Despite the considerable interest for antiferromagnets that appeared with the perspective of using them for spintronics, their experimental study, including the imaging of antiferromagnetic textures, remains a challenge. To address this issue, quantum sensors, and, in particular, the nitrogen-vacancy (NV) defects in diamond have become a widespread technical solution. We review here the recent applications of single NV centers to study a large variety of antiferromagnetic materials, from quantitative imaging of antiferromagnetic domains and non-collinear states, to the detection of spin waves confined in antiferromagnetic textures and the non-perturbative measurement of spin transport properties. We conclude with recent developments improving further the magnetic sensitivity of scanning NV microscopy, opening the way to detailed investigations of the internal texture of antiferromagnetic objects.

In the room-temperature magnetoelectric multiferroic, BiFeO3, the non-collinear antiferromagnetic state is coupled to the ferroelectric order, opening applications for low-power electric-field-controlled magnetic devices. While several strategies have been explored to simplify the ferroelectric landscape, here we directly stabilize a single domain ferroelectric and spin cycloid state in epitaxial BiFeO3(111) thin films grown on orthorhombic DyScO3(011). Comparing with films grown on SrTiO3(111), we identify anisotropic in-plane strain as a powerful handle to tailor the single antiferromagnetic state. In this single domain multiferroic state, we establish the thickness limit of the coexisting electric and magnetic orders and directly visualize the suppression of the spin cycloid induced by the magnetoelectric interaction below the ultrathin limit of 1.4 nanometers. This as-grown single domain multiferroic configuration in BiFeO3 thin films opens an avenue both for fundamental investigations and for electrically-controlled non-collinear antiferromagnetic spintronics.

BiFeO3 is a rich room-temperature multiferroic material in which noncollinear antiferromagnetic spin cycloids can be deterministically controlled by an electric field through the magnetoelectric interaction, opening perspectives for low-power reconfigurable antiferromagnetic spintronics. Using a commercial scanning nitrogen-vacancy (N-V) magnetometer, we are able to image two different types of spin cycloids stabilized in strain-engineered BiFeO3 epitaxial thin films. We show that, in these samples harboring two ferroelectric variants, each ferroelectric domain is coupled to a single spin cycloid, giving rise to a zigzag magnetic pattern. These ferroelectric domains can be manipulated at the local scale by piezoresponse force microscopy, allowing the design of micron-sized single domains. Thanks to its coupled optical microscope and fast-imaging capabilities, the scanning N-V magnetometer enables a quick repositioning in such areas of interest. Finally, quantitative imaging on single ferroelectric domains provides insights into the physical parameters of each spin-cycloid type and their impact on the magnetic-stray-field measurements.

We report on the formation of topological defects emerging from the cycloidal antiferromagnetic order at the surface of bulk BiFeO3 crystals. Combining reciprocal and real-space magnetic imaging techniques, we first observe, in a single ferroelectric domain, the coexistence of antiferromagnetic domains in which the antiferromagnetic cycloid propagates along different wave vectors. We then show that the direction of these wave vectors is not strictly locked to the preferred crystallographic axes as continuous rotations bridge different wave vectors. At the junctions between the magnetic domains, we observe topological line defects identical to those found in a broad variety of lamellar physical systems with rotational symmetries. Our work establishes the presence of these magnetic objects at room temperature in the multiferroic antiferromagnet BiFeO3, offering new possibilities for their use in spintronics

The nitrogen-vacancy (NV) defect in diamond is an efficient quantum sensor of randomly fluctuating signalsvia relaxometry measurements. In particular, the longitudinal spin relaxation of the NV defect accelerates in thepresence of magnetic noise with a spectral component at its electron spin resonance frequency.We look into thiseffect quantitatively by applying a calibrated and tunable magnetic noise on a single NV defect.We show that anincrease of the longitudinal spin relaxation rate translates into a reduction of the photoluminescence (PL) signalemitted under continuous optical illumination, which can be explained using a simplified three-level model of theNV defect. This PL quenching mechanism offers a simple, all-optical method to detect magnetic noise sourcesat the nanoscale.

Antiferromagnetic materials are promising platforms for next-generation spintronics owing to their fast dynamics and high robustness against parasitic magnetic fields. However, nanoscale imaging of the magnetic order in such materials with zero net magnetization remains a major experimental challenge. Here we show that non-collinear antiferromagnetic spin textures can be imaged by probing the magnetic noise they locally produce via thermal populations of magnons. To this end, we perform nanoscale, all-optical relaxometry with a scanning quantum sensor based on a single nitrogen-vacancy (NV) defect in diamond. Magnetic noise is detected through an increase of the spin relaxation rate of the NV defect, which results in an overall reduction of its photoluminescence signal under continuous laser illumination. As a proof-of-concept, the efficiency of the method is demonstrated by imaging various spin textures in synthetic antiferromagnets, including domain walls, spin spirals and antiferromagnetic skyrmions. This imaging procedure could be extended to a large class of intrinsic antiferromagnets and opens up new opportunities for studying the physics of localized spin wave modes for magnonics.