Abstract Chromia (Cr2O3) is a magnetoelectric oxide that permits voltage‐control of the antiferromagnetic (AFM) order, but it suffers technological constraints due to its low Néel Temperature (TN≈307 K) and the need of a symmetry‐breaking applied magnetic field to achieve reversal of the Néel vector. Recently, boron (B) doping of Cr2O3films led to an increaseTN>400 K and allowed the realization of voltage magnetic‐field free controlled Néel vector rotation. Here, the impact of B doping is directly imaged on the formation of AFM domains in Cr2O3thin films and elucidates the mechanism of voltage‐controlled manipulation of the spin structure using nitrogen‐vacancy (NV) scanning probe magnetometry. A stark reduction and thickness dependence of domain size in B‐doped Cr2O3(B:Cr2O3) films is found, explained by the increased germ density, likely associated with the B doping. By reconstructing the surface magnetization from the NV stray‐field maps, a qualitative distinction between the undoped and B‐doped Cr2O3films is found, manifested by the histogram distribution of the AFM ordering, that is, 180°domains for pure films, and 90°domains for B:Cr2O3films. Additionally, NV imaging of voltage‐controlled B‐doped Cr2O3devices corroborates the 90°rotation of the AFM domains observed in magnetotransport measurement. 
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                            Nanoscale imaging of antiferromagnetic domains in epitaxial films of Cr 2 O 3 via scanning diamond magnetic probe microscopy
                        
                    
    
            We report direct imaging of boundary magnetization associated with antiferromagnetic domains in magnetoelectric epitaxial Cr 2 O 3 thin films using diamond nitrogen vacancy microscopy. We found a correlation between magnetic domain size and structural grain size which we associate with the domain formation process. We performed field cooling, i.e. , cooling from above to below the Néel temperature in the presence of a magnetic field, which resulted in the selection of one of the two otherwise degenerate 180° domains. Lifting of such a degeneracy is achievable with a magnetic field alone due to the Zeeman energy of a weak parasitic magnetic moment in Cr 2 O 3 films that originates from defects and the imbalance of the boundary magnetization of opposing interfaces. This boundary magnetization couples to the antiferromagnetic order parameter enabling selection of its orientation. Nanostructuring the Cr 2 O 3 film with mesa structures revealed reversible edge magnetic states with the direction of magnetic field during field cooling. 
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                            - PAR ID:
- 10393119
- Date Published:
- Journal Name:
- RSC Advances
- Volume:
- 13
- Issue:
- 1
- ISSN:
- 2046-2069
- Page Range / eLocation ID:
- 178 to 185
- Format(s):
- Medium: X
- Sponsoring Org:
- National Science Foundation
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