D‐Band Engineering in Pd‐Based Nanowire Networks for Further Enhancement in Ethanol Electrooxidation Reaction

Abstract The development of highly efficient electrocatalysts for the ethanol oxidation reaction (EOR) is essential for the commercialization of direct ethanol fuel cells, yet challenges remain. In this study, a one‐pot solution‐phase method to synthesize Pd nanowire networks (NNWs) with very high surface‐to‐volume ratio having numerous twin and grain boundaries is developed. Using the same method, the Pd lattice is further engineered by introducing Ag and Cu atoms to produce AgPd, and CuPd alloy structure which significantly shifts the Pd d‐band center upward and downward, respectively due to strain and ligand effects. Theoretical analysis employing density functional theory (DFT) demonstrates that such modification of the d‐band center significantly influences the adsorption energies of reactants on the catalytic surface. Owing to their notably high surface‐to‐volume ratio and the presence of multiple twin and grain boundaries, Pd NNWs demonstrate significantly enhanced electrocatalytic activity toward EOR, ≈7.2 times greater than that of commercial Pd/C. Remarkably, compared to Pd NNWs, AgPd, and CuPd NNWs display enlarged and reduced electrocatalytic activity toward EOR, respectively. Specifically, Ag 4 Pd 7 NNWs achieve a remarkable mass activity of 9.00 A mg pd −1 for EOR, which is 13.6 times higher than commercial Pd/C.