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Facile Synthesis of Worm-like Micelles by Visible Light Mediated Dispersion Polymerization Using Photoredox Catalyst
Published on: June 8, 2016
Conjugated donor-acceptor (D-A) supramolecule catalyst for visible-light-driven photocatalytic removal of bromate in
Guoshuai Liu1, Shijie You2, Yujian Zhang3
1State Key Laboratory of Urban Water Resource and Environment, School of Environment, Harbin Institute of Technology, Harbin 150090, PR China; Department of Water Management, Section Sanitary Engineering, Delft University of Technology, PO Box 5048, 2600 GA Delft, the Netherlands.
Abstract:
To guarantee drinking water security, removal of bromate (BrO3-) has garnered plenty of attention in water treatment. In current study, we have developed a novel conjugated donor-acceptor (D-A) photocatalyst (4,4''-bis(diphenylamino)-[1,1':4',1''-terphenyl]-2',5'-dicarbaldehyde, BDTD) with supramolecule architecture assembling via intermolecular CH···O hydrogen bonds and CH···π interactions. Both diffuse reflectance spectrum (DRS) and density functional theoretical (DFT) calculations gave the bandgap of Eg = 2.21 eV, clearly indicating the visible-light response of BDTD supramolecule. The calculations showed that BDTD supramolecule could induce nearly 100% removal of BrO3- stably at pH-neutral condition driven by visible light, accounting for a first-order kinetic constant being one order of magnitude higher than most of the photocatalysts previous reported. As demonstrated by our electron scavenger experiment and DFT calculations, the BDTD supramolecule should undergo the photocatalytic reduction of BrO3- through direct reduced by the lowest unoccupied molecular orbital of conduction band (potential of -1.705 V versus standard hydrogen electrode) electron. The BDTD supramolecule may serve as an attractive photocatalyst by virtue of response to visible light, efficient charge transfer and separation as well as high photocatalytic activity, which will make the removal of BrO3- in water much easier, more economical and more sustainable.
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