Interrogation of cobaloxime-based supramolecular photocatalyst architectures

被引:13
|
作者
Mulfort, Karen L. [1 ]
机构
[1] Argonne Natl Lab, Div Chem Sci & Engn, 9700 South Cass Ave, Argonne, IL 60439 USA
关键词
Artificial photosynthesis; Supramolecular; Cobaloxime; X-ray scattering; Photocatalysis; ELECTROCATALYTIC HYDROGEN EVOLUTION; ULTRAFAST CHARGE-TRANSFER; STRUCTURAL-CHARACTERIZATION; FUNCTIONAL MODELS; ELECTRON-TRANSFER; WATER OXIDATION; H-2; EVOLUTION; PHOTOSYSTEM-I; CATALYST; COMPLEXES;
D O I
10.1016/j.crci.2015.12.010
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
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.
引用
收藏
页码:221 / 229
页数:9
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