Jörg Wrachtrup

Single dopant atoms or dopant-related defect centers in a solid state matrix provide an attractive platform for quantum simulation of topological states, for quantum computing and communication, due to their potential to realize a scalable architecture compatible with electronic and photonic integrated circuits. The production of such quantum devices calls for deterministic single atom doping techniques because conventional stochastic doping techniques are cannot deliver appropriate architectures. Here, we present the fabrication of arrays of praseodymium color centers in YAG substrates, using a deterministic source of single laser-cooled Pr$^+$ ions. The beam of single Pr$^+$ ions is extracted from a Paul trap and focused down to 30(9) nm. Using a confocal microscope we determine a conversion yield into active color centers up to 50% and realizing a placement accuracy of better than 50 nm.

Identifying weakly coupled nuclear spins around single electron spins is a key step of implementing quantum information processing using coupled electron-nuclei spin systems or sensing like single spin nuclear magnetic resonance detection using diamond defect spins. Dynamical decoupling control of the center electron spin with periodic pulse sequences [e.g., the Carre-Purcell-Meiboom-Gill (CPMG) sequence] has been successfully used to identify single nuclear spins and to resolve structure of nuclear spin clusters. Here, we design a new type of pulse sequences by replacing the repetition unit (a single $π$-pulse) of the CPMG sequence with a group of nonuniformly-spaced $π$-pulses. Using nitrogen-vacancy center system in diamond, we show that the designed pulse sequence improves the resolution of nuclear spin noise spectroscopy, and more information about the surrounding nuclear spins is extracted. The principle of dynamical decoupling design proposed in this paper is useful in many systems (e.g., defect spin qubit in solids, trapped ion and superconducting qubit) for high-resolution noise spectroscopy.