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Carbon-Coated Ni-Fe Nanocatalysts: Bridging the Gap in Cinnamaldehyde Hydrogenation Performance and Durability

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This study focuses on the synthesis and evaluation of carbon−coated Ni−Fe alloy catalysts (NiFex@C, x = 0, 0.3, 0.7, 1.1) for the hydrogenation of cinnamaldehyde. The catalysts were characterized using Transmission Electron Microscopy (TEM), X-ray Diffraction (XRD), Raman spectroscopy, and X-ray Photoelectron Spectroscopy (XPS). The introduction of Fe was found to increase the average particle size of the bimetallic catalysts compared to the monometallic Ni@C. Ni existed in both metallic and oxide states, while Fe exhibited multiple oxidation states in the bimetallic catalysts. The carbon layer, approximately 2–3 nm thick, was confirmed to envelop the alloy particles. The catalytic performance of carbon−coated Ni−Fe alloy catalysts indicated that the addition of Fe to Ni@C enhanced the selectivity towards hydrocinnamaldehyde (HCAL), with NiFe0.7@C showing the highest selectivity (~88.6%) but at a reduced conversion rate. The carbon layer played a pivotal role in the stability and reusability of the catalysts. NiFe0.7@C maintained consistent performance over multiple reaction cycles, while NiFe0.7 NPs (without a carbon layer) exhibited significant deactivation. Both catalysts displayed strong magnetism, facilitating easy separation from the reaction mixture. This study sheds light on the significance of the carbon layer in bimetallic catalysts and provides valuable insights for designing efficient catalysts for hydrogenation processes.
Title: Carbon-Coated Ni-Fe Nanocatalysts: Bridging the Gap in Cinnamaldehyde Hydrogenation Performance and Durability
Description:
This study focuses on the synthesis and evaluation of carbon−coated Ni−Fe alloy catalysts (NiFex@C, x = 0, 0.
3, 0.
7, 1.
1) for the hydrogenation of cinnamaldehyde.
The catalysts were characterized using Transmission Electron Microscopy (TEM), X-ray Diffraction (XRD), Raman spectroscopy, and X-ray Photoelectron Spectroscopy (XPS).
The introduction of Fe was found to increase the average particle size of the bimetallic catalysts compared to the monometallic Ni@C.
Ni existed in both metallic and oxide states, while Fe exhibited multiple oxidation states in the bimetallic catalysts.
The carbon layer, approximately 2–3 nm thick, was confirmed to envelop the alloy particles.
The catalytic performance of carbon−coated Ni−Fe alloy catalysts indicated that the addition of Fe to Ni@C enhanced the selectivity towards hydrocinnamaldehyde (HCAL), with NiFe0.
7@C showing the highest selectivity (~88.
6%) but at a reduced conversion rate.
The carbon layer played a pivotal role in the stability and reusability of the catalysts.
NiFe0.
7@C maintained consistent performance over multiple reaction cycles, while NiFe0.
7 NPs (without a carbon layer) exhibited significant deactivation.
Both catalysts displayed strong magnetism, facilitating easy separation from the reaction mixture.
This study sheds light on the significance of the carbon layer in bimetallic catalysts and provides valuable insights for designing efficient catalysts for hydrogenation processes.

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