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Charge-state transitions of a single Cu-phthalocyanine molecule adsorbed on an insulating layer of NaCl on Cu(111) are probed by means of alternate charging scanning tunneling microscopy. Real-space imaging of the electronic transitions reveals the Jahn--Teller distortion occurring upon formation of the first and second anionic charge states. The experimental findings are rationalized by a theoretical many-body model which highlights the crucial role played by the substrate. The latter enhances and stabilizes the intrinsic Jahn--Teller distortion of the negatively charged molecule hosting a degenerate pair of single-particle frontier orbitals. Consequently, two excess electrons are found to occupy, in the ground state, the same localized orbital, despite a larger Coulomb repulsion than the one for the competing delocalized electronic configuration. Control over the charging sequence by varying the applied bias voltage is also predicted.

In polarizable materials, electronic charge carriers interact with the surrounding ions, leading to quasiparticle behaviour. The resulting polarons play a central role in many materials properties including electrical transport, optical properties, surface reactivity and magnetoresistance, and polaron properties are typically investigated indirectly through such macroscopic characteristics. Here, noncontact atomic force microscopy (nc-AFM) is used to directly image polarons in Fe2O3 at the single quasiparticle limit. A combination of Kelvin probe force microscopy (KPFM) and kinetic Monte Carlo (KMC) simulations shows that Ti doping dramatically enhances the mobility of electron polarons, and density functional theory (DFT) calculations indicate that a metallic transition state is responsible for the enhancement. In contrast, hole polarons are significantly less mobile and their hopping is hampered further by the introduction of trapping centres.

Understanding and controlling decoherence in open quantum systems is of fundamental interest in science, while achieving long coherence times is critical for quantum information processing. Although great progress was made for individual, isolated systems, and electron spin resonance (ESR) of single spins with nanoscale resolution has been demonstrated, the construction of complex solid-state quantum devices requires ultimately controlling the environment down to atomic scales, as potentially enabled by scanning probe microscopy with its atomic and molecular characterization and manipulation capabilities. Consequently, the recent implementation of ESR in scanning tunneling microscopy (STM) represents a milestone towards this goal and was quickly followed by the demonstration of coherent oscillations, tunable dipolar and exchange couplings and access to nuclear spins with real-space atomic resolution. Atomic manipulation even fueled the ambition to realize first artificial atomic-scale quantum devices. However, the current-based sensing inherent to this method limits coherence times. Here, we demonstrate pump-probe ESR atomic force microscopy detection of electron spin transitions between non-equilibrium triplet states of individual pentacene molecules. Spectra of these transitions exhibit sub-nanoelectronvolt energy resolution, allowing local discrimination of molecules that only differ in their isotopic configuration. Furthermore, the electron spins can be coherently manipulated over tens of microseconds, likely not limited by the detection method but by the molecular properties. Single-molecule ESR atomic force microscopy can be combined with atomic manipulation and characterization, and thereby paves the way for atomically well-defined quantum components with long coherence times and local quantum-sensing experiments., Comment: 28 pages, 3 figures, 4 extended-data figures

In scanning tunneling microscopy (STM) experiments of molecules on insulating films, tunneling through molecular resonances implies transiently charging the molecule. The transition back to the charge ground state by tunneling through the insulating film is crucial, for example, for understanding STM-induced electroluminescence. Here, using STM, we report on the charge-state lifetimes of individual molecules adsorbed on NaCl films of different thicknesses on Cu(111) and Au(111). To that end, we approached the tip to the molecule at resonant tunnel conditions up to a regime where charge transport was limited by tunneling through the NaCl film. The resulting saturation of tunnel current is a direct measure of the molecule's charge-state lifetime, thus providing a means to study charge dynamics and, thereby, exciton dynamics. Comparison of anion and cation lifetimes on different substrates reveals the critical role of the level alignment with the insulator's conduction and valence band, and the metal-insulator interface state.

Controlling selectivity of reactions is a quest in chemistry. Here, we demonstrate reversible and selective bond formation and dissociation promoted by tip-induced reduction-oxidation reactions on a surface. Molecular rearrangements leading to different constitutional isomers are selected by the polarity and magnitude of applied voltage pulses from the tip of a combined scanning tunneling and atomic force microscope. Characterization of voltage dependence of the reactions and determination of reaction rates demonstrate selectivity in constitutional isomerization reactions and provide insight into the underlying mechanisms. With support of density functional theory calculations, we find that the energy landscape of the isomers in different charge states is important to rationalize the selectivity. Tip-induced selective single-molecule reactions increase our understanding of redox chemistry and could lead to novel molecular machines.