Thin film surface nanostructures of semicrystalline diblock copolymer are promising for the fabrication of photonic crystals and bioanalytical devices because they might be tailorable by controlled crystallization. One approach to systematically control polymer crystallization is a self-nucleation experiment. The self-nucleation experiment for block copolymers has only been reported for the bulk and so far not for thin films. Considering the versatility of a tailorable surface nanostructure, it is promising to apply the controlled crystallization of a bulk self-nucleation experiment to thin films of a diblock copolymer. In the current study we tested the hypothesis that within two self-nucleation experiments, i.e., in the bulk and thin film, the calorimetric bulk properties of a polybutadiene-block-poly(ethylene oxide) can be correlated to the resulting thin film surface nanostructures and to understand as well as predict their formation. The calorimetric bulk properties measured by differential scanning calorimetry in the bulk self-nucleation experiment were correlated to surface nanostructures measured by atomic force microscopy of the thin film self-nucleation experiment samples. In analogy to the bulk self-nucleation experiment, we introduced a crystalline standard for the thin film self-nucleation experiment where the crystalline lamellae consisted of once-folded chains. Annealing the thin film crystalline standard promoted the thickening of crystalline lamellae on the film surface which is explained by the formation of less folded chain crystals that obtain higher melting temperatures. The crystalline lamellae thickness was steplessly variable within the range of 8-16 nm. In analogy to the Hoffman Weeks and Gibbs Thomson plots, we derived a function which can be used to predict the lamellae thickness as a function of the annealing temperature. Bulk and thin film self-nucleation experiments were successfully related, since thin film surface nanostructures were consistently correlated to calorimetric results. We established the dual self-nucleation experiment as a powerful tool to predictably tailor thin film nanostructures in the range of several nanometers.