Functionalization of carbon supports with heteroatom dopants is now widely regarded as a promising route for stabilizing and strengthening the interactions between the support and metal catalysts. Tuning the type and density of heteroatom dopants allows for the tailoring of nanoscale catalyst−support interactions; however, an understanding of these phenomena has not yet been fully realized because of the complexity of the system. In this work, computational modeling, materials synthesis, and advanced nanomaterial characterization are used to systematically investigate the intriguing effect of the two most common nitrogen functionalities in the carbon-based supports on the interactions with selected transition metals toward realizing catalytic applications. Specifically, this study utilized density functional theory to evaluate adsorption energies and modes of adsorption for 12 metals located in groups 8−11 and periods 4−6 with pyridinic and graphitic N defects. Based on these results, further electronic structure investigation of the period 4 metals was conducted to elucidate periodic group trends. Experimental work included synthesis and nanomaterial characterization of a subset of materials featuring three metals each supported on two types of N-doped carbon supports and undoped graphene. Characterization of nanomaterials with scanning transmission electron microscopy and energy-dispersive X-ray spectroscopy confirmed that N functionalities enhanced the interactions with the selected transition metals when compared to the undoped support and demonstrated that the nature of the defect influences these interactions. Both computations and experiments agreed that Fe and Co are biased toward the graphitic sites over pyridinic sites, while Ni has an affinity to both defects without a statistically significant preference. This work established a correlation between computational and experimental work and a framework that can be expanded to other metals and alternative dopants beyond nitrogen in tailoring nanoscale catalyst−support interactions for a breadth of catalytic applications.
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