化学
催化作用
纳米孔
氧化物
电化学
化学工程
选择性催化还原
纳米技术
吸附
氮氧化物
还原(数学)
电池(电)
氨
产量(工程)
沸石
储能
电催化剂
功率密度
氮氧化物
氨生产
数码产品
无机化学
阳极
表面工程
工作(物理)
高效能源利用
能量转换
化学能
作者
Dongdong Wang,Yan Guo,Deyan Luan,Xiaojun Gu,Xiong Wen David Lou
摘要
High Resolution Image Download MS PowerPoint Slide 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.
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