Zhan Yi, Buffa Andrea, Yu Linghui, Xu Zhichuan J, Mandler Daniel
School of Materials Science and Engineering, Nanyang Technological University, Singapore, 639798, Singapore.
Campus for Research Excellence and Technological Enterprise (CREATE), Singapore-HUJ Alliance for Research and Enterprise (SHARE), Singapore, 138602, Singapore.
Nanomicro Lett. 2020 Jul 3;12(1):141. doi: 10.1007/s40820-020-00479-1.
Lithium-sulfur batteries (LSBs) are considered as the next generation of advanced rechargeable batteries because of their high energy density. In this study, sulfur and CoS electrocatalyst are deposited on carbon nanotube buckypaper (S/CoS/BP) by a facile electrodeposition method and are used as a binder-free high-performance cathode for LSBs. Elemental sulfur is deposited on buckypaper by electrooxidation of a polysulfide solution (~ S). This approach substantially increased the current and time efficiency of sulfur electrochemical deposition on conductive material for LSBs. S/CoS/BP cathode could deliver an initial discharge capacity as high as 1650 mAh g at 0.1 C, which is close to the theoretical capacity of sulfur. At current rate of 0.5 C, the S/CoS/BP has a capacity of 1420 mAh g at the first cycle and 715 mAh g after 500 cycles with a fading rate of 0.099% per cycle. The high capacity of S/CoS/BP is attributed to both the homogeneous dispersion of nanosized sulfur within BP and the presence of CoS catalyst. The sodium dodecyl sulfate (SDS) pretreatment of BP renders it polarity to bind polysulfides and thus facilitates the good dispersibility of nanosized sulfur within BP. CoS catalyst accelerates the kinetics of polysulfide conversion and reduces the presence of polysulfide in the cathode, which suppresses the polysulfide diffusion to anode, i.e., the shuttle effect. The mitigation of the active material loss improves not only the capacity but also the cyclability of S/CoS/BP.
锂硫电池(LSBs)因其高能量密度而被视为下一代先进的可充电电池。在本研究中,通过简便的电沉积方法将硫和CoS电催化剂沉积在碳纳米管巴基纸上(S/CoS/BP),并用作LSBs的无粘结剂高性能阴极。通过多硫化物溶液(~S)的电氧化将元素硫沉积在巴基纸上。这种方法显著提高了LSBs导电材料上硫电化学沉积的电流和时间效率。S/CoS/BP阴极在0.1 C时可提供高达1650 mAh g的初始放电容量,接近硫的理论容量。在0.5 C的电流速率下,S/CoS/BP在第一个循环时的容量为1420 mAh g,在500次循环后的容量为715 mAh g,每循环衰减率为0.099%。S/CoS/BP的高容量归因于纳米级硫在BP中的均匀分散以及CoS催化剂的存在。BP的十二烷基硫酸钠(SDS)预处理使其具有极性以结合多硫化物,从而促进纳米级硫在BP中的良好分散性。CoS催化剂加速了多硫化物转化的动力学,并减少了阴极中多硫化物 的存在,这抑制了多硫化物向阳极的扩散,即穿梭效应。活性材料损失的减轻不仅提高了S/CoS/BP的容量,还提高了其循环性能。