Facile Synthesis of a Micro–Nano-Structured FeOOH/BiVO4/WO3 Photoanode with Enhanced Photoelectrochemical Performance

10Citations
Citations of this article
10Readers
Mendeley users who have this article in their library.
Get full text

Abstract

In the realm of photoelectrocatalytic (PEC) water splitting, the BiVO4/WO3 photoanode exhibits high electron–hole pair separation and transport capacity, rendering it a promising avenue for development. However, the charge transport and reaction kinetics at the heterojunction interface are suboptimal. This study uses the hydrothermal–electrodeposition–dip coating–calcination method to prepare a microcrystalline WO3 photoanode thin film as the substrate material and combines it with nanocrystalline BiVO4 to form a micro–nano-structured heterojunction photoanode to enhance the intrinsic and surface/interface charge transport properties of the photoanode. Under the condition of 1.23 V vs. RHE, the photoelectric current density reaches 1.09 mA cm−2, which is twice that of WO3. Furthermore, by using a simple impregnation–mineralization method to load the amorphous FeOOH catalyst, a noncrystalline–crystalline composite structure is formed to increase the number of active sites on the surface and reduce the overpotential of water oxidation, lowering the onset potential from 0.8 V to 0.6 V (vs. RHE). The photoelectric current density is further increased to 2.04 mA cm−2 (at 1.23 V vs. RHE). The micro–nano-structure and noncrystalline–crystalline composite structure proposed in this study will provide valuable insights for the design and synthesis of high-efficiency photoelectrocatalysts.

Cite

CITATION STYLE

APA

Li, R., Zhan, F., Wen, G., Wang, B., Qi, J., Liu, Y., … La, P. (2024). Facile Synthesis of a Micro–Nano-Structured FeOOH/BiVO4/WO3 Photoanode with Enhanced Photoelectrochemical Performance. Catalysts, 14(11). https://doi.org/10.3390/catal14110828

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free