Fe‐VS2 Electrocatalyst with Organic Matrix‐Mediated Electron Transfer for Highly Efficient Nitrogen Fixation

Electrochemical N2 fixation is considered to be a promising alternative to Haber–Bosch technology. Inspired by the composition and structure of natural nitrogenase, Fe‐doped VS2 nanosheets were prepared via one‐step solvothermal method. The electron transfer system mediated by organic conductive pol...

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Veröffentlicht in:ChemSusChem 2022-08, Vol.15 (16), p.e202200741-n/a
Hauptverfasser: Xiu, Ziyuan, Zheng, Ming, Li, Jiadong, Wei, Feng, Dong, Changchang, Zhang, Mingrui, Zhou, Xin, Han, Xiaojun
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Sprache:eng
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Zusammenfassung:Electrochemical N2 fixation is considered to be a promising alternative to Haber–Bosch technology. Inspired by the composition and structure of natural nitrogenase, Fe‐doped VS2 nanosheets were prepared via one‐step solvothermal method. The electron transfer system mediated by organic conductive polymer (1‐AAQ‐PA) was constructed to promote the electron transfer between Fe‐VS2 nanosheets and the electrode in electrocatalytic N2 reduction reaction (NRR). The obtained 1‐AAQ‐PA−Fe‐VS2 electrode converted N2 to NH3 with a yield of 31.6 μg h−1 mg−1 at −0.35 V vs. reversible hydrogen electrode and high faradaic efficiency of 23.5 %. The introduction of Fe dopants favored N2 adsorption and activation, while the Li−S bond between Fe‐VS2 and Li2SO4 effectively inhibited hydrogen evolution. The highly efficient electron utilization in the electrocatalytic NRR process was realized using the 1‐AAQ‐PA as the electron transfer medium. Density functional theory calculations showed that N2 was preferentially adsorbed on Fe and reduced to NH3 via both distal and alternating mechanism. Nitrogen reduction: A bionic nitrogen fixation system composed of Fe‐VS2 nanosheets and 1‐aminoanthraquinone‐functionalized polymethacrylic acid (1‐AAQ‐PA) matrix is fabricated with 1‐AAQ‐PA as the electron medium to achieved high NH3 yield rate of 31.6 μg h−1 mg−1 and faradaic efficiency to NH3 of 23.1 % in 0.05 m Li2SO4 electrolyte at −0.35 V vs. reversible hydrogen electrode. This work provides inspiration and insights for the development of effective catalyst systems for nitrogen reduction.
ISSN:1864-5631
1864-564X
DOI:10.1002/cssc.202200741