Visible Light Driven Hydrogen Evolution by Molecular Nickel Catalysts with Time-Resolved Spectroscopic and DFT Insights.

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ID: 37682
2019
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Abstract
Hydrogen (H) is a clean fuel that can potentially be a future solution for the storage of intermittent renewable energy. However, current H production is mainly dominated by the energy intensive steam reforming reaction, which consumes a fossil fuel, methane, and emits copious amounts of carbon dioxide as one of the byproducts. To address this challenge, we report a molecular catalyst that produces H from aqueous solutions, is composed of affordable, earth-abundant elements such as nickel, and has been incorporated into a system driven by visible light. Under optimized conditions, we observe a turnover number of 3880, among the best for photocatalytic H evolution with nickel complexes from water-methanol solutions. Through nanosecond transient absorption, electron paramagnetic resonance, and UV-vis spectroscopic measurements, and supported by density functional theory calculations, we report a detailed study of this photocatalytic H evolution cycle. We demonstrate that a one-electron reduced, predominantly ligand-centered, reactive Ni intermediate can be accessed under visible light irradiation using triethylamine as the sacrificial electron donor and reductive quencher of the initial photosensitizer excited state. In addition, the computational calculations suggest that the second coordination sphere ether arms can enhance the catalytic activity by promoting proton relay, similar to the mechanism among [FeFe] hydrogenases in nature. Our study can form the basis for future development of H evolution molecular catalysts that incorporate both ligand redox noninnocence and alternative second coordination sphere effects in artificial photosynthetic systems driven by visible light.
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ho2019visibleinorganic Use this key to autocite in the manuscript while using SciMatic Manuscript Manager or Thesis Manager
Authors Ho, Xian Liang;Shao, Haiyan;Ng, Yik Yie;Ganguly, Rakesh;Lu, Yunpeng;Soo, Han Sen;
Journal Inorganic chemistry
Year 2019
DOI
10.1021/acs.inorgchem.8b03003
URL
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