Non‐Carbonized Pd Single‐Atom Catalyst Supported on Lignin‐Functionalized Phenolic Resin for Potent Catalytic Transfer Hydrogenation of Lignin‐Derived Aldehydes

Single-atom catalysts (SACs) depend significantly on their support properties, and organic polymers have emerged as promising candidates due to their tunable physicochemical properties and diverse functional groups. However, the high-temperature carbonization commonly required for conventional organic polymer-supported SAC fabrication often leads to the loss of these functional groups, thus weakening metal-support interactions and catalytic performance accordingly. Herein, we report a sustainable strategy to synthesize nitrogen-functionalized lignin-based phenolic resin (N-LPR) supports for stabilizing atomically dispersed palladium (Pd) without carbonization. Using ammonia solution (NH<sub>3</sub>·H<sub>2</sub>O) as both the nitrogen source and catalyst, high molecular weight lignin fractions (L3) were transformed into N-L3PR-50% supports with a unique nano-chain-like structure, high surface area, and abundant amine groups, which can directly anchor Pd sites under room temperature. The resulting Pd@N-L3PR-50% catalyst achieved approximately 100% vanillin conversion and 97.91% selectivity for 2-methoxy-4-methylphenol at 80 °C with excellent cycle stability and adaptability to lignin-derived aldehydes, benefiting from the stable Pd-N coordination and the good adsorption capacity provided by the N-L3PR-50% support. Consequently, this work not only demonstrates a straightforward non-carbonation strategy to prepare lignin-based SACs for potent biomass-derived chemical transformations but also provides a novel avenue for the application of conventional multifunctional organic polymers as support for SACs.

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Publication Details

Journal
Angewandte Chemie International Edition
Published
2025-03-27
DOI
https://doi.org/10.1002/anie.202503195
Citations
48
Primary Topic
Catalysis and Hydrodesulfurization Studies
Type
article
Field-Weighted Citation Impact
34.24
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article

Non‐Carbonized Pd Single‐Atom Catalyst Supported on Lignin‐Functionalized Phenolic Resin for Potent Catalytic Transfer Hydrogenation of Lignin‐Derived Aldehydes

Wenjie Sui, Tairan Pang, Guanhua Wang, Chuanling Si et al.
48 citations
Angewandte Chemie International Edition
Catalysis and Hydrodesulfurization Studies
34.24
article

Non‐Carbonized Pd Single‐Atom Catalyst Supported on Lignin‐Functionalized Phenolic Resin for Potent Catalytic Transfer Hydrogenation of Lignin‐Derived Aldehydes

Wenjie Sui, Tairan Pang, Guanhua Wang, Chuanling Si, Junkai Li, Zhenglong Xue
article en
48 citations

Abstract

Single-atom catalysts (SACs) depend significantly on their support properties, and organic polymers have emerged as promising candidates due to their tunable physicochemical properties and diverse functional groups. However, the high-temperature carbonization commonly required for conventional organic polymer-supported SAC fabrication often leads to the loss of these functional groups, thus weakening metal-support interactions and catalytic performance accordingly. Herein, we report a sustainable strategy to synthesize nitrogen-functionalized lignin-based phenolic resin (N-LPR) supports for stabilizing atomically dispersed palladium (Pd) without carbonization. Using ammonia solution (NH<sub>3</sub>·H<sub>2</sub>O) as both the nitrogen source and catalyst, high molecular weight lignin fractions (L3) were transformed into N-L3PR-50% supports with a unique nano-chain-like structure, high surface area, and abundant amine groups, which can directly anchor Pd sites under room temperature. The resulting Pd@N-L3PR-50% catalyst achieved approximately 100% vanillin conversion and 97.91% selectivity for 2-methoxy-4-methylphenol at 80 °C with excellent cycle stability and adaptability to lignin-derived aldehydes, benefiting from the stable Pd-N coordination and the good adsorption capacity provided by the N-L3PR-50% support. Consequently, this work not only demonstrates a straightforward non-carbonation strategy to prepare lignin-based SACs for potent biomass-derived chemical transformations but also provides a novel avenue for the application of conventional multifunctional organic polymers as support for SACs.

Angewandte Chemie International EditionVol. 64(23)
Tianjin University of Science and Technology (CN), Tianjin Economic-Technological Development Area (CN)
Responsible consumption and production
Openalex Percentile: Top 0%
Catalysis and Hydrodesulfurization Studies
34.24
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