The physical properties of epitaxial films can fundamentally differ from those of bulk single crystals even above the critical thickness. By a combination of non-resonant x-ray magnetic scattering, neutron diffraction and vector-mapped x-ray magnetic linear dichroism photoemission electron microscopy, we show that epitaxial (111)-BiFeO 3 films support sub-micron antiferromagnetic domains, which are magneto-elastically coupled to a coherent crystallographic monoclinic twin structure. This unique texture, which is absent in bulk single crystals, should enable control of magnetism in BiFeO 3 film devices via epitaxial strain.PACS numbers: 77.55. Nv, 68.37.Yz, 75.60.Ch, Electrical manipulation of spins in insulators is a promising route to a new generation of fast, low consumption electronics [1][2][3]. Although direct electrical control of ferromagnets is challenging, much progress has been made towards electrical switching of antiferromagnetic spins [4]. Multiferroic BiFeO 3 (BFO) is one of the most promising materials: at room temperature, BFO is both ferroelectric and antiferromagnetic, and its spins can be rotated by switching the direction of the electrical polarisation [5,6]. Thus far, a fundamental limitation towards practical BFO devices has been the lack of understanding of the interplay between ferroelectricity, ferromagnetism and lattice distortions (ferroelasticity). Using a combination of non-resonant x-ray magnetic scattering (NXMS), neutron diffraction and vectormapped x-ray magnetic linear dichroism photoemission electron microscopy (XMLD-PEEM), we show that the antiferromagnetic domain structure of 1 µm thick, epitaxial (111)-oriented BFO films displays a ≈100 nm-scale texture, dramatically different from the mm-size features in bulk single crystals. We also demonstrate that this magnetic texture is coherent (having matching topography and symmetry elements) with a pattern of monoclinic domains at the nanoscale. This texture is reminiscent of the dense polydomain states that are thermodynamically stable in ferroelectric perovskites such as PbTiO 3 in the presence of strain misfit [7]. This strongly suggests that the relaxed (111)-oriented BFO structure is not trigonal, but is a texture of coherent monoclinic micro twins. Besides providing a new pathway towards strainengineering multiferroic domains in BFO, our approach yielded a detailed picture of the interplay between magnetism and lattice over 5 orders of magnitude in length * p.g.radaelli@physics.ox.ac.uk scales, and could be applied to many classes of functional magnetic oxide devices.Below its ferroelectric Curie temperature of T C = 1103 K, bulk BFO is generally believed to possess a rhombohedrally-distorted perovskite structure with space group R3c (pictured in fig. 1(a) and (b)) [8,9], although very recent high-resolution synchrotron measurements have suggested a small monoclinic distortion [10]. The Bi 3+ and Fe 3+ cations are displaced away from their centrosymmetric positions along the (111) (pseudocubic setting) axis [11], producing a ...