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

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

Research output: Contribution to journalArticlepeer-review

73 Scopus citations

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.
Original languageEnglish (US)
Pages (from-to)2126-2132
Number of pages7
JournalNano Letters
Volume11
Issue number5
DOIs
StatePublished - May 11 2011
Externally publishedYes

Fingerprint

Dive into the research topics of 'Control of Electron Transfer from Lead-Salt Nanocrystals to TiO 2'. Together they form a unique fingerprint.

Cite this