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首页> 外文期刊>ACS nano >Linker-induced anomalous emission of organic-molecule conjugated metal-oxide nanoparticles
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Linker-induced anomalous emission of organic-molecule conjugated metal-oxide nanoparticles

机译:接头引起的有机分子共轭金属氧化物纳米粒子的异常发射

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Semiconductor nanoparticles conjugated with organic- and dye-molecules to yield high efficiency visible photoluminescence (PL) hold great potential for many future technological applications. We show that folic acid (FA)-conjugated to nanosize TiO _2 and CeO _2 particles demonstrates a dramatic increase of photoemission intensity at wavelengths between 500 and 700 nm when derivatized using aminopropyl trimethoxysilane (APTMS) as spacer-linker molecules between the metal oxide and FA. Using density-functional theory (DFT) and time-dependent DFT calculations we demonstrate that the strong increase of the PL can be explained by electronic transitions between the titania surface oxygen vacancy (OV) states and the low-energy excited states of the FA/APTMS molecule anchored onto the surface oxygen bridge sites in close proximity to the OVs. We suggest this scenario to be a universal feature for a wide class of metal oxide nanoparticles, including nanoceria, possessing a similar band gap (~3 eV) and with a large surface-vacancy-related density of electronic states. We demonstrate that the molecule-nanoparticle linker can play a crucial role in tuning the electronic and optical properties of nanosystems by bringing optically active parts of the molecule and of the surface close to each other.
机译:与有机分子和染料分子共轭以产生高效可见光致发光(PL)的半导体纳米颗粒在许多未来技术应用中具有巨大潜力。我们表明,当使用氨基丙基三甲氧基硅烷(APTMS)作为金属氧化物与金属之间的间隔基连接分子进行衍生化时,与纳米级TiO _2和CeO _2颗粒共轭的叶酸(FA)在500至700 nm的波长处显示出光发射强度的急剧增加。 F A。使用密度泛函理论(DFT)和随时间变化的DFT计算,我们证明了PL的强烈增加可以通过二氧化钛表面氧空位(OV)状态与FA /的低能激发态之间的电子跃迁来解释APTMS分子锚定在与OV紧密相邻的表面氧桥位点上。我们建议这种情况对于包括纳米氧化铈在内的各种金属氧化物纳米粒子具有普遍的特征,这些纳米粒子具有类似的带隙(〜3 eV)并且具有大的与空位相关的电子态密度。我们证明了分子-纳米粒子连接体可以通过使分子和表面的光学活性部分彼此靠近来在调节纳米系统的电子和光学性质中发挥关键作用。

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