Sulfate-mediated reactive oxygen species for efficient photocatalytic nitrogen fixation over TiO2

Abstract

Direct photocatalytic N2 fixation under mild conditions (compared to the harsh conditions of the Haber–Bosch process) is hindered by N[triple bond, length as m-dash]N inertness and lack of controllable activation. Here, a sulfate-modified TiO2 catalyst (S-TiO2) achieves an NH3 production rate of 217.24 µmol h−1 g−1 at 200 °C in simulated air. The mechanism follows an “oxidation-first, reduction-later” pathway: sulfate-derived ROS oxidize N2 to NOx intermediates, which are then hydrogenated to NH3 (confirmed by in situ FTIR and MS). This work provides new insights into solar-driven N2 fixation.

Graphical abstract: Sulfate-mediated reactive oxygen species for efficient photocatalytic nitrogen fixation over TiO2

Supplementary files

Article information

Article type
Communication
Submitted
06 Apr 2026
Accepted
05 May 2026
First published
06 May 2026

Chem. Commun., 2026, Advance Article

Sulfate-mediated reactive oxygen species for efficient photocatalytic nitrogen fixation over TiO2

X. Zhang, L. Zhang, Y. Hu, X. Li, X. Yang, P. Wang, H. Yu, S. Song, B. Zhang and X. Ding, Chem. Commun., 2026, Advance Article , DOI: 10.1039/D6CC02106A

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