Abstract
In this study, ZnO nanorods (NRs) were hydrothermally grown on an Au-coated glass substrate at a relatively low temperature (90 °C), followed by the deposition of Ag(2)CrO(4) particles via a successive ionic layer adsorption and reaction (SILAR) route. The content of the Ag(2)CrO(4) particles on ZnO NRs was controlled by changing the number of SILAR cycles. The fabricated ZnO-Ag(2)CrO(4) heterojunction photoelectrodes were subjected to morphological, structural, compositional, and optical property analyses; their photoelectrochemical (PEC) properties were investigated under simulated solar light illumination. The photocurrent responses confirmed that the ability of the ZnO-Ag(2)CrO(4) heterojunction photoelectrodes to separate the photo-generated electron-hole pairs is stronger than that of bare ZnO NRs. Impressively, the maximum photocurrent density of about 2.51 mA cm(-2) at 1.23 V (vs. Ag/AgCl) was measured for the prepared ZnO-Ag(2)CrO(4) photoelectrode with 8 SILAR cycles (denoted as ZnO-Ag(2)CrO(4)-8), which exhibited about 3-fold photo-enhancement in the current density as compared to bare ZnO NRs (0.87 mA cm(-2)) under similar conditions. The improvement in photoactivity was attributed to the ideal band gap and high absorption coefficient of the Ag(2)CrO(4) particles, which resulted in improved solar light absorption properties. Furthermore, an appropriate annealing treatment was proven to be an efficient process to increase the crystallinity of Ag(2)CrO(4) particles deposited on ZnO NRs, which improved the charge transport characteristics of the ZnO-Ag(2)CrO(4)-8 photoelectrode annealed at 200 °C and increased the performance of the photoelectrode. The results achieved in the present work present new insights for designing n-n heterojunction photoelectrodes for efficient and cost-effective PEC applications and solar-to-fuel energy conversions.