Interfacial Water Frustration for Nitrate Semireduction to Hydroxylamine at Industrial-Relevant Currents
Shunhan Jia1,2, Ruhan Wang1,2, Weixiang Li1,2
1Beijing National Laboratory for Molecular Sciences, CAS Laboratory of Colloid and Interface and Thermodynamics, CAS Research/Education Center for Excellence in Molecular Sciences, Center for Carbon Neutral Chemistry, Institute of Chemistry, Chinese Academy of Sciences, Beijing 100190, China.
None:
Hydroxylamine (NH2OH) has a broad range of applications. Electrocatalytic semireduction of nitrate (NO3-) to NH2OH is a promising pathway for its sustainable production. However, the reported route typically led to either insufficient or excessive hydrogenation because the mismatch between supply and demand of active species during electrocatalysis remains a critical challenge, resulting in poor selectivity to NH2OH. Herein, we demonstrate an interfacial water (H2O) frustration strategy to achieve highly selective electrocatalytic semireduction of nitrate (NO3-) to hydroxylamine (NH2OH). By engineering the electric double layer (EDL) through alkali metal cation modulation, we precisely regulated the activation of interfacial H2O to inhibit excessive active hydrogen (*H) generation, thereby controlling the *H supply. In addition, tensile-strained bibased catalysts promoted *NO intermediate formation, enhancing *H demand and suppressing over-reduction to NH3. It achieved a Faradaic efficiency (FE) of 93.9% for NH2OH at 120 mA cm-2 under acidic conditions, which enabled the gram-scale synthesis of industrially relevant oximes with high nitrogen selectivity. Remarkably, this work achieved the highest NH2OH FE under industrial-level current densities (>100 mA cm-2). This work provided a generalizable approach for steering semireduction pathways through interfacial H2O frustration, which constructs the supply-demand balance of essential active species involved in electrocatalytic reactions.
Related Concept Videos
Preparation of Amines: Reduction of Oximes and Nitro Compounds
Though catalytic hydrogenation can reduce nitrobenzenes, the reduction is nonselective in the presence of other functional groups. For instance, if nitrobenzene contains an aldehyde group,...
1° Amines to Diazonium or Aryldiazonium Salts: Diazotization with NaNO2 Overview
The nitrous acid is unstable. Hence, it is formed in situ from a solution of sodium nitrite and cold aqueous acids such as hydrochloric or sulfuric acid. In an acidic solution, the –OH group of nitrous acid undergoes protonation to give oxonium ion, followed by...
2° Amines to N-Nitrosamines: Reaction with NaNO2
1° Amines to Diazonium or Aryldiazonium Salts: Diazotization with NaNO2 Mechanism
Nitriles to Carboxylic Acids: Hydrolysis
Nitriles to Amines: LiAlH4 Reduction
As shown below, the mechanism involves three steps. Firstly, the hydride ion acting as a nucleophile attacks the nitrile carbon to form an anion. In the second step, a second equivalent of the hydride ion attacks the anion to...


