In situ Detection of Cobaloxime Intermediates During Photocatalysis Using Hollow-Core Photonic Crystal Fiber Microreactors

被引:6
作者
Lawson, Takashi [1 ,2 ]
Gentleman, Alexander S. [1 ,2 ]
Pinnell, Jonathan [1 ]
Eisenschmidt, Annika [2 ]
Anton-Garcia, Daniel [2 ]
Frosz, Michael H. [3 ]
Reisner, Erwin [2 ]
Euser, Tijmen G. [1 ]
机构
[1] Univ Cambridge, NanoPhoton Ctr, Cavendish Lab, JJ Thomson Ave, Cambridge CB3 0HE, England
[2] Univ Cambridge, Yusuf Hamied Dept Chem, Lensfield Rd, Cambridge CB2 1EW, England
[3] Max Planck Inst Sci Light, Staudtstr 2, D-91058 Erlangen, Germany
基金
英国工程与自然科学研究理事会;
关键词
Cobaloximes; Hollow-Core Photonic Crystal Fibers; Laser Spectroscopy; Optofluidics; Photocatalysis; HYDROGEN EVOLUTION; MOLECULAR CATALYSTS; OPERANDO SPECTROSCOPY; PHOTOREDOX CATALYSTS; HOMOGENEOUS SYSTEM; WATER; REDUCTION; MECHANISM; LIGAND; PH;
D O I
10.1002/anie.202214788
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Hollow-core photonic crystal fibers (HC-PCFs) provide a novel approach for in situ UV/Vis spectroscopy with enhanced detection sensitivity. Here, we demonstrate that longer optical path lengths than afforded by conventional cuvette-based UV/Vis spectroscopy can be used to detect and identify the Co-I and Co-II states in hydrogen-evolving cobaloxime catalysts, with spectral identification aided by comparison with DFT-simulated spectra. Our findings show that there are two types of signals observed for these molecular catalysts; a transient signal and a steady-state signal, with the former being assigned to the Co-I state and the latter being assigned to the Co-II state. These observations lend support to a unimolecular pathway, rather than a bimolecular pathway, for hydrogen evolution. This study highlights the utility of fiber-based microreactors for understanding these and a much wider range of homogeneous photocatalytic systems in the future.
引用
收藏
页数:8
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