The dissolution of nano-sized Ni3Al-based γ′ precipitates was investigated in the newly developed polycrystalline nickel-based VDM^® Alloy 780 at the surface and in the bulk region with in-situ lab-source and synchrotron X-ray diffraction. These studies are important in obtaining a deeper understanding of the strengthening mechanism responsible for the stability and long service lives of such superalloys. We found that the dissolution behavior of the γ′ phase is very similar at the surface and in the bulk region, but small deviations were detected. The dissolution of γ′ starts at around 800 °C and no γ′ was found at temperatures exceeding 970 °C. As a result, the elements Al and Nb, which were bound in the γ′ phase, dissolved into the γ matrix and strongly increased the γ lattice parameter, as their atomic size is larger than the γ-forming elements Ni, Co, and Cr. However, this effect was suppressed in the surface area. A second matrix γ phase was detected at the same temperature range as that of the dissolution of the γ′ phase in the lab-source XRD measurements. The newly formed γ-2 phase had a smaller lattice parameter than that of the initial γ matrix. We propose that the γ-2 matrix phase is a result of high-temperature surface oxidation, which consumes, among other elements, Al and Nb and, therefore, leads to the smaller γ lattice parameter.

The development of widely applicable methods for the synthesis of C-C-bonded nanostructures on inert and insulating surfaces is a challenging yet rewarding milestone in the field of on-surface synthesis. This would enable studies of nearly unperturbed covalent nanostructures with unique electronic properties as graphene nanoribbons (GNR) and π-conjugated 2D polymers. The prevalent Ullmann-type couplings are almost exclusively carried out on metal surfaces to lower the temperature required for initial dehalogenation well below the desorption threshold. To overcome the necessity for the activation of monomers on the target surface, we employ a recently developed Radical Deposition Source (RaDeS) for the direct deposition of radicals onto inert surfaces for subsequent coupling by addition reactions. The radicals are generated en route by indirect deposition of halogenated precursors through a heated reactive tube, where the dehalogenation reaction proceeds. Here, we use the ditopic 6,11-diiodo-1,2,3,4-tetraphenyltriphenylene (DITTP) precursor that afforded chevron-like GNR on Au(111) via the usual two-staged reaction comprised of monomer-coupling into covalent polymers and subsequent formation of an extended GNR by intramolecular cyclodehydrogenation (CDH). As a model system for inert surfaces, we use Ag(111) passivated with a closed monolayer of chemisorbed iodine that behaves in an inert manner with respect to dehalogenation reactions and facilitates the progressive coupling of radicals into extended covalent structures. We deposit the DITTP-derived biradicals onto both iodine-passivated and pristine Ag(111) surfaces. While on the passivated surface, we directly observe the formation of covalent polymers, on pristine Ag(111) organometallic intermediates emerge instead. This has decisive consequences for the further progression of the reaction: heating the organometallic chain directly on Ag(111) results in complete desorption, whereas the covalent polymer on iodine-passivated Ag(111) can be transformed into the GNR. Yet, the respective CDH proceeds directly on Ag(111) after thermal desorption of the iodine passivation. Accordingly, future work is aimed at the further development of approaches for the complete synthesis of GNR on inert surfaces.

Ni-based superalloys are indispensable for applications in demanding environments, such as the heavily stressed rotating discs in the hot sections of modern gas turbines or jet engines. In this paper, the microstructure evolution during hot deformation to mimic the forging process was investigated in the polycrystalline VDM® Alloy 780 via in situ X-ray diffraction at temperatures of 950, 1000, and 1050 °C. For the tested temperatures, the hot forming led to subgrain formation, the built-up of a texture by rotation of the matrix grains into preferred orientations, and dynamic recrystallization. The influence of the deformation was analyzed depending on the direction of the lattice plane normals to the load direction, for the first five γ-reflections in the diffraction pattern. During uniaxial compressive deformation intensity, maxima develop in the loading direction solely for the γ-(220) reflections, while intensity minima develop for the other reflections which correspond to the formation of a fiber texture. In the transverse direction, all γ-reflections except the (220) have an increased intensity at the maximum specimen strain of 20 pct. Directly after the hot forming, three different cooling rates of 10, 100, and 1000 °C/min and their influence on the microstructure were investigated. The fast and medium cooling rates lead to low recrystallized fractions and a largely preserved deformation texture, whereas the low cooling rate leads to a high recrystallized fraction and a slight remaining texture. Additionally, the diffraction data are complemented by electron microscopy measurements.