Electron Transfer from Photoexcited Naphthalene Diimide Radical Anion to Electrocatalytically Active Re(bpy)(CO)3Cl in a Molecular Triad

Jose F. Martinez, Nathan T. La Porte, Michael R. Wasielewski

Research output: Contribution to journalArticle

11 Citations (Scopus)

Abstract

Electron donor-acceptor photosensitizers having long charge separation lifetimes and high-reducing potentials that can be easily appended to thermodynamically difficult to reduce catalysts hold great promise for driving CO2 reduction. This study presents a new molecular triad utilizing a naphthalene diimide radical anion (NDI•-) donor chromophore appended to a 9,10-diphenylanthracene (DPA) acceptor, which is in turn linked to Re(bpy)(CO)3Cl. The NDI•- chromophore is readily generated by mild chemical or electrochemical reduction, absorbs at wavelengths as long as 800 nm, and has an excited state oxidation potential (-2.1 V vs SCE), which rivals or exceeds those of metalorganic and organometallic chromophores. Photoexcitation of NDI•- to∗NDI•- is followed by ultrafast reduction of DPA to DPA•-, which then rapidly reduces the metal complex. The overall quantum yield for reduction of Re(bpy)(CO)3Cl is approximately 90% using visible light. The overall time constant for the forward electron transfer to reduce the metal complex is τ = 14.5 ps, while the time constant for back-electron transfer is τ = 24.5 ns. Under typical electrocatalytic conditions, the molecular triad demonstrates electrochemical reduction of CO2.

Original languageEnglish
Pages (from-to)2608-2617
Number of pages10
JournalJournal of Physical Chemistry C
Volume122
Issue number5
DOIs
Publication statusPublished - Feb 8 2018

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ASJC Scopus subject areas

  • Electronic, Optical and Magnetic Materials
  • Energy(all)
  • Physical and Theoretical Chemistry
  • Surfaces, Coatings and Films

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