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高效近红外激活三重态-三重态湮灭上转换用于光氧化还原催化。

Highly Effective Near-Infrared Activating Triplet-Triplet Annihilation Upconversion for Photoredox Catalysis.

机构信息

Department of Biochemistry and Molecular Pharmacology, University of Massachusetts Medical School, Worcester, Massachusetts 01605, United States.

State Key Laboratory of Heavy Oil Processing School of Chemical Engineering, China University of Petroleum, Qingdao 266580, P. R. China.

出版信息

J Am Chem Soc. 2020 Oct 28;142(43):18460-18470. doi: 10.1021/jacs.0c06976. Epub 2020 Oct 19.

Abstract

Organic triplet-triplet annihilation upconversion (TTA-UC) materials have considerable promise in areas as broad as biology, solar energy harvesting, and photocatalysis. However, the development of highly efficient near-infrared (NIR) light activatable TTA-UC systems remains extremely challenging. In this work, we report on a method of systematically tailoring an annihilator to attain such outstanding systems. By chemical modifications of a commonly used perylene annihilator, we constructed a family of perylene derivatives that have simultaneously tailored triplet excited state energy (T) and singlet excited state energy (S), two key annihilator factors to determine TTA-UC performance. this method, we were able to tune the TTA-UC system from an endothermic type to an exothermic one, thus significantly elevating the upconversion performance of NIR light activatable TTA upconversion systems. In conjunction with the photosensitizer PdTNP (10 μM), the upconversion efficiency using the optimal annihilator (100 μM) identified in this study was measured to be 14.1% under the low-power density of NIR light (100 mW/cm, 720 nm). Furthermore, using such a low concentration of perylene derivative, we demonstrated that the optimal TTA-UC pair developed in our study can act as a highly effective light wavelength up-shifter to enable NIR light to drive a photoredox catalysis that otherwise requires visible light. We found that such an NIR driven method is highly effective and can even surpass directly visible light driven photoredox catalysis. This method is important for photoredox catalysis as NIR light can penetrate much deeper in colored photoredox catalysis reaction solutions, especially when done in a large-scale manner. Furthermore, this TTA-UC mediated photoredox catalysis reaction is found to be outdoor sunlight operable. Thus, our study provides a solution to enhance NIR activatable organic upconversion and set the stage for a wide array of applications that have previously been limited by the suboptimal efficiency of the existing TTA upconversion materials.

摘要

有机三重态-三重态湮灭上转换(TTA-UC)材料在生物学、太阳能收集和光催化等广泛领域具有相当大的应用前景。然而,开发高效的近红外(NIR)光激活 TTA-UC 系统仍然极具挑战性。在这项工作中,我们报告了一种系统地修饰湮灭剂以获得此类卓越系统的方法。通过对常用苝湮灭剂进行化学修饰,我们构建了一系列具有同时调整三重态激发态能量(T)和单重态激发态能量(S)的苝衍生物,这两个关键的湮灭剂因素决定了 TTA-UC 性能。通过这种方法,我们能够将 TTA-UC 系统从吸热型调整为放热型,从而显著提高了近红外光激活 TTA 上转换系统的上转换性能。与光敏剂 PdTNP(10 μM)结合,使用本研究中确定的最佳湮灭剂(100 μM),在低功率密度的近红外光(100 mW/cm,720nm)下,测量到的上转换效率为 14.1%。此外,使用如此低浓度的苝衍生物,我们证明了我们研究中开发的最佳 TTA-UC 对可以用作高效的光波长上转换器,以实现近红外光驱动原本需要可见光的光还原催化。我们发现这种近红外驱动方法非常有效,甚至可以超过直接可见光驱动的光还原催化。对于光还原催化来说,这种方法很重要,因为近红外光可以在有色光还原催化反应溶液中穿透得更深,尤其是在大规模进行时。此外,这种 TTA-UC 介导的光还原催化反应被发现可在户外阳光条件下运行。因此,我们的研究提供了一种增强近红外可激活有机上转换的解决方案,并为一系列以前受到现有 TTA 上转换材料效率不佳限制的应用奠定了基础。

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