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重新审视碳化钼和碳化铁上的电化学氮还原:有前景的催化剂还是误报?

Revisiting the Electrochemical Nitrogen Reduction on Molybdenum and Iron Carbides: Promising Catalysts or False Positives?

作者信息

Izelaar Boaz, Ripepi Davide, Asperti Simone, Dugulan A Iulian, Hendrikx Ruud W A, Böttger Amarante J, Mulder Fokko M, Kortlever Ruud

机构信息

Large Scale Energy Storage, Process and Energy Department, Faculty of Mechanical, Maritime and Materials Engineering, Delft University of Technology, Delft2628 CB, The Netherlands.

Materials for Energy Conversion and Storage, Chemical Engineering Department, Faculty of Applied Sciences, Delft University of Technology, Delft2629 HZ, The Netherlands.

出版信息

ACS Catal. 2023 Jan 12;13(3):1649-1661. doi: 10.1021/acscatal.2c04491. eCollection 2023 Feb 3.

Abstract

The electrochemical dinitrogen reduction reaction (NRR) has recently gained much interest as it can potentially produce ammonia from renewable intermittent electricity and replace the Haber-Bosch process. Previous literature studies report Fe- and Mo-carbides as promising electrocatalysts for the NRR with activities higher than other metals. However, recent understanding of extraneous ammonia and nitrogen oxide contaminations have challenged previously published results. Here, we critically assess the NRR performance of several Fe- and Mo-carbides reported as promising by implementing a strict experimental protocol to minimize the effect of impurities. The successful synthesis of α-MoC decorated carbon nanosheets, α-MoC nanoparticles, θ-FeC nanoparticles, and χ-FeC nanoparticles was confirmed by X-ray diffraction, scanning and transmission electron microscopy, and X-ray photoelectron and Mössbauer spectroscopy. After performing NRR chronoamperometric tests with the synthesized materials, the ammonia concentrations varied between 37 and 124 ppb and are in close proximity with the estimated ammonia background level. Notwithstanding the impracticality of these extremely low ammonia yields, the observed ammonia did not originate from the electrochemical nitrogen reduction but from unavoidable extraneous ammonia and NO impurities. These findings are in contradiction with earlier literature studies and show that these carbide materials are not active for the NRR under the employed conditions. This further emphasizes the importance of a strict protocol in order to distinguish between a promising NRR catalyst and a false positive.

摘要

电化学固氮反应(NRR)近来备受关注,因为它有可能利用可再生的间歇性电力生产氨,从而取代哈伯-博施工艺。先前的文献研究报道,铁和钼的碳化物是很有前景的NRR电催化剂,其活性高于其他金属。然而,最近对外源氨和氮氧化物污染的认识对先前发表的结果提出了挑战。在这里,我们通过实施严格的实验方案来尽量减少杂质的影响,从而严格评估了几种据报道很有前景的铁和钼碳化物的NRR性能。通过X射线衍射、扫描和透射电子显微镜以及X射线光电子能谱和穆斯堡尔谱,证实了α-MoC修饰的碳纳米片、α-MoC纳米颗粒、θ-FeC纳米颗粒和χ-FeC纳米颗粒的成功合成。在用合成材料进行NRR计时电流测试后,氨浓度在37至124 ppb之间变化,与估计的氨背景水平相近。尽管这些极低的氨产率不切实际,但观察到的氨并非来自电化学氮还原,而是来自不可避免的外源氨和NO杂质。这些发现与早期的文献研究相矛盾,表明在所采用的条件下,这些碳化物材料对NRR没有活性。这进一步强调了严格方案对于区分有前景的NRR催化剂和假阳性的重要性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a45d/9903294/3e953c9da9c6/cs2c04491_0002.jpg

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