Definitive evidence is presented for the favourable electrochemical properties of carbon nanotube modified electrodes arising from the ends of SWNTs due to oxygenated carbon species in general, and carboxylic acid moieties in particular, produced during acid purification.
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http://dx.doi.org/10.1039/b415051a | DOI Listing |
J Environ Manage
January 2025
School of Environment Science and Engineering, Donghua University, Shanghai, 201620, PR China; Shanghai Institution of Pollution Control and Ecological Security, Shanghai, 200092, PR China; State Environmental Protection Engineering Center for Pollution Treatment and Control in Textile Industry, Donghua University, Shanghai, 201620, PR China.
The pivotal role of electrolytes such as NaSO and NaCl in electrochemical treatment of dyeing wastewater was investigated by comparing recalcitrant Reactive Red X-3B (RRX-3B) degradation rates, active species formation and intermediates generation in a double-chamber cell. It was found that similar reactive oxygen species (ROS) formed in the anodic chamber are OH and O, in the cathodic chamber is O with different electrolytes, while this is not the case for ROS contribution, RRX-3B degradation kinetic and intermediates. NaCl favored the generation of O, faster decolorization (-N=N- cleavage), and organic intermediates degradation in the anodic chamber.
View Article and Find Full Text PDFAppl Microbiol Biotechnol
January 2025
Environmental Microbiology Group, Institute of Water Research, University of Granada, 18003, Granada, Spain.
Microbial fuel cell (MFC) technology has received increased interest as a suitable approach for treating wastewater while producing electricity. However, there remains a lack of studies investigating the impact of inoculum type and hydraulic retention time (HRT) on the efficiency of MFCs in treating industrial saline wastewater. The effect of three different inocula (activated sludge from a fish-canning industry and two domestic wastewater treatment plants, WWTPs) on electrochemical and physicochemical parameters and the anodic microbiome of a two-chambered continuous-flow MFC was studied.
View Article and Find Full Text PDFAdv Mater
January 2025
School of Chemistry, Chemical Engineering and Biotechnology, Nanyang Technological University, 62 Nanyang Drive, Singapore, 637459, Singapore.
Developing highly efficient catalysts to accelerate sluggish electrode reactions is critical for the deployment of sustainable aqueous electrochemical technologies, yet remains a great challenge. Rationally integrating functional components to tailor surface adsorption behaviors and adsorbate dynamics would divert reaction pathways and alleviate energy barriers, eliminating conventional thermodynamic constraints and ultimately optimizing energy flow within electrochemical systems. This approach has, therefore, garnered significant interest, presenting substantial potential for developing highly efficient catalysts that simultaneously enhance activity, selectivity, and stability.
View Article and Find Full Text PDFJ Am Chem Soc
January 2025
Materials Science and Engineering Division, National Institute of Standards and Technology, 100 Bureau Drive, Gaithersburg, Maryland 20899, United States.
Cu electrodeposition and the electrocatalysis of hydrogenation reactions thereupon involve significant interactions with adsorbed hydrogen. Electrochemical mass spectrometry (EC-MS) is used to explore the formation and decomposition of surface hydride on Cu(111) in 0.1 mol L HClO.
View Article and Find Full Text PDFAngew Chem Int Ed Engl
January 2025
Peking University Shenzhen Graduate School, Shool of Chemical Biology and Biotechnology, Lishui Road, Nanshan District, -, Shenzhen, CHINA.
Regulating the coordination environment of active sites has proved powerful for tapping into their catalytic activity and selectivity in homogeneous catalysis, yet the heterogeneous nature of copper single-atom catalysts (SACs) makes it challenging. This work reports a bottom-up approach to construct a SAC (rGO@Cu-N(Hx)-C) by inlaying preformed amine coordinated Cu2+ units into reduced graphene oxide (rGO), permitting molecular level revelation on how the proximal N-site functional groups (N-H or N-CH3) impact on the carbon dioxide reduction reaction (CO2RR). It is demonstrated that the N-H moiety of rGO@Cu-NHx-C can serve as an in-situ protonation agent to accelerate the CO2-to-methane reduction kinetics, delivering a methane current density (163 mA/cm2) 2.
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