Garapati Meenakshi Seshadhri, Sundara Ramaprabhu
Alternative Energy and Nanotechnology Laboratory (AENL), Nano Functional Materials Technology Center (NFMTC), Department of Physics, Indian Institute of Technology Madras, Chennai 600036, India.
ACS Omega. 2020 Aug 27;5(35):22379-22388. doi: 10.1021/acsomega.0c02778. eCollection 2020 Sep 8.
Lithium-sulfur (Li-S) batteries are the potential candidates for developing high-energy-density electric vehicles. However, poor electrical conductivity of sulfur/discharged products, low active material utilization, shuttle mechanism, and poor cycle life remain the major challenges for the development of Li-S batteries. Herein, we report the nitrogen-doped highly porous carbon (NC) with interconnected pores as the sulfur host (NC-S), which is synthesized by a facile one-step process without using any template and activation agents. The highly interconnected porous structure of NC can accommodate a high amount of sulfur loading and provide space for sulfur volume expansion during redox reactions. Besides, to mitigate the lithium polysulfide dissolution and shuttle mechanism, metallic and polar magnesium diboride (MgB) is used as an interlayer. Consequently, the NC-S/MgB cathode delivers higher specific capacity, rate capability, and excellent cyclic stability than the NC-S cathode and bulk sulfur cathode with MgB interlayer. The lithium polysulfide (LPS) adsorption test shows that MgB has strong chemisorption toward lithium polysulfides, which can inhibit the dissolution of LPS into the electrolyte and minimizes the shuttle effect. The dynamic electrochemical impedance spectroscopy analysis investigates the electrochemical reaction kinetics of the NC-S/MgB cathode during the charging and discharging processes. Overall, this work demonstrates that the synergy between the nitrogen-doped porous carbon-sulfur host and polar metallic MgB improves the performance of the Li-S battery, which is beneficial for the development of high-energy-density batteries for the future.
锂硫(Li-S)电池是开发高能量密度电动汽车的潜在候选者。然而,硫/放电产物的导电性差、活性材料利用率低、穿梭机制以及循环寿命短仍然是锂硫电池发展的主要挑战。在此,我们报道了一种具有相互连通孔隙的氮掺杂高孔隙率碳(NC)作为硫宿主(NC-S),它是通过一种简便的一步法合成的,无需使用任何模板和活化剂。NC高度相互连通的多孔结构可以容纳大量的硫负载,并为氧化还原反应过程中硫的体积膨胀提供空间。此外,为了减轻多硫化锂的溶解和穿梭机制,金属性和极性的二硼化镁(MgB)被用作中间层。因此,与具有MgB中间层的NC-S阴极和块状硫阴极相比,NC-S/MgB阴极具有更高的比容量、倍率性能和优异的循环稳定性。多硫化锂(LPS)吸附测试表明,MgB对多硫化锂具有很强的化学吸附作用,这可以抑制LPS溶解到电解液中,并使穿梭效应最小化。动态电化学阻抗谱分析研究了NC-S/MgB阴极在充放电过程中的电化学反应动力学。总体而言,这项工作表明氮掺杂多孔碳硫宿主与极性金属MgB之间的协同作用提高了锂硫电池的性能,这有利于未来高能量密度电池的发展。