The electroconversion of polyethylene terephthalate (PET) into C2 fine chemicals and hydrogen (H) presents a promising solution for advancing the circular plastics economy. In this study, we report the electrooxidation of ethylene glycol (EG) to glycolic acid (GA) using a Pt-Ni(OH) catalyst, achieving a high Faraday efficiency (>90 %) even at high current densities (250 mA cm at 0.8 V vs. RHE). Notably, this catalyst outperforms most existing Pt-based catalysts in terms of catalytic activity. Experimental analyses reveal that: 1) Ni(OH) enhances the adsorption of OH ions and promotes the rapid generation of *OH active species, which are essential for the efficient oxidation of EG to GA; 2) the oxygenophilic nature of Pt improves EG adsorption, and in synergy with Ni, accelerates the oxidation process. Furthermore, Pt lowers the electrolysis potential, preventing excessive oxidation and ensuring high selectivity for GA. This work offers a promising pathway for the electrooxidation-based upgrading of PET plastics and provides valuable insights for future research in this area.
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http://dx.doi.org/10.1002/asia.202401843 | DOI Listing |
J Colloid Interface Sci
February 2025
College of Chemistry, Chemical Engineering and Materials Science, Soochow University, Suzhou 215123, China. Electronic address:
One-dimensional (1D) Pd-based nanowire materials, characterized by high aspect ratios and exposed high-index crystal surfaces, are widely developed in the field of direct fuel cells. However, their synthesis methods are often not universal and necessitate demanding conditions, including high temperatures and metal templates, leading to resource consumption. In this study, we present a simple and universal one-step method for synthesizing PdM (Sb, Ir, and Bi) nanowire networks (NNWs) at room temperature.
View Article and Find Full Text PDFAdv Mater
March 2025
School of Materials Science and Engineering, University of Science and Technology Beijing, Beijing, 100083, China.
The upcycling of polyethylene terephthalate (PET)-derived ethylene glycol (EG) to glycolic acid (GA, a biodegradable polymer monomer) via electrocatalysis not only produces valuable chemicals but also mitigates plastic pollution. However, the current reports for electrooxidation of EG-to-GA usually operate at reaction potentials of >1.0 V vs reversible hydrogen electrode (RHE), much higher than the theoretical potential (0.
View Article and Find Full Text PDFJACS Au
February 2025
Shanghai Key Laboratory of Rare Earth Functional Materials and Education Ministry Key Laboratory of Resource Chemistry, Shanghai Normal University, Shanghai 200234, P. R. China.
Electro-upgrading of low-cost alcohols such as ethylene glycol is a promising and sustainable approach for the production of value-added chemicals while substituting energy-consuming OER in water splitting. However, the sluggish kinetics and possibility of C-C dissociation make the design of selective and efficient electrocatalysts challenging. Herein, we demonstrate the synthesis of a hollowed bimetallic PtAg nanostructure through an in situ dynamic evolution method that could efficiently drive the selective electrochemical ethylene glycol oxidation reaction (EGOR).
View Article and Find Full Text PDFJ Am Chem Soc
March 2025
Materials Sciences Division, Lawrence Berkeley National Laboratory, Berkeley, California 94720, United States.
Lithium-ion batteries (LIBs) with nonaqueous liquid electrolytes are prone to gas generation at elevated voltages and temperatures, degrading battery performance and posing serious safety risks. Organosilicon (OS) additives are an emerging candidate solution for gassing problems in LIBs, but a detailed understanding of their functional mechanisms remains elusive. In this work, we present a combined computational and experimental study to elucidate the gas-reducing effects of OS additives.
View Article and Find Full Text PDFChem Sci
March 2025
Center of Advanced Electrochemical Energy, State Key Laboratory of Advanced Chemical Power Sources, School of Chemistry and Chemical Engineering, Chongqing University Chongqing 40004 P. R. China
The electrocatalytic oxidation of ethylene glycol (EG) to produce valuable glycolic acid (GLYA) is a promising strategy to tackle EG overcapacity. Despite the good selectivity of Pd for EG oxidation, its performance is constrained by limited mass activity and toxicity of intermediates like CO or CO-analogues. This study reports the alloying of Pd with Ni and Mo metals to enhance the activity and durability of EG oxidation in alkaline media.
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