DRIFT study of deuterium-exchanged graphite oxide

石墨烯 氧化物 氧化石墨 化学工程 阴极 纳米颗粒 材料科学 硫黄 石墨 法拉第效率 纳米复合材料 多硫化物 电化学 化学 纳米技术 电解质 复合材料 电极 物理化学 工程类 冶金
作者
Tamás Szabó,Ottó Berkesi,Imre Dékány
出处
期刊:Carbon [Elsevier BV]
卷期号:43 (15): 3186-3189 被引量:460
标识
DOI:10.1016/j.carbon.2005.07.013
摘要

Reduced graphene oxide (rGO/polycation/sulfur) composites are promising cathode materials for Li-S battery applications because homogeneously dispersed sulfur nano/micro clusters in suitable carbon hosts enable remarkable cycle life for Li-S battery cells. New, benign and economic synthesis methods based only on aqueous colloidal dispersions are demanded for achieving high dispersity grade of sulfur within the carbon host. Colloidal interactions leading to heteroaggregation between carbonaceous lamellae and polycation-modified sulphur nanoparticles at ambient conditions in water are foreseen to afford nanocomposite cathodes, which maintain excellent electrochemical performance.Hydrophilic sulfur nanoparticles (SNPs) were coated by low doses of polycation (PDDA) until reaching the isoelectric point (IEP), and in high dose to achieve charge reversal. Streaming potential titrations were performed to reveal appropriate mass ratios of PPDA, SNP and GO. Positively charged SNPs formed stable heteroaggregated structures with GO, and were employed to fabricate rGO/polycation/sulphur cathodes.Charge reversal characteristics of SNPs, polycation and GO were characterized quantitatively and mass ratios of PDDA to SNP beyond IEP were found to mediate attractive interactions leading to rapid heteroaggregation between SNPs and GO and also alleviate lithium polysulfide migration. The composite cathode showed an initial discharge capacity of 522 mAhg−1 at 0.2C rate with an excellent capacity retention of 91.4 % and coulombic efficiency of 98.5% after 100 charge–discharge cycles.
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