Abstract
The development of efficient and durable nonplatinum-based electrocatalysts for the hydrogen evolution reaction (HER) remains a key challenge. This study explores the heterojunction between titanium dioxide nanotubes (TiO(2) NTs) and molybdenum disulfide quantum dots (MoS(2) QDs) as a viable alternative to platinum-based HER electrocatalysts. TiO(2) NTs were synthesized via anodization, while MoS(2) QDs were electrosynthesized chronopotentiometrically, followed by heterojunction formation via immersion/adsorption. The optimized TiO(2) NTs/MoS(2) QDs electrocatalyst exhibited significantly enhanced HER activity, achieving an overpotential of 617 mV at 100 mA cm(-2) (η(100)), a notable improvement over 927 mV observed for bare TiO(2) NTs. Electrochemical impedance spectroscopy (EIS) revealed a dramatic reduction in charge transfer resistance from 475 to 9.9 Ω after MoS(2) QDs deposition. A Tafel slope of 106 mV dec(-1) indicated a Volmer-Heyrovsky HER mechanism with second-order kinetics, as confirmed by kinetic modeling. Structural and morphological characterization (XRD, SEM, TEM, and EDX) confirmed the successful heterojunction formation. This work highlights the potential of TiO(2) NTs/MoS(2) QDs as scalable and efficient electrocatalysts for sustainable hydrogen production, offering a promising alternative to platinum-based systems.