4.8 Article

Photocatalytic generation of hydrogen from water using a cobalt pentapyridine complex in combination with molecular and semiconductor nanowire photosensitizers

期刊

CHEMICAL SCIENCE
卷 4, 期 1, 页码 118-124

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ROYAL SOC CHEMISTRY
DOI: 10.1039/c2sc21163g

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  1. DOE/LBNL [403801]
  2. NSF [CHE-1111900]
  3. Office of Science, Office of Basic Energy Sciences, Materials Sciences and Engineering Division, of the US Department of Energy [DE-AC02-05CH11231]

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Recently, a family of cobalt pentapyridine complexes of the type [(R-PY5Me(2))Co(H2O)])(CF3SO3)(2), (R = CF3, H, or NMe2; PY5Me(2) = 2,6-bis(1,1-di(pyridin-2-yl)ethyl)pyridine) were shown to catalyze the electrochemical generation of hydrogen from neutral aqueous solutions using a mercury electrode. We now report that the CF3 derivative of this series, [(CF(3)PY5Me(2))Co(H2O)](CF3SO3)(2) (1), can also operate in neutral water as an electrocatalyst for hydrogen generation under soluble, diffusion-limited conditions on a glassy carbon electrode, as well as a photocatalyst for hydrogen production using either molecular or semiconductor nanowire photosensitizers. Owing to its relatively low overpotential compared to other members of the PY5 family, complex 1 exhibits multiple redox features on glassy carbon, including a one-proton, one-electron coupled oxidative wave. Further, rotating disk electrode voltammetry measurements reveal the efficacy of 1 as a competent hydrogen evolution catalyst under soluble, diffusion-limited conditions. In addition, we establish that 1 can also generate hydrogen from neutral water under photocatalytic conditions with visible light irradiation (lambda(irr) >= 455 nm), using [Ru(bpy)(3)](2+) as a molecular inorganic chromophore and ascorbic acid as a sacrificial donor. Dynamic light scattering measurements show no evidence for nanoparticle formation for the duration of the photolytic hydrogen evolution experiments. Finally, we demonstrate that 1 is also able to enhance the hydrogen photolysis yield of GaP nanowires in water, showing that this catalyst is compatible with solid-state photosensitizers. Taken together, these data establish that the well-defined cobalt pentapyridine complex [(CF(3)PY5Me(2))Co(H2O)](2+) is a versatile catalyst for hydrogen production from pure aqueous solutions using either solar or electrical input, providing a starting point for integrating molecular systems into sustainable energy generation devices.

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