Impact of polymorphism shape of titania nanocrystals on the hydrogen evolution reaction

Herein, we investigated the impact of polymorphism vs. dimension control of titania nanocrystals towards hydrogen generation. Two different forms of titania nanoparticles have been synthesized following the solvothermal method, leading to the formation of two distinct physicochemical features. Detailed structural, morphological, and optical studies revealed that the formation of titania nanorods correspond to rutile while granular particles correspond to the anatase phase. Among various titania polymorphs, anatase is well known for its superior photocatalytic activity; however, to our surprise, the as-synthesized rutile nanorods exhibited higher catalytic activity in comparison to anatase spheres, and hydrogen evolution was considerably enhanced after the addition of a minute amount of Pt as the co-catalyst. Thus, despite the higher catalytic activity of anatase, the enhanced hydrogen evolution of rutile nanorods may be related to the creation of a 1D structure. Our study highlights the importance of considering not only TiO 2 polymorphism but also shape and dimension in optimizing photocatalytic H 2 production. Two polymorphs of titania were synthesized by varying the reaction conditions. Enhanced HER in rutile nanorods was seen compared to that in anatase granules due to enhanced charge separation and faster diffusion of charge.