Manganese tetra-pyridyl-porphyrins are found to self-organize in an ordered monolayer on graphene. Moreover, post deposition of cobalt ad-atoms steers the geometric reordering of the layer, yielding the formation of a self-assembled bimetallic network, where both Mn and Co are tetra-coordinated with nitrogen. While manganese shifts from Mn(ii) towards the +2/+3 oxidation state range, depending on the local Co concentration and not reaching a full Mn(iii) configuration, pyridinic cobalt is stabilized in the rarer +1 oxidation state. The actual geometric and electronic structures of the framework are defined by lateral interactions, dominating over the weaker network-graphene bonding.
Single atom coordination in a manganese–cobalt bi-metallic framework on graphene: geometric and electronic structures / Baronio, Stefania; De Col, Michela; Yadav, Asha; Roondhe, Basant; Mischke, Valentin; Resel, Olga; Bidoggia, Davide; Namar, Alessandro; Vinogradov, Nikolay; Scardamaglia, Mattia; Valvidares, Manuel; Gargiani, Pierluigi; Cinchetti, Mirko; Zamborlini, Giovanni; Giannozzi, Paolo; Vesselli, Erik. - In: NANOSCALE. - ISSN 2040-3364. - (2025), pp. 16946-16963. [10.1039/d5nr01383f]
Single atom coordination in a manganese–cobalt bi-metallic framework on graphene: geometric and electronic structures
Baronio, Stefania;De Col, Michela;Bidoggia, Davide;Namar, Alessandro;Scardamaglia, Mattia;Cinchetti, Mirko;Zamborlini, Giovanni;Giannozzi, Paolo
;Vesselli, Erik
2025-01-01
Abstract
Manganese tetra-pyridyl-porphyrins are found to self-organize in an ordered monolayer on graphene. Moreover, post deposition of cobalt ad-atoms steers the geometric reordering of the layer, yielding the formation of a self-assembled bimetallic network, where both Mn and Co are tetra-coordinated with nitrogen. While manganese shifts from Mn(ii) towards the +2/+3 oxidation state range, depending on the local Co concentration and not reaching a full Mn(iii) configuration, pyridinic cobalt is stabilized in the rarer +1 oxidation state. The actual geometric and electronic structures of the framework are defined by lateral interactions, dominating over the weaker network-graphene bonding.| File | Dimensione | Formato | |
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