Jiang De-en, Dai Sheng
Chemical Sciences Division and Center for Nanophase Materials Sciences, Oak Ridge National Laboratory, Oak Ridge, Tennessee 37831, USA.
J Phys Chem A. 2008 Jan 17;112(2):332-5. doi: 10.1021/jp0765087. Epub 2007 Dec 18.
We examine the electronic ground states of acenes with different numbers of fused benzene rings (up to 40) by using first principles density functional theory. Their properties are compared with those of infinite polyacene. We find that the ground state of acenes that consist of more than seven fused benzene rings is an antiferromagnetic (in other words, open-shell singlet) state, and we show that this singlet is not necessarily a diradical, because the spatially separated magnetizations for the spin-up and spin-down electrons increase with the size of the acene. For example, our results indicate that there are about four spin-up electrons localized at one zigzag edge of 20-acene. The reason that both acenes and polyacene have the antiferromagnetic ground state is due to the zigzag-shaped boundaries, which cause pi-electrons to localize and form spin orders at the edges. Both wider graphene ribbons and large rectangular-shaped polycyclic aromatic hydrocarbons have been shown to share this antiferromagnetic ground state. Therefore, we demonstrate that the pi-electronic structures of higher acenes and polyacene are still dictated by the zigzag edges, and our results provide a consistent description of their electronic ground state.
我们运用第一性原理密度泛函理论研究了具有不同苯环稠合数(至多40个)的并苯的电子基态。将它们的性质与无限长聚并苯的性质进行了比较。我们发现,由七个以上苯环稠合而成的并苯的基态是反铁磁(换句话说,开壳层单重态)态,并且我们表明这种单重态不一定是双自由基,因为自旋向上和自旋向下电子的空间分离磁矩会随着并苯尺寸的增加而增大。例如,我们的结果表明,在20并苯的一个锯齿形边缘处约有四个自旋向上的电子局域化。并苯和聚并苯都具有反铁磁基态的原因是锯齿形边界,这会导致π电子在边缘处局域化并形成自旋有序。较宽的石墨烯带和大型矩形多环芳烃都已被证明具有这种反铁磁基态。因此,我们证明了高级并苯和聚并苯的π电子结构仍然由锯齿形边缘决定,并且我们的结果为它们的电子基态提供了一致的描述。