Stability and Electronic Properties of 1D and 2D Ca@C60 Oligomers and Polymers

Yabei Wu, Zhonghao Zhou, Zhiyong Wang
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Abstract

The polymerization of fullerenes is a significant method for obtaining fullerene-based materials that possess intriguing properties. Metallofullerenes, as a notable type of fullerene derivatives, are also capable of undergoing polymerization, potentially resulting in the creation of metallofullerene polymers. However, there is currently limited knowledge regarding the polymerization process of metallofullerenes. In this study, we have selected Ca@C 60 as a representative compound to investigate the polymerization process of metallofullerenes. The objective of this research is to determine whether the polymerization process is energetically favorable and to examine how the electronic properties of the metallofullerene are altered throughout the polymerization process. Ca@C 60 is a unique metallofullerene molecule that exhibits insolubility in common fullerene solvents like toluene and carbon disulfide but is soluble in aniline. This behavior suggests a potential tendency for Ca@C 60 to form oligomers and polymers that resist dissolution. However, the structures and properties of polymerized Ca@C 60 remain unknown. We employed density functional theory calculations to investigate the stability and electronic properties of one-dimensional and two-dimensional Ca@C 60 oligomers and polymers. Our findings indicate that the coalescence of Ca@C 60 monomers is energetically favorable, with a significant contribution from van der Waals interactions between the fullerene cages. The polymerization process of Ca@C 60 also involves the formation of covalent linkages, including four-atom rings and C-C single bonds. The increase in the number of the Ca@C 60 units to three and four in the oligomer leads to a significant decrease in the HOMO-LUMO gap. In the two-dimensional polymerized Ca@C 60, the organization of the monomers closely resembles the spatial configuration of carbon atoms in graphene. With a direct bandgap of 0.22 eV, the polymerized Ca@C 60 holds potential for utilization in optoelectronic devices.
一维和二维 Ca@C60 低聚物和聚合物的稳定性和电子特性
富勒烯的聚合是获得具有奇妙特性的富勒烯基材料的重要方法。金属富勒烯作为富勒烯衍生物的一个重要类型,也能够进行聚合,从而可能产生金属富勒烯聚合物。然而,目前有关金属富勒烯聚合过程的知识还很有限。在本研究中,我们选择了 Ca@C 60 作为研究金属富勒烯聚合过程的代表性化合物。本研究的目的是确定聚合过程在能量上是否有利,并研究在整个聚合过程中金属富勒烯的电子特性是如何改变的。Ca@C 60 是一种独特的金属富勒烯分子,它在甲苯和二硫化碳等常见富勒烯溶剂中表现出不溶性,但可溶于苯胺。这种行为表明,Ca@C 60 有可能形成抗溶解的低聚物和聚合物。然而,聚合 Ca@C 60 的结构和性质仍然未知。我们利用密度泛函理论计算研究了一维和二维 Ca@C 60 低聚物和聚合物的稳定性和电子特性。我们的研究结果表明,Ca@C 60 单体的凝聚在能量上是有利的,其中富勒烯笼之间的范德华相互作用起了重要作用。Ca@C 60 的聚合过程还涉及共价键的形成,包括四原子环和 C-C 单键。低聚物中 Ca@C 60 单元的数量增加到三个和四个后,HOMO-LUMO 间隙显著减小。在二维聚合 Ca@C 60 中,单体的组织结构与石墨烯中碳原子的空间构型非常相似。聚合 Ca@C 60 的直接带隙为 0.22 eV,有望用于光电设备。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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