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The current industrial ammonia synthesis relies on Haber–Bosch process that is initiated by the dissociative mechanism, in which the adsorbed N 2  dissociates directly, and thus is limited by Brønsted–Evans–Polanyi (BEP) relation. Here we propose a new strategy that an anchored Fe 3  cluster on the θ-Al 2 O 3 (010) surface as a heterogeneous catalyst for ammonia synthesis from first-principles theoretical study and microkinetic analysis. We have studied the whole catalytic mechanism for conversion of N 2  to NH 3  on Fe 3 /θ-Al 2 O 3 (010), and find that an associative mechanism, in which the adsorbed N 2  is first hydrogenated to NNH, dominates over the dissociative mechanism, which we attribute to the large spin polarization, low oxidation state of iron, and multi-step redox capability of Fe 3  cluster. The associative mechanism liberates the turnover frequency (TOF) for ammonia production from the limitation due to the BEP relation, and the calculated TOF on Fe 3 /θ-Al 2 O 3 (010) is comparable to Ru B5 site.

Heterogeneous Fe3 single-cluster catalyst for ammonia synthesis via an associative mechanism