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Issue 43, 2018
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The excess electron in polymer nanocomposites

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We have used ab initio molecular dynamics and density-functional theory (DFT) calculations at the B3LYP/6-31G** level of theory to evaluate the energy and localisation of excess electrons at a number of representative interfaces of polymer nanocomposites. These modelled interfaces are made by combining liquid water and amorphous slabs of polyethylene and silica. The walls of the amorphous silica slabs are built with two surface chemistries: Q4 or fully-dehydroxylated and Q3/Q4 or partially-hydroxylated with a silanol content between 1.62 and 6.86 groups per nm2. Our results indicate that in silica/polyethylene systems an excess electron would sit at the interface with energies between −1.75 eV with no hydroxylation and −0.99 eV with the highest silanol content. However, in the presence of a free water film, the chemistry of the silica surface has a negligible influence on the behaviour of the excess electron. The electron sits preferentially at the water/vapour interface with an energy of minus a few tenths of an eV. We conclude that the moisture content in a wet polymer nanocomposite has a profound influence on the electron trapping behaviour as it produces much lower trapping energies and a higher excess-electron mobility compared to the dry material.

Graphical abstract: The excess electron in polymer nanocomposites

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The article was received on 25 Jul 2018, accepted on 18 Sep 2018 and first published on 29 Oct 2018

Article type: Paper
DOI: 10.1039/C8CP04741C
Phys. Chem. Chem. Phys., 2018,20, 27528-27538
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    The excess electron in polymer nanocomposites

    F. Saiz and N. Quirke, Phys. Chem. Chem. Phys., 2018, 20, 27528
    DOI: 10.1039/C8CP04741C

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