Rational Design of Photoelectrodes for the Fully Integrated Polymer Electrode Membrane–Photoelectrochemical Water-Splitting System: A Case Study of Bismuth Vanadate

Abstract

Photoelectrochemical (PEC) reactors based on polymer electrolyte membrane (PEM) electrolyzers are an attractive alternative to improve scalability compared to conventional monolithic devices. To introduce narrow band gap photoabsorbers such as BiVO4 in PEM-PEC system requires cost-effective and scalable deposition techniques beyond those previously demonstrated on monolithic FTO-coated glass substrates, followed by the preparation of membrane electrode assemblies. Herein, we address the significant challenges in coating narrow band gap metal-oxides on porous substrates as suitable photoelectrodes for the PEM-PEC configuration. In particular, we demonstrate the deposition and integration of W-doped BiVO4 on porous conductive substrates by a simple, cost-effective, and scalable deposition based on the SILAR (successive ionic layer adsorption and reaction) technique. The resultant W-doped BiVO4 photoanode exhibits a photocurrent density of 2.1 mA·cm–2, @1.23V vs RHE, the highest reported so far for the BiVO4 on any porous substrates. Furthermore, we integrated the BiVO4 on the PEM-PEC reactor to demonstrate the solar hydrogen production from ambient air with humidity as the only water source, retaining 1.55 mA·cm–2, @1.23V vs RHE. The concept provides insights into the features necessary for the successful development of materials suitable for the PEM-PEC tandem configuration reactors and the gas-phase operation of the reactor, which is a promising approach for low-cost, large-scale solar hydrogen production.