{"title":"Insight into the improvement of rate capability and cyclability in LiFePO4/polyaniline composite cathode","authors":"Wei-Min Chen, Long Qie, Li-Xia Yuan, Sheng-An Xia, Xian-Luo Hu, Wu-Xing Zhang, Yun-Hui Huang","doi":"10.1016/j.electacta.2010.12.041","DOIUrl":null,"url":null,"abstract":"<div><p>A simple and efficient strategy was employed to enhance high-rate performance for carbon-coated LiFePO<sub>4</sub> (C-LFP) by incorporating with conducting polymer polyaniline (PANI). C-LFP was synthesized via a solid state reaction whereas PANI was formed in situ by chemical oxidative polymerization of aniline with ammonium persulfate as an oxidizer to achieve the C-LFP/PANI composites. Specific capacities as high as 165<!--> <!-->mAh<!--> <!-->g<sup>−1</sup> at 0.2<!--> <!-->C, 133<!--> <!-->mAh<!--> <!-->g<sup>−1</sup> at 7<!--> <!-->C and 123<!--> <!-->mAh<!--> <!-->g<sup>−1</sup> at 10<!--> <!-->C were obtained in C-LFP/7<!--> <!-->wt.% PANI composite. Moreover, the composite exhibits remarkably improved cyclability as compared with the parent C-LFP. The mechanism has been carefully investigated for the improvement in the electrochemical performance. Experimental results show that the charge transfer impedance decreases significantly and the cathode surface becomes much smooth over cycling with modification of conductive PANI. The incorporated PANI can work not only as an additional host for Li<sup>+</sup>-ion insertion/extraction, but also as a binder to modify the electrode surface and a container for electrolyte to penetrate into C-LFP particles.</p></div>","PeriodicalId":305,"journal":{"name":"Electrochimica Acta","volume":"56 6","pages":"Pages 2689-2695"},"PeriodicalIF":5.5000,"publicationDate":"2011-02-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/j.electacta.2010.12.041","citationCount":"74","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Electrochimica Acta","FirstCategoryId":"88","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0013468610016749","RegionNum":3,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"ELECTROCHEMISTRY","Score":null,"Total":0}
引用次数: 74
Abstract
A simple and efficient strategy was employed to enhance high-rate performance for carbon-coated LiFePO4 (C-LFP) by incorporating with conducting polymer polyaniline (PANI). C-LFP was synthesized via a solid state reaction whereas PANI was formed in situ by chemical oxidative polymerization of aniline with ammonium persulfate as an oxidizer to achieve the C-LFP/PANI composites. Specific capacities as high as 165 mAh g−1 at 0.2 C, 133 mAh g−1 at 7 C and 123 mAh g−1 at 10 C were obtained in C-LFP/7 wt.% PANI composite. Moreover, the composite exhibits remarkably improved cyclability as compared with the parent C-LFP. The mechanism has been carefully investigated for the improvement in the electrochemical performance. Experimental results show that the charge transfer impedance decreases significantly and the cathode surface becomes much smooth over cycling with modification of conductive PANI. The incorporated PANI can work not only as an additional host for Li+-ion insertion/extraction, but also as a binder to modify the electrode surface and a container for electrolyte to penetrate into C-LFP particles.
采用一种简单有效的策略,通过与导电聚合物聚苯胺(PANI)结合,提高碳包覆LiFePO4 (C-LFP)的高性能。C-LFP采用固相法合成,聚苯胺采用过硫酸铵作为氧化剂原位化学氧化聚合制备聚苯胺/聚苯胺复合材料。C- lfp /7 wt.% PANI复合材料在0.2 C、7 C和10 C下的比容量分别高达165 mAh g−1、133 mAh g−1和123 mAh g−1。此外,与母体C-LFP相比,复合材料表现出明显改善的循环性。为了提高电化学性能,对其机理进行了细致的研究。实验结果表明,导电聚苯胺改性后的阴极在循环过程中电荷转移阻抗明显降低,阴极表面光滑。加入的聚苯胺不仅可以作为Li+离子插入/提取的附加载体,还可以作为修饰电极表面的粘合剂和电解质渗透到C-LFP颗粒中的容器。
期刊介绍:
Electrochimica Acta is an international journal. It is intended for the publication of both original work and reviews in the field of electrochemistry. Electrochemistry should be interpreted to mean any of the research fields covered by the Divisions of the International Society of Electrochemistry listed below, as well as emerging scientific domains covered by ISE New Topics Committee.