仍然是一个巨大的挑战。在此,我们设计了一种富含腈基、羧基和羟基的可交联粘合剂,用于硅-石墨(Si-C)复合负极。腈基和羟基可通过里特反应在电池中原位交联。交联后的粘合剂具有优异的回弹性,与活性材料和集流器的粘附性良好。交联粘合剂电池的循环性能远远优于同类电池。循环硅-碳阳极的扫描电子显微镜结果表明,交联粘结剂可抑制体积膨胀和粉化。此外,X 射线光电子能谱研究和密度函数理论计算表明,酯溶剂和 LiPF6 在硅阳极上的分解得到了缓解,Si-C 阳极上形成了更稳定的 SEI 膜。我们在电池中原位交联粘合剂的策略为设计比容量更大、循环寿命更长的下一代硅基阳极提供了一种可行的方法。
期刊介绍:
Giant is an interdisciplinary title focusing on fundamental and applied macromolecular science spanning all chemistry, physics, biology, and materials aspects of the field in the broadest sense. Key areas covered include macromolecular chemistry, supramolecular assembly, multiscale and multifunctional materials, organic-inorganic hybrid materials, biophysics, biomimetics and surface science. Core topics range from developments in synthesis, characterisation and assembly towards creating uniformly sized precision macromolecules with tailored properties, to the design and assembly of nanostructured materials in multiple dimensions, and further to the study of smart or living designer materials with tuneable multiscale properties.