材料科学
镍
硫化物
催化作用
电化学
电催化剂
硫化镍
电合成
聚对苯二甲酸乙二醇酯
乙二醇
电解
格式化
无机化学
电解质
化学工程
电解水
碳纤维
酯交换
原电池
二氧化碳电化学还原
阴极
氧化还原
阴极保护
聚苯胺
纳米技术
作者
Jun Qi,Jiachun Li,Xiangtong Meng,Zhanhao Jiang,Zhenhao Wang,Yi Ma,Hongqi Zou,Yadong Du,Zhiqun Lin,Jieshan Qiu
标识
DOI:10.1002/aenm.202504208
摘要
Abstract Despite recent stunning progress in electrocatalytic valorization of plastics, it remains a huge challenge to develop highly active electrocatalysts for achieving industrial‐level current density. Herein, a flocculent chromium‐modified nickel sulfide (Cr‐Ni 3 S 2 ‐Ni(OH) 2 /NF) immobilizing on nickel foam and scrutinize its electrocatalytic activity for oxidation of ethylene glycol monomers (EOR) of polyethylene terephthalate (PET) is crafted. The Cr‐Ni 3 S 2 ‐Ni(OH) 2 /NF catalyst facilitates efficient formate production at an industrial‐level current density of 1200 mA cm −2 , requiring a record low potential of 1.561 V (vs. RHE). A series of in‐situ spectroscopy in conjunction with theoretical calculations substantiates that the high activity of the catalyst originates from the regulated d‐band center of Ni by Cr and S species. Hybrid electrosynthesis systems coupling EOR and cathodic CO 2 or H 2 O reduction reaction (CO 2 RR or HER) are subsequently assembled. When reaching 400 mA cm −2 , CO 2 RR//EOR electrolyzer enables coproduction of formate at an impressively low cell voltage of 2.694 V, avoiding ion‐exchange membrane and product crossover. Rigorous techno‐economic evaluation reveals that the attractive profitability of these two electrosynthesis routes reverses the long‐term dilemma of negative profits. This work paves a green and sustainable avenue toward the valorization of low‐grade carbon resources.
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