Mechanism of N sub(2) Reduction to NH sub(3) by Aqueous Solvated Electrons

Recently a novel approach to the photocatalytic reduction of molecular nitrogen under ambient conditions was reported in which hydrated electrons generated from ultraviolet illumination of diamond served as the reducing agent [Zhu, D.; Zhang, L.; Ruther, R. E.; Hamers, R. J. Photo-Illuminated Diamond as a Solid-State Source of Solvated Electrons in Water for Nitrogen Reduction. Nat. Mater. 2013, 12, 836-841]. This surprising reduction of N sub(2) by aqueous solvated electrons is absent from the vast existing radiolysis literature and thus has little mechanistic precedent. In this work, a combination of experimental and computational approaches is used to elucidate the detailed molecular-level mechanistic pathway from nitrogen to ammonia. A variety of approaches, including electronic structure calculations, molecular dynamics simulations, kinetic modeling, and pH-dependent experimental measures of NH sub(3) and competing H sub(2) production, implicate a hydrogen atom addition mechanism at early reduction steps and sequential protonation/direct reduction by a solvated electron at later steps, thus involving both direct and indirect reactions with solvated electrons. This work provides a framework for understanding the possible application of solvated electrons as energetic reducing agents for chemically inert species under mild conditions.