pH-Mediated Collective and Selective Solar Photocatalysis by a Series of Layered Aurivillius Perovskites

[Image: see text] Semiconductor photocatalysis under natural sunlight is an emergent area in contemporary materials research, which has attracted considerable attention toward the development of catalysts for environmental remediation using solar energy. A series of five-layer Aurivillius-phase perovskites, Bi(5)ATi(4)FeO(18) (A = Ca, Sr, and Pb), are synthesized for the first time. Rietveld refinements of the powder X-ray diffraction data indicated orthorhombic structure for the Aurivillius phases with Fe largely occupying the central octahedral layer, whereas the divalent cations (Ca, Sr, and Pb) are statistically distributed over the cubo-octahedral A-sites of the perovskite. The compounds with visible-light-absorbing ability (E(g) ranging from ∼2.0 to 2.2 eV) not only exhibit excellent collective photocatalytic degradation of rhodamine B–methylene blue (MB) and rhodamine B–rhodamine 6G mixture at pH 2 but also show almost 100% photocatalytic selective degradation of MB from the rhodamine B–MB mixture at pH 11 under natural solar irradiation. The selectivity in the alkaline medium is believed to originate from the combined effect of the photocatalytic degradation of MB by the Aurivillius-phase perovskites and the photolysis of MB. Although a substantial decrease in MB adsorption from the mixed dye solution (MB + RhB) together with slower MB photolysis at the neutral pH makes the selective MB degradation sluggish, the compounds showed excellent photocatalytic degradation activity and chemical oxygen demand removal efficacy toward individual RhB (at pH 2) and MB (at pH 11) under sunlight irradiation. The catalysts are exceptionally stable and retain good crystallinity even after five successive cyclic runs without any noticeable loss of activity in both the acidic and alkaline media. The present work provides an important insight into the development of layered perovskite photocatalysts for collective degradation of multiple pollutants and selective removal of one or multiple pollutants from a mixture. The later idea may open up new possibilities for recovery/purification of useful chemical substances from the contaminated medium through selective photocatalysis.