纳米片
乙二醇
催化作用
材料科学
脱氢
蚀刻(微加工)
化学工程
尿素
电化学
普鲁士蓝
超声
色散(光学)
无机化学
纳米技术
电极
化学
有机化学
光学
物理
工程类
物理化学
图层(电子)
作者
Hongfeng Zhao,Yan Zhang,Chaoyue Xie,Jiachen Wang,Tingsheng Zhou,Changhui Zhou,Jinhua Li,Jing Bai,Xinyuan Zhu,Baoxue Zhou
标识
DOI:10.1021/acs.est.2c07282
摘要
As the primary source of nitrogen pollutants in domestic sewage, urine is also an alternative for H2 production via electrochemical processes. However, it suffers from sluggish kinetics and noble-metal catalyst requirement. Here, we report a non-precious ultrathin NiFe-layered double hydroxide catalyst for the remarkable conversion of urea into N2 and H2, which is in situ grown on a Ni foam via ultrasonic self-etching in Fe3+/ethylene glycol (EG). EG regulates the etching rate of Fe3+, resulting in an ultrathin nanosheet structure with the aid of ultrasonication. This structure dramatically promotes the dehydrogenation process via decreasing the nanolayer thickness from 120 to 3.4 nm and leads to a 4.8-fold increase in the generation of active sites. It exhibits record urea oxidation kinetics (390.8 mA·cm–2 at 1.5 V vs RHE) with excellent stability (120 h), which is 11.8 times better than that of commercial Pt/C catalyst (33.1 mA·cm–2). Tests with real urine at 20 mA cm–2 achieve 74% total nitrogen removal and 2853 μmol·h–1 of H2 production. This study provides an attractive landscape for producing H2 by consuming urine biowastes.
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