Bidirectional Nitrogen Neutralization via Coupled Electrocatalytic Processes of Nitrate Reduction and Hydrazine Oxidation

中和 联氨(抗抑郁剂) 材料科学 硝酸盐 氮气 电催化剂 还原(数学) 无机化学 电化学 电极 有机化学 化学 物理化学 抗体 几何学 免疫学 生物 色谱法 数学
作者
Fasheng Chen,Xinyu Zhou,Huaizhu Wang,Xinyu Liu,Qingxiu Yang,Xi Chen,Qiaoqiao Mu,Jitian Liu,Xiao Li,Xuemei Liao,Zhenju Jiang,Zhong Jin,Minghang Jiang
出处
期刊:Advanced Functional Materials [Wiley]
卷期号:35 (26) 被引量:24
标识
DOI:10.1002/adfm.202421405
摘要

Abstract The electrocatalytic coupling of the nitrate reduction reaction (NO 3 − RR) and the hydrazine oxidation reaction (HzOR), denoted as NO 3 − RR||HzOR, not only holds promise for the synthesis of high‐value‐added products (such as NH 3 ) but also facilitates bidirectional nitrogen neutralization. Here, the synthesis of sponge‐like porous nitrogen‐doped carbon encapsulated Cu nanoparticles electrocatalysts is presented for the electrochemical NO 3 − RR||HzOR. Substituting the traditional oxygen evolution reaction (OER) with the HzOR as the anode reaction notably accelerates the kinetic process of NH 3 synthesis via NO 3 − RR. Moreover, the spatial confinement of Cu nanoparticles within a sponge‐like porous nitrogen‐doped carbon (NDC) structure not only addresses the aggregation and detachment issues of Cu NPs from the catalyst support surface but also effectively modulates the electronic structure of Cu NPs through electronic interactions between NDC and Cu NPs. This, in turn, enhances the adsorption and activation of nitrate ions. Consequently, the combined advantages of optimized surface electronic structure and spatial confinement of Cu NPs significantly improve the activity and stability for the electrocatalytic NO 3 − RR to NH 3 . This work offers significant reference value for sustainable nitrogen neutrality development by leveraging a mild, energy‐efficient, and environmentally friendly electrocatalytic process that concurrently eliminates nitrogen pollutants in both high and low oxidation states.
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