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首页> 外文期刊>Chemphyschem: A European journal of chemical physics and physical chemistry >Ultrafast Dynamics of Photogenerated Electrons in CdS Nanocluster Multilayers Assembled on Solid Substrates:Effects of Assembly and Electrode Potential
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Ultrafast Dynamics of Photogenerated Electrons in CdS Nanocluster Multilayers Assembled on Solid Substrates:Effects of Assembly and Electrode Potential

机译:在固体基材上组装CDS纳米光幕多层的光发化电子的超快动力学:组装和电极电位的影响

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摘要

The ultrafast dynamics of photogenerated electrons in multilayer assemblies of CdS nanoparticles prepared on quartz and indium-tin oxide (ITO) substrates were followed by femtosecond (fs) visible-pump/mid-IR probe spectroscopy. Based on the observation of the photoinduced transient absorption spectra in the broad mid-IR range at the multilayer assembly of CdS nanoparticles, the occupation and fast relaxation of higher electronic states (1P_e) were clarified. As compared with the electron dynamics of isolated (dispersed in solution) nanoparticles, the decay of photoexcited electrons in the multilayer assembly was clearly accelerated probably due to both electron hopping and scattering during interparticle electron tunneling. By using an ITO electrode as a substrate, the effect of the electric field on the photoelectron dynamics in the multilayer assembly was also investigated in situ. Both the amplitude and lifetime of photoexcited electrons gradually reduced as the potential became more positive. This result was explained by considering the reduction of the interparticle tunneling probability and the increase in the electron-transfer rate from the CdS nanoparticle assembly to the ITO electrode.
机译:在石英和氧化铟锡(ITO)衬底上制备的CDS纳米粒子的多层组件中的光静脉电子的超快动力学次次是Femtosecond(FS)可见泵/中红外探针光谱。基于在CDS纳米颗粒的多层组装的宽半IR范围内观察光致瞬态吸收光谱,阐明了更高电子状态(1P_E)的占用和快速松弛。与隔离(分散在溶液中的溶液中的电子动力学相比,多层组件中的光屏蔽电子的衰减可能由于电子跳跃和在颗粒电子隧道中的电子跳跃和散射而显然加速。通过使用ITO电极作为基板,还研究了多层组件中的光电子动力学对光电子动力学的影响。当电位变得更积极时,光屏蔽电子的幅度和寿命均逐渐减小。通过考虑将颗粒隧穿概率和从CDS纳米颗粒组件的电转移速率的增加来解释该结果是通过从CDS纳米颗粒组件到ITO电极的替换。

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