Abstract
The electrochemical nitric oxide (NO) valorization strategy reconciles industrial emission mitigation with distributed ammonia (NH(3)) production, offering a dual solution for deteriorating urban air quality and fertilizer-deprived agricultural regions. Rational engineering of active sites constitutes the cornerstone for overcoming this catalytic bottleneck. Herein, we report a chemical etching-coordination strategy that enables the precise construction of hollow-architected high-entropy oxides (HEOs) with a nanoporous shell and customizable multimetallic compositions spanning quinary to decenary systems. Employing RuFeCoNiCuZnO as the first HEO catalyst for electrocatalytic low-concentration NO (1 vol %) reduction delivers record-breaking Faraday efficiency of 99.08% and 104.03 μg h(-1) mg(cat)(-1) production rate for NH(3) synthesis, outperforming FeCoNiCuZnO and some reported catalysts. The Zn-NO battery with RuFeCoNiCuZnO achieves a power density of 1.18 mW cm(-2) and an NH(3) yield of 69.87 μg h(-1) mg(cat)(-1). Experimental results demonstrate that the incorporation of Ru modifies the electronic structure and enhances NO adsorption capacity of FeCoNiCuZnO, thereby promoting NO electroreduction. This work establishes a general method to engineer HEO nanostructures, whose unique configuration offers new possibilities in catalysis and energy conversion.