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DOI | 10.1039/c9ee00336c |
Asymmetric allyl-activation of organosulfides for high-energy reversible redox flow batteries | |
Weng G.-M.; Yang B.; Liu C.-Y.; Du G.-Y.; Li E.Y.; Lu Y.-C. | |
发表日期 | 2019 |
ISSN | 1754-5692 |
起始页码 | 2244 |
结束页码 | 2252 |
卷号 | 12期号:7 |
英文摘要 | Organosulfides (R-Sn-R) exhibit a high theoretical capacity and low cost, but suffer from sluggish kinetics and poor reversibility. Here, we demonstrate an effective and universal strategy to improve their redox activity by replacing one organic functional group with an allyl (A) to form asymmetric allyl-substituted organosulfides (R-Sn-A). This promotes the cleavage of the A-S bond owing to facile generation of allyl radials, thereby improving the reduction kinetics and capacity. We verified the formation of asymmetric organosulfides by gas-chromatography-mass spectrometry and show that the allyl-activation strategy is universal to a series of functional groups. We successfully increased the discharge potential (up to 280 mV) and discharge capacity (up to 200%) of the organosulfide compared to its symmetric counterpart. A highly-concentrated liquid electrolyte (5 M) with a volumetric capacity of 224 A h L-1 was realized, demonstrating a substantial improvement in volumetric capacity compared to other reported liquid electrolytes to date. This strategy revitalizes organosulfides for high-energy and low-cost energy storage applications. © The Royal Society of Chemistry 2019. |
语种 | 英语 |
scopus关键词 | Chemical activation; Costs; Electrolytes; Gas chromatography; Mass spectrometry; Redox reactions; Concentrated liquids; Discharge capacities; Discharge potential; Gas chromatography-mass spectrometry; Liquid electrolytes; Organic functional groups; Theoretical capacity; Volumetric capacity; Flow batteries; electrolyte; energy storage; equipment; radical; reaction kinetics; spectrometry |
来源期刊 | Energy and Environmental Science |
文献类型 | 期刊论文 |
条目标识符 | http://gcip.llas.ac.cn/handle/2XKMVOVA/162836 |
作者单位 | Electrochemical Energy and Interfaces Laboratory, Department of Mechanical and Automation Engineering, Chinese University of Hong Kong, Shatin N. T., 999077, Hong Kong; Department of Chemistry, National Taiwan Normal University, No. 88, Tingchow Road, Taipei, 116, Taiwan |
推荐引用方式 GB/T 7714 | Weng G.-M.,Yang B.,Liu C.-Y.,et al. Asymmetric allyl-activation of organosulfides for high-energy reversible redox flow batteries[J],2019,12(7). |
APA | Weng G.-M.,Yang B.,Liu C.-Y.,Du G.-Y.,Li E.Y.,&Lu Y.-C..(2019).Asymmetric allyl-activation of organosulfides for high-energy reversible redox flow batteries.Energy and Environmental Science,12(7). |
MLA | Weng G.-M.,et al."Asymmetric allyl-activation of organosulfides for high-energy reversible redox flow batteries".Energy and Environmental Science 12.7(2019). |
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