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The electrocatalytic nitrate reduction reaction represents a promising technology for wastewater treatment while enabling electrochemical ammonia (NH<sub>3</sub>) synthesis. However, electrostatic repulsion between nitrate (NO<sub>3</sub><sup>-</sup>) and the cathode impedes NO<sub>3</sub><sup>-</sup> diffusion into the electric double layer, thereby hindering the reaction. Herein, the diffusion limitation is mitigated by introducing a trace CsOH additive to the electrolyte, and the underlying mechanism is systematically elucidated. CsOH not only weakens the static repulsion between NO<sub>3</sub><sup>-</sup> and the cathode but also enhances the selectivity of NH<sub>3</sub> by preventing the formation of adsorbed H<sup>+</sup> on the electrode. Remarkably, the addition of CsOH enables an NH<sub>3</sub> production rate of 456.2 μmol cm<sup>-2</sup> h<sup>-1</sup> at 150 mA cm<sup>-2</sup> with a faradaic efficiency of 65.2% in 20 mM NO<sub>3</sub><sup>-</sup>. Furthermore, the Zn-NO<sub>3</sub> battery with a CsOH additive achieves a peak power density of 30.16 mW cm<sup>-2</sup>. This work not only provides fundamental insights of additive-enhanced NO<sub>3</sub><sup>-</sup> reduction but also successfully demonstrates a Zn-NO<sub>3</sub> battery capable of simultaneous high-efficiency NH<sub>3</sub> synthesis and electric power generation.
Published in: ACS Applied Materials & Interfaces
Volume 18, Issue 8, pp. 12609-12618