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首页> 外文期刊>Nanoscale >Fluorescence enhancement of fungicide thiabendazole by van der Waals interaction with transition metal dichalcogenide nanosheets for highly specific sensors
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Fluorescence enhancement of fungicide thiabendazole by van der Waals interaction with transition metal dichalcogenide nanosheets for highly specific sensors

机译:荧光增强的杀菌剂噻苯咪唑通过范德华相互作用过渡金属dichalcogenide nanosheets非常具体的传感器

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摘要

Many molecules quench their fluorescence upon adsorption on surfaces. Herein we show that the interaction of thiabendazole, a widespread used fungicide of the benzimidazole family, with nanosheets of transition metal dichalcogenides, particularly of WS2, leads to a significant increase, more than a factor of 5, of the fluorescence yield. This surprising effect is rationalized by DFT calculations and found to be related to the inhibition of the intramolecular rotation between the benzimidazole and thiazole groups due to a bonding rigidization upon interaction with the MoS2 surface. This non-covalent adsorption leads to a redistribution of the molecular LUMO that blocks the non-radiative energy dissipation channel. This unusual behaviour does not operate either for other molecules of the same benzimidazole family or for other 2D materials (graphene or graphene oxide). Moreover, we found that a linear dependence of the emission with the concentration of thiabendazole in solution, which combined with the specificity of the process, allows the development of a highly sensitive and selective method towards thiabendazole determination that can be applied to real river water samples. An excellent detection limit of 2.7 nM, comparable to the best performing reported methods, is obtained with very good accuracy (E-r <= 6.1%) and reproducibility (RSD <= 4.1%) in the concentration range assayed.
机译:许多分子熄灭他们的荧光吸附在表面上。噻苯咪唑的交互,广泛使用杀菌剂苯并咪唑的家庭过渡金属dichalcogenides nanosheets,尤其是二硫化钨,导致一个重要的增加,超过5倍的荧光产额。合理化的DFT计算和发现分子内的抑制有关苯并咪唑、噻唑之间的旋转组织由于粘结rigidization与二硫化钼表面的交互。非共价吸附导致重新分配分子LUMO的街区无辐射能量耗散通道。不寻常的行为也不操作其他分子相同的苯并咪唑的家庭或其他二维材料(石墨烯和石墨烯氧化)。依赖的排放浓度噻苯咪唑的解决方案,结合过程的特异性,允许开发的高度敏感和选择性方法对噻苯咪唑的决心可以应用到真正的河水样品。优秀的检测极限为2.7纳米,具有可比性表现最好的报道方法,获得非常精确(e - r < = 6.1%)和再现性(RSD < = 4.1%)浓度范围化验。

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