铂金
氧化还原
电合成
氧化剂
化学
电解
聚对苯二甲酸乙二醇酯
吸附
乙二醇
化学工程
无机化学
乙烯
聚乙二醇
饮用水
组合化学
材料科学
纳米技术
阴极
氧化还原
白金黑
化学反应
核化学
有机化学
高分子化学
电化学
化学稳定性
铂纳米粒子
高氯酸
催化作用
作者
Zehao Xiao,Hong-Yu Guo,Yu Gu,Changze Wei,Zheng Lin,Mingchuan Luo,Shaojun Guo
出处
期刊:Science Advances
[American Association for the Advancement of Science]
日期:2026-11-04
卷期号:12 (45): eaei5545-eaei5545
标识
DOI:10.1126/sciadv.aei5545
摘要
Glycolates are indispensable in the health, chemical and pharmaceutical industries, whereas their mainstream production involve toxic chemicals and harsh operating condition. An alternative route for glycolate production is electrifying ethylene glycol (EG) that originates from polyethylene terephthalate (PET) but suffers from poor durability of active platinum site that tend to deactivate. Herein, we demonstrate a dynamic redox reactivation strategy, which alternates between working potential for oxidizing EG to glycolate and nonworking potential for reviving active platinum sites by the chemical reduction of adsorbed EG, realizing an unprecedented stability for over 3000 hours under average current density of ∼220 milliamperes per square centimeter. Upscaling this approach, the assembled electrolyzer drives a record current of 10 amperes at 1.18 volts for repeatable 40 batches of glycolates electrosynthesis, with each batch converting 48.0 grams of PET to 11.6 grams of glycolates (52.8% yield), 37.7 grams of p -phthalic acid (95.8% yield), 248.7 grams of NaHSO 4 (95.2% yield) and ∼11.5 liters of hydrogen, showcasing a considerable revenue of ∼$1072 per ton glycolate.
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