合成气
催化作用
电极
3D打印
材料科学
化学工程
还原(数学)
纳米技术
化学还原
氧还原反应
化学
选择性催化还原
燃料电池
工作(物理)
一氧化碳
氧还原
作者
Na Zhao,Yuxue Zhou,Yuyi Huang,Yaoan Shi,Qianxi Zhao,Wei Wang
出处
期刊:Fuel
[Elsevier BV]
日期:2026-05-04
卷期号:427: 139709-139709
标识
DOI:10.1016/j.fuel.2026.139709
摘要
3D printing has gained great attention in electrochemical CO 2 reduction (CO 2 RR), however, its use in constructing self-supported catalytic electrodes with well-dispersed coordination active sites is still underdeveloped. In this study, a catalytic electrode with CoN X coordination structures (3D-CE-CoN X ) was successfully fabricated using 3D printing for syngas production via CO 2 RR. The CO 2 RR reaction was conducted in a H-type electrolyzer, which was equipped with a conventional three-electrode system. Electrochemical tests show that 3D-CE-CoN X , carbonized at 700 °C, exhibits good CO 2 reduction activity within the potential range of −0.6 V to −1.0 V, producing syngas with a H 2 :CO ratio ranging from 0.53 to 1.79, which is tunable mainly by the applied potential. At −0.7 V, the current density for CO ( J CO ) is −0.19 mA cm −2 , while for H 2 ( J H2 )is −0.14 mA cm −2 . After 24 h of continuous electrolysis, 3D-CE-CoN X maintains 91.5% of its initial CO faradaic efficiency (FE CO ). Furthermore, X-ray absorption fine structure (XAFS) characterization confirms the successful incorporation of CoN X sites, validating the electrode’s effectiveness. This study highlights the unique advantages of 3D printing in catalytic electrode construction and provides a feasible pathway for obtaining high-performance catalytic electrodes for future energy conversion applications.
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