Electrocatalytic filtration process adopting the electrocatalytic membrane as both filtration membrane and active electrode showed great prospect on the organic pollutant removal from water. In this work, a high-performance metal-free polypyrrole (PPy) coated carbon-based electrocatalytic membrane (PPy@CCM) was developed through the facile and controllable electro-polymerization deposition method. Structural properties and electrochemical performance of the prepared PPy@CCM were characterized systematically. The influences of preparation parameters and operational parameters on water treatment performance of PPy@CCM were also investigated. Results indicates that the spherical PPy particles uniformly distributed on the surface of PPy@CCM. Coating with PPy particles can significantly improve the hydrophilicity and electrochemical activity of CCM, therefore PPy@CCM has lower hydraulic resistance and higher water treatment performance than CCM. The phenol and chemical oxygen demand (COD) removal rates obtained by PPy@CCM are up to 99.51% and 89.90%, respectively, under the optimal condition of 2.0 V cell potential, 2.50 g·L NaSO, 1.5 ml·min flow rate and 50 mg·L phenol, and only 0.5 kWh·kgCOD energy consumption is consumed. In addition, PPy@CCM also exhibits good treatment performance in different water matrixes. Moreover, PPy@CCM has good stability for several cycle operation and considerable applicability for different types of organic pollutants removal. The oxidation mechanism study reveals that PPy@CCM has both direct and indirect oxidation activity during the electrocatalytic filtration treatment, and the coating of PPy can improve the direct oxidation ability and ·OH yield of CCM.
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http://dx.doi.org/10.1016/j.jcis.2022.06.138 | DOI Listing |
ACS Nano
January 2025
State Key Laboratory of Silicate Materials for Architectures & State Key Laboratory of Advanced Technology for Materials Synthesis and Processing & School of Chemistry, Chemical Engineering and Life Sciences & Laoshan Laboratory & School of Materials Science and Engineering & International School of Materials Science and Engineering, Wuhan University of Technology, Wuhan 430070, China.
Electrolysis of seawater for hydrogen (H) production to harvest clean energy is an appealing approach. In this context, there is an urgent need for catalysts with high activity and durability. RuO electrocatalysts have shown efficient activity in the hydrogen and oxygen evolution reactions (HER and OER), but they still suffer from poor stability.
View Article and Find Full Text PDFJ Am Chem Soc
January 2025
School of Chemistry, Beijing Advanced Innovation Center for Biomedical Engineering, Key Laboratory of Bio-Inspired Smart Interfacial Science and Technology, Beihang University, Beijing 100191, China.
The dual-site synergistic catalytic mechanism on NiFeOOH suggests weak adsorption of Ni sites and strong adsorption of Fe sites limited its activity toward alkaline oxygen evolution reaction (OER). Large-scale density functional theory (DFT) calculations confirm that Co doping can increase Ni adsorption, while the metal vacancy can reduce Fe adsorption. The combined two factors can further modulate the atomic environment and optimize the free energy toward oxygen-containing intermediates, thus enhancing the OER activity.
View Article and Find Full Text PDFAngew Chem Int Ed Engl
January 2025
Inner Mongolia University, College of Chemistry and Chemical Engineering, 235 West University Street, Saihan District, 010021, Hohhot, CHINA.
Electrocatalytic glycerol oxidation reaction (GOR) to produce high-value formic acid (FA) is hindered by high formation potential of active species and sluggish C-C bond cleavage kinetics. Herein, Ni single-atom (NiSA) and Co single-atom (CoSA) dual sites anchored on nitrogen-doped carbon nanotubes embedded with Ni0.1Co0.
View Article and Find Full Text PDFACS Appl Mater Interfaces
January 2025
Department of Chemistry, University of Victoria, 3800 Finnerty Road, Victoria, BC V8P 5C2, Canada.
One of the key technical challenges before the widespread adoption of proton exchange membrane fuel cells (PEMFCs) is increasing the durability of the platinum catalyst layer to meet a target of 8000 operating hours with only a 10% loss of performance. Carbon corrosion, one of the primary mechanisms of degradation in fuel cells, has attracted attention from researchers interested in solving the durability problem. As such, the development of catalyst supports to avoid this issue has been a focus in recent years, with interest in hydrophobic supports such as highly graphitized carbons.
View Article and Find Full Text PDFSmall
January 2025
Faculty of Materials Science and Engineering, Analysis and Testing Research Center, Kunming University of Science and Technology, Kunming, 650093, P. R. China.
Modulating electronic structure to balance the requirement of both hydrogen evolution reaction (HER) and oxygen evolution reaction (OER) is crucial for developing bifunctional catalysts. Herein, phase transformation engineering is utilized to separately regulate catalyst structure, and the designed NiFe@Ni/Fe-MnOOH schottky heterojunction exhibits remarkable bifunctional electrocatalytic activity with low overpotentials of 19 and 230 mV at 10 mA cm for HER and OER in 1M KOH, respectively. Meanwhile, an anion-exchange membrane water electrolyzer employing NiFe@Ni/Fe-MnOOH as electrodes shows low voltages of 1.
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