Ahn Junho, Park Byeongho, Kim Jongsoon, Um Moon-Kwang, Yi Jin Woo, Yoo Jung-Keun
Carbon Composites Department, Korea Institute of Materials Science (KIMS), 797 Changwondaero, Changwon 51508, Republic of Korea.
Department of Energy Science, Sungkyunkwan University, Suwon 440-746, Republic of Korea.
ACS Appl Mater Interfaces. 2021 May 5;13(17):19970-19982. doi: 10.1021/acsami.1c00848. Epub 2021 Apr 21.
Cylindrical-type cells have been widely adopted by major battery and electric vehicle manufacturers owing to their price competitiveness, safety, and easy expandability. However, placement of electrodes at the core of cylindrical cells is currently restricted because of high electrode curvature and the lack of specialized electrodes and electrode materials. Here, we report the realization of highly flexible high-energy-density electrodes (active material loading of >98.4%) that can be used at the cores of cylindrical cells. The improved properties result from the introduction of a multifunctional poly(melamine--formaldehyde) (MF copolymer) additive, which yields a relatively more fluidic and well-dispersed slurry using only 0.08 wt %. MF copolymer-mediated formation of completely wrapped CNT/PVDF networks on LiCoO (LCO) and accompanying contact enhancement between LCO and carbon nanotubes (CNTs) resulted in an increase of electrical and mechanical properties of the two types (composites with or without collectors) of electrodes compared with those of additive-free electrodes. Flexibility tests were carried out by rolling electrodes onto cylinder substrates (diameters of ca. 1 and 10 mm); this process resulted in relatively lower resistance changes of the MF copolymer-containing electrodes than for the reference electrodes. In addition, capacity retention after 100 cycles for cells with and without MF copolymers was approximately 10-20% better for the samples with the MF copolymer than for those without. CNT/PVDF networks with MF copolymers were proven to induce a relatively thin and stable cathode electrolyte interface layer accompanying the chemical bond formation during cycling.
圆柱形电池因其价格竞争力、安全性和易于扩展性,已被各大电池和电动汽车制造商广泛采用。然而,由于电极曲率高以及缺乏专用电极和电极材料,目前圆柱形电池核心部位电极的放置受到限制。在此,我们报告了一种可用于圆柱形电池核心部位的高柔韧性、高能量密度电极(活性材料负载量>98.4%)的实现。性能的提升源于引入了一种多功能聚(三聚氰胺-甲醛)(MF共聚物)添加剂,该添加剂仅使用0.08 wt%就能产生流动性相对更好且分散均匀的浆料。MF共聚物介导在LiCoO(LCO)上形成完全包裹的CNT/PVDF网络,并伴随LCO与碳纳米管(CNTs)之间接触增强,与无添加剂电极相比,两种类型(有或无集流体)电极的电学和力学性能均有所提高。通过将电极卷绕到圆柱形基材(直径约1和10 mm)上进行柔韧性测试;该过程导致含MF共聚物电极的电阻变化相对低于参比电极。此外,含MF共聚物的样品在100次循环后的容量保持率比不含MF共聚物的样品高约10 - 20%。事实证明,含MF共聚物的CNT/PVDF网络在循环过程中伴随化学键形成会诱导出相对较薄且稳定的阴极电解质界面层。