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Wavelength-controlled manipulation of colloidal quasi-resonant quantum dots under pulsed laser irradiation

机译:脉动激光照射下胶体准谐振量子点的波长控制操纵

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Production of nanostructures consisting of semiconductor nanoparticles (NPs) is of interest for number of applications. Development of new methods of NPs' manipulation and aggregation of NPs into nanostructures with pre-defined geometry is also of considerable interest from the fundamental point of view. Under laser irradiation with properly chosen wavelengths excitonic excitations of semiconductor NPs will be induced. Electrodynamical interaction between excited NPs is rather universal and allows formation of wide variety of nanostructures both of homo- and heterogeneous content. Theoretical approach for study of interaction of NPs' ensembles with laser light includes dipole-dipole approximation for NPs' attraction. Experimental results are obtained for TGA stabilized CdTe QDs with the excitonic resonance at 520 nm. Six different samples of the same colloid solution were irradiated at wavelengths from 540 to 570 nm. Modifications of absorption spectra of solutions after irradiation was detected, being most prominent at 555 and 560 nm irradiation wavelengths. Analysis of spectra shows that up to 47% of QDs were assembled into pairs with 10 nm inter-QD distance. Therefore, possibility of precise QDs manipulation via laser-induced electrodynamical interaction is demonstrated.
机译:由半导体纳米颗粒(NPS)组成的纳米结构的产生对于应用数量。新的NPS操纵方法和NPS聚集到具有预定几何形状的纳米结构的新方法也是相当大的兴趣来自根本的观点。 Under laser irradiation with properly chosen wavelengths excitonic excitations of semiconductor NPs will be induced.激发的NPS之间的电动相互作用是相当普遍的,并且允许形成各种纳米结构,两种均匀含量。 L激光研究NPS合奏相互作用的理论方法包括对NPS的吸引力的偶极偶极近似。对于TGA稳定的CDTEQDS获得实验结果,具有520nm的激发器共振。将六种不同的相同胶体溶液样品以540-570nm的波长照射。检测到照射后溶液吸收光谱的修饰,在555和560nm辐照波长下突出。光谱分析表明,高达47%的QDS组装成具有10nm QD距离的对成对。因此,证明了通过激光诱导的电动相互作用精确QDS操纵的可能性。

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