Kang Hui-Ju, Bari Gazi A K M Rafiqul, Lee Tae-Gyu, Khan Tamal Tahsin, Park Jae-Woo, Hwang Hyun Jin, Cho Sung Yong, Jun Young-Si
Department of Advanced Chemicals & Engineering, Chonnam National University, 77 Yongbong-ro, Buk-gu, Gwangju 61186, Korea.
Department of Materials Science and Engineering, Chonnam National University, 77 Yongbong-ro, Buk-gu, Gwangju 61186, Korea.
Nanomaterials (Basel). 2020 Oct 12;10(10):2012. doi: 10.3390/nano10102012.
Rechargeable lithium-sulfur batteries (LSBs) are emerging as some of the most promising next-generation battery alternatives to state-of-the-art lithium-ion batteries (LIBs) due to their high gravimetric energy density, being inexpensive, and having an abundance of elemental sulfur (S). However, one main, well-known drawback of LSBs is the so-called polysulfide shuttling, where the polysulfide dissolves into organic electrolytes from sulfur host materials. Numerous studies have shown the ability of porous carbon as a sulfur host material. Porous carbon can significantly impede polysulfide shuttling and mitigate the insulating passivation layers, such as LiS, owing to its intrinsic high electrical conductivity. This work suggests a scalable and straightforward one-step synthesis method to prepare a unique interconnected microporous and mesoporous carbon framework via salt templating with a eutectic mixture of LiI and KI at 800 °C in an inert atmosphere. The synthesis step used environmentally friendly water as a washing solvent to remove salt from the carbon-salt mixture. When employed as a sulfur host material, the electrode exhibited an excellent capacity of 780 mAh g at 500 mA g and a sulfur loading mass of 2 mg cm with a minor capacity loss of 0.36% per cycle for 100 cycles. This synthesis method of a unique porous carbon structure could provide a new avenue for the development of an electrode with a high retention capacity and high accommodated sulfur for electrochemical energy storage applications.
可充电锂硫电池(LSB)正成为一些最有前景的下一代电池,有望替代最先进的锂离子电池(LIB),因为其具有高重量能量密度、成本低廉且元素硫(S)储量丰富。然而,锂硫电池一个主要的、众所周知的缺点是所谓的多硫化物穿梭效应,即多硫化物从硫主体材料溶解到有机电解质中。大量研究表明多孔碳作为硫主体材料的能力。多孔碳由于其固有的高导电性,能够显著阻碍多硫化物穿梭,并减轻诸如LiS等绝缘钝化层的影响。这项工作提出了一种可扩展且直接的一步合成方法,通过在惰性气氛中于800℃下用LiI和KI的低共熔混合物进行盐模板化,制备独特的相互连接的微孔和介孔碳骨架。合成步骤使用环境友好的水作为洗涤溶剂,从碳 - 盐混合物中去除盐分。当用作硫主体材料时,该电极在500 mA g的电流密度和2 mg cm的硫负载量下表现出780 mAh g的优异容量,并且在100次循环中每次循环的容量损失仅为0.36%。这种独特多孔碳结构的合成方法可为开发具有高保持容量和高容纳硫量的电极用于电化学储能应用提供一条新途径。