“… , The crystalline phases of the as-synthesized HKUST-1 and Pd–HKUST-1 were nicely matched with the simulated XRD data (Figure S3) as obtained using Rietveld refinement (conducted by Materials studio, Accelrys Software, Inc.), demonstrating that the as-synthesized materials comprise the crystal structure of HKUST-1. After carbonization of Pd–HKUST-1, a MOF structural change was also reflected in the XRD pattern of Cu–Pd@C where the distinguished diffraction peaks appeared at 2θ = 38.8, 40.5, 47.1 49.1, 61.5, 68.5, and 75.3°, respectively, which could be readily indexed to the Cu 2 O (111), Pd (111), Pd (220), Cu 2 O (220), Pd (220), and Cu (220) crystalline planes, is in good agreement with the previous report . The PXRD pattern of Cu–Pd@C- A (Figure a) exhibited characteristic diffractions peaks at 2θ = 40.2, 43.4, 46.8, 50.4, 68.4, and 74.1° which could be indexed to Pd (111), Cu (111), Pd (200), Cu (200), Pd (220), and Cu (220) reflections, corresponding to the face-centered cubic ( fcc ) lattice arrangement of Pd 0 and Cu 0 nanoparticles (Powder Diffraction File (PDF) nos.…”