Yeast-derived N, P co-doped porous green carbon materials as metal-free catalysts for selective hydrogenation of chloronitrobenzene

Biomass provides a promising source of carbon for obtaining environment-friendly carbon materials, but obtaining heteroatom-doped carbon materials (HDCMs) from biomass directly by a green method still remains challenging. This study successfully synthesized nitrogen and phosphorus co-doped porous ca...

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Veröffentlicht in:Green chemistry : an international journal and green chemistry resource : GC 2024-07, Vol.26 (13), p.7958-797
Hauptverfasser: Wang, Xiaohua, Zhao, Hongfan, Zhou, Yebin, Yin, Chunyu, He, Wei, Feng, Feng, Wang, Fengli, Lu, Chunshan, Li, Xiaonian
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container_issue 13
container_start_page 7958
container_title Green chemistry : an international journal and green chemistry resource : GC
container_volume 26
creator Wang, Xiaohua
Zhao, Hongfan
Zhou, Yebin
Yin, Chunyu
He, Wei
Feng, Feng
Wang, Fengli
Lu, Chunshan
Li, Xiaonian
description Biomass provides a promising source of carbon for obtaining environment-friendly carbon materials, but obtaining heteroatom-doped carbon materials (HDCMs) from biomass directly by a green method still remains challenging. This study successfully synthesized nitrogen and phosphorus co-doped porous carbon materials (Y-NPC) by the simple in situ pyrolysis of renewable yeast mixed with water from 800 to 950 °C. Various characterization methods show that nitrogen and phosphorus are doped into the carbon skeleton and mainly exist in the forms of graphite-N, pyridine-N, C-P, P-N, and P-O states. The catalyst Y-NPC-900 °C with a 3D hierarchical porous structure and high P-N content exhibited superior nitro hydrogenation performance and reaction stability using molecular hydrogen and hydrazine hydrate as hydrogen sources under mild conditions. Density functional theory (DFT) calculations and experiments attributed the exceptional catalytic performance to hydrogen activation and the good adsorption ability of substrates over N, P co-doped carbon (NPC). Therefore, this research proposes an eco-friendly and simple synthesis strategy for in situ N, P co-doping metal-free carbon catalysts derived from biomass, showing the significance of N, P co-doping and single N- or P-monodoping in the charge distribution of carbon materials. The N, P co-doped porous carbon materials were synthesized via the in situ pyrolysis of yeast post-water treatment and exhibited superior nitro hydrogenation performance using molecular hydrogen and hydrazine hydrate as hydrogen sources.
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This study successfully synthesized nitrogen and phosphorus co-doped porous carbon materials (Y-NPC) by the simple in situ pyrolysis of renewable yeast mixed with water from 800 to 950 °C. Various characterization methods show that nitrogen and phosphorus are doped into the carbon skeleton and mainly exist in the forms of graphite-N, pyridine-N, C-P, P-N, and P-O states. The catalyst Y-NPC-900 °C with a 3D hierarchical porous structure and high P-N content exhibited superior nitro hydrogenation performance and reaction stability using molecular hydrogen and hydrazine hydrate as hydrogen sources under mild conditions. Density functional theory (DFT) calculations and experiments attributed the exceptional catalytic performance to hydrogen activation and the good adsorption ability of substrates over N, P co-doped carbon (NPC). Therefore, this research proposes an eco-friendly and simple synthesis strategy for in situ N, P co-doping metal-free carbon catalysts derived from biomass, showing the significance of N, P co-doping and single N- or P-monodoping in the charge distribution of carbon materials. 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source Royal Society Of Chemistry Journals; Alma/SFX Local Collection
subjects Biomass
Carbon
Catalysts
Charge distribution
Charge materials
Chloronitrobenzene
Density functional theory
Doping
Hydrazine
Hydrazines
Hydrogen
Hydrogenation
Nitrogen
Phosphorus
Porous materials
Pyrolysis
Substrates
Yeast
Yeasts
title Yeast-derived N, P co-doped porous green carbon materials as metal-free catalysts for selective hydrogenation of chloronitrobenzene
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