RESUMEN
We report a comparative computational investigation on the first six members of linear poly-C,Si,Ge-acenes (X4n+2H2n+4, X = C,Si,Ge; n = 1, 2, 3, 4, 5, 6). We performed density functional theory (DFT) and time-dependent DFT calculations to compare morphological, electronic, and optical properties. While C-acenes are planar, Si- and Ge-acenes assume a buckled configuration. Electronic properties show similar trends as a function of size for all families. In particular, differently from C-based compounds, in the case of both Si- and Ge-acenes, the excitation energies of the strongest low-lying electronic transition (ß peaks) span the visible region of the spectrum, demonstrating their size tunability. For all families, we assessed the plasmonic character of this transition and found a linear relationship for the wavelength-dependence of the ß peaks as a function of the number of rings. A similar slope of about 56 nm is observed for Si- and Ge-acenes, although the peak positions of the former are located at lower wavelengths. Outcomes of this study are compared with existing theoretical results for 2D lattices and nanoribbons, and experiments where available.
RESUMEN
We report a comparative and systematic computational analysis on the electronic and optical properties of the boron-nitride-made (BN) counterparts of the carbon-made circumacenes. Recently, these planar molecules have attracted interest for applications in the condensed matter physics domain. In particular, we focus on the five first members of this BN-family (from BN-coronene to BN-circumpentacene) presenting a comparison with their carbon analogues. For all the systems investigated, we calculate different electronic properties and the optical absorption spectra, performing all electron Density Functional Theory (DFT) and Time Dependent-DFT (TD-DFT) calculations. In the context of ab initio calculations we select a localized Gaussian basis-set matched with a hybrid exchange-correlation functional. We discuss possible implications of the observed BN cluster properties, which could be an alternative material or complementar as compared to their carbon analogues. In particular, concerning the optical properties, we have found that the main difference between the two families is that the BN molecules absorb in the UV, rather than in the visible as happens for the C-made parents. Moreover, we demonstrate that the electronic and optical observables of the BN clusters are nearly independent of the cluster size in contrast to what happens for their carbonaceous counterparts.