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Visible‐Light Photocatalytic Activity of Ionic Liquid TiO 2 Spheres: Effect of the Ionic Liquid's Anion Structure
Author(s) -
Łuczak Justyna,
PaszkiewiczGawron Marta,
Długokęcka Marta,
Lisowski Wojciech,
Grabowska Ewelina,
Makurat Samanta,
Rak Janusz,
ZaleskaMedynska Adriana
Publication year - 2017
Publication title -
chemcatchem
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.497
H-Index - 106
eISSN - 1867-3899
pISSN - 1867-3880
DOI - 10.1002/cctc.201700861
Subject(s) - ionic liquid , anatase , photocatalysis , bromide , photochemistry , ion , ionic bonding , visible spectrum , chemistry , inorganic chemistry , oxygen , materials science , catalysis , organic chemistry , optoelectronics
Abstract The effect of the ionic liquid's (IL) anion type ([BMIM][X], where BMIM=1‐butyl‐3‐methylimidazolium and X=[Br], [PF 6 ], or octylsulfonate [OctSO 4 ]) and IL content on the morphology, surface properties, and photoactivity of TiO 2 obtained by the solvothermal method has been systematically investigated. Our results revealed that the presence of [Br] and [OctSO 4 ] anions favor the formation of anatase phase, whereas the presence of [PF 6 ] causes formation of anatase and Ti(OH)PO 4 phase mixtures. The highest photocatalytic activity under visible radiation (approximately four times higher than pristine TiO 2 ) was observed for the TiO 2 sample grown in the presence of 1‐butyl‐3‐methylimidazolium bromide for ionic liquid to TiO 2 precursor molar ratio 1:2. Visible‐light‐induced phenol degradation was found to be realized mainly by oxygen radical anions, whereas the contributions of the other processes involving reactions with trapped electrons, holes, and hydroxyl radical, are limited in the overall reaction mechanism. Quantum chemical calculations on a model of anatase vacancy suggest that the charge transfer between the bromide anion and molecular oxygen interacting with the vacancy is a source of photoactivity induced by visible photons.