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Electrochemical response of metal complexes in homogeneous solution under photoirradiation

机译:金属配合物在光辐照下在均相溶液中的电化学响应

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摘要

The electrochemical detection of metal complexes in the photoexcited state is important for understanding photoinduced electron transfer (PET) processes, which play a central role in photo-energy conversion systems. In general, however, the redox potentials of excited states have been indirectly estimated by a combination of spectroscopic properties and ground-state redox potentials. To establish a simple method for directly determining the redox potentials of the photoexcited states of metal complexes, electrochemical measurements under several conditions were performed. The electrochemical response was largely influenced not only by the generation of photoexcited molecules but also by the convection induced by photoirradiation, even when the global temperature of the sample solution was unchanged. The suppression of these unfavourable electrochemical responses was successfully achieved by adopting well-established electrochemical techniques. Furthermore, as an initial demonstration, the photoexcited state of a Ru-based metal complex was directly detected, and its redox potential was determined using a thin layer electrochemical method.
机译:在光激发态下对金属配合物的电化学检测对于理解光诱导电子转移(PET)过程非常重要,该过程在光能转换系统中起着核心作用。然而,通常,激发态的氧化还原电势是通过光谱性质和基态氧化还原电势的组合间接估计的。为了建立直接确定金属络合物光激发态氧化还原电势的简单方法,在几种条件下进行了电化学测量。电化学反应不仅受光激发分子的产生影响,而且受光辐照引起的对流的影响很大,即使样品溶液的整体温度不变。通过采用公认的电化学技术成功地抑制了这些不利的电化学反应。此外,作为初步证明,直接检测Ru基金属络合物的光激发态,并使用薄层电化学方法测定其氧化还原电位。

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