Abstract

Ultrafast, multi-dimensional spectroscopic measurements of photosynthetic light-harvesting complexes have revealed quantum coherences with timescales comparable to those of energy-transfer processes. These observations have led to a debate regarding the states that give rise to the coherences and whether the presence of the coherences has implications for photosynthetic light harvesting. In these experiments, laser pulses create a coherent superposition of quantum states with a defined phase relationship across an ensemble, which gives rise to the quantum coherence and associated quantum beating signal. Dephasing of these quantum coherences, seen as a decay of the beating signal, is among the most sensitive probes of the interactions between a system and its surrounding environment. In this Review, we discuss the proposed origin and assignment of the observed quantum coherences in photosynthetic systems as electronic, vibronic or vibrational. We describe the latest experimental efforts towards unravelling the nature of the coherences, in particular ultrafast, two-dimensional electronic spectroscopy, as well as the accompanying theoretical and computational results. We discuss how measuring coherences can inform us about the excited-state dynamics of biophysical and chemical systems relevant to natural light harvesting and how these measurements reveal electronic structure beyond that captured by simplistic models. Femtosecond spectroscopy of photosynthetic systems reveals long-lived quantum coherences. This Review focuses on efforts to understand the microscopic origins of these signals and discusses how such coherences may be exploited to probe design principles of photosynthetic light harvesting.

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