Krause Stefan, Cerretani Cecilia, Vosch Tom
Nanoscience Center , Department of Chemistry , University of Copenhagen , Universitetsparken 5 , Copenhagen 2100 , Denmark . Email:
Chem Sci. 2019 Apr 24;10(20):5326-5331. doi: 10.1039/c9sc00865a. eCollection 2019 May 28.
Optically activated delayed fluorescence (OADF) is a powerful tool for generating background-free, anti-Stokes fluorescence microscopy modalities. Recent findings, using DNA-stabilized silver nanoclusters (DNA-AgNCs), indicate that OADF is usually accompanied by a dark state-mediated consecutive photon absorption process leading to upconversion fluorescence (UCF). In this study, we disentangle the OADF and UCF process by means of wavelength-dependent NIR excitation spectroscopy. We demonstrate that, by appropriate choice of secondary NIR excitation wavelength, the dark state population can be preferentially depleted through OADF, minimizing the UCF contribution. These findings show that dark state depletion by OADF might enable background-free STED-like nanoscopy.
光激活延迟荧光(OADF)是一种用于产生无背景、反斯托克斯荧光显微镜模式的强大工具。最近使用DNA稳定的银纳米团簇(DNA-AgNCs)的研究结果表明,OADF通常伴随着暗态介导的连续光子吸收过程,从而导致上转换荧光(UCF)。在本研究中,我们通过波长相关的近红外激发光谱法解开了OADF和UCF过程。我们证明,通过适当选择二次近红外激发波长,可以通过OADF优先耗尽暗态粒子数,从而将UCF的贡献降至最低。这些发现表明,OADF引起的暗态耗尽可能实现类似受激发射损耗(STED)的无背景纳米显微镜技术。