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Phase Engineering of High-Entropy Alloy for Enhanced Electrocatalytic Nitrate Reduction to Ammonia

Research output: Journal Publications and Reviews › RGC 21 - Publication in refereed journal › peer-review

Abstract

Directly electrochemical conversion of nitrate (NO3−) is an efficient and environmentally friendly technology for ammonia (NH3) production but is challenged by highly selective electrocatalysts. High-entropy alloys (HEAs) with unique properties are attractive materials in catalysis, particularly for multi-step reactions. Herein, we first reported the application of HEA (FeCoNiAlTi) for electrocatalytic NO3− reduction to NH3 (NRA). The bulk HEA is active for NRA but limited by the unsatisfied NH3 yield of 0.36 mg h−1 cm−2 and Faradaic efficiency (FE) of 82.66 %. Through an effective phase engineering strategy, uniform intermetallic nanoparticles are introduced on the bulk HEA to increase electrochemical active surface area and charge transfer efficiency. The resulting nanostructured HEA (n-HEA) delivers enhanced electrochemical NRA performance in terms of NH3 yield (0.52 mg h−1 cm−2) and FE (95.23 %). Further experimental and theoretical investigations reveal that the multi-active sites (Fe, Co, and Ni) dominated electrocatalysis for NRA over the n-HEA. Notably, the typical Co sites exhibit the lowest energy barrier for NRA with *NH2 to *NH3as the rate-determining step. © 2024 Wiley-VCH GmbH.
Original languageEnglish
Article numbere202407589
JournalAngewandte Chemie - International Edition
Volume63
Issue number35
Online published4 May 2024
DOIs
Publication statusPublished - 26 Aug 2024

Funding

This work is supported by a grant from the Research Grants Council of the Hong Kong Special Administrative Region, China [Project No. T23-713/22-R]. We thank Dr. M. K. TSE from the Department of Chemistry of the City University of Hong Kong for the NMR measurements.

Research Keywords

  • density functional theory
  • electrocatalysis
  • high-entropy alloy
  • NH3 synthesis
  • NO3− reduction

RGC Funding Information

  • RGC-funded

ESI Highly Cited Papers

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ESI Highly Cited Paper Designation Date(s)

  • 20260108
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  • 20250911
  • 20250710
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  • 20250313
  • 20251113
  • 20260312
  • 20260709
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