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Cu nanoclusters steer the self-assembly of Fe phthalocyanines from a substrate- to a laterally-driven regime

M. Corva et al., ACS Nano 12, 10755 (2018); DOI: 10.1021/acsnano.8b05992


By artificially modifying the potential energy surface that governs the self-assembly of a 2D metallorganic crystal of iron phthalocyanines, we show that it is possible to switch from substrate- to laterallydriven regimes. By exploiting the capability of an ultra-thin alumina film to host metallic nanoparticle seeds, we achieve the tunability of the process, ultimately determined by the average nanocluster size. Long-range self-assembly mechanisms are attractive for applications in the synthesis of novel nanotechnological devices, and our work provides an original contribution to this field.

Ultima modifica il Venerdì, 08 Maggio 2020 20:07