{"title":"Pre-embedded Strategy for Anti-NOM Poisoning Performance of Palladium Nanoparticles in Electrocatalytic Dechlorination","authors":"Linpiao Cheng, Shuyue Liu, Yinan Liu, Xiangyi Tang, Mue Tang, Xinhua Xu, Xiaoshu Lv","doi":"10.1016/j.electacta.2025.145642","DOIUrl":null,"url":null,"abstract":"Electrocatalytic hydrodechlorination (EHDC) represents a sustainable approach to detoxifying the chlorinated organic pollutants (COPs). However, electrodes often suffer from fouling due to the ubiquitous natural organic matters (NOM) in surface water bodies. Herein we demonstrated that pre-mixing humic acid (HA) with palladium nanoparticles (Pd NPs) is an ingenious approach to address this issue. The introduction of HA improved dispersion of Pd NPs, enhanced surface hydrophilicity to promote H* generation, and increased electrostatic repulsion and steric-hinerance against NOM in solution. As a result, the as-synthesized HA<sub>0.2</sub>-Pd electrode exhibits significantly improved EHDC performance and anti-NOM poisoning ability. In the batch experiment, the HA<sub>0.2</sub>-Pd NPs achieved removal efficiencies of 91.3 and 80.8% respectively, for treating 50.0 mg L<sup>−1</sup> of 2,4-dichlorophenol (2,4-DCP, a probe COP) from contaminated water in the absence or presence of 20 mg L<sup>−1</sup> HA (representative of NOM) at -0.85 V <em>vs.</em> Ag/AgCl. Compared to that, the pure Pd/C electrode experienced a marked efficacy decline from 82.9 to 56.5% in the presence of HA. Moreover, the HA<sub>0.2</sub>-Pd/C electrode maintained a steady efficiency above 92.0% over 12 h EHDC in a continuous-flow cell, while only 60.0% for the Pd/C electrode. When subjected to contaminated natural water, the HA<sub>0.2</sub>-Pd/C electrode afforded an EHDC efficiency of 75.4%, significantly surpassing the 39.4% efficiency of Pd/C electrode.","PeriodicalId":305,"journal":{"name":"Electrochimica Acta","volume":"34 1","pages":""},"PeriodicalIF":5.5000,"publicationDate":"2025-01-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Electrochimica Acta","FirstCategoryId":"88","ListUrlMain":"https://doi.org/10.1016/j.electacta.2025.145642","RegionNum":3,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"ELECTROCHEMISTRY","Score":null,"Total":0}
引用次数: 0
Abstract
Electrocatalytic hydrodechlorination (EHDC) represents a sustainable approach to detoxifying the chlorinated organic pollutants (COPs). However, electrodes often suffer from fouling due to the ubiquitous natural organic matters (NOM) in surface water bodies. Herein we demonstrated that pre-mixing humic acid (HA) with palladium nanoparticles (Pd NPs) is an ingenious approach to address this issue. The introduction of HA improved dispersion of Pd NPs, enhanced surface hydrophilicity to promote H* generation, and increased electrostatic repulsion and steric-hinerance against NOM in solution. As a result, the as-synthesized HA0.2-Pd electrode exhibits significantly improved EHDC performance and anti-NOM poisoning ability. In the batch experiment, the HA0.2-Pd NPs achieved removal efficiencies of 91.3 and 80.8% respectively, for treating 50.0 mg L−1 of 2,4-dichlorophenol (2,4-DCP, a probe COP) from contaminated water in the absence or presence of 20 mg L−1 HA (representative of NOM) at -0.85 V vs. Ag/AgCl. Compared to that, the pure Pd/C electrode experienced a marked efficacy decline from 82.9 to 56.5% in the presence of HA. Moreover, the HA0.2-Pd/C electrode maintained a steady efficiency above 92.0% over 12 h EHDC in a continuous-flow cell, while only 60.0% for the Pd/C electrode. When subjected to contaminated natural water, the HA0.2-Pd/C electrode afforded an EHDC efficiency of 75.4%, significantly surpassing the 39.4% efficiency of Pd/C electrode.
期刊介绍:
Electrochimica Acta is an international journal. It is intended for the publication of both original work and reviews in the field of electrochemistry. Electrochemistry should be interpreted to mean any of the research fields covered by the Divisions of the International Society of Electrochemistry listed below, as well as emerging scientific domains covered by ISE New Topics Committee.