Efficient electrocatalytic valorization of chlorinated organic water pollutant to ethylene.
Chungseok ChoiXiaoxiong WangSoonho KwonJames L HartConor L RooneyNia J HarmonQuynh P SamJudy J ChaWilliam A Goddard IiiMenachem ElimelechHailiang WangPublished in: Nature nanotechnology (2022)
Electrochemistry can provide an efficient and sustainable way to treat environmental waters polluted by chlorinated organic compounds. However, the electrochemical valorization of 1,2-dichloroethane (DCA) is currently challenged by the lack of a catalyst that can selectively convert DCA in aqueous solutions into ethylene. Here we report a catalyst comprising cobalt phthalocyanine molecules assembled on multiwalled carbon nanotubes that can electrochemically decompose aqueous DCA with high current and energy efficiencies. Ethylene is produced at high rates with unprecedented ~100% Faradaic efficiency across wide electrode potential and reactant concentration ranges. Kinetic studies and density functional theory calculations reveal that the rate-determining step is the first C-Cl bond breaking, which does not involve protons-a key mechanistic feature that enables cobalt phthalocyanine/carbon nanotube to efficiently catalyse DCA dechlorination and suppress the hydrogen evolution reaction. The nanotubular structure of the catalyst enables us to shape it into a flow-through electrified membrane, which we have used to demonstrate >95% DCA removal from simulated water samples with environmentally relevant DCA and electrolyte concentrations.
Keyphrases
- carbon nanotubes
- ionic liquid
- density functional theory
- reduced graphene oxide
- metal organic framework
- room temperature
- molecular dynamics
- photodynamic therapy
- gold nanoparticles
- highly efficient
- carbon dioxide
- machine learning
- human health
- visible light
- gas chromatography
- gene expression
- molecular dynamics simulations
- mass spectrometry
- high resolution
- climate change
- neural network