Furfural electrovalorisation to hydrofuroin with near-unity faradaic efficiency on a single-atom zinc catalyst†

EES catalysis Pub Date : 2025-06-23 DOI:10.1039/D5EY00113G
Jiaxiang Chen, Songbo Ye, Fangxin She, Xin Yang, Fangzhou Liu, Zixun Yu, Zhi Zheng, Ming Hong, Qiang Wang, Yuan Chen, Hao Li and Li Wei
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Abstract

Electrochemical valorisation of biomass to value-added chemical feedstocks holds great potential to reduce the reliance on fossil fuels and accelerate the realisation of a sustainable future. In this work, we show that hydrofuroin, an important feedstock for sustainable aviation fuels, can be selectively produced on a zinc (Zn) single-atom catalyst via the electrochemical furfural reduction reaction (FRR). Initial theoretical results show that the weak binding capability of a zinc (Zn) single-atom active center effectively suppresses the parasitic hydrogen evolution reaction (HER) while enabling fast desorption and dimerization of furfural radicals towards hydrofuroin formation, which was proved by our experimental validation. The catalyst, obtained by depositing zinc phthalocyanine on purified multi-walled carbon nanotubes, exhibits near-unity faradaic efficiency for hydrofuroin production in a wide potential window, e.g., −0.5 to −0.8 VRHE. The kinetic study further provides mechanistic insights into hydrofuroin formation on the single-atom site. This catalyst can be integrated into a flow cell electrolyser to achieve highly efficient furfural conversion to sustainable fuel precursors, which is beneficial for biomass electrovalorisation to value-added green products and chemicals.

Abstract Image

在单原子锌催化剂上以接近统一的法拉第效率将糠醛电价化为氢呋喃
生物质的电化学增值为增值化学原料具有巨大的潜力,可以减少对化石燃料的依赖,加速实现可持续的未来。在这项工作中,我们证明了氢呋喃是可持续航空燃料的重要原料,可以通过电化学糠醛还原反应(FRR)在锌(Zn)单原子催化剂上选择性地生产。初步的理论结果表明,锌(Zn)单原子活性中心的弱结合能力有效地抑制了寄生析氢反应(HER),同时使糠醛自由基快速解吸和二聚形成氢呋喃,实验验证了这一点。通过将酞菁锌沉积在纯化的多壁碳纳米管上获得的催化剂,在- 0.5至- 0.8 VRHE的宽电位窗口内表现出接近统一的氢呋喃生产效率。动力学研究进一步提供了氢呋喃在单原子位置形成的机理见解。该催化剂可以集成到液流电池电解槽中,实现高效的糠醛转化为可持续燃料前体,这有利于生物质电价值转化为增值的绿色产品和化学品。
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