Probing boron vacancy defects in hBN via single spin relaxometry.

Abstract

Spin defects in solids offer promising platforms for quantum sensing and memory due to their long coherence times and optical addressability. Here, we integrate a single nitrogen-vacancy (NV) center in diamond with scanning probe microscopy to detect, read out, and spatially map spin-based quantum sensors at the nanoscale. Using the boron vacancy ( <math xmlns="http://www.w3.org/1998/Math/MathML"> <msubsup><mrow><mi>V</mi></mrow> <mrow><mi>B</mi></mrow> <mrow><mo>-</mo></mrow> </msubsup> </math> ) center in hexagonal boron nitride-an emerging two-dimensional spin system-as a model, we detect its electron spin resonance indirectly via changes in the spin relaxation time (T₁) of a nearby NV center, eliminating the need for optical excitation or fluorescence detection of the <math xmlns="http://www.w3.org/1998/Math/MathML"> <msubsup><mrow><mi>V</mi></mrow> <mrow><mi>B</mi></mrow> <mrow><mo>-</mo></mrow> </msubsup> </math> . Cross-relaxation between NV and <math xmlns="http://www.w3.org/1998/Math/MathML"> <msubsup><mrow><mi>V</mi></mrow> <mrow><mi>B</mi></mrow> <mrow><mo>-</mo></mrow> </msubsup> </math> ensembles significantly reduces NV T₁, enabling quantitative nanoscale mapping of defect densities beyond the optical diffraction limit and clear resolution of hyperfine splitting in isotopically enriched h¹⁰B¹⁵N. Our method demonstrates interactions between spin sensors in 3D and 2D materials, establishing NV centers as versatile probes for characterizing otherwise inaccessible spin defects.