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本文引用的文献

1
Vibronically coherent ultrafast triplet-pair formation and subsequent thermally activated dissociation control efficient endothermic singlet fission.振动相干超快三重态对形成和随后的热激活解离控制有效的吸热单重态裂变。
Nat Chem. 2017 Dec;9(12):1205-1212. doi: 10.1038/nchem.2856. Epub 2017 Sep 11.
2
The entangled triplet pair state in acene and heteroacene materials.并五苯和杂并五苯材料中的纠缠三线态对态。
Nat Commun. 2017 Jul 12;8:15953. doi: 10.1038/ncomms15953.
3
Unified model for singlet fission within a non-conjugated covalent pentacene dimer.非共轭共价五并苯二聚体中单态裂变的统一模型。
Nat Commun. 2017 May 18;8:15171. doi: 10.1038/ncomms15171.
4
Tuning the effective spin-orbit coupling in molecular semiconductors.调控分子半导体中的有效自旋轨道耦合。
Nat Commun. 2017 May 11;8:15200. doi: 10.1038/ncomms15200.
5
The quantum needle of the avian magnetic compass.鸟类磁罗盘的量子指针
Proc Natl Acad Sci U S A. 2016 Apr 26;113(17):4634-9. doi: 10.1073/pnas.1600341113. Epub 2016 Apr 4.
6
Cooperative singlet and triplet exciton transport in tetracene crystals visualized by ultrafast microscopy.超快显微镜可视化的并五苯晶体中的协同单重态和三重态激子输运。
Nat Chem. 2015 Oct;7(10):785-92. doi: 10.1038/nchem.2348. Epub 2015 Sep 14.
7
Identification of a triplet pair intermediate in singlet exciton fission in solution.溶液中单线态激子裂变过程中三重态对中间体的鉴定。
Proc Natl Acad Sci U S A. 2015 Jun 23;112(25):7656-61. doi: 10.1073/pnas.1503471112. Epub 2015 Jun 9.
8
Resonant energy transfer of triplet excitons from pentacene to PbSe nanocrystals.三重激子从并五苯到 PbSe 纳米晶体的共振能量转移。
Nat Mater. 2014 Nov;13(11):1033-8. doi: 10.1038/nmat4093. Epub 2014 Oct 5.
9
Energy harvesting of non-emissive triplet excitons in tetracene by emissive PbS nanocrystals.PbS 纳米晶体对四并苯非辐射三重激子的能量收集。
Nat Mater. 2014 Nov;13(11):1039-43. doi: 10.1038/nmat4097. Epub 2014 Oct 5.
10
Short-lived charge-transfer excitons in organic photovoltaic cells studied by high-field magneto-photocurrent.通过强磁场光电流研究有机光伏电池中的短寿命电荷转移激子。
Nat Commun. 2014 Jul 29;5:4529. doi: 10.1038/ncomms5529.

有机半导体中耦合自旋对的位置选择性测量。

Site-selective measurement of coupled spin pairs in an organic semiconductor.

机构信息

Laboratoire de Physique des Solides, Université Paris-Sud, CNRS, UMR 8502, F-91405 Orsay, France.

Cavendish Laboratory, University of Cambridge, Cambridge CB3 0HE, United Kingdom.

出版信息

Proc Natl Acad Sci U S A. 2018 May 15;115(20):5077-5082. doi: 10.1073/pnas.1718868115. Epub 2018 May 2.

DOI:10.1073/pnas.1718868115
PMID:29720443
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5960292/
Abstract

From organic electronics to biological systems, understanding the role of intermolecular interactions between spin pairs is a key challenge. Here we show how such pairs can be selectively addressed with combined spin and optical sensitivity. We demonstrate this for bound pairs of spin-triplet excitations formed by singlet fission, with direct applicability across a wide range of synthetic and biological systems. We show that the site sensitivity of exchange coupling allows distinct triplet pairs to be resonantly addressed at different magnetic fields, tuning them between optically bright singlet ([Formula: see text]) and dark triplet quintet ([Formula: see text]) configurations: This induces narrow holes in a broad optical emission spectrum, uncovering exchange-specific luminescence. Using fields up to 60 T, we identify three distinct triplet-pair sites, with exchange couplings varying over an order of magnitude (0.3-5 meV), each with its own luminescence spectrum, coexisting in a single material. Our results reveal how site selectivity can be achieved for organic spin pairs in a broad range of systems.

摘要

从有机电子学到生物系统,理解自旋对之间的分子间相互作用的作用是一个关键挑战。在这里,我们展示了如何通过自旋和光学灵敏度的组合来选择性地处理这些对。我们通过由单态裂变形成的束缚自旋三重态激发对证明了这一点,这在广泛的合成和生物系统中具有直接的适用性。我们表明,交换耦合的位点敏感性允许不同的三重态对在不同的磁场中共振地被寻址,将它们调谐在光学上明亮的单态([Formula: see text])和暗三重态 quintet ([Formula: see text])构型之间:这在宽的光学发射光谱中诱导出窄孔,揭示了交换特异性发光。使用高达 60 T 的磁场,我们确定了三个不同的三重态对位点,交换耦合变化幅度为一个数量级(0.3-5 meV),每个位点都有自己的发光光谱,在单个材料中共存。我们的结果揭示了在广泛的系统中如何为有机自旋对实现位点选择性。