Solvent assisted shape dependent MAPbI3/polyfluorene heterostructures with a larger surface area for improved photocatalytic H2 evolution

Abstract

Although lead based MAPbI3 has been used as a material for photocatalytic hydrogen evolution, conventionally synthesized MAPbI3 in HI solution suffers from very low HER activity with a hydrogen evolution rate of 30 μmol h−1 g−1. Several efforts have been made to boost the HER performance by tagging a co-catalyst. But no such significant approach was developed to improve the HER activity of pristine MAPbI3. In this work, the shape and morphology of MAPbI3 have been modified by a simple solvent change route. This led to substantial transformation in shape and morphology affecting various facets of photocatalytic and photoelectrochemical performance. DMF assisted pristine MAPbI3 exhibited an HER activity of 830 μmol h−1 g−1, almost 28-fold better than that of typical HI based MAPbI3. This work highlights how solvent transition from HI to DMF can influence the shape and surface morphologies which impact the photocatalytic and photoelectrochemical performances of pristine MAPbI3. To further enhance the HER activity of DMF assisted MAPbI3, the as-synthesized polyfluorene co-catalyst was integrated on the MAPbI3 surface. Under optimized conditions, the hydrogen evolution of MAPbI3/polyfluorene composites can reach up to 6200 μmol h−1 g−1.

Graphical abstract: Solvent assisted shape dependent MAPbI3/polyfluorene heterostructures with a larger surface area for improved photocatalytic H2 evolution

Supplementary files

Article information

Article type
Paper
Submitted
17 iyl 2024
Accepted
21 okt 2024
First published
22 okt 2024
This article is Open Access
Creative Commons BY-NC license

Energy Adv., 2024, Advance Article

Solvent assisted shape dependent MAPbI3/polyfluorene heterostructures with a larger surface area for improved photocatalytic H2 evolution

T. Pal, S. Bhowmik, A. S. Tanwar, A. Suhail, N. R. Peela, C. V. Sastri and P. K. Iyer, Energy Adv., 2024, Advance Article , DOI: 10.1039/D4YA00457D

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