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从胶体硫化铅量子点向二氧化钛纳米颗粒的电子注入。

Electron injection from colloidal PbS quantum dots into titanium dioxide nanoparticles.

作者信息

Hyun Byung-Ryool, Zhong Yu-Wu, Bartnik Adam C, Sun Liangfeng, Abruña Hector D, Wise Frank W, Goodreau Jason D, Matthews James R, Leslie Thomas M, Borrelli Nicholas F

机构信息

Department of Applied Physics, Cornell University, Ithaca, New York 14850, USA.

出版信息

ACS Nano. 2008 Nov 25;2(11):2206-12. doi: 10.1021/nn800336b.

Abstract

Injection of photoexcited electrons from colloidal PbS quantum dots into TiO(2) nanoparticles is investigated. The electron affinity and ionization potential of PbS quantum dots, inferred from cyclic voltammetry measurements, show strong size dependence due to quantum confinement. On the basis of the measured energy levels, photoexcited electrons should transfer efficiently from the quantum dots into TiO(2) only for quantum-dot diameter below approximately 4.3 nm. Continuous-wave fluorescence spectra and fluorescence transients of PbS quantum dots coupled to titanium dioxide nanoparticles are consistent with electron transfer for small quantum dots. The measured electron transfer time is surprisingly slow ( approximately 100 ns), and implications of this for future photovoltaics will be discussed. Initial results obtained from solar cells sensitized with PbS quantum dots are presented.

摘要

研究了从胶体硫化铅量子点向二氧化钛纳米颗粒注入光激发电子的过程。通过循环伏安法测量推断出的硫化铅量子点的电子亲和势和电离势,由于量子限制而表现出强烈的尺寸依赖性。基于测量的能级,仅当量子点直径低于约4.3纳米时,光激发电子才应有效地从量子点转移到二氧化钛中。与二氧化钛纳米颗粒耦合的硫化铅量子点的连续波荧光光谱和荧光瞬态与小量子点的电子转移一致。测量得到的电子转移时间出奇地慢(约100纳秒),并将讨论其对未来光伏的影响。还展示了用硫化铅量子点敏化的太阳能电池获得的初步结果。

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