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Electrically-powered synthesis provides a sustainable approach for propylene oxidation to propylene oxide and propylene glycol in aqueous medium using water as the oxygen source, which can substitute conventional energy-intensive process that relies on hazardous oxidants. However, current electrosynthesis is suffering from expensive catalysts, low current density and Faradaic efficiency. Herein, guided by accidental finding of Ag+ showing activity for propylene electrooxidation to propylene glycol and following mechanistic understanding, we report 1,2,3-triazole-chelated Ag catalyst with improved current density (15.8 mA/cm2) and Faradaic efficiency (62.5%), comparable with heterogeneous Pt and Pd catalysts using 30-fold less expensive metal. We experimentally and theoretically demonstrate that triazole coordination modulates the oxidative ability of the in-situ formed Ag-oxo species, suppressing overoxidation and oxygen evolution. Furthermore, by employing a high-pressure electrolyzer, we strengthen propylene mass transfer and attain an enhanced current density of 61.1 mA/cm2 with Faradaic efficiency of 73.4%. By circulating electro-deposition/dissolution of Ag, the catalyst shows reusability in 10 cycles. This work demonstrates the potential of using cost-effective homogeneous catalyst for propylene electrooxidation.
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Simin Xu
Harbin Medical University
Xiang Liu
University of Science and Technology of China
An-Zhen Li
Unité Matériaux et Transformations
Nature Communications
Tsinghua University
Sinopec (China)
Gannan Normal University
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Xu et al. (Mon,) studied this question.
synapsesocial.com/papers/69403b822d562116f290c1b3 — DOI: https://doi.org/10.1038/s41467-025-65253-6