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Interrogation of cobaloxime-based supramolecular photocatalyst architectures

Journal

COMPTES RENDUS CHIMIE
Volume 20, Issue 3, Pages 221-229

Publisher

centre Mersenne pour ldition scientifique ouverte
DOI: 10.1016/j.crci.2015.12.010

Keywords

Artificial photosynthesis; Supramolecular; Cobaloxime; X-ray scattering; Photocatalysis

Funding

  1. Division of Chemical Sciences, Geosciences, and Biosciences
  2. Office of Basic Energy Sciences of the U.S. Department of Energy [DE-AC02-06CH11357]

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This perspective provides a discussion of recent work focused on elucidating the fundamental interactions of artificial photosynthesis in newly developed supramolecular photocatalysts composed of linked chromophore and catalyst modules. Supramolecular photocatalyst architectures are of particular interest because of their potential to overcome many of the limitations of molecular or multimolecular systems and amenability to conventional and emerging physical characterization techniques. As such, changes to the oxidation state and/or physical structure of either chromophore or catalyst modules in response to light excitation is readily monitored with high spatial and temporal resolution. To illustrate this approach, the design evolution of photocatalysts based on Ru(II) poly(pyridyl) chromophores linked to cobaloxime-based H-2 catalysts is discussed. In this work, new synthesis, transient optical spectroscopy, and X-ray scattering were combined to develop next generation photocatalysts capable of ultrafast charge transfer and identification of a key intermediate for hydrogen photocatalysis. Recent and upcoming advances in light source capabilities are ideally suited to monitor light-generated transient structures and well-poised to dramatically impact the drive toward technologically relevant systems for artificial photosynthesis. (C) 2016 Academie des sciences. Published by Elsevier Masson SAS. All rights reserved.

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