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Effective green electro-Fenton process induced by atomic hydrogen for rapid oxidation of organic pollutants over a highly active and reusable carbon based palladium nanocatalyst
Journal article   Peer reviewed

Effective green electro-Fenton process induced by atomic hydrogen for rapid oxidation of organic pollutants over a highly active and reusable carbon based palladium nanocatalyst

Ling Yang, Chen Chen, Ruiyu Bao, Zhegang Huang, Wenzhong Wang, Chen Zhang, Jianxin Xia, Junfeng Geng and Hua Li
Applied surface science, Vol.602, p.154325
15/11/2022

Abstract

Atomic hydrogen Heterogeneous electro-Fenton Hydroxyl radical Palladium nanoparticles Wastewater treatment
[Display omitted] •Pd nanoparticles dispersed in carbon black were further loaded on carbon felt (Pd/C@CF) can catalyze the production of atomic hydrogen (H*).•H* can replace the Fe2+ to reduce H2O2 in a Fenton-like reaction with H2O as byproduct.•The effects of various influence factors on the electro-Fenton process induced by H* reactivity were investigated.•The Pd/C@CF cathode was proved to be a little pH dependent, highly stable, and potentially practical applications in wastewater treatment. Heterogeneous electro-Fenton (HEF) reaction is a highly efficient process for the degradation and mineralization of refractory organic pollutants in water. Since atomic hydrogen H*, currently widely used in electrocatalytic hydrogen dechlorination (ECHD) domains, can rapidly transfer one electron to H2O2 to generate OH and H2O, it has been considered as a promising species instead of Fe2+ for HEF reactions. However, H* is extremely unstable as it can be easily combined into hydrogen gas (H2), appropriate electro-catalytic material would be needed in order to speed up the production of H* on the one hand, and stabilize this in-situ formed species on the other. Here we show that house-synthesized Pd nanoparticles dispersed in carbon black (∼8 % Pd on carbon) which were further loaded on carbon felt (Pd/C@CF) exhibited an excellent performance in HEF process for degradation of a variety of organic compounds (with the best of ∼99 % in 75 min). Radical scavenging experiments revealed that hydroxyl radical (OH) was the key reactive species, and cyclic voltammetry tests proved the stabilization of H* by Pd nanoparticles which in turn resulted in a significant increase in the yield of OH via the reduction of H2O2. The superior performance could be attributed to the Pd nanoparticles dispersed uniformly in carbon with a large number of active sites, thereby lowering the over potential to create a suitable microenvironment for H* generation and stabilization. In addition, the Pd/C@CF composite was proved to be a little pH dependent, highly stable, and well recyclable for effective utilization of H* towards a rapid HEF oxidation for potentially many practical applications in wastewater treatment.

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