纳米片
电极
催化作用
材料科学
浸出(土壤学)
电化学
可逆氢电极
化学工程
标准氢电极
硫黄
化学
纳米技术
无机化学
工作电极
有机化学
工程类
物理化学
环境科学
土壤科学
土壤水分
作者
Junxi Li,Yiyin Peng,Wendong Zhang,Xuelin Shi,Min Chen,Peng Wang,Xianming Zhang,Hailu Fu,Xiaoshu Lv,Fan Dong,Guangming Jiang
标识
DOI:10.1016/j.apsusc.2020.145369
摘要
Abstract Electrocatalytic hydrodechlorination (EHDC) is deemed as one promising approach for efficient and safe detoxification of the trace halogenated organic pollutants in water. Here we prepared one advanced Pd/MnO2-Ni foam electrode via the construction of oxygen-deficient MnO2 nanosheet arrays on Ni foam skeleton, which then served as the support and electron donator to capture and reduce Pd precursor to nanoparticles. With the three-dimensional porous structure, hierarchical skeleton surfaces and improved Pd dispersion, the Pd/MnO2-Ni foam electrode delivered an unprecedented large mass activity (kobs) of 0.883 min−1 mmolPd−1 for EHDC of 2,4-dichlorophenol (2,4-DCP), in comparison to 0.081 min−1 mmolPd−1 of the Pd/Ni foam electrode and those reported in literatures. The Pd/MnO2-Ni foam electrode also displayed high durability during the repeated batch EHDC experiments without the efficiency decay and the leaching of Mn/Ni/Pd, unless some reduced sulfur compounds and nitrite were included. The mechanism study revealed the MnO2 in electrode served as a mediator to transfer H* from Pd to 2,4-DCP, which extended the reactive area beyond Pd and hindered the molecular hydrogen evolution, leading to the enhanced reactions between H* and 2,4-DCP. The Pd/MnO2-Ni foam electrode was also tested in a continuous-flow EHDC system, and displayed the potential and retention time-dependent performances.
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