Kiseleva Natalia, Nazari Pariya, Dee Carolin, Busko Dmitry, Richards Bryce S, Seitz Michael, Howard Ian A, Turshatov Andrey
Institute of Microstructure Technology, Karlsruhe Institute of Technology, Hermann-von-Helmholtz-Platz 1, 76344 Eggenstein-Leopoldshafen, Germany.
Institute of Inorganic Chemistry, University of Tübingen, Auf der Morgenstelle 18, 72076 Tübingen, Germany.
J Phys Chem Lett. 2020 Apr 2;11(7):2477-2481. doi: 10.1021/acs.jpclett.0c00221. Epub 2020 Mar 13.
The upconversion of near-infrared (NIR) to visible (vis) photons is of interest for display technologies and energy conversion. Although triplet-triplet annihilation (TTA) offers a mechanism for upconversion that works efficiently at low incident irradiance flux densities, current strategies for NIR-vis upconversion based on TTA have fundamental limitations. Herein, we report a strategy for NIR-vis TTA based on lanthanide-containing complexes to sensitize the upconversion. We demonstrate a β-diketonate complex of Yb paired with rubrene that emits yellow (λ = 559 nm) under NIR excitation (λ = 980 nm). This corresponds to an exceptional anti-Stokes shift of just less than 1 eV. Thus, lanthanide complexes could unlock high-performance NIR-vis upconversion, with lanthanide sensitizers overcoming the energy loss, reabsorption, and short triplet lifetime that fundamentally limit porphyrin, nanocrystals, and direct S-T sensitizers.
将近红外(NIR)光子上转换为可见光(vis)光子在显示技术和能量转换领域备受关注。尽管三重态-三重态湮灭(TTA)提供了一种在低入射辐照通量密度下有效工作的上转换机制,但目前基于TTA的近红外-可见光上转换策略存在根本局限性。在此,我们报告一种基于含镧系元素配合物的近红外-可见光TTA策略,以敏化上转换。我们展示了一种与红荧烯配对的镱β-二酮配合物,在近红外激发(λ = 980 nm)下发射黄色光(λ = 559 nm)。这对应于仅略小于1 eV的异常反斯托克斯位移。因此,镧系元素配合物可以实现高性能的近红外-可见光上转换,镧系元素敏化剂克服了从根本上限制卟啉、纳米晶体和直接单重态-三重态敏化剂的能量损失、再吸收和短三重态寿命问题。