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Recent experiments have shown that polypropylene (PP) with a small fraction of hydroxyl (-OH) side groups displays a two-fold increase in the dielectric permittivity. It has been suggested that both the -OH groups and trapped water molecules may contribute to the dielectric constant increase. In this first principles computational study, using short polyolefin chains as models of PP, we shed light on the role played by -OH functional groups and the trapped moisture. Our results reveal that the trapped water molecules will inevitably accompany -OH incorporation (due to hydrogen bonding) and that both the -OH groups and water molecules will contribute cooperatively to the increase of the PP dielectric constant. These findings also provide insights into the effects of moisture on other molecularly functionalized materials systems. V C 2013 AIP Publishing LLC [http://dx.

Being in the group with the most diverse set of properties among all in the periodic table, the Group 14 elements (C, Si, Ge, Sn, and Pb) are particularly interesting candidates for structure-property investigation. Motivated by the need to create new insulators for energy storage and electronics applications, we study a few compounds based on Group 14 elements in this work, namely the dihydrides, dichlorides, and difluorides. Using density functional theory (DFT) calculations, we establish patterns in their properties, including favored coordination chemistry, stability, electronic structure, and dielectric behavior. While a coordination number (CN) of 4 is commonly associated with Group 14 elements, there is a significant deviation from it down the group, with CNs as high as 7 and 8 common in Pb. Further, there is an increase in the relative stability of the ?2 oxidation state as opposed to ?4 when we go from C to Pb, a direct consequence of which is the existence of the di-compounds of C and Si as polymers, whereas the compounds of Ge, Sn, and Pb are strictly 3D crystalline solids. The coordination chemistries are further linked with the band gaps and dielectric constants (divided into two components: the electronic part and the ionic part) of these compounds. We also see that the more stable difluorides and dichlorides have large band gaps and small electronic dielectric constants, and most of the Ge and Sn compounds have remarkably large ionic dielectric constants by virtue of having polar and more flexible bonds. The staggering variation in properties displayed by these parent compounds offers opportunities for designing derivative materials with a desired combination of properties.