Electrosynthesis of 2,5-Furandicarboxylic Acid from 5-Hydroxymethylfurfural: Mechanisms, Advanced Catalysts, and Reaction Microenvironments

Abstract

As the sole renewable source of organic carbon, biomass is indispensable to the green transition, offering both abundance and carbon neutrality. The biomass-derived platform molecule, 5-hydroxymethylfurfural (HMF), can be valorized into various high-value chemicals via oxidation. Most notably, 2,5-furandicarboxylic acid (FDCA) has emerged as a crucial sustainable alternative to fossil-based terephthalic acid for polyester production. This review provides a comprehensive analysis of the electrocatalytic oxidation of HMF to FDCA. We begin by dissecting the reaction pathways and mechanisms to clarify key kinetic steps and current bottlenecks. To establish benchmarks for the field, we summarize standard evaluation metrics that enable rigorous comparison among disparate studies. The review then systematically categorizes diverse catalyst systems and engineering strategies, with a specific focus on how reaction parameters (pH, electrolyte composition, and applied potential) dictate product selectivity. Concluding with a forward-looking perspective, we propose future directions to accelerate the development of efficient, controllable, and low-cost technologies for FDCA production.

Article information

Article type
Review Article
Submitted
11 Dec 2025
Accepted
12 Jan 2026
First published
12 Jan 2026
This article is Open Access

All publication charges for this article have been paid for by the Royal Society of Chemistry
Creative Commons BY-NC license

Chem. Sci., 2026, Accepted Manuscript

Electrosynthesis of 2,5-Furandicarboxylic Acid from 5-Hydroxymethylfurfural: Mechanisms, Advanced Catalysts, and Reaction Microenvironments

J. Zhang, S. Wang, J. Liu, J. Chen, G. Zhang, Y. Hou, M. Zheng, S. Wang and X. F. Lu, Chem. Sci., 2026, Accepted Manuscript , DOI: 10.1039/D5SC09723A

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