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Face-on-oriented formation of bis(diimino)metal coordination nanosheets on gold electrodes by electrochemical oxidation
Bis(diimino)metal complex nanosheets composed of metal ions and hexaaminobenzene ligands (MHABs) are fascinating two-dimensional materials which have been gaining significant attention as electrode materials and electrocatalysts owing to their electrical conductivities, redox properties, and porous structures obtained by the π-conjugated system and regular metal complex arrangement. Although electrochemical oxidation enables the simple and direct formation of MHABs on electrodes within a couple of minutes only, the obtained MHABs are relatively rough and of low crystallinity. This study investigated the effects of the applied potential during the synthesis, the type of base, and the concentrations of bases and building blocks on the synthesis of NiHAB nanosheets. Optical microscopy (OM), atomic force microscopy (AFM), Raman spectroscopy, X-ray photoelectron spectroscopy (XPS), and grazing-incidence X-ray scattering (GIXS) results revealed that a low oxidation potential, high concentration of the ammonia solution, and low concentration of the building blocks in the reaction solution provided a nanometre-thick NiHAB layer. Under the optimal reaction conditions, NiHAB nanosheets were successfully synthesized in a face-on orientation manner on gold electrodes using electrochemical oxidation methods. Furthermore, the anisotropic electrochemical synthesis of CuHAB was achieved under the optimised conditions. The mechanism of the MHAB growth process with an anisotropic orientation and nanometre thickness was proposed and attributed to the flat adsorption of π-conjugated oligomers composed of bis(diamino)metal moieties in a solution onto an electrode surface and the electrochemical oxidation and deprotonation of the adsorbates on the electrode.
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- 12/03/2024
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- CC BY 3.0 Deed
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Face-on-oriented formation of bis(diimino)metal coordination nanosheets on gold electrodes by electrochemical oxidation.pdf | 3.49 MB | MDR Open |
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Supplementary file.pdf | 2.13 MB | MDR Open |
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