Single-shot gradient-assisted photon echo electronic spectroscopy.

Two-dimensional electronic spectroscopy (2D ES) maps the electronic structure of complex systems on a femtosecond time scale. While analogous to multidimensional NMR spectroscopy, 2D optical spectroscopy differs significantly in its implementation. Yet, 2D Fourier spectroscopies still require point-by-point sampling of the time delay between two pulses responsible for creating quantum coherence among states. Unlike NMR, achieving the requisite phase stability at optical frequencies between these pulse pairs remains experimentally challenging. Nonetheless, 2D optical spectroscopy has been successfully demonstrated by combining passive and active phase stabilization along with precise control of optical delays and long-term temperature stability, although the widespread adoption of 2D ES has been significantly hampered by these technical challenges. Here, we exploit an analogy to magnetic resonance imaging (MRI) to demonstrate a single-shot method capable of acquiring the entire 2D spectrum in a single laser shot using only conventional optics. Unlike point-by-point sampling protocols typically used to record 2D spectra, this method, which we call GRadient-Assisted Photon Echo (GRAPE) spectroscopy, largely eliminates phase errors while reducing the acquisition time by orders of magnitude. By incorporating a spatiotemporal encoding of the nonlinear polarization along the excitation frequency axis of the 2D spectrum, GRAPE spectroscopy achieves no loss in signal while simultaneously reducing overall noise. Here, we describe the principles of GRAPE spectroscopy and discuss associated experimental considerations.

[1]  Graham R. Fleming,et al.  Two-dimensional spectroscopy of electronic couplings in photosynthesis , 2005, Nature.

[2]  Emma Springate,et al.  Instantaneous mapping of coherently coupled electronic transitions and energy transfers in a photosynthetic complex using angle-resolved coherent optical wave-mixing. , 2009, Physical review letters.

[3]  Minhaeng Cho,et al.  Coherent two-dimensional optical spectroscopy. , 2008, Chemical reviews.

[4]  Rick Trebino,et al.  Spatially encoded, single-shot ultrafast spectroscopies , 1995 .

[5]  D. Jonas Optical Analogs of 2D NMR , 2003, Science.

[6]  P. Hamm,et al.  Active phase stabilization in Fourier-transform two-dimensional infrared spectroscopy. , 2005, Optics Letters.

[7]  E. Hahn Concepts of NMR in quantum optics , 1997 .

[8]  T. Mančal,et al.  Evidence for wavelike energy transfer through quantum coherence in photosynthetic systems , 2007, Nature.

[9]  D. Kane,et al.  Single-shot measurement of the intensity and phase of an arbitrary ultrashort pulse by using frequency-resolved optical gating. , 1993, Optics letters.

[10]  Jennifer P. Ogilvie,et al.  Two-dimensional spectroscopy using diffractive optics based phased-locked photon echoes , 2004 .

[11]  Graham R Fleming,et al.  Phase-stabilized two-dimensional electronic spectroscopy. , 2004, The Journal of chemical physics.

[12]  Lucio Frydman,et al.  The acquisition of multidimensional NMR spectra within a single scan , 2002, Proceedings of the National Academy of Sciences of the United States of America.

[13]  Ralph Weissleder,et al.  Emerging concepts in molecular MRI. , 2007, Current opinion in biotechnology.

[14]  K. Nelson,et al.  Irreversible Organic Crystalline Chemistry Monitored in Real Time , 2006, Science.

[15]  David M. Jonas,et al.  Two-dimensional Fourier transform electronic spectroscopy , 2001 .

[16]  Graham R. Fleming,et al.  Femtosecond solvation dynamics of water , 1994, Nature.

[17]  Peifang Tian,et al.  Femtosecond Phase-Coherent Two-Dimensional Spectroscopy , 2003, Science.

[18]  Peter Simon,et al.  Single-shot TG FROG for the characterization of ultrashort DUV pulses. , 2009, Optics express.

[19]  Igor V. Stiopkin,et al.  Tunable two-dimensional femtosecond spectroscopy. , 2004, Optics letters.

[20]  Thomas Hornung,et al.  Diffraction-based femtosecond pulse shaping with a two-dimensional spatial light modulator. , 2005, Optics letters.

[21]  S. Mukamel,et al.  Tracing exciton dynamics in molecular nanotubes with 2D electronic spectroscopy , 2009 .

[22]  C. Dorrer,et al.  Spectral resolution and sampling issues in Fourier-transform spectral interferometry , 2000 .

[23]  S. Mukamel,et al.  Excitonic couplings and interband energy transfer in a double-wall molecular aggregate imaged by coherent two-dimensional electronic spectroscopy. , 2009, The Journal of chemical physics.

[24]  M. Maroncelli,et al.  Polar Solvent Dynamics and Electron-Transfer Reactions , 1989, Science.

[25]  D. Jonas Two-dimensional femtosecond spectroscopy. , 2003, Annual review of physical chemistry.

[26]  L. Frydman,et al.  Principles and progress in ultrafast multidimensional nuclear magnetic resonance. , 2009, Annual review of physical chemistry.

[27]  P. Rentzepis,et al.  Time resolved picosecond emission spectroscopy of organic dye lasers , 1971 .

[28]  Daniel B. Turner,et al.  Two-Quantum 2D FT Electronic Spectroscopy of Biexcitons in GaAs Quantum Wells , 2009, Science.

[29]  A. Tokmakoff,et al.  Single-shot two-dimensional infrared spectroscopy. , 2007, Optics express.

[30]  R. R. Ernst,et al.  Two‐dimensional spectroscopy. Application to nuclear magnetic resonance , 1976 .

[31]  R. Turner,et al.  Echo-planar imaging: magnetic resonance imaging in a fraction of a second. , 1991, Science.