Wang Changlong, Peng Yujie, Xu Ziyi, Yu Jiamei, Wu Yufeng
Institute of Circular Economy, College of Materials Science and Engineering, Beijing University of Technology, Beijing, 100124, P. R. China.
State Key Laboratory of Materials Low-Carbon Recycling, Beijing University of Technology, Beijing, 100124, China.
Small Methods. 2025 Jul 9:e2500187. doi: 10.1002/smtd.202500187.
Green electrochemical synthesis of 2,5-furandicarboxylic acid (FDCA) from biomass is an essential alternative for the substitution of petroleum-based terephthalic acid. The rational design and application of high-performance electrocatalysts are the key to advance this technique. In this work, mesoporous carbon encapsulated ultrafine ScO nanoparticles are reported as a new, highly efficient and selective electrocatalyst that realizes the concurrent electrochemical oxidation of biomass-derived 5-hydroxymethylfurfural (HMF) to FDCA coupled with hydrogen evolution. The performance of the optimum electrocatalyst, ScO@C-900, is suppressed its counterparts, including the mesoporous ScO and the state-of the art electrocatalyst, Ni(OH), NiOOH, and some other noble metal electrocatalysts. The high performance is attributed to the ultrafine ScO nanoparticles with abundant oxygen vacancies, and the mesoporous carbon layer synergistically promotes electrochemical oxidation by accelerating the adsorption and confinement of key intermediates for electro-oxidation, and facilitating the transportations of reactants/products within/out of the electrocatalyst. Moreover, experiments including the electrochemical and in situ measurements, as well as theoretical studies, provide insights into the origin of high efficiency and the preference of the diformylfuran (DFF) pathway.
从生物质中绿色电化学合成2,5-呋喃二甲酸(FDCA)是替代石油基对苯二甲酸的重要选择。高性能电催化剂的合理设计与应用是推进该技术的关键。在这项工作中,报道了介孔碳包裹的超细ScO纳米颗粒作为一种新型、高效且选择性的电催化剂,它实现了将生物质衍生的5-羟甲基糠醛(HMF)同时电化学氧化为FDCA并伴有析氢反应。最优电催化剂ScO@C-900的性能优于其同类催化剂,包括介孔ScO以及最先进的电催化剂Ni(OH)、NiOOH和其他一些贵金属电催化剂。其高性能归因于具有大量氧空位的超细ScO纳米颗粒,并且介孔碳层通过加速电氧化关键中间体的吸附和限制,以及促进反应物/产物在电催化剂内外的传输,协同促进了电化学氧化。此外,包括电化学和原位测量以及理论研究在内的实验,为高效的起源和二甲酰基呋喃(DFF)途径的偏好提供了深入见解。