0000000000012473

AUTHOR

Valentin Diez-cabanes

0000-0002-6234-2749

Iron’s Wake: The Performance of Quantum Mechanical-Derived Versus General-Purpose Force Fields Tested on a Luminescent Iron Complex

Recently synthetized iron complexes have achieved long-lived excited states and stabilities which are comparable, or even superior, to their ruthenium analogues, thus representing an eco-friendly and cheaper alternative to those materials based on rare metals. Most of computational tools which could help unravel the origin of this large efficiency rely on ab-initio methods which are not able, however, to capture the nanosecond time scale underlying these photophysical processes and the influence of their realistic environment. Therefore, it exists an urgent need of developing new low-cost, but still accurate enough, computational methodologies capable to deal with the steady-state and trans…

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Photomodulation of Two-Dimensional Self-Assembly of Azobenzene-Hexa-peri-hexabenzocoronene-Azobenzene Triads

International audience; Achieving exquisite control over self-assembly of functional polycyclic aromatic hydrocarbons (PAH) and nanographene (NG) is essential for their exploitation as active elements in (nano)technological applications. In the framework of our effort to leverage their functional complexity, we designed and synthesized two hexa-peri-hexabenzocoronene (HBC) triads, pAHA and oAHA, decorated with two light-responsive azobenzene moieties at the pseudo-para and ortho positions, respectively. Their photoisomerization in solution is demonstrated by UV–vis absorption. 1H NMR measurements of oAHA suggested 23% of Z-form can be obtained at a photostationary state with UV irradiation …

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Reversible switching of the Au(111) work function by near infrared irradiation with a bistable SAM based on a radical donor–acceptor dyad

We describe the modification of the work function (WF) of Au(111) upon deposition of self-assembled monolayers (SAMs) with two donor–acceptor (D–A) systems, one based on a ferrocene-polychlorotriphenylmethyl radical (Fc–PTM) dyad and another on its non-radical dyad analogue. Kelvin Probe Force Microscopy (KPFM) has been used to measure the changes in the Contact Potential Difference (CPD) between the tip and the SAM under application of a cycling sweep of direct current (DC) voltage bias. These measurements showed that both SAMs exhibit a hysteretic behaviour in their WF changes. Interestingly, the hysteresis loop of the radical SAM is notably reduced when irradiated with NIR light, which w…

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