Composition-driven morphological evolution of BaTiO3 nanowires for efficient piezocatalytic hydrogen production

Abstract

Hydrogen production from water by piezocatalysis is very attractive owing to its high energy efficiency and novelty. BaTiO3, a highly piezoelectric material, is particularly suitable for this application due to its high piezoelectric potential, non-toxic nature, and physicochemical stability. Owing to the critical role of morphology on properties, one-dimensional (1D) materials are expected to exhibit superior water-splitting performance and thus there is a need to optimise the processing conditions to develop outstanding piezocatalysts. In the present work, piezoelectric BaTiO3 nanowires (NWs) were hydrothermally synthesised with precursor Ba:Ti molar ratios of 1:1, 2:1, and 4:1. The morphology, defect chemistry, and hydrogen evolution reaction (HER) efficiency of the as-synthesised BaTiO3 NWs were systematically investigated. The results showed that the morphological features, aspect ratio, structural stability and defect contents of the 1D morphologies collectively have a significant impact on the HER efficiency. The morphological evolution mechanism of the 1D structures were described in terms of ion exchange and dissolution-growth processes of template-grown BaTiO3 NWs for different Ba:Ti molar ratios. Notably, the BaTiO3 NWs synthesised with Ba:Ti molar ratio of 2:1 displayed high crystallinity, good defect concentrations, and good structural integrity under ultrasonication, resulting in an outstanding HER efficiency of 149.24 μmol h−1g−1 which is the highest obtained for nanowire morphologies. These results highlight the importance of synthesis conditions for BaTiO3 NWs for generating excellent piezocatalytic water splitting performance. Additionally, post-ultrasonication tested BaTiO3 NWs demonstrated unexpected photocatalytic activity, with the BTO-1 sample (1:1 Ba:Ti) exhibiting 56% photodegradation of RhB in 2 h of UV irradiation.