Photoelectrochemical detection behavior of porous MoO3 nanorods synthesized via facile hydrothermal method
摘要
The growing demand for reliable photoelectrochemical detection in environmental monitoring, biomedical sensing, and emerging optoelectronic technologies has stimulated extensive research on wide-bandgap transition metal oxides such as molybdenum trioxide (MoO3). In this work, porous MoO3 nanorods were synthesized via a facile hydrothermal method and systematically investigated for their structural, optical, morphological, and electrochemical properties. X-ray diffraction analysis confirmed the formation of an orthorhombic crystalline phase, while UV–Visible spectroscopy revealed strong optical absorption with an estimated bandgap of 2.9 eV. Brunauer–Emmett–Teller (BET) analysis demonstrated a mesoporous nature with a moderate specific surface area and a volume-weighted average pore diameter of ~ 3.4 nm, which is consistent with the porous nanorod-like morphology observed from field-emission scanning electron microscopy. Electrochemical studies indicated predominantly diffusion-controlled charge transfer behavior. Photoelectrochemical detection studies, carried out using chronoamperometry under simulated illumination, exhibited clear and reproducible photocurrent responses. The MoO3 nanorods demonstrated a maximum responsivity of 7.08 mA/W at 2.0 V bias with a fast response time of 1.2 s, highlighting efficient light-induced charge separation and transport. The combined structural, optical, and photoelectrochemical characteristics establish porous MoO3 nanorods as promising photoactive materials for future photodetection and optoelectronic applications.