首页> 外文期刊>Langmuir: The ACS Journal of Surfaces and Colloids >Photosensitization Dynamics of Stable Copper Nanoclusters inside the Aqueous Core of Reverse Micelles with Different Pool Sizes
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Photosensitization Dynamics of Stable Copper Nanoclusters inside the Aqueous Core of Reverse Micelles with Different Pool Sizes

机译:不同泳池尺寸的反向胶束水芯内稳定铜纳米能器的光敏动力学

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摘要

The perennial problem of instability of fluorescent copper nanoclusters (Cu NCs), stemming principally from aerial oxidation, has prevented their vivid usage in energy harvesting compared to the other metal NCs. However, replacement of the much expensive metal NCs with the cheaper Cu NCs is desirable if the functions are met with. Although thiolate protection of Cu NCs could bring some stability to them, appreciably decentlystable Cu NCs were produced inside the aqueous core of reverse micelles (RMs). However, this recent development has not been further explored on the photosensitization of the Cu NCs inside the RMs and their controlled modulation as energy antenna. Here we have synthesized stable Cu NCs inside the aqueous core of RMs with three different pool sizes and established photoinduced electron transfer (PET) to an electron acceptor. Considering the bulk quencher concentration, it appears that the extent of PET increases with decrease in the size of the aqueous core of RMs. However, calculating the effective concentration of the electron acceptor inside the RMs and considering the polarity of the microheterogeneous systems, it becomes clear that the extent of PET actually decreases with decrease in the size of the aqueous pool (w(0), i.e., [H2O]/[AOT]) = 5-20) in the RMs. This proof of concept and the results are promising toward applications in PET-driven phenomena such as solar cells or batteries.
机译:与其他金属纳米团簇相比,主要源于空气氧化的荧光铜纳米团簇(Cu-NCs)长期存在的不稳定性问题阻碍了它们在能量收集中的生动应用。然而,如果功能得到满足,则需要用更便宜的铜NCs替换昂贵的金属NCs。虽然硫氰酸盐对铜纳米颗粒的保护可以给它们带来一定的稳定性,但在反胶束(RMs)的水核内产生了明显的可分散的铜纳米颗粒。然而,这一最新进展尚未在RMs内铜纳米晶的光敏化及其作为能量天线的受控调制方面得到进一步探索。在这里,我们在RMs的水核内合成了具有三种不同池大小的稳定Cu NCs,并建立了光诱导电子转移(PET)到电子受体的模型。考虑到整体淬火剂浓度,PET的范围似乎随着RMs水核尺寸的减小而增大。然而,通过计算RMs内电子受体的有效浓度,并考虑到微非均相系统的极性,可以清楚地看出,PET的范围实际上随着RMs中的水池(w(0),即[H2O]/[AOT]=5-20)尺寸的减小而减小。这一概念证明和结果有望应用于太阳能电池或电池等PET驱动现象。

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