AbstractUnderstanding and manipulating complex spin texture in multiferroics can offer new perspectives for electric field-controlled spin manipulation. In BiFeO₃, a well-known room temperature multiferroic, the competition between various exchange interactions manifests itself as non-collinear spin order, i.e., an incommensurate spin cycloid with period 64 nm. We report on the stability and systematic expansion of the length of the spin cycloid in (110)-oriented epitaxial Co-doped BiFeO₃ thin films. Neutron diffraction shows (i) this cycloid, despite its partly out-of-plane canted propagation vector, can be stabilized in thinnest films; (ii) the cycloid length expands significantly with decreasing film thickness; (iii) theory confirms a unique [$11\bar 2$ 11 2 ¯ ] cycloid propagation direction; and (iv) in the temperature dependence the cycloid length expands significantly close to T_N. These observations are supported by Monte Carlo simulations based on a first-principles effective Hamiltonian method. Our results therefore offer new opportunities for nanoscale magnonic devices based on complex spin textures.