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超小PbS纳米晶体作为红到蓝三重态融合上转换的敏化剂。

Ultra-small PbS nanocrystals as sensitizers for red-to-blue triplet-fusion upconversion.

作者信息

Imperiale Christian J, Green Philippe B, Hasham Minhal, Wilson Mark W B

机构信息

University of Toronto, Department of Chemistry Toronto ON M5S 3H6 Canada

出版信息

Chem Sci. 2021 Oct 11;12(42):14111-14120. doi: 10.1039/d1sc04330g. eCollection 2021 Nov 3.

Abstract

Photon upconversion is a strategy to generate high-energy excitations from low-energy photon input, enabling advanced architectures for imaging and photochemistry. Here, we show that ultra-small PbS nanocrystals can sensitize red-to-blue triplet-fusion upconversion with a large anti-Stokes shift (Δ = 1.04 eV), and achieve max-efficiency upconversion at near-solar fluences ( = 220 mW cm) despite endothermic triplet sensitization. This system facilitates the photo-initiated polymerization of methyl methacrylate using only long-wavelength light ( : 637 nm); a demonstration of nanocrystal-sensitized upconversion photochemistry. Time-resolved spectroscopy and kinetic modelling clarify key loss channels, highlighting the benefit of long-lifetime nanocrystal sensitizers, but revealing that many (48%) excitons that reach triplet-extracting carboxyphenylanthracene ligands decay before they can transfer to free-floating acceptors-emphasizing the need to address the reduced lifetimes that we determine for molecular triplets near the nanocrystal surface. Finally, we find that the inferred thermodynamics of triplet sensitization from these ultra-small PbS quantum dots are surprisingly favourable-completing an advantageous suite of properties for upconversion photochemistry-and do not vary significantly across the ensemble, which indicates minimal effects from nanocrystal heterogeneity. Together, our demonstration and study of red-to-blue upconversion using ultra-small PbS nanocrystals in a quasi-equilibrium, mildly endothermic sensitization scheme offer design rules to advance implementations of triplet fusion, especially where large anti-Stokes wavelength shifts are sought.

摘要

光子上转换是一种从低能量光子输入产生高能量激发的策略,可实现用于成像和光化学的先进架构。在此,我们表明超小的硫化铅纳米晶体能够敏化具有大反斯托克斯位移(Δ = 1.04 eV)的红到蓝三重态融合上转换,并且尽管三重态敏化是吸热的,但在近太阳通量( = 220 mW cm)下仍能实现最大效率的上转换。该系统仅使用长波长光( : 637 nm)就能促进甲基丙烯酸甲酯的光引发聚合;这是纳米晶体敏化上转换光化学的一个实例。时间分辨光谱和动力学建模阐明了关键的损失通道,突出了长寿命纳米晶体敏化剂的优势,但也揭示了许多(48%)到达三重态提取羧基苯基蒽配体的激子在转移到自由漂浮受体之前就发生了衰减,这强调了需要解决我们所确定的纳米晶体表面附近分子三重态寿命缩短的问题。最后,我们发现从这些超小的硫化铅量子点推断出的三重态敏化热力学令人惊讶地有利,这为上转换光化学完善了一套有利的特性,并且在整个集合中变化不显著,这表明纳米晶体异质性的影响最小。总之,我们在准平衡、温和吸热的敏化方案中使用超小硫化铅纳米晶体进行红到蓝上转换的演示和研究提供了设计规则,以推进三重态融合的实现,特别是在寻求大反斯托克斯波长位移的情况下。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cd1f/8565365/a22d6c40a8b9/d1sc04330g-f1.jpg

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