Enhanced solar water oxidation and unassisted water splitting using graphite-protected bulk heterojunction organic photoactive layers

Polymer donors and non-fullerene acceptors have played an important role as photoactive materials in the development of high-efficiency organic solar cells and have immense potential in devices for direct solar hydrogen generation. However, their use in direct solar water-splitting devices has been limited by their instability in aqueous environment and recombination losses at the interface with catalysts. Here we report anodes containing PM6:D18:L8-BO photoactive layers reaching high solar water oxidation photocurrent density over 25 mA cm<sup>-2</sup> at +1.23 V versus reversible hydrogen electrode and days-long operational stability. This was achieved by integrating the organic photoactive layer with a graphite sheet functionalized with earth-abundant NiFeOOH water oxidation catalyst, which provides both water resistance and electrical connection between the catalyst and the photoactive layer without any losses. Using monolithic tandem anodes containing organic PM6:D18:L8-BO and PTQ10:GS-ISO photoactive layers, we achieve a solar-to-hydrogen efficiency of 5%. These results pave the way towards high-efficiency, stable and unassisted solar hydrogen generation by low-cost organic photoactive materials.

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Publication Details

Journal
Nature Energy
Published
2025-03-18
DOI
https://doi.org/10.1038/s41560-025-01736-6
Citations
14
Primary Topic
Advanced Photocatalysis Techniques
Type
article
Field-Weighted Citation Impact
5.09

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article

Enhanced solar water oxidation and unassisted water splitting using graphite-protected bulk heterojunction organic photoactive layers

Salvador Eslava, Joel Luke, Mengya Yang, Flurin D. Eisner et al.
14 citations
Nature Energy
Advanced Photocatalysis Techniques
5.09
article

Enhanced solar water oxidation and unassisted water splitting using graphite-protected bulk heterojunction organic photoactive layers

Salvador Eslava, Joel Luke, Mengya Yang, Flurin D. Eisner, Jenny Nelson, Shi Wei Yuan, Mátyás Dabóczi, Jolanda Simone Müller, Noof Al Lawati, Ji‐Seon Kim, Katherine Stewart, Maoqing Zhi
article en
14 citations

Abstract

Polymer donors and non-fullerene acceptors have played an important role as photoactive materials in the development of high-efficiency organic solar cells and have immense potential in devices for direct solar hydrogen generation. However, their use in direct solar water-splitting devices has been limited by their instability in aqueous environment and recombination losses at the interface with catalysts. Here we report anodes containing PM6:D18:L8-BO photoactive layers reaching high solar water oxidation photocurrent density over 25 mA cm<sup>-2</sup> at +1.23 V versus reversible hydrogen electrode and days-long operational stability. This was achieved by integrating the organic photoactive layer with a graphite sheet functionalized with earth-abundant NiFeOOH water oxidation catalyst, which provides both water resistance and electrical connection between the catalyst and the photoactive layer without any losses. Using monolithic tandem anodes containing organic PM6:D18:L8-BO and PTQ10:GS-ISO photoactive layers, we achieve a solar-to-hydrogen efficiency of 5%. These results pave the way towards high-efficiency, stable and unassisted solar hydrogen generation by low-cost organic photoactive materials.

Nature EnergyVol. 10(5)
Queen Mary University of London (GB), HUN-REN Centre for Energy Research (HU), Imperial College London (GB)
Imperial College London, European Commission, Engineering and Physical Sciences Research Council, H2020 Marie Skłodowska-Curie Actions
Openalex Percentile: Top 4%
Advanced Photocatalysis Techniques
5.09
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