Tiago Buckup

Highly sensitive single-beam heterodyne coherent anti-Stokes Raman scattering

Single-beam coherent anti-Stokes Raman-scattering (CARS) microspectroscopy achieves a complete CARS scheme with a femtosecond laser. Here, we introduce heterodyne detection in a simple experimental extension: the optical fields driving the CARS process and the local oscillator used for heterodyning are derived from a single beam of ultrashort laser pulses by pulse shaping. The heterodyne signal is amplified by more than 3 orders of magnitude and is linearly dependent on the concentration of Raman scatterers. This dramatically increases the sensitivity of chemically selective detection at microscopic resolution while maintaining the simplicity of the single-beam setup.

Shaper-assisted collinear SPIDER: fast and simple broadband pulse compression in nonlinear microscopy

In situ characterization and control of the phase of broadband femtosecond pulses in microscopy can be achieved with a novel simplified scheme based on spectral shear interferometry for direct electric field reconstruction (SPIDER): the use of a femtosecond pulse shaper eliminates the need for an interferometer setup, allows dispersion-free SPIDER operation and at the same time compression even of complex pulses. Beyond compression, the scheme allows precise phase control at the site of the microscopic experiment. We present the underlying principles, design considerations, and details of the experimental implementation, and show the successful operation of the shaper-assisted collinear (SAC) SPIDER to characterize, compress, and tailor broadband femtosecond pulses in situ. The reliability is demonstrated by comparison with independent cross-frequency-resolved optical gating measurement, and improved multiphoton imaging with SAC-SPIDER-compressed pulses is shown. Its simplicity and versatility make SAC-SPIDER an extremely useful tool for next-generation broadband nonlinear microscopy.

Controlling the efficiency of an artificial light-harvesting complex.

Adaptive femtosecond pulse shaping in an evolutionary learning loop is applied to a bioinspired dyad molecule that closely mimics the early-time photophysics of the light-harvesting complex 2 (LH2) photosynthetic antenna complex. Control over the branching ratio between the two competing pathways for energy flow, internal conversion (IC) and energy transfer (ET), is realized. We show that by pulse shaping it is possible to increase independently the relative yield of both channels, ET and IC. The optimization results are analyzed by using Fourier analysis, which gives direct insight to the mechanism featuring quantum interference of a low-frequency mode. The results from the closed-loop experiments are repeatable and robust and demonstrate the power of coherent control experiments as a spectroscopic tool (i.e., quantum-control spectroscopy) capable of revealing functionally relevant molecular properties that are hidden from conventional techniques.

Mapping multidimensional excited state dynamics using pump-impulsive-vibrational-spectroscopy and pump-degenerate-four-wave-mixing

Pump-impulsive vibrational spectroscopy (pump-IVS) is used to record excited state vibrational dynamics following photoexcitation of two carotenoids, β-carotene and lycopene, with <30 fs temporal resolution, and covering the full vibrational spectrum of the investigated chromophores. The results record the course of S2-S1 internal conversion, followed by vibrational relaxation and decay to the electronic ground state. This interpretation is corroborated by comparison with pump-degenerate-four-wave-mixing (pump-DFWM) experiments on the same systems. The results demonstrate the potential of both time-domain spectroscopic techniques to resolve photochemical dynamics, including fingerprint frequencies which directly reflect changes in bonding and structure in the nascent sample. The exclusive strengths and limitations of these two methods are compared with those presented by the frequency-domain Femtosecond Stimulated Raman Scattering (FSRS) technique, highlighting the complementary nature of the three, and the benefits of using them in concert to investigate vibrational dynamics in reactive species.

Chemoselective imaging of mouse brain tissue via multiplex CARS microscopy.

The fast and reliable characterization of pathological tissue is a debated topic in the application of vibrational spectroscopy in medicine. In the present work we apply multiplex coherent anti-Stokes Raman scattering (MCARS) to the investigation of fresh mouse brain tissue. The combination of imaginary part extraction followed by principal component analysis led to color contrast between grey and white matter as well as layers of granule and Purkinje cells. Additional quantitative information was obtained by using a decomposition algorithm. The results perfectly agree with HE stained references slides prepared separately making multiplex CARS an ideal approach for chemoselective imaging.

In situ broadband pulse compression for multiphoton microscopy using a shaper-assisted collinear SPIDER

The characterization and control of the phase of broadband femtosecond pulses in nonlinear microscopy are successfully demonstrated with a collinear configuration of spectral shear interferometry for direct electric field reconstruction (SPIDER). A femtosecond-pulse shaper is used as a dispersionless interferometer for the measurement of the spectral phase and to actively compress a broadband supercontinuum from a photonic crystal fiber. This allows in situ online phase management and enables the application of quantum control spectroscopy in microenvironments.

Acceleration of Singlet Fission in an Aza-Derivative of TIPS-Pentacene.

The influence of the carbon to nitrogen substitution on the photoinduced dynamics of TIPS-pentacene was investigated by ultrafast transient absorption measurements on spin-coated thin films in the visible and in the near-infrared spectral region. A global target analysis was performed to provide a detailed picture of the excited-state dynamics. We found that the chemical modification has a high impact on the triplet formation and leads to shorter dynamics; hence it speeds up the singlet fission process. A faster relaxation from the singlet into the triplet manifold implies a higher efficiency because other relaxation channels are avoided. The air-stable aza-derivatives have the potential to exceed the energy conversion efficiency of TIPS-pentacene.

Multidimensional spectroscopy of β-carotene: Vibrational cooling in the excited state

Pump-degenerate four wave mixing (Pump-DFWM) is used for investigating the vibrational dynamics in the excited state of beta-carotene in solution. In this 2D technique, an initial pump pulse promotes the system to the excited state, which is then probed by the succeeding DFWM sequence. We focus particularly on the internal conversion between the S(2) and S(1) state with high temporal and spectral resolution. The frequency shift of the excited state vibrations is measured and is explained as mode-specific vibrational cooling. Our results suggest an internal conversion in a time range between 260 and 500 fs without any intermediate states.

Direct Observation of a Dark State in Lycopene Using Pump-DFWM

We apply pump-degenerate four-wave-mixing (pump-DFWM) for the investigation of the ultrafast internal relaxation of the excited states of lycopene. A unique feature in the pump-DFWM signal, appearing at small temporal delays between the initial pump pulse and the DFWM sequence, provides direct evidence for the participation of an additional excited state located between the S(2) and S(1) states. Our experimental findings are corroborated by a detailed numerical simulation of lycopenes pump-DFWM signal using the Brownian oscillator model. A very fast dynamics directly after excitation of the S(2) state manifests as a component populated with a time constant of about 20 fs and which decays to S(1) with a lifetime of 110 fs. This ultrafast dynamics is discussed under the light of several different models suggested for the relaxation pathway of carotenoids. In this context, we show that the dynamics can be explained in terms of a dark electronic state between the S(2) and S(1) states.

Enhancement of molecular modes by electronically resonant multipulse excitation: further progress towards mode selective chemistry.

We show that molecular vibrations induced by resonant excitation pulses can be enhanced by pulse trains, compared to Fourier-limited pulses of equal pulse energy. As a proof-of-principle, a low frequency mode of Nile Blue at 600 cm(-1) is observed and amplified in a pump and probe experiment. In addition to previous experiments in our group, an increased population transfer to the excited electronic state is identified as an important element of the underlying physical mechanism. These results suggest an enhancement on the level of individual molecules rather than a macroscopic effect.