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Synthesis of ammonia through photo- and electrocatalysis is a rapidly growing field. Titania-based catalysts are widely reported for photocatalytic ammonia synthesis and have also been suggested as electrocatalysts. The addition of transition-metal dopants is one strategy for improving the performance of titania- based catalysts. In this work, we screen d-block transition- metal dopants for surface site stability and evaluate trends in their performance as the active site for the reduction of nitrogen to ammonia on TiO2. We find a linear relationship between the d-band center and metal substitution energy of the dopant site, while the binding energies of N2, N2H, and NH2 all are strongly correlated with the cohesive energies of the dopant metals. The activity of the metal-doped systems shows a volcano type relationship with the NH2 and N2H energies as descriptors. Some metals such as Co, Mo, and V are predicted to slightly improve photo- and electrocatalytic performance, but most metals inhibit the ammonia synthesis reaction. The results provide insight into the role of transition-metal dopants for promoting ammonia synthesis, and the trends are based on unexpected electronic structure factors that may have broader implications for single-atom catalysis and doped oxides.

Computational Study of Transition-Metal Substitutions in Rutile TiO2 (110) for Photoelectrocatalytic Ammonia Synthesis