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使用石墨保护的本体异质结有机光活性层增强太阳能水氧化和无辅助水分解。

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

作者信息

Daboczi Matyas, Eisner Flurin, Luke Joel, Yuan Shi Wei, Lawati Noof Al, Zhi Maoqing, Yang Mengya, Müller Jolanda Simone, Stewart Katherine, Kim Ji-Seon, Nelson Jenny, Eslava Salvador

机构信息

Department of Chemical Engineering and Centre for Processable Electronics, Imperial College London, London, UK.

Institute of Technical Physics and Materials Science, HUN-REN Centre for Energy Research, Budapest, Hungary.

出版信息

Nat Energy. 2025;10(5):581-591. doi: 10.1038/s41560-025-01736-6. Epub 2025 Mar 18.

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 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.

摘要

聚合物供体和非富勒烯受体作为光活性材料在高效有机太阳能电池的发展中发挥了重要作用,并且在直接太阳能制氢装置中具有巨大潜力。然而,它们在直接太阳能水分解装置中的应用受到其在水性环境中的不稳定性以及与催化剂界面处的复合损失的限制。在此,我们报道了含有PM6:D18:L8-BO光活性层的阳极,在相对于可逆氢电极+1.23 V时达到超过25 mA cm的高太阳能水氧化光电流密度以及长达数天的运行稳定性。这是通过将有机光活性层与用储量丰富的NiFeOOH水氧化催化剂功能化的石墨片集成来实现的,该石墨片既提供了耐水性,又在催化剂和光活性层之间实现了电连接且没有任何损失。使用包含有机PM6:D18:L8-BO和PTQ10:GS-ISO光活性层的单片串联阳极,我们实现了5%的太阳能到氢能效率。这些结果为通过低成本有机光活性材料实现高效、稳定和无辅助的太阳能制氢铺平了道路。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8fde/12116381/29f45d2b7e6b/41560_2025_1736_Fig1_HTML.jpg

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