Control of Electron Transfer from Lead-Salt Nanocrystals to TiO 2

Type
Article

Authors
Hyun, Byung-Ryool
Bartnik, A. C.
Sun, Liangfeng
Hanrath, Tobias
Wise, F. W.

KAUST Grant Number
KUS-C1-018-02

Date
2011-05-11

Abstract
The roles of solvent reorganization energy and electronic coupling strength on the transfer of photoexcited electrons from PbS nanocrystals to TiO 2 nanoparticles are investigated. We find that the electron transfer depends only weakly on the solvent, in contrast to the strong dependence in the nanocrystal-molecule system. This is ascribed to the larger size of the acceptor in this system, and is accounted for by Marcus theory. The electronic coupling of the PbS and TiO 2 is varied by changing the length, aliphatic and aromatic structure, and anchor groups of the linker molecules. Shorter linker molecules consistently lead to faster electron transfer. Surprisingly, linker molecules of the same length but distinct chemical structures yield similar electron transfer rates. In contrast, the electron transfer rate can vary dramatically with different anchor groups. © 2011 American Chemical Society.

Citation
Hyun B-R, Bartnik AC, Sun L, Hanrath T, Wise FW (2011) Control of Electron Transfer from Lead-Salt Nanocrystals to TiO 2 . Nano Lett 11: 2126–2132. Available: http://dx.doi.org/10.1021/nl200718w.

Acknowledgements
The authors thank Professor Masa-aki Haga (Chuo University, Japan) for providing MBPA. This work was supported by the Cornell Center for Materials Research (CCMR) with funding from the Materials Research Science and Engineering Center program of the National Science Foundation (cooperative agreement DMR 0520404) and in part by Award No. KUS-C1-018-02, made by King Abdullah University of Science and Technology (KAUST).

Publisher
American Chemical Society (ACS)

Journal
Nano Letters

DOI
10.1021/nl200718w

PubMed ID
21506588

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