This study demonstrated efficient solar-to-H2O2 conversion through a photoelectrochemical (PEC) cell that maximizes the utilization of solar energy by having double side generation of H2O2 on both the photoanode and cathode. This work was accomplished by preparing (i) efficient BiVO4 (BVO) photoanodes modified with various metal dopants (Mo, W, or Cr), (ii) surface-treatment with phosphate on the as-synthesized photoanodes, and (iii) single-walled carbon nanotube (CNT) electrodes with anchored anthraquinone (AQ-CNT), a reversible H2O2-evolving catalyst that has been widely used in the H2O2 production industry. The introduction of Mo into BVO and surface phosphate treatment on BVO (P-Mo-BVO) enhanced the faradaic efficiency (FE) of H2O2 production from water oxidation and slowed the H2O2 decomposition kinetics with achieving highly durable PEC reactions over 100 h (90% photocurrent remained), while bare Mo-BVO experienced the rapid decline of the photocurrent during irradiation with the dissolution of BiVO4. The utilization of AQ on the cathode made the H2O2 production by oxygen reduction highly selective and suppressed competing H2 production completely. Consequently, the optimized configuration of a BVO photoanode modified with Mo (10 atom%) and phosphate and an AQ-CNT cathode enabled H2O2 production on both electrodes, yielding H2O2 production with FE values of 40-50% and ∼100%, respectively, across a broad range of potentials (0.75 to 2 VRHE) and a net H2O2 production rate of 0.66 μmol min-1 cm-2 at 1.0 VRHE. This dual electrode system also successfully demonstrated H2O2 production under an external bias-free condition with a net H2O2 production rate of 0.16 μmol min-1 cm-2 and FE value of ∼43% and ∼100% for photoanodic and cathodic production, respectively. To the best of our knowledge, this is the most durable PEC system for H2O2 production obtained using a BiVO4-based photoanode that enabled the simultaneous photoanodic and cathodic production of H2O2.
|Number of pages||13|
|Journal||Energy and Environmental Science|
|Publication status||Published - 2020 Jun|
Bibliographical noteFunding Information:
This research was financially supported by the Global Research Laboratory (GRL) Program (NRF-2014K1A1A2041044), Basic Science Research Program (NRF-2017R1A2B2008952), and Basic Research Lab (BRL) Program (NRF-2018R1A4A1022194), which were funded by the Korea government (MSIT) through the National Research Foundation (NRF).
© The Royal Society of Chemistry.
All Science Journal Classification (ASJC) codes
- Environmental Chemistry
- Renewable Energy, Sustainability and the Environment
- Nuclear Energy and Engineering