Published June 7, 2015 | Version v1
Journal article

Ultra-broadband 2D electronic spectroscopy of carotenoid-bacteriochlorophyll interactions in the LH1 complex of a purple bacterium

  • 1. Department of Chemistry, Princeton University, Washington Road, Princeton, New Jersey 08544 (United States)
  • 2. CNR-IFN, Dipartimento di Fisica, Politecnico di Milano, P.zza L. da Vinci 32, Milano 20133 (Italy)
  • 3. Glasgow Biomedical Research Centre, IBLS, University of Glasgow, 126 Place, Glasgow G12 8TA, Scotland (United Kingdom)
  • 4. CNRS, Institut de Chimie de Lyon, École Normale Supérieure de Lyon, Université de Lyon, 46 Allée d'Italie, F-69364 Lyon Cedex 07 (France)
  • 5. Dipartimento di Chimica "G. Ciamician," Università di Bologna, Via Selmi 2, IT-40126 Bologna (Italy)
  • 6. Madrid Institute for Advanced Studies, IMDEA Nanociencia, Madrid (Spain)

Description

We investigate the excitation energy transfer (EET) pathways in the photosynthetic light harvesting 1 (LH1) complex of purple bacterium Rhodospirillum rubrum with ultra-broadband two-dimensional electronic spectroscopy (2DES). We employ a 2DES apparatus in the partially collinear geometry, using a passive birefringent interferometer to generate the phase-locked pump pulse pair. This scheme easily lends itself to two-color operation, by coupling a sub-10 fs visible pulse with a sub-15-fs near-infrared pulse. This unique pulse combination allows us to simultaneously track with extremely high temporal resolution both the dynamics of the photoexcited carotenoid spirilloxanthin (Spx) in the visible range and the EET between the Spx and the B890 bacterio-chlorophyll (BChl), whose Qx and Qy transitions peak at 585 and 881 nm, respectively, in the near-infrared. Global analysis of the one-color and two-color 2DES maps unravels different relaxation mechanisms in the LH1 complex: (i) the initial events of the internal conversion process within the Spx, (ii) the parallel EET from the first bright state S2 of the Spx towards the Qx state of the B890, and (iii) the internal conversion from Qx to Qy within the B890

Additional details

Identifiers

Publishing Information

Journal Title
Journal of Chemical Physics
Journal Volume
142
Journal Issue
21
Journal Page Range
p. 212433-212433.10
ISSN
0021-9606
CODEN
JCPSA6

Optional Information

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