Department of Chemistry, University of Waterloo, Waterloo, Ontario N2L 3G1, Canada.
J Phys Chem Lett. 2023 Jun 22;14(24):5586-5591. doi: 10.1021/acs.jpclett.3c01042. Epub 2023 Jun 12.
Fullerene cages allow the confinement of single molecules and the construction of molecular assemblies whose properties strongly differ from those of free species. In this work, we employ the density-matrix renormalization group method to show that chains of fullerenes filled with polar molecules (LiF, HF, and HO) can form dipole-ordered quantum phases. In symmetry broken environments, these ordered phases are ferroelectric, a property that makes them promising candidates for quantum devices. We demonstrate that for a given guest molecule, the occurrence of these quantum phases can be enforced or influenced either by changing the effective electric dipole moment or by isotopic substitution. In the ordered phase, all systems under consideration are characterized by universal behavior that depends only on the ratio of the effective electric dipole and of the rotational constant. A phase diagram is derived, and further molecules are proposed as candidates for dipole-ordered endofullerene chains.
富勒烯笼允许单个分子的限制和分子组装的构建,其性质与游离物种有很大的不同。在这项工作中,我们采用密度矩阵重整化群方法表明,充满极性分子(LiF、HF 和 HO)的富勒烯链可以形成偶极有序的量子相。在对称破缺环境中,这些有序相是铁电的,这一性质使它们成为量子器件的有前途的候选者。我们证明,对于给定的客体分子,通过改变有效电偶极矩或同位素取代,可以强制或影响这些量子相的出现。在有序相中,所考虑的所有系统都具有仅取决于有效电偶极矩与旋转常数之比的通用行为。得出了一个相图,并进一步提出了作为偶极有序endo 富勒烯链候选物的分子。