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用于将2,5-双(羟甲基)呋喃热催化和电催化氧化为2,5-呋喃二甲酸的钴@氮掺杂碳链状纳米线

Co@NC Chainmail Nanowires for Thermo- and Electrocatalytic Oxidation of 2,5-Bis(hydroxymethyl)furan to 2,5-Furandicarboxylic Acid.

作者信息

Zhu Bin, Wang Qiuge, Wang Jinggang, Yu Xiao, Zhang Jian, Chen Chunlin

机构信息

Ningbo Institute of Materials Technology and Engineering, Chinese Academy of Sciences, 1219 Zhongguan West Road, Ningbo, 315201, P.R. China.

University of Chinese Academy of Sciences, Beijing, 100049, P.R. China.

出版信息

ChemSusChem. 2025 Feb 16;18(4):e202401422. doi: 10.1002/cssc.202401422. Epub 2024 Nov 6.

Abstract

2,5-Furandicarboxylic acid (FDCA) has emerged as an important bio-based furanic compound, which has broad application prospects in renewable energy and materials, especially in the preparation of polyethylene 2,5-furandicarboxylate (PEF). While the conventional synthesis of FDCA involves oxidation of 5-hydroxymethylfurfural (HMF) as a substitute, the thermal and chemical instability of HMF due to its aldehyde group poses challenges. A more favorable alternative is the utilization of 2,5-bis(hydroxymethyl)furan (BHMF), a non-aldehyde and more stable precursor. This study pioneeringly reports nitrogen-doped-carbon encapsulated cobalt (Co@NC) chainmail nanowires for the thermal and electrocatalytic oxidation of BHMF to FDCA. The Co@NC/NF achieved a 97.9 % conversion of BHMF with a 93.3 % yield of FDCA at 1.475 V vs. RHE, whereas thermal catalysis only obtained 14.9 % FDCA yield after 10 hours. Kinetic studies indicated that the large electrochemically active surface area and excellent kinetic parameters contribute its superior electrochemical performance. Mechanistic analysis revealed that the migration of inner electrons to the exterior modified the electronic properties of the carbon layer, thereby facilitating the oxidation of BHMF. Furthermore, the in-situ generation of high-valent cobalt species markedly accelerated the BHMF oxidation. This research underscores the potential of carbon-encapsulated metal chainmail catalysts in thermal and electrochemical biomass conversion.

摘要

2,5-呋喃二甲酸(FDCA)已成为一种重要的生物基呋喃类化合物,在可再生能源和材料领域具有广阔的应用前景,尤其是在聚2,5-呋喃二甲酸乙二酯(PEF)的制备方面。虽然传统的FDCA合成方法涉及以5-羟甲基糠醛(HMF)的氧化作为替代,但由于其醛基导致HMF的热稳定性和化学稳定性较差,带来了挑战。一种更有利的替代方法是利用2,5-双(羟甲基)呋喃(BHMF),一种无醛且更稳定的前体。本研究首次报道了氮掺杂碳包覆钴(Co@NC)链状纳米线用于将BHMF热催化氧化和电催化氧化为FDCA。在相对于可逆氢电极(RHE)为1.475 V的条件下,Co@NC/NF实现了BHMF 97.9%的转化率,FDCA产率为93.3%,而热催化在10小时后仅获得14.9%的FDCA产率。动力学研究表明,较大的电化学活性表面积和优异的动力学参数有助于其卓越的电化学性能。机理分析表明,内部电子向外部的迁移改变了碳层的电子性质,从而促进了BHMF的氧化。此外,高价钴物种的原位生成显著加速了BHMF的氧化。这项研究强调了碳包覆金属链状催化剂在热催化和电化学生物质转化中的潜力。

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