标题:Manipulating Polysulfide Conversion with Strongly Coupled Fe3O4 and Nitrogen Doped Carbon for Stable and High Capacity Lithium-Sulfur Batteries
作者:Lu, Ke; Zhang, Hong; Gao, Siyuan; Ma, Houyi; Chen, Junzheng; Cheng, Yingwen
作者机构:[Lu, Ke; Gao, Siyuan; Cheng, Yingwen] Northern Illinois Univ, Dept Chem & Biochem, De Kalb, IL 60115 USA.; [Zhang, Hong; Ma, Houyi] Shandong Univ, S 更多
通讯作者:Cheng, YW;Ma, HY
通讯作者地址:[Cheng, YW]Northern Illinois Univ, Dept Chem & Biochem, De Kalb, IL 60115 USA;[Ma, HY]Shandong Univ, Sch Chem & Chem Engn, Key Lab Colloid & Interface 更多
来源:ADVANCED FUNCTIONAL MATERIALS
出版年:2019
卷:29
期:4
DOI:10.1002/adfm.201807309
关键词:high sulfur loading; iron oxide; Li-S battery; strong coupling
摘要:Li-S batteries are among the most promising energy storage technologies but their commercialization faces substantial challenges, largely due to difficulties in controlling their reaction pathways under practical conditions. Here, the synthesis of strongly coupled Fe3O4 and N-doped carbon directly in flexible carbon cloth is demonstrated, as well as their novel use for hosting sulfur with outstanding performance for Li-S batteries. It is discovered that the synergistic effects of Fe3O4 and N-carbon bring strong adsorption toward lithium polysulfide, and ensure nearly complete conversion of short-chain polysulfide to Li2S during discharge. The Li2S solids generated on these novel hosts are extremely reactive and can be readily charged back to S without a noticeable overpotential. The critical roles of Fe3O4 and N-doped carbon are studied and direct correlations are established between their surface concentration/crystallinity and the Li2S4 to Li2S conversion capacity. This novel manipulation of polysulfide conversion allows to fabricate freestanding and flexible sulfur cathodes that deliver a specific capacity of 1316 mAh g(-1) at 0.1C and stable cycling for 1000 cycles at 0.2C under a high sulfur loading of approximate to 4.7 mg cm(-2).
收录类别:SCOPUS;SCIE
Scopus被引频次:1
资源类型:期刊论文
原文链接:https://www.scopus.com/inward/record.uri?eid=2-s2.0-85057822161&doi=10.1002%2fadfm.201807309&partnerID=40&md5=2ba1316f8b653e42f6219488c34062b9
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