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Przemyslaw Gawel

Publications and source records attributed to Przemyslaw Gawel.

2 recordsLinked to original sources

Memristive Switches in Rigid Conjugated Single-Molecule Junctions

Voltage-driven memristive switching has been reported in molecular junctions, yet its microscopic origin often remains elusive. Here, we study three rigid OPE-like derivatives that lack an obvious internal switching pathway using mechanically controlled break junctions (MCBJs) and observe non-volatile, bistable hysteretic IV characteristics at cryogenic temperature. We introduce a quantitative analysis workflow that classifies memristive IVs, clusters the two conductance states, and extracts switching features and stability metrics from repeated measurements at fixed displacement. While all molecules exhibit memristive behavior, stability and hysteresis reproducibility depend strongly on anchoring and connectivity: the linear biphenyl backbone with thiolate (SAc) anchoring shows the most reproducible, predominantly field-driven hysteresis, whereas the meta-phenyl variant with thioether (SMe) anchoring is dominated by stochastic, current-driven events. The resulting conductance statistics point to an extrinsic, mechanically mediated origin involving contact rearrangements, multi-molecule transport, blinking (open-closed) contacts, injection-point shifts, and $π$-$π$-stacking dimerization.

cond-mat.mes-hall↗

An sp-hybridized molecular carbon allotrope, cyclo[18]carbon

Carbon allotropes built from rings of two-coordinate atoms, known as cyclo[n]carbons, have fascinated chemists for many years, but until now they could not be isolated or structurally characterized, due to their high reactivity. We generated cyclo[18]carbon (C18) using atom manipulation on bilayer NaCl on Cu(111) at 5 Kelvin by eliminating carbon monoxide from a cyclocarbon oxide molecule C24O6. Characterization of cyclo[18]carbon by high-resolution atomic force microscopy revealed a polyynic structure with defined positions of alternating triple and single bonds. The high reactivity of cyclocarbon and cyclocarbon oxides allows covalent coupling between molecules to be induced by atom manipulation, opening an avenue for the synthesis of other carbon allotropes and carbon-rich materials from the coalescence of cyclocarbon molecules.

physics.chem-ph↗