While the nucleation of two-dimensional polymer domains is not initiated by the applied electric field, their depolymerization and subsequent desorption, are a consequence of the change in the polarity of the substrate bias within the area scanned by the STM tip.
A collaborative effort! A rapid method is demonstrated for creating porphyrin-containing single-layered 2D-covalent organic frameworks (s2D-COFs) on a graphite surface. The s2D-COF films, characterized with molecular precision using scanning tunneling microscopy (STM), are used as a cathode for electrochemical CO2 reduction.
Glad to see this collaborative effort on the design and self-assembly of molecular switches on surfaces published.
See our recent publication in Nanoscale on nanopatterning graphite at two different length scales in one step
Enjoy our paper published in J. Am. Chem. Soc. on "Metal Ion and Guest-Mediated Spontaneous Resolution and Solvent-Induced Chiral Symmetry Breaking in Guanine-Based Metallosupramolecular Networks"
We used scanning tunnelling microscopy to follow in real-time, as bonds form and break, molecule by molecule, the birth and growth of 2D dynamic covalent polymers on a solid support immersed in a reactive solution.
We reveal the superior sensing capability of covalently modified graphene layers for ammonia detection
We report on the detection and stabilization of a previously unknown two-dimensional (2D) pseudopolymorph.
We demonstrate spatially resolved multicomponent covalent chemical patterning of single layer graphene using a facile and efficient method.
In this paper, published in Nanoscale, we demonstrate that the ascorbic acid mediated dediazoniation of aryldiazonium salts leads to self-limiting growth of monolayers with high grafting densities