Hydride materials have a significant ability to promote ammonia synthesis over supported transition metal (TM) nanoparticles due to the unique properties of lattice H- ions. Here, we report that lanthanum oxyhydride (LaH3-2xOx) facilitates ammonia synthesis on the supported TM catalyst under visible light irradiation. Ru-loaded LaH3-2xOx exhibited an order of magnitude higher ammonia synthesis rate at 180 °C with an ∼18 kJ mol-1 lower activation energy under visible light irradiation (λ = 405 nm, 1.04 W cm-2) than that under dark conditions. The enhanced catalytic performance can be explained by photoionization of H- (H- → H0 + e-) constituting the valence band maximum (VBM) of LaH3-2xOx, in which photogenerated electrons are transferred to supported Ru, and neutral hydrogen (H0) facilitates the hydrogenation of nitrogen species. Moreover, the photoexcitation of LaH3-2xOx enables shifting of the optimum TM catalyst from Ru to Ni in the volcano-shaped relationship between ammonia synthesis activity and metal-nitrogen binding energy.
Abe et al. (Thu,) studied this question.