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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