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Materials Science in Additive Manufacturing                                   Directed energy deposition




                         A                                   B














            Figure 2. Localized surface morphology of (A) high-speed directed energy deposition (H-DED) and (B) broad-beam laser-directed energy deposition
            (B-DED). Scale bars: 500 μm

                         A                                            B











                         C                                            D










            Figure 3. Cross-sectional macroscopic morphology (A and C) and binding zone microstructure (B and D) of the coatings through various directed energy
            deposition (DED) technology. Scale bars: 1000 μm (A and C); 40 μm (B and D)
            Abbreviations: B-DED: Broad-beam laser-directed energy deposition; H-DED: High-speed directed energy deposition
            stacked structure with higher roughness, whereas the   during the solidification of the molten pool, the carbide
            B-DED coating surface is smoother. Although the shape   with the highest affinity for carbon forms first. The Gibbs
            of the binding line varies, both coatings exhibit strong   free energy of M C  remains lower than that of carbides,
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            metallurgical bonding with the substrate (Figure 3B and D).   such as M C  and M C  over a wide temperature range,
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            As the H-DED coating has a smaller melt pool diameter, it   causing M C  to precipitate first. However, the overall
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            has a more curved binding line than the B-DED coating.  carbide content in the deposited coating is low, possibly
                                                               indicating insufficient carbon atoms in the molten pool
            3.2. X-ray diffraction of the coatings             to form other carbides. As key hardening phases, these
            Figure 4A displays the XRD patterns of B-DED, H-DED,   carbides feature complex structures, high melting points,
            and the deposition powder. The powder and coatings   and hardness, enhancing the coating’s wear resistance and
            primarily consist of a face-centered cubic austenitic phase   hardness. 23,25
            (γ-Fe), along with a small amount of carbides. The  γ-Fe   The different DED process influences the preferred
            phase corresponds to the (111), (200), (220), and (311)   orientation of the surface grains but does not change the
            crystal faces. The carbides are present in the form of   phase composition of the coating. The peak shape and
            interstitial phases, mainly M C  (M = Fe, Cr). Given the   position of the H-DED coating are similar to those of the
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            similar lattice and electronic structures of Fe, Cr, and Fe   deposition powder, but the intensity of the diffraction
            atoms, some Cr atoms in Cr C  can be easily replaced,   peaks has increased, particularly for the (111) crystal
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            forming M C -type carbides. Research  revealed that   face, where both the intensity and the full width at half
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            Volume 3 Issue 4 (2024)                         4                              doi: 10.36922/msam.4974
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