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使用单原子铱修饰的α-FeO光阳极选择性光电化学合成己二酸。

Selective photoelectrochemical synthesis of adipic acid using single-atom Ir decorated α-FeO photoanode.

作者信息

Si Shenghe, Mao Yuyin, Liu Ying-Ao, Ma Jun, Jiang Weiyi, Zhao En-Dian, Song Kepeng, Cheng Hefeng, Huang Baibiao, Liu Dong, Xiong Yujie

机构信息

School of Chemistry and Materials Science, University of Science and Technology of China, Hefei, Anhui, China.

State Key Laboratory of Bioinspired Interfacial Materials Science, Sustainable Energy and Environmental Materials Innovation Center, School of Nano Science and Technology, Suzhou Institute for Advanced Research, University of Science and Technology of China, Suzhou, Jiangsu, China.

出版信息

Nat Commun. 2025 Jun 2;16(1):5128. doi: 10.1038/s41467-025-60506-w.

Abstract

Photoelectrochemical (PEC) synthesis offers a sustainable route for fine chemicals production, yet comprehending and modulating the reaction processes at the atomic level remains a challenge. Herein, we develop a single-atom Ir decorated Ti-doped α-FeO photoanode for selective PEC synthesis of adipic acid from cyclohexanone using water as the oxygen source. The PEC system achieves 6.0 μmol cm h adipic acid production with ~60% Faradaic efficiency and ~88% selectivity. The single-atom Ir promotes the photogenerated carrier separation and transfer, while regulating the electronic structure of Ti-doped α-FeO photoanode to optimize its adsorption strength of OH and cyclohexanone. Mechanistic studies reveal a non-free-radical reaction pathway at the atomic level, driven by photogenerated holes through an adsorbed hydroxyl transfer. Notably, integrating the photoanode and an amorphous silicon-based photocathode leads to a bias-free PEC device that enables stable adipic acid production for over 80 hours, underscoring the potential for sustainable light-driven synthesis.

摘要

光电化学(PEC)合成提供了一条生产精细化学品的可持续途径,然而在原子水平上理解和调控反应过程仍然是一项挑战。在此,我们开发了一种单原子铱修饰的掺钛α-氧化铁光阳极,用于以水作为氧源从环己酮选择性PEC合成己二酸。该PEC系统实现了6.0 μmol cm⁻² h⁻¹的己二酸产量,法拉第效率约为60%,选择性约为88%。单原子铱促进了光生载流子的分离和转移,同时调节掺钛α-氧化铁光阳极的电子结构,以优化其对OH和环己酮的吸附强度。机理研究揭示了在原子水平上由光生空穴通过吸附的羟基转移驱动的非自由基反应途径。值得注意的是,将光阳极与非晶硅基光阴极集成,得到了一种无偏压的PEC装置,能够稳定生产己二酸超过80小时,突出了可持续光驱动合成的潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1c99/12130220/4c772858e76b/41467_2025_60506_Fig1_HTML.jpg

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