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This work develops a bifunctional support that enhances ammonia synthesis efficiency in catalyst systems, suggesting new possibilities for mild reactions.
Toward enhancing the NH₃ synthesis activity of Ru-based catalysts under mild conditions, various electron donors have been intensively investigated. The electron donation typically originates from either the support itself or the external promoter that transforms into a near-metallic state during the reaction, yet single materials combining both pathways remain rarely reported. This work develops such a bifunctional support — strontium carbonate (SrCO₃). Over the Ru-SrCO₃/CNTs catalyst, surface SrCO₃ is partially reduced in situ to form near-metallic Sr⁰ species, which together with the unreduced basic Sr²⁺ in the bulk SrCO₃ donate electrons to Ru sites, achieving highly efficient N₂ activation. Moreover, the SrCO₃ support can also boost NH₃ desorption and mitigate hydrogen poisoning. The potassium-promoted catalyst K-Ru-SrCO₃/CNTs even delivers an outstanding NH₃-synthesis rate of 61.6 mmolNH3 gcat⁻¹ h⁻¹ at 400 °C and 0.9 MPa, outperforming most state-of-the-art Ru-based catalysts with Ru mass-loading ≤ 5 wt. % reported to date.
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Hu et al. (2026) studied this question.
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