材料科学
法拉第效率
堆栈(抽象数据类型)
氧化还原
碳纤维
电解水
聚酯纤维
电解
化学工程
乙二醇
乙烯
耐久性
氢
聚对苯二甲酸乙二醇酯
格式化
高压
对苯二甲酸
电极
电催化剂
电解质
纳米技术
电解法
聚乙烯
膜电极组件
电压
复合材料
选择性
硫黄
生物量(生态学)
作者
Guangtao Ma,Lejuan Cai,Yifan Li,Zhenzhong Liu,Jiawei Li,Li Xiong,Hengjie Liu,Jingxiang Low,Askar Parmanov,Olim Ruzimuradov,Yi Cui,Ning Zhang,Yujie Xiong
摘要
ABSTRACT The electrooxidation of ethylene glycol (EG) from polyethylene terephthalate (PET) waste to produce valuable commodities offers a novel approach to the circular plastic economy. However, reaction efficiency is significantly limited by uncontrollable side reactions and competitive water oxidation, particularly at high or fluctuating voltages. Here, we present an efficient EG‐to‐formate evolution at an ultrawide potential range of 1.4–2.3 V versus reversible hydrogen electrode, with Faradaic efficiencies of over 95% persisting on a sulfur‐modified NiCo‐based catalyst. It has been revealed that structural reconstruction engineering, governed by sulfur redox electrochemistry, provides active (oxy)hydroxide sites that promote key C–C scission with good robustness. Accordingly, this system exhibits exceptional durability of over 1100 h in a membrane electrode assembly (MEA) electrolyzer and good tolerance to voltage intermittences and fluctuations. Deployment on a larger scale through a 5 × 4 cm 2 MEA series stack affords a formate productivity of 193.1 mmol h −1 at 4.0 A from real‐world PET waste hydrolysate, together with high carbon selectivity of 97% and stable operation for 500 h. This electrified process demonstrates great profitability and a negative carbon budget, highlighting its significant potential to advance the circular plastic economy and achieve carbon neutrality.
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