Dual-time scale photoinduced electron transfer from PbS quantum dots to a molecular acceptor

Kathryn E. Knowles, Michał Malicki, Emily A Weiss

Research output: Contribution to journalArticle

66 Citations (Scopus)

Abstract

A combination of picosecond and microsecond transient absorption dynamics reveals the involvement of two mechanisms by which 1,4-benzoquinone (BQ) induces the decay of the excited state of PbS quantum dots (QDs): (i) electron transfer to BQ molecules adsorbed to the surfaces of PbS QDs and (ii) collisionally gated electron transfer to freely diffusing BQ. Together, these two mechanisms quantitatively describe the quenching of photoluminescence upon addition of BQ to PbS QDs in dichloromethane solution. This work represents the first quantitative study of a QD-ligand system that undergoes both adsorbed and collisionally gated photoinduced charge transfer within the same sample. The availability of a collisionally gated pathway improves the yield of electron transfer from PbS QDs to BQ by an average factor of 2.5 over that for static electron transfer alone.

Original languageEnglish
Pages (from-to)12470-12473
Number of pages4
JournalJournal of the American Chemical Society
Volume134
Issue number30
DOIs
Publication statusPublished - Aug 1 2012

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Quantum Dots
Semiconductor quantum dots
Electrons
Methylene Chloride
Dichloromethane
Excited states
Charge transfer
Quenching
Photoluminescence
Ligands
benzoquinone
Availability
Molecules

ASJC Scopus subject areas

  • Chemistry(all)
  • Catalysis
  • Biochemistry
  • Colloid and Surface Chemistry

Cite this

Dual-time scale photoinduced electron transfer from PbS quantum dots to a molecular acceptor. / Knowles, Kathryn E.; Malicki, Michał; Weiss, Emily A.

In: Journal of the American Chemical Society, Vol. 134, No. 30, 01.08.2012, p. 12470-12473.

Research output: Contribution to journalArticle

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