Liu Wei, Yang Shenshen, Fan Dongsheng, Wu Yang, Zhang Jingbo, Lu Yaozong, Fu Linping
School of Material Science and Engineering, Henan University of Science and Technology, Luoyang 471023, China.
Collaborative Innovation Center for New Materials and Advanced Processing Technologies of Nonferrous Metals, Luoyang 471023, China.
ACS Omega. 2024 Feb 16;9(8):9792-9802. doi: 10.1021/acsomega.3c10031. eCollection 2024 Feb 27.
Molybdenum disulfide shows promise as an anode material for lithium-ion batteries. However, its commercial potential has been constrained due to the poor conductivity and significant volume expansion during the charge/discharge cycles. To address these issues, in this study, N-doped MoS/C composites (NMC) were prepared via an enhanced hydrothermal method, using ammonium molybdate and thiourea as molybdenum and sulfur sources, respectively. Polyethylene glycol 400 (PEG400) and polyvinylpyrrolidone (PVP) were added in the hydrothermal procedure as soft template surfactants and nitrogen/carbon sources. The crystal structure, morphology, elemental composition, and surface valence state of the N-doped MoS/C composites were characterized by X-ray diffraction (XRD), field emission scanning electron microscopy (FESEM), high-resolution transmission electron microscopy (HRTEM), and X-ray photoelectron spectroscopy (XPS), respectively. The results indicate that the NMC prepared by this method are spherical particles with a nanoflower-like structure composed of MoS flakes, having an average particle size of about 500 nm. XPS analysis shows the existence of C and N elements in the samples as C-N, C-C, and pyrrolic N. As anodes for LIBs, the NMC without annealing deliver an initial discharge capacity of 548.2 mAh·g at a current density of 500 mA·g. However, this capacity decays in the following cycles with a discharge capacity of 66.4 mAh·g and a capacity retention rate of only 12% after 50 cycles. In contrast, the electrochemical properties of the counterparts are enhanced after annealing, which exhibits an initial discharge capacity of 575.9 mAh·g and an ultimate discharge capacity of 669.2 mAh·g after 70 cycles. The capacity retention rate decreases initially but later increases and elevated afterward to reach 116% at the 70th cycle, indicating an improvement in charge-discharge performance. The specimens after annealing have a smaller impedance, which indicates better charge transport and lithium-ion diffusion performance.
二硫化钼作为锂离子电池的负极材料展现出了潜力。然而,由于其导电性差以及在充放电循环过程中显著的体积膨胀,其商业潜力受到了限制。为了解决这些问题,在本研究中,通过一种改进的水热法制备了氮掺杂的MoS/C复合材料(NMC),分别使用钼酸铵和硫脲作为钼源和硫源。在水热过程中加入聚乙二醇400(PEG400)和聚乙烯吡咯烷酮(PVP)作为软模板表面活性剂以及氮/碳源。分别通过X射线衍射(XRD)、场发射扫描电子显微镜(FESEM)、高分辨率透射电子显微镜(HRTEM)和X射线光电子能谱(XPS)对氮掺杂的MoS/C复合材料的晶体结构、形貌、元素组成和表面价态进行了表征。结果表明,通过该方法制备的NMC是由MoS薄片组成的具有纳米花状结构的球形颗粒,平均粒径约为500nm。XPS分析表明样品中存在作为C-N、C-C和吡咯氮形式的C和N元素。作为锂离子电池的负极,未退火的NMC在电流密度为500mA·g时的初始放电容量为548.2mAh·g。然而,该容量在随后的循环中衰减,50次循环后的放电容量为66.4mAh·g,容量保持率仅为12%。相比之下,退火后的对应物的电化学性能得到了增强,其初始放电容量为575.9mAh·g,70次循环后的最终放电容量为669.2mAh·g。容量保持率最初下降,但随后上升,在第70次循环时升至116%,表明充放电性能有所改善。退火后的样品具有较小的阻抗,这表明其电荷传输和锂离子扩散性能更好。