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Coral-like Fe-doped MoO/C heterostructures with rich oxygen vacancies for efficient electrocatalytic N reduction. | LitMetric

Coral-like Fe-doped MoO/C heterostructures with rich oxygen vacancies for efficient electrocatalytic N reduction.

Dalton Trans

Key Laboratory of Chemical Engineering Processes&Technology for High-efficiency Conversion (College of Heilongjiang Province), School of Chemistry and Material Science, Heilongjiang University, Harbin, 150080, China.

Published: February 2023

AI Article Synopsis

Article Abstract

Molybdenum (Mo) is one of the most important constituent elements in natural nitrogenase and theoretical calculation results show that Mo-based materials can be used as potential NRR electrocatalysts. The design of advanced catalysts with a special structure is very essential for promoting the development of electrocatalytic N into NH. In this paper, Fe-doped MoO/C heterostructured nanoparticles with rich oxygen vacancies (Vo) are designed and they exhibit highly efficient catalytic activity for artificial N fixation in neutral electrolytes under ambient conditions. The influence of the atomic ratio of the Fe source to the Mo source and the NaBH ethanol solution treatment on the structure and electrocatalytic performance are systematically investigated. The Vo-Fe-MoO/C (1 : 50) catalyst with rich oxygen vacancies shows a satisfactory electrocatalytic N reduction reaction (e-NRR) activity in 0.1 M NaSO with a high ammonia yield rate of 15.87 ± 0.3 μg h mg at -0.5 V the reversible hydrogen electrode ( the RHE) and a FE of 13.4% at -0.3 V ( the RHE). According to the results of DFT calculations, the active center of the electro-catalytic nitrogen reduction reaction is the molybdenum atom between the iron atom and the O vacancy. Oxygen vacancies can not only reduce the energy barrier of the RDS but also facilitate the desorption of ammonia and the first step hydrogenation of nitrogen. The doping of Fe will change the electronic state of the Mo atom in MoO.

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http://dx.doi.org/10.1039/d2dt03275aDOI Listing

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