4.8 Article

A practical FeP nanoarrays electrocatalyst for efficient catalytic reduction of nitrite ions in wastewater to ammonia

Journal

APPLIED CATALYSIS B-ENVIRONMENTAL
Volume 325, Issue -, Pages -

Publisher

ELSEVIER
DOI: 10.1016/j.apcatb.2022.122353

Keywords

Electrocatalysis; Nitrite reduction; Ammonia production; Iron phosphide; Theoretical calculations

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The conversion of nitrite ions into ammonia via an electrochemical process is significant due to its potential in addressing the energy-intensive ammonia production and substantial environmental pollution caused by nitrite ions. A study successfully prepared iron phosphide nanoarrays on a Ti plate and utilized it as an efficient catalyst for the conversion of nitrite ions into ammonia. The optimized parameters and mechanistic studies revealed that atomic hydrogen greatly influenced the reaction rate and selectivity, and specific facets of FeP were identified as the main active sites for nitrite reduction.
Ammonia production is an energy-intensive process while nitrite ions are a substantial environmental pollutant, therefore the conversion of nitrite ions (NO2- ) into ammonia (NH3) via an electrochemical process is of great significance. Using a hydrothermal method plus a low temperature phosphating process, iron phosphide nanoarrays (FeP NA) were prepared on a Ti plate to form FeP NA|Ti, which was then used to efficiently convert NO2ions into NH3. In a single-chamber cell using a neutral pH electrolyte, the Faradaic efficiency for nitrite to ammonia conversion reached 82.5 & PLUSMN; 2.3 %. Various parameters were optimized to ensure the high performance of FeP NA|Ti which were explained with mechanistic studies. It was found that atomic hydrogen (H*) greatly impacts both the reaction rate and selectivity. Furthermore, density functional theory (DFT) calculations reveal that the (211) and (011) facets of FeP are the main active faces for nitrite reduction where the nitrite ions tend to bind with two adjacent Fe atoms of FeP to ensure maximum performance.

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