ABSTRACT
1D-molybdenum disulfide (MoS2) nanoscrolls displayed enhanced electrochemical properties compared to 2D-MoS2 nanosheet counterparts. Rolling of nanosheets is the main fabrication route to nanoscrolls. However, owing to the conflict between chemical stability and multiple bending, the morphology transition from nanosheets to nanoscrolls is quite challenging. Herein we describe a reversible morphology transition from nanosheets to nanoscrolls by utilizing non-covalent interactions between MoS2 nanosheets and phenothiazine based organic dye. Interestingly, nanoscrolls can easily be opened back into nanosheets by destroying the non-covalent interactions with organic solvents. The prepared nanoscrolls exhibited enhanced electrochemical properties than nanosheets. Compared to nanosheets, nanoscrolls exhibited comparatively lower overpotential with a Tafel slope of 141 mV dec-1 and high specific capacitance of 1868 F g-1. Hydrogen evolution by the Volmer-Heyrovsky mechanism being superior for the nanoscrolls is envisaged by the relatively increased availability of Hads sites at MoS2 edges induced by scrolling. Whereas the high specific capacitance value of nanoscrolls is ascribed to the enhanced electrical double-layer capacitance mediated charge storage, which arises due to the synergistic effect of both scrolled structure and the electron-rich phenothiazine-based dye.
ABSTRACT
Nanostructured photocatalysts have always offered opportunities to solve issues concerned with the environmental challenges caused by rapid urbanization and industrialization. These materials, due to their tunable physicochemical characteristics, are capable of providing a clean and sustainable ecosystem to humanity. One of the current thriving research focuses of visible-light-driven photocatalysts is on the nanocomposites of titanium dioxide (TiO2) with carbon nanostructures, especially graphene. Coupling TiO2 with graphene has proven more active by photocatalysis than TiO2 alone. It is generally considered that graphene sheets act as an electron acceptor facilitating the transfer and separation of photogenerated electrons during TiO2 excitation, thereby reducing electron-hole recombination. This study briefly reviews the fundamental mechanism and interfacial charge-transfer dynamics in TiO2/graphene nanocomposites. Design strategies of various graphene-based hybrids are highlighted along with some specialized synthetic routes adopted to attain preferred properties. Importantly, the enhancing interfacial charge transfer of photogenerated e¯CB through the graphene layers by morphology orientation of TiO2, predominated exposure of their high energy crystal facets, defect engineering, enhancing catalytic sites in graphene, constructing dedicated architectures, tuning the nanomaterial dimensionality at the interface, and employing the synergism adopted through various modifications, are systematically compiled. Portraying the significance of these photocatalytic hybrids in environmental remediation, important applications including air and water purification, self-cleaning surfaces, H2 production, and CO2 reduction to desired fuels, are addressed.
