电合成
材料科学
催化作用
乙二醇
乙醇酸
化学工程
电化学
吸附
对苯二甲酸
齿合度
电解质
钯
选择性
键裂
铂金
电催化剂
膜电极组件
水溶液
贵金属
聚对苯二甲酸乙二醇酯
无机化学
溶解
乙烯
锐钛矿
浸出(土壤学)
电极
纳米技术
金属
降级(电信)
阴极
组合化学
膜
产量(工程)
纳米颗粒
作者
Yuqiao Zhou,Feng Yu,Yang Peng,Shuai Wang,Yifan Tian,Kai Zhang,Wenjing Huang,Bo Chen
标识
DOI:10.1002/adfm.202528195
摘要
ABSTRACT Electrochemical upcycling of polyethylene terephthalate (PET) into value‐added chemicals offers a sustainable pathway for mitigating plastic pollution and advancing the global energy transition. However, conventional noble metal catalysts often exhibit severe performance degradation arising from surface oxidation and the accumulation of poisoning intermediates, which ultimately limits catalytic activity and durability. Herein, we employ a rapid microwave‐irradiation strategy to construct coral‐like Pd 3 Pb nanocrystals with a precisely engineered architecture. In situ spectroscopic and kinetic analyses revealed that Pb incorporation disrupts continuous Pd ensembles, thereby suppressing bridged and bidentate adsorption motifs and retarding undesired C─C bond cleavage. Meanwhile, enhanced interfacial * OH availability and electron injection from oxophilic Pb alleviate carbonaceous poisoning and PdO passivation, thereby enabling exceptional long‐term robustness. As a result, Pd 3 Pb achieves a low onset potential (0.28 V vs. RHE), high glycolic acid selectivity (95.2%), and excellent durability (>77 h) in both model electrolytes and real PET hydrolysate. Moreover, a Pd 3 Pb‐based membrane electrode assembly operates stably at 1.0 V at 100 mA cm −2 for 72 h, maintaining an average yield rate of 6.46 mmol h −1 cm −2 . This work elucidates pathways that inhibit catalyst deactivation and informs the rational design of robust catalysts for PET valorization.
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