Nicholas Chisholm

Room-Temperature Quantum Bit Memory Exceeding One Second

Extending Quantum Memory Practical applications in quantum communication and quantum computation require the building blocks—quantum bits and quantum memory—to be sufficiently robust and long-lived to allow for manipulation and storage (see the Perspective by Boehme and McCarney). Steger et al. (p. 1280) demonstrate that the nuclear spins of 31P impurities in an almost isotopically pure sample of 28Si can have a coherence time of as long as 192 seconds at a temperature of ∼1.7 K. In diamond at room temperature, Maurer et al. (p. 1283) show that a spin-based qubit system comprised of an isotopic impurity (13C) in the vicinity of a color defect (a nitrogen-vacancy center) could be manipulated to have a coherence time exceeding one second. Such lifetimes promise to make spin-based architectures feasible building blocks for quantum information science. Defects in diamond can be operated as quantum memories at room temperature. Stable quantum bits, capable both of storing quantum information for macroscopic time scales and of integration inside small portable devices, are an essential building block for an array of potential applications. We demonstrate high-fidelity control of a solid-state qubit, which preserves its polarization for several minutes and features coherence lifetimes exceeding 1 second at room temperature. The qubit consists of a single 13C nuclear spin in the vicinity of a nitrogen-vacancy color center within an isotopically purified diamond crystal. The long qubit memory time was achieved via a technique involving dissipative decoupling of the single nuclear spin from its local environment. The versatility, robustness, and potential scalability of this system may allow for new applications in quantum information science.

All-Optical Sensing of a Single-Molecule Electron Spin

We demonstrate an all-optical method for magnetic sensing of individual molecules in ambient conditions at room temperature. Our approach is based on shallow nitrogen-vacancy (NV) centers near the surface of a diamond crystal, which we use to detect single paramagnetic molecules covalently attached to the diamond surface. The manipulation and readout of the NV centers is all-optical and provides a sensitive probe of the magnetic field fluctuations stemming from the dynamics of the electronic spins of the attached molecules. As a specific example, we demonstrate detection of a single paramagnetic molecule containing a gadolinium (Gd(3+)) ion. We confirm single-molecule resolution using optical fluorescence and atomic force microscopy to colocalize one NV center and one Gd(3+)-containing molecule. Possible applications include nanoscale and in vivo magnetic spectroscopy and imaging of individual molecules.