Issue 31, 2023

Photogenerated charge separation at BiVO4 photoanodes enhanced by a Ag-modified porphyrin polymer skeleton

Abstract

Bismuth vanadate (BiVO4) has been considered a promising photoactive material in photoelectrochemical (PEC) water-splitting systems. However, the performance of BiVO4-based photoanodes is currently unsatisfactory, indicating the need for new architectural designs to improve their efficiency. In this paper, a porphyrin-phosphazene polymer (THPP-HCCP) was synthesized with a sizeable conjugated structure, and Ag particles were deposited on its surface as an organic–inorganic composite interface improvement layer. The deposition of the composite polymer film on BiVO4 resulted in a significant increase in photocurrent density, reaching up to 2.2 mA cm−2 (1.23 V vs. RHE), almost three times higher than pristine BiVO4, which benefits from the synergistic effect of Ag nanoparticles and porphyrin-phosphazene. Furthermore, photophysical and intensity-modulated photocurrent analysis demonstrated that the Ag–THPP-HCCP heterostructures could broaden the light-absorbing range and facilitate hole transfer to the semiconductor surface, resulting in an improved water oxidation process. The dynamic charge transport behavior of Ag–THPP-HCCP/BiVO4 was investigated using scanning photoelectrochemical microscopy, which showed that the rate constant (Keff) exhibits an almost 4-fold increase compared to pristine BiVO4, indicating a significant improvement in the transport of photogenerated holes. This experiment presents a novel strategy for designing high-efficiency polymer-based photoanodes.

Graphical abstract: Photogenerated charge separation at BiVO4 photoanodes enhanced by a Ag-modified porphyrin polymer skeleton

Supplementary files

Article information

Article type
Paper
Submitted
05 Jun 2023
Accepted
11 Jul 2023
First published
19 Jul 2023

Dalton Trans., 2023,52, 10911-10917

Photogenerated charge separation at BiVO4 photoanodes enhanced by a Ag-modified porphyrin polymer skeleton

H. Ye, H. Xiao, R. Zhang, S. Zhang, Z. Wang, W. Luo, R. Xie, Y. Feng and X. Lu, Dalton Trans., 2023, 52, 10911 DOI: 10.1039/D3DT01728A

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