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通过与人工光合作用相关的单脉冲和双脉冲激光实验对电荷分离态进行定量洞察。

Quantitative insights into charge-separated states from one- and two-pulse laser experiments relevant for artificial photosynthesis.

作者信息

Neumann Svenja, Kerzig Christoph, Wenger Oliver S

机构信息

Department of Chemistry , University of Basel , St. Johanns-Ring 19 , 4056 Basel , Switzerland . Email:

出版信息

Chem Sci. 2019 May 9;10(21):5624-5633. doi: 10.1039/c9sc01381d. eCollection 2019 Jun 7.

DOI:10.1039/c9sc01381d
PMID:31293747
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6553010/
Abstract

Charge-separated states (CSSs) are key intermediates in photosynthesis and solar energy conversion. However, the factors governing the formation efficiencies of CSSs are still poorly understood, and light-induced electron-hole recombinations as deactivation pathways competing with desired charge accumulations are largely unexplored. This greatly limits the possibility to perform efficient multi-electron transfer, which is essential for artificial photosynthesis. We present a systematic investigation of two donor-sensitizer-acceptor triads (with different donor-acceptor distances) capable of storing as much as 2.0 eV in their CSSs upon the absorption of a visible photon. Using quantitative one- and two-pulse laser flash photolysis, we provide deep insights into both the CSS formation quantum yield, which can reach up to 80%, and the fate of the CSS upon further (secondary) excitation with green photons. The triad with shorter intramolecular distances shows a remarkable excitation wavelength dependence of the CSS formation quantum yield, and the CSS of this triad undergoes more efficient light-induced charge recombination than the longer equivalent by about one order of magnitude, whilst thermal charge recombination shows the exact opposite behavior. The unexpected results of our detailed photophysical study can be rationalized by detrimental singlet charge transfer states or structural considerations, and could significantly contribute to the future design of CSS precursors for accumulative multi-electron transfer and artificial photosynthesis.

摘要

电荷分离态(CSSs)是光合作用和太阳能转换中的关键中间体。然而,目前人们对决定CSSs形成效率的因素仍知之甚少,并且作为与所需电荷积累相竞争的失活途径的光致电子 - 空穴复合在很大程度上尚未得到充分研究。这极大地限制了进行高效多电子转移的可能性,而多电子转移对于人工光合作用至关重要。我们对两个供体 - 敏化剂 - 受体三联体(具有不同的供体 - 受体距离)进行了系统研究,它们在吸收一个可见光子后,其CSSs中能够存储高达2.0电子伏特的能量。通过定量单脉冲和双脉冲激光闪光光解,我们深入了解了CSS形成量子产率(可达80%)以及用绿色光子进一步(二次)激发后CSS的命运。分子内距离较短的三联体显示出CSS形成量子产率对激发波长有显著依赖性,并且该三联体的CSS比分子内距离较长的等效三联体经历更高效的光致电荷复合,效率高出约一个数量级,而热电荷复合则表现出相反的行为。我们详细的光物理研究的意外结果可以通过有害的单线态电荷转移态或结构因素来解释,并且可能对未来用于累积多电子转移和人工光合作用的CSS前体的设计做出重大贡献。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7a2d/6553010/b2e4fa5d54b3/c9sc01381d-f5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7a2d/6553010/84b8baa72ba6/c9sc01381d-s1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7a2d/6553010/19178b849c97/c9sc01381d-f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7a2d/6553010/dafbbf6737a7/c9sc01381d-f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7a2d/6553010/77fe893baaec/c9sc01381d-f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7a2d/6553010/4830c1a476fe/c9sc01381d-f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7a2d/6553010/b2e4fa5d54b3/c9sc01381d-f5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7a2d/6553010/84b8baa72ba6/c9sc01381d-s1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7a2d/6553010/19178b849c97/c9sc01381d-f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7a2d/6553010/dafbbf6737a7/c9sc01381d-f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7a2d/6553010/77fe893baaec/c9sc01381d-f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7a2d/6553010/4830c1a476fe/c9sc01381d-f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7a2d/6553010/b2e4fa5d54b3/c9sc01381d-f5.jpg

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