4.7 Article

Conjugated donor-acceptor (D-A) supramolecule catalyst for visible light-driven photocatalytic removal of bromate in water

Journal

JOURNAL OF COLLOID AND INTERFACE SCIENCE
Volume 553, Issue -, Pages 666-673

Publisher

ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.jcis.2019.06.072

Keywords

Bromate; BDTD supramolecule; Photocatalyst; Visible light

Funding

  1. National Natural Science Foundation of China [51822806, 51678184, 51761145031]
  2. Fundamental Research Funds for the Central Universities [HIT.BRETIV.201905]
  3. China Scholarship Council [201806120344]

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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 C-H...O hydrogen bonds and C-H...pi interactions. Both diffuse reflectance spectrum (DRS) and density functional theoretical (DFT) calculations gave the bandgap of E-g = 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. (C) 2019 Elsevier Inc. All rights reserved.

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