Kawade Ujjwala V, Kadam Sunil R, Kulkarni Milind V, Kale Bharat B
Centre for Materials for Electronics Technology (C-MET), Ministry of Electronics and Information Technology (MeitY) Panchavati Pune 411008 India
Ben-Gurion University of the Negev, Department of Chemistry Beer-Sheva Israel.
Nanoscale Adv. 2020 Jan 6;2(2):823-832. doi: 10.1039/c9na00727j. eCollection 2020 Feb 18.
Significant efforts continue to be directed toward the construction of anode materials with high specific capacity and long cycling stability for lithium-ion batteries (LIBs). In this context, silicon is preferred due to its high capacity even though it has a problem of excessive volume expansion during electrochemical reactions as well as poor cyclability due to a reduction in conductivity. Hence, the hybridization of silicon with suitable materials could be a promising approach to overcome the abovementioned problems. Herein, we demonstrate the uniform decoration of nickel oxide (NiO) nanoparticles (15-20 nm) on silicon nanosheets using bis(cyclopentadienyl) nickel(ii) (CHNi) at low temperatures, taking advantage of the presence of two unpaired electrons in an antibonding orbital in the cyclopentadienyl group. The formation and growth mechanism are discussed in detail. The electrochemical study of the nanocomposite revealed an initial delithiation capacity of 2507 mA h g with a reversible capacity of 2162 mA h g, having 86% retention and better cycling stability for up to 500 cycles. At the optimum concentration, NiO nanoparticles facilitate Li-ion adsorption, which in turn accelerates the transport of Li-ions to active sites of silicon. The Warburg coefficient and Li-ion diffusion at the electrodes confirm the enhancement in the charge transfer process at the electrode/electrolyte interface with NiO nanoparticles. Further, the NiO nanoparticles with uniform distribution suppress the agglomeration of Si nanosheets and provide sufficient space to accommodate a volume change in Si during cycling, which also reduces the diffusion path length of the Li-ions. It also helps to strengthen the mechanical stability, which might be helpful in preventing the cracking of silicon due to volume expansion and maintains the Li-ion transport pathway of the active material, resulting in enhanced cycling stability. Due to the synergic effect between NiO nanoparticles and Si sheets, the nanocomposite delivers high reversible capacity.
人们仍在付出巨大努力来构建用于锂离子电池(LIBs)的具有高比容量和长循环稳定性的负极材料。在这种背景下,硅因其高容量而成为首选,尽管它在电化学反应过程中存在体积过度膨胀的问题,并且由于导电性降低导致循环性能较差。因此,将硅与合适的材料进行杂化可能是克服上述问题的一种有前景的方法。在此,我们利用环戊二烯基中反键轨道上两个未成对电子的存在,在低温下使用双(环戊二烯基)镍(II)(CHNi)在硅纳米片上均匀装饰氧化镍(NiO)纳米颗粒(15 - 20纳米)。详细讨论了其形成和生长机制。对该纳米复合材料的电化学研究表明,其初始脱锂容量为2507 mA h g,可逆容量为2162 mA h g,保留率为86%,并且在高达500次循环中具有更好的循环稳定性。在最佳浓度下,NiO纳米颗粒促进锂离子吸附,这反过来又加速了锂离子向硅活性位点的传输。Warburg系数和电极处的锂离子扩散证实了NiO纳米颗粒增强了电极/电解质界面处的电荷转移过程。此外,分布均匀的NiO纳米颗粒抑制了硅纳米片的团聚,并提供了足够的空间来适应循环过程中硅的体积变化,这也缩短了锂离子的扩散路径长度。它还有助于增强机械稳定性,这可能有助于防止硅因体积膨胀而开裂,并维持活性材料的锂离子传输路径,从而提高循环稳定性。由于NiO纳米颗粒与硅片之间的协同效应,该纳米复合材料具有高可逆容量。