乙二醇
催化作用
选择性
乙烯
乙醇酸
吸附
电解
材料科学
化学
无机化学
化学工程
核化学
电解质
电极
有机化学
乳酸
生物
工程类
物理化学
遗传学
细菌
作者
Zijian Li,Shao Wang,Yijun Yin,Rui Qin,Chenyang Wei,Hongxia Luo,Tiancheng Mu
标识
DOI:10.1002/asia.202401843
摘要
The electroconversion of polyethylene terephthalate (PET) into C2 fine chemicals and hydrogen (H2) 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)2 catalyst, achieving a high Faraday efficiency (>90%) even at high current densities (250 mA cm−2 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)2 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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