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Ultrafast Photoinduced Electron Transfer from Cyclometalated Rhodium and Iridium Complexes to Cyan Emitting Copper Nanoclusters: Footsteps toward Light Harvesting

机译:超快速光诱导的电子从环数钟阳和虹膜络合物转移到铜发射铜纳米簇:朝着光收集的脚步

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摘要

In recent times, copper nanocluster (Cu NC) has become a promising candidate as an interesting nanomaterial for its potential applications in optoelectronics, sensing, catalysis and bioimaging. Herein, we have synthesized L-Cysteine protected Cu NC in 1:1 water:acetonitrile (ACN) solvent possessing bright cyan emission (λem=495 nm) with 10.4% quantum yield. Furthermore, the cyclometalated complexes of Ir(III) and Rh(III) are light harvesters, which are applied in photoinduced electron and energy transfer and photocatalysis. Three such cyclometalated complexes of Rh and Ir have been employed herein, which on electrostatic interaction with Cu NCs in 1:1 water:ACN medium, quench the fluorescence from Cu NC dramatically. This quenching could be suitably attributed to photoinduced electron transfer (PET) where Cu NC acts as an electron acceptor. PET has been confirmed by steady state and time resolved fluorescence spectroscopy as well as by ultrafast femtosecond upconversion and transient absorption spectro- scopy.
机译:最近,铜纳米簇(CU NC)已成为有前途的候选人,作为其在光电子,感应,催化和生物成像中的潜在应用,成为有趣的纳米材料。本文中,我们在1:1水中合成了L-半胱氨酸保护的Cu NC:乙腈(ACN)溶剂具有亮氰发射(λem= 495 nm),量子为10.4%。此外,IR(III)和RH(III)的环数复合物是光收割者,它们用于光诱导的电子以及能量转移和光催化。本文已经采用了三种此类RH和IR的环化复合物,它们与1:1水中的Cu NC相互作用:ACN培养基:ACN培养基,从Cu NC急剧解散了荧光。这种淬火可以适当地归因于光诱导的电子转移(PET),其中Cu NC充当电子受体。 PET已通过稳态和时间分辨的荧光光谱以及超快飞秒上转换和瞬时吸收光谱证实。

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