Mapping Excited-State Dynamics by Coherent Control of a Dendrimer's Photoemission Efficiency

• Published in: Science (American Association for the Advancement of Science) Vol. 326; no. 5950; pp. 263 - 267
• Main Authors: Kuroda, Daniel G, Singh, C.P, Peng, Zhonghua, Kleiman, Valeria D
• Format: Journal Article
• Language: English
• Published: Washington, DC American Association for the Advancement of Science 09.10.2009; The American Association for the Advancement of Science
• Subjects: Chemical engineering; Chemistry; Dendrimers; Electric fields; Electric pulses; Emissions; Energy transfer; Exact sciences and technology; Fundamental areas of phenomenology (including applications); General and physical chemistry; Lasers; Macromolecules; Mapping; Molecules; Nonlinear optics; Optics; Photochemistry; Photons; Physical chemistry of induced reactions (with radiations, particles and ultrasonics); Physics; Q1; Quantum mechanics; Quantum theory; Step functions; Theory of reactions, general kinetics; Theory of reactions, general kinetics. Catalysis. Nomenclature, chemical documentation, computer chemistry; Ultrafast processes; optical pulse generation and pulse compression; Pulse shaping; Photoemission; Quantum optics; Photoinduced effect; Radiation matter interactions; Laser beam applications; Excited states; Optical pulse; Quantum interference phenomena; Donor acceptor interaction; Dendritic structure
• ISSN: 0036-8075; 1095-9203
• DOI: 10.1126/science.1176524

Adaptive laser pulse shaping has enabled impressive control over photophysical processes in complex molecules. However, the optimal pulse shape that emerges rarely offers straightforward insight into the excited-state properties being manipulated. We have shown that the emission quantum yield of a donor-acceptor macromolecule (a phenylene ethynylene dendrimer tethered to perylene) can be enhanced by 15% through iterative phase modulation of the excitation pulse. Furthermore, by analyzing the pulse optimization process and optimal pulse features, we successfully isolated the dominant elements underlying the control mechanism. We demonstrated that a step function in the spectral phase directs the postexcitation dynamics of the donor moiety, thus characterizing the coherent nature of the donor excited state. An accompanying pump-probe experiment implicates a 2+1 photon control pathway, in which the optimal pulse promotes a delayed excitation to a second excited state through favorable quantum interference.