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SnS 2 /Bi 4 Ti 3 O 12 Heterostructure Material: A UV‐Visible Light Active Direct Z‐Scheme Photocatalyst for Aqueous Phase Degradation of Diazinon
Author(s) -
Das Krishnendu,
Majhi Dibyananda,
Bariki Ranjit,
Mishra Braja G.
Publication year - 2020
Publication title -
chemistryselect
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.437
H-Index - 34
ISSN - 2365-6549
DOI - 10.1002/slct.201904532
Subject(s) - photocatalysis , materials science , visible spectrum , heterojunction , photodegradation , aqueous solution , photochemistry , radical , band gap , optoelectronics , chemistry , catalysis , organic chemistry
In this study, a series of Z‐scheme SnS 2 /Bi 4 Ti 3 O 12 heterostructure photocatalyst materials were synthesized by a two‐step process. Initially, Bi 4 Ti 3 O 12 (BT) nanopellets with planar dimension of 350–400 nm were prepared by a facile combustion synthesis route. The SnS 2 nanoparticles (10–20 nm) were subsequently decorated over BT surface using a hydrothermal method. The heterostrucure materials possess orthorhombic BT and hexagonal SnS 2 crystalline phases with high interfacial contact and strong interaction at microscopic level. Optical and photoelectrochemical (PEC) measurements suggest improved UV‐visible light absorption and enhanced charge carrier separation and migration properties. The SnS 2 /Bi 4 Ti 3 O 12 materials displayed excellent photocatalytic activity for degradation of diazinon insecticide (>90 % with k app ∼0.019 min −1 ) in aqueous media under UV‐visible light illumination. The valence band (VB) holes and • OH radicals were identified as major transient species responsible for photodegradation of diazinon. A Z‐scheme electron transfer process has been proposed to explain adequately the generation of these radicals which was deduced from PEC measurements, scavenger and radical trapping experiments. Mechanistic study revealed that diazinon degradation occured in a series of steps to produce 2‐isopropyl‐6‐methyl‐pyrimidin‐4‐ol as a major intermediate which was further mineralized over the photocatalyst surface. The process potential of the developed photocatalytic method has been tested for different water matrices and interfering anionic species with radical quenching activity.