Related Experiment Video
Updated: May 23, 2025

A Complete Method for Evaluating the Performance of Photocatalysts for the Degradation of Antibiotics in Environmental Remediation
Published on: October 6, 2022
B-Modified Pd Cathodes for the Efficient Detoxification of Halogenated Antibiotics: Enhancing C-F Bond Breakage
Zefang Chen1, Lin Du2, Victor Fung3
1School of Civil and Environmental Engineering, Georgia Institute of Technology, Atlanta, Georgia 30332, United States.
Abstract:
Halogenated antibiotics pose a great threat to aqueous environments because of their persistent biotoxicity from carbon-halogen bonds. Electrochemical reduction (ER) is an efficient technology for dehalogenation, but it still suffers from limited efficiencies in breaking C-F bonds. Herein, we present a strategy to enhance C-F cleavage and promote detoxification by loading benchmark palladium cathodes onto boron-doped carbon. This improves the florfenicol (FLO) degradation rate constant and defluorination efficiency by 1.24 and 1.05 times, respectively, and improves the defluorination of various fluorinated compounds. The cathode with optimal B content shows superior mass activity for FLO degradation (1.11 mmol g-1 Pd min-1), which is 5.9 times that of commercial Pd/C and is among the best-reported cathodes. Notably, the exclusive formation of the direct defluorination product (i.e., FLO-F) on Pd/B-C implies a higher intrinsic C-F cleavage ability endowed by B doping. As revealed by experiments and theoretical calculations, boron modification enhances palladium binding and induces stronger strain effects and higher electron density for surface palladium atoms, which boosts H* generation and reduces the energy barrier for C-F cleavage. This study provides an effective cathode design strategy to enhance C-F activation, which may broadly benefit the destruction and detoxification of fluorinated organics that are limited by sluggish C-F cleavage kinetics.
More Related Videos
09:12[DPEPhosbcpCu]PF6: A General and Broadly Applicable Copper-Based Photoredox Catalyst
Published on: May 21, 2019
12:05Preparation of Hydrophobic Metal-Organic Frameworks via Plasma Enhanced Chemical Vapor Deposition of Perfluoroalkanes for the Removal of Ammonia
Published on: October 10, 2013
Related Concept Videos
ortho–para-Directing Deactivators: Halogens
Electrophilic Aromatic Substitution: Fluorination and Iodination of Benzene
Radical Substitution: Hydrogenolysis of Alkyl Halides with Tributyltin Hydride
The bonds formed in this reaction are stronger than the bonds broken, making it energetically favorable. The reaction follows a radical chain mechanism similar to radical halogenation...
Electrophilic 1,2- and 1,4-Addition of X2 to 1,3-Butadiene
Halogenation of Alkenes
Consider the bromination of cyclopentene. Molecular bromine is polarized in the proximity of the π electrons of cyclopentene. An electrophilic bromine atom adds across the double bond, forming a cyclic bromonium ion intermediate.
Phase II Reactions: Miscellaneous Conjugation Reactions
A key example involves the conjugation of cyanide ions, which impair cellular respiration and alter hemoglobin into non-oxygen-carrying cyanmethemoglobin. To neutralize this threat, a sulfur atom from thiosulphate is transferred to the cyanide ion, catalyzed by the enzyme rhodanese, resulting in an inactive compound called thiocyanate. The production of...