Control of single electron spins constitutes one of the most promising platforms for spintronics, quantum sensing, and quantum information processing. Utilizing single molecular magnets as their hosts establishes an interesting framework since their molecular structure is highly flexible and chemistry-based large-scale synthesis directly provides a way toward scalability. Here, we demonstrate coherent spin manipulation of single molecules on a surface, which we control individually using a scanning tunneling microscope in combination with electron spin resonance. We previously found that iron phthalocyanine (FePc) molecules form a spin-1/2 system when placed on an insulating thin film of magnesium oxide (MgO). Performing Rabi oscillation and Hahn echo measurements, we show that the FePc spin can be coherently manipulated with a phase coherence time T₂^Echo of several hundreds of nanoseconds. Tunneling current-dependent measurements demonstrate that interaction with the tunneling electrons is the dominating source of decoherence. In addition, we perform Hahn echo measurements on small self-assembled arrays of FePc molecules. We show that, despite additional intermolecular magnetic coupling, spin resonance and T₂^Echo are much less perturbed by T₁ spin flip events of neighboring spins than by the tunneling current. This will potentially allow for individual addressable molecular spins in self-assemblies and with application for quantum information processing.

Individual electron spins in solids are promising candidates for quantum science and technology, where bottom-up assembly of a quantum device with atomically precise couplings has long been envisioned. Here, we realized atom-by-atom construction, coherent operations, and readout of coupled electron-spin qubits using a scanning tunneling microscope. To enable the coherent control of “remote” qubits that are outside of the tunnel junction, we complemented each electron spin with a local magnetic field gradient from a nearby single-atom magnet. Readout was achieved by using a sensor qubit in the tunnel junction and implementing pulsed double electron spin resonance. Fast single-, two-, and three-qubit operations were thereby demonstrated in an all-electrical fashion. Our angstrom-scale qubit platform may enable quantum functionalities using electron spin arrays built atom by atom on a surface.

We investigated spin-1/2 hydrogenated titanium (Ti) atoms on MgO using scanning tunneling microscopy (STM) combined with electron spin resonance (ESR) in vector magnetic fields. Rotating external magnetic fields, we observed rather drastic changes in both amplitude and frequency of resonance signals for single Ti atoms. While the variation of ESR amplitudes reflects the effects of the spin polarization of a magnetic tip and local magnetic fields created by the interaction between the tip and Ti, the change of resonance frequencies shows the anisotropy of $g$ values for Ti atoms. Using the Ti atoms at the low-symmetry bridge adsorption site of the MgO lattice allowed for identifying the $g$ values in all three spatial directions. Multiplet calculations confirmed the origin of this anisotropy as the spin-orbit coupling induced effects of crystal. Our results show the capability of single atomic spins as a sensor to probe magnetic surroundings and highlight the precision of ESR-STM to identify the single atom's spin states in a solid-state environment.