4.8 Article

Two-Color Nonlinear Spectroscopy for the Rapid Acquisition of Coherent Dynamics

Journal

JOURNAL OF PHYSICAL CHEMISTRY LETTERS
Volume 6, Issue 13, Pages 2413-2420

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acs.jpclett.5b00861

Keywords

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Funding

  1. National Science Foundation [PHY-1305450]
  2. Office of Basic Energy Sciences, U.S. Department of Energy [DE-FG02-07ER15904]
  3. U.S. Department of Energy (DOE) [DE-FG02-07ER15904] Funding Source: U.S. Department of Energy (DOE)
  4. Direct For Mathematical & Physical Scien [1305450] Funding Source: National Science Foundation
  5. Division Of Physics [1305450] Funding Source: National Science Foundation
  6. Division Of Physics
  7. Direct For Mathematical & Physical Scien [1607570] Funding Source: National Science Foundation

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There has been considerable recent interest in the observation of coherent dynamics in photosynthetic systems by 2D electronic spectroscopy (2DES). In particular, coherences that persist during the waiting time in a 2DES experiment have been attributed to electronic, vibrational, and vibronic origins in various systems. The typical method for characterizing these coherent dynamics requires the acquisition of 2DES spectra as a function of waiting time, essentially a 3DES measurement. Such experiments require lengthy data acquisition times that degrade the signal-to-noise of the recorded coherent dynamics. We present a rapid and high signal-to-noise pulse-shaping-based approach for the characterization of coherent dynamics. Using chlorophyll a, we demonstrate that this method retains much of the information content of a 3DES measurement and provides insight into the physical origin of the coherent dynamics, distinguishing between ground and excited state coherences. It also enables high resolution determination of ground and excited state frequencies.

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