Theoretical insight into electrochemical nitrate reduction on transition metal iron doped graphdiyne

Author:

Xie Shuyi1,Ruan Wenqi1,Liu Qianqian1,Zhang Yongfan12,Guo Xiangyu3ORCID,Ding Kaining12ORCID

Affiliation:

1. College of Chemistry, Research Institute of Photocatalysis State Key Laboratory of Photocatalysis on Energy and Environment, Fuzhou University Fuzhou China

2. College of Chemistry, Fujian Provincial Key Laboratory of Electrochemical Energy Storage Materials Fuzhou University Fuzhou China

3. School of Science Constructor University Bremen Germany

Abstract

AbstractProduction of ammonia (NH3) by electrocatalytic reduction of nitrate (NO3RR) not only eliminates harmful pollution, but also provides a way to reduce the energy consumption associated with predominated Haber‐Bosch process. However, realization of this process still faces many challenges because of the complexity of the reaction mechanism. Here we investigated the catalytic activity and selectivity of a series of graphdiyne supported single atom catalysts (SACs), namely TM/GDY, for the reduction of N to NH3 by first‐principles calculations. Among the 10 SACs studied, Fe/GDY was found to have good catalytic performance, consistent with the fact that the Fe‐doped GDY molecular layer was located near the top of the volcano plot, with a reaction limit potential of −0.44 V and showed excellent selectivity in inhibiting the competitive hydrogen evolution reaction (HER). The formation of the by‐products NO2, NO, N2O and N2 on Fe/GDY requires a considerable energy barrier, which ensures high selectivity. Furthermore, detailed electronic property analyses indicate that the GDY can work as an electron repository to effectively balance the charge transfers during the reaction process. This study not only offers an eligible NO3RR electrocatalyst but also provides an atomic understanding of the mechanisms of the NO3RR process behind.

Funder

National Natural Science Foundation of China

Natural Science Foundation of Fujian Province

Publisher

Wiley

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