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首页> 外文期刊>The journal of physical chemistry, C. Nanomaterials and interfaces >Modulation of Semiconducting Behavior and a Change in Morphology upon Gelation of a Peptide Appended Naphthalenediimide
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Modulation of Semiconducting Behavior and a Change in Morphology upon Gelation of a Peptide Appended Naphthalenediimide

机译:半导体行为的调节及肽凝胶化凝胶化萘二亚胺的凝胶化变化

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摘要

A dipeptide-appended naphthalenediimide (NDI) is self-assembled in an aqueous phosphate buffer medium of pH 7.5 to form nanovesicular structures. Interestingly, these molecules are assembled to form hydrogels in the presence of glucono-delta-lactone (at pH 4.7) or Ru3+ solution (at pH 4.6). The gel formation is associated with a sharp morphological change from nanospheres to a nano fibrous network structure, and this nanofibrous network is responsible to trapping of many solvent molecules to form hydrogels. These gels and aggregates are well characterized by different spectroscopic and microscopic tools including UV-vis absorption and fluorescence spectroscopy, Fourier transformed infrared spectroscopy (FTIR), X-ray powder diffraction (XRPD), rheological studies, and high resolution transmission electron microscopic (HR-TEM) studies. The peptide-appended NDI was found to form J-aggregate as is evident from the UV-vis absorption studies of the aggregated species. Upon excitation at 384 nm wavelength, the glucono-delta-lactone-based hydrogel shows a greenish blue fluorescence, and similar fluorescence is observed for the aggregates of NDI-appended peptide in aqueous buffer medium at pH 7.5. The soluble aggregates and both gels (obtained from the treatment of glucono-delta-lactone and Ru3+) show wonderful current conduction and photoswitching properties. The photoconductivity and the gain in photocurrent values are enhanced in the GDL and Ru3+ mediated gels by several orders. This indicates that the morphological change from nanovesicles to ordered network of fibers has an important role in the enhancement of photocurrent gain in photoswitching experiments.
机译:将含二肽附加的萘二酰亚胺(NDI)在pH7.5的磷酸水溶液缓冲介质中自组装,以形成纳米窝结构。有趣的是,这些分子组装成在葡萄糖醇 - δ-内酯(在pH4.7)或Ru3 +溶液(在pH4.6时)形成水凝胶。凝胶形成与从纳米球到纳米纤维网络结构的尖锐形态变化相关,并且该纳米纤维网络负责捕获许多溶剂分子以形成水凝胶。这些凝胶和聚集体具有很好的特征,其具有不同的光谱和微观工具,包括UV-Vis吸收和荧光光谱,傅里叶变换的红外光谱(FTIR),X射线粉末衍射(XRPD),流变研究和高分辨率透射电子显微镜(HR -tem)研究。发现肽附加的NDI在聚集物种的UV-Vis吸收研究中明显形成J-骨料。在激发2004nm波长时,葡聚糖醇 - 内酯基水凝胶显示出绿色的蓝色荧光,并且在pH7.5的水性缓冲培养基中的NDI附加肽的聚集体观察到类似的荧光。可溶性聚集体和两个凝胶(从Glucono-delta-内酯和Ru3 +的处理中获得)显示出精彩的电流传导和光学性能。通过几个顺序在Gd1和Ru3 +介导的凝胶中增强光电导性和光电流的增益。这表明从纳米寡粒碱到有序纤维网络的形态变化在光电流在光电实验中的光电流增益中具有重要作用。

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