journal article·2016-07-08Open access

Electron Transfer from Single Semiconductor Nanocrystals to Individual Acceptor Molecules

Haixu Leng, James Loy, Victor Amin, Emily A. Weiss, Matthew Pelton

ACS Energy Letters· Volume 1· Issue 1

Abstract

This Letter reports the measurement of photoinduced electron-transfer rates from individual CdSe/CdS nanocrystals, or quantum dots (QDs), to methyl viologen acceptor molecules adsorbed on the QD surfaces, using time-resolved photoluminescence at the single-nanocrystal level. For each QD measured, the electron-transfer rate is constant over time, and the photoluminescence blinking dynamics are independent of the measured transfer rate. The total electron-transfer rate is distributed in discrete, constant increments, corresponding to discrete numbers of adsorbed molecules on each QD. The results thus validate previous assumptions that viologen molecules adsorb independently on QD surfaces and that the total electron-transfer rate from a single QD to multiple molecules on its surface is simply the sum of the transfer rates to the individual molecules. The measurement provides an optical method to count the number of active acceptor molecules bound to a single nanocrystal and opens up new possibilities for mechanistic studies of charge transfer at the nanoscale.
Source: openalex_inverted_index · Quality: baseline

Research context

OpenAlex topics: Quantum Dots Synthesis And Properties · Molecular Junctions and Nanostructures · Chalcogenide Semiconductor Thin Films

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

Affiliations

Department of Physics, University of Maryland, Baltimore County, 1000 Hilltop Circle, Baltimore, Maryland 21250, United States

Department of Chemistry, Northwestern University, 145 Sheridan Road, Evanston, Illinois 60208, United States

Center for Nanoscale Materials, Argonne National Laboratory, 9700 South Cass Avenue, Argonne, Illinois 60639, United States

Funding

National Institute of Standards and Technology · W.M. Keck Foundation · Office of Science · National Science Foundation · Institute for Sustainability and Energy at Northwestern

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