Cobalt single-atom and nano catalysts for efficient transfer hydrodeoxygenation of vanillin with formic acid

This study presents a Co catalyst with coexisting single-atoms and nanoparticles on N-doped carbon (Co<sub>1</sub>+Co<sub>n</sub>/N-C). Synthesized via a sacrificial MgO-template method, it achieves 100% vanillin conversion and >99% selectivity to 2-methoxy-4-methylphenol at 160°C using formic acid, outperforming single-component catalysts. Kinetic studies reveal a water-mediated dual hydrogen transfer pathway, lowering the apparent activation energy to 61.7 kJ/mol. Isotopic studies suggest a water-mediated mechanism, wherein water molecules facilitate proton transfer and hydrogen spillover through a hydrogen-bonding network. This process synergizes with formic acid dehydrogenation to enable a dual hydrogen transfer pathway, involving protonation of the aldehyde group and hydride (H⁻) attack. The catalyst maintains 95% conversion over ten cycles, demonstrating high stability for biomass upgrading.

Authors

Institutions

Publication Details

Journal
Communications Chemistry
Published
2026-02-23
DOI
https://doi.org/10.1038/s42004-026-01947-2
Primary Topic
Catalysis for Biomass Conversion
Type
article
Field-Weighted Citation Impact
0.00

Funders

Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Cobalt single-atom and nano catalysts for efficient transfer hydrodeoxygenation of vanillin with formic acid

Zisheng Xu, Guitao Shi, Linlin Wang, Jie Li et al.
Communications Chemistry
Catalysis for Biomass Conversion
article

Cobalt single-atom and nano catalysts for efficient transfer hydrodeoxygenation of vanillin with formic acid

Zisheng Xu, Guitao Shi, Linlin Wang, Jie Li, Maofei Ran, Tao Dai
article en

Abstract

This study presents a Co catalyst with coexisting single-atoms and nanoparticles on N-doped carbon (Co<sub>1</sub>+Co<sub>n</sub>/N-C). Synthesized via a sacrificial MgO-template method, it achieves 100% vanillin conversion and >99% selectivity to 2-methoxy-4-methylphenol at 160°C using formic acid, outperforming single-component catalysts. Kinetic studies reveal a water-mediated dual hydrogen transfer pathway, lowering the apparent activation energy to 61.7 kJ/mol. Isotopic studies suggest a water-mediated mechanism, wherein water molecules facilitate proton transfer and hydrogen spillover through a hydrogen-bonding network. This process synergizes with formic acid dehydrogenation to enable a dual hydrogen transfer pathway, involving protonation of the aldehyde group and hydride (H⁻) attack. The catalyst maintains 95% conversion over ten cycles, demonstrating high stability for biomass upgrading.

Communications Chemistry
Qinghai Tibetan Hospital (CN), Southwest Minzu University (CN)
National Natural Science Foundation of China, Southwest Minzu University
Clean water and sanitation
Openalex Percentile: Top 48%
Catalysis for Biomass Conversion
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.