Nanoscale Magnetism Probed in a Matter-Wave Interferometer.

We explore a wide range of fundamental magnetic phenomena by measuring the dephasing of matter-wave interference fringes upon application of a variable magnetic gradient. The versatility of our interferometric Stern-Gerlach technique enables us to study the magnetic properties of alkali atoms, organic radicals, and fullerenes in the same device, with magnetic moments ranging from a Bohr magneton to less than a nuclear magneton. We find evidence for magnetization of a supersonic beam of organic radicals and, most notably, observe a strong magnetic response of a thermal C_{60} beam consistent with high-temperature atomlike deflection of rotational magnetic moments.

Quantum-assisted diamagnetic deflection of molecules.

We measure the diamagnetic deflection of anthracene and adamantane in a long-baseline matter-wave interferometer. From the nanometer-level deflection we extract the magnetic susceptibilities of the molecules which we compare with calculations and previous results. Adamantane yields an isotropic average mass susceptibility of -8.0 ± 1.1 m3 kg-1, consistent with expectations, while anthracene yields a higher-than-anticipated value of -13.6 ± 1.3 m3 kg-1. We attribute the high anthracene value to the planar aromatic molecule's magnetic anisotropy and partial alignment in the molecular beam, and estimate the magnitude of the effect on the observed deflection.

Matter-wave interference and deflection of tripeptides decorated with fluorinated alkyl chains.

Studies of neutral biomolecules in the gas phase allow for the study of molecular properties in the absence of solvent and charge effects, thus complementing spectroscopic and analytical methods in solution or in ion traps. Some properties, such as the static electronic susceptibility, are best accessed in experiments that act on the motion of the neutral molecules in an electric field. Here, we screen seven peptides for their thermal stability and electron impact ionizability. We identify two tripeptides as sufficiently volatile and thermostable to be evaporated and interfered in the long-baseline universal matter-wave interferometer. Monitoring the deflection of the interferometric molecular nanopattern in a tailored external electric field allows us to measure the static molecular susceptibility of Ala-Trp-Ala and Ala-Ala-Trp bearing fluorinated alkyl chains at C- and N-termini. The respective values are 4 π ε 0 × 330 ± 150 Å 3 and 4 π ε 0 × 270 ± 80 Å 3 .

Quantum measurement of a rapidly rotating spin qubit in diamond.

A controlled qubit in a rotating frame opens new opportunities to probe fundamental quantum physics, such as geometric phases in physically rotating frames, and can potentially enhance detection of magnetic fields. Realizing a single qubit that can be measured and controlled during physical rotation is experimentally challenging. We demonstrate quantum control of a single nitrogen-vacancy (NV) center within a diamond rotated at 200,000 rpm, a rotational period comparable to the NV spin coherence time T2. We stroboscopically image individual NV centers that execute rapid circular motion in addition to rotation and demonstrate preparation, control, and readout of the qubit quantum state with lasers and microwaves. Using spin-echo interferometry of the rotating qubit, we are able to detect modulation of the NV Zeeman shift arising from the rotating NV axis and an external DC magnetic field. Our work establishes single NV qubits in diamond as quantum sensors in the physically rotating frame and paves the way for the realization of single-qubit diamond-based rotation sensors.