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Relationships between Exciton Dissociation and Slow Recombination within ZnSe/CdS and CdSe/CdS Dot-in-Rod Heterostructures

机译:ZnSe / Cds和Cdse / Cds点滴落型异质结构中激子解离和缓慢重组之间的关系

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Type-II and,, quasi type-II heterostructure nanocrystals ate known- to, exhibit extended excited-state lifetimes compared to their single material counterparts because of reduced wave function overlap between the electron and hole. However, due to fast and efficient hole trapping and nonuniform morphologies, the photophysics of dot-in-rod heterostructures are more rich and complex than this simple picture. Using transient absorption spectroscopy, we observe that the behavior of electrons in the CdS "rod" or "bulb" regions of nonuniform ZnSe/CdS and CdSe/CdS dot-in-rods is Similar regardless of the "dot" material,-which supports previous work demonstrating that hole trapping and particle morphology drive electron dynamics. Furthermore, we show that the longest lived 'state in these dot-in rods. IS. not generated by the type-II or quasi type-II band alignment between the dot and the rod, but rather by electron hole dissociation that occurs due to fast hole trapping in the CdS rod and electron localization to the bulb. We propose that specific variations in partide morphology and surface chemistry determine the mechanism and efficiency of charge separation and recombination in these nanostructures, and therefore impact their excited-state dynamics to a greater extent than the heterostructure energy level alignment alone.
机译:型号II和,准型-I型异质结构纳米晶体,其已知 - 与它们的单个材料对应物相比,表现出延长的激发状态寿命,因为在电子和孔之间重叠的波函数重叠。然而,由于快速高效的孔捕获和不均匀的形态,点杆状异性结构的光药更丰富和复杂,而不是这种简单的图片。使用瞬态吸收光谱,我们观察到,无论“点”材料,CDS“杆”或“CDS / CDS点杆的CDS”杆“或”灯泡“区域中的电子的行为是相似的 - 无论是”点“材料 - 以前的工作证明了孔捕获和粒子形态驱动电子动力学。此外,我们表明这些点在杆中最长的居住状态。是。不是由点和杆之间的II型或准型 - II带对准而产生,而是通过电子孔解离,其由于CDS棒中的快速捕获和灯泡的电子定位而发生。我们提出伴随形态和表面化学的特定变化决定了这些纳米结构中的电荷分离和重组的机制和效率,因此在更大程度上仅仅将它们的激发状态动力学造成单独的异质能量水平对准。

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