电催化剂
材料科学
气凝胶
硝酸盐
氨
无机化学
化学工程
电极
电化学
纳米技术
物理化学
有机化学
化学
工程类
作者
Zheng Jiang,Shujuan Jiang,Wei Huang,Shurong Li,Simin Chen,Huifang Li,Guangping Zheng,Jing Yang
标识
DOI:10.1002/adfm.202507903
摘要
Abstract Renewable energy‐driven electroreduction of nitrate to ammonia presents a low‐carbon and promising route for sustainable ammonia synthesis. For Cu‐based electrocatalysts, due to their sluggish kinetics of the hydrogenation steps, nitrite often accumulates on the electrocatalysts surface, resulting in low ammonia yield rate and selectivity, as well as serious deactivation of electrocatalysts. Herein, a continuous relay site construction strategy that integrates the Cu─Co relay sites into an interconnected porous network is proposed. Owing to the adequately exposed interconnected Cu─Co relay sites, regulated adsorption energy of the nitrate and intermediates, promoted hydrogenation ability, and excellent self‐supportability of 3D skeleton, the Cu 50 Co 50 aerogel realizes the high‐efficiency relay catalysis with an ultrahigh NH 3 yield rate of 3.3 ± 0.27 mmol·h −1 ·cm −2 (2110 ± 173 mmol·h −1 ·g cat −1 ) and a large NH 3 Faraday efficiency of ≈100% at −0.2 V vs. RHE. The potential need for the Cu 50 Co 50 aerogel in the electrocatalysis at an industrial‐level current density remains stable even after 100‐h chronopotentiometry measurement, demonstrating excellent long‐term stability. Besides, the large‐scale preparation (>1 g) of the Cu 50 Co 50 aerogel can be easily achieved, and its exceptional performance is maintained consistently. Such a continuous relay site construction strategy opens a new way for developing advanced electrocatalysts for high‐efficiency relay catalysis.
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