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Fe(II)-rich catalytic interfaces boost nitrate adsorption and hydrogenation for selective electrochemical ammonia synthesis

delete2025-08-05
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PRE
AI
H
H. Wang
S
Shiyin Yuan
J
Jia Yan
Y
Yinghao Xue
赵东琦 (Dongqi Zhao)
J
Jianwei Fan *
张伟贤 (Wei‐xian Zhang)
DOI:10.1016/j.cej.2025.166686delete
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Abstract

Abstract

En 中文
• Fe@CF-1 achieves 98.46% NO3− conversion within 2 h across a wide pH range (3–12). • Stabilized Fe(II) sites have the ability to effectively adsorb and activate NO3−. • Fe sites promote hydrogenation of nitrogenous intermediates while inhibiting HER. • Fe@CF-1 shows dynamic evolution of Fe(II) and Fe(III) species during NO3RR.
Keywords:
Fe@CF-1
NO3− reduction
Fe(II) sites
hydrogenation
HER inhibition

Journal

Chemical Engineering Journal cover
Chemical Engineering Journal
IF:
13.2
Papers:
7.4W
Citations:
48.5W

Organization

T
tsinghua university
Scholars:
11.6W
Papers: 9.9W
Citations: 137
T
tongji university
Scholars:
7.6W
Papers: 5.9W
Citations: 98