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Torben Steenbock

Publications and source records attributed to Torben Steenbock.

2 recordsLinked to original sources

Superexchange Mechanism in Coupled Triangulenes Forming Spin-1 Chains

We show that the origin of the antiferromagnetic coupling in spin-1 triangulene chains, which were recently synthesized and measured by Mishra et al. Nature 598, 287-292 (2021) originates from a superexchange mechanism. This process, mediated by inter-triangulene states, opens the possibility to control parameters in the effective bilinear-biquadratic spin model. We start from the derivation of an effective tight-binding model for triangulene chains using a combination of tight-binding and Hartree-Fock methods fitted to hybrid density functional theory results. Next, correlation effects are investigated within the configuration interaction method. Our low-energy many-body spectrum for $N_{\rm Tr}=2$ and $N_{\rm Tr}=4$ triangulene chains agree well with the bilinear-biquadratic spin-1 chain antiferromagnetic model when indirect coupling processes, and superexchange coupling between triangulene spins are taken into account.

cond-mat.mtrl-sci

Structural diradical character

A reliable first-principles description of singlet diradical character is essential for predicting nonlinear optical and magnetic properties of molecules. Since diradical and closed-shell electronic structures differ in their distribution of single, double, triple and aromatic bonds, modeling electronic diradical character requires accurate bond-length patterns, in addition to accurate absolute bond lengths. We therefore introduce structural diradical character, which we suggest as an additional measure for comparing first-principles calculations with experimental data. We employ this measure to identify suitable exchange-correlation functionals for predicting the bond length patterns and electronic diradical character of a biscobaltocene with the potential for photoswitchable nonlinear optical activity. Out of four popular approximate exchange-correlation functionals with different exact-exchange admixtures (BP86, TPSS, B3LYP, TPSSh), the two hybrid functionals TPSSh and B3LYP perform best for diradical bond length patterns, with TPSSh being best for the organometallic validation systems and B3LYP for the organic ones. Still, none of the functionals is suitable for correctly describing relative bond lengths across the range of molecules studied, so that none can be recommended for predictive studies of (potential) diradicals without reservation.

physics.comp-ph