Department of Chemistry, School of Natural Science, ‡School of Energy and Chemical Engineering, and §School of Materials Science and Engineering, Ulsan National Institute of Science and Technology (UNIST) , Ulsan, 689-798, South Korea.
ACS Appl Mater Interfaces. 2014 Oct 22;6(20):18001-7. doi: 10.1021/am504854x. Epub 2014 Oct 1.
This work demonstrates the design, synthesis, characterization, and study of the electrochemical performance of a novel binder for silicon (Si) anodes in lithium-ion batteries (LIBs). Polymeric binders with three different functional groups, namely, carboxylic acid (COOH), carboxylate (COO(-)), and hydroxyl (OH), in a single polymer backbone have been synthesized and characterized via (1)H NMR and FTIR spectroscopies. A systematic study that involved varying the ratio of the functional groups indicated that a material with an acid-to-alcohol molar ratio of 60:40 showed promise as an efficient binder with an initial columbic efficiency of 89%. This exceptional performance is attributed to the strong adhesion of the binder to the silicon surface and to cross-linking between carboxyl and hydroxyl functional groups, which minimize the disintegration of the Si anode structure during the large volume expansion of the lithiated Si nanoparticle. Polymers with multiple functional groups can serve as practical alternative binders for the Si anodes of LIBs, resulting in higher capacities with less capacity fade.
这项工作展示了一种新型锂离子电池 (LIB) 硅 (Si) 负极用聚合物粘结剂的设计、合成、表征和电化学性能研究。通过 (1)H NMR 和 FTIR 光谱学,合成并表征了具有三种不同官能团(羧酸 (COOH)、羧酸盐 (COO(-)) 和羟基 (OH))的单一聚合物主链的聚合物粘结剂。系统的研究涉及改变官能团的比例,结果表明,酸醇摩尔比为 60:40 的材料具有作为高效粘结剂的潜力,初始库仑效率为 89%。这种优异的性能归因于粘结剂与硅表面的强附着力以及羧基和羟基官能团之间的交联,这最大限度地减少了锂化硅纳米颗粒的大体积膨胀过程中 Si 阳极结构的解体。具有多种官能团的聚合物可以作为 LIBs 的 Si 阳极的实用替代粘结剂,从而实现更高的容量和更小的容量衰减。