Journal Article FZJ-2026-04258

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Observing the Spatial and Temporal Evolution of Exciton Wave Functions in Organic Semiconductors

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2026
APS College Park, Md.

Physical review / X 16(3), 031054 () [10.1103/3zmg-276c]

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Abstract: Excitons, the correlated electron-hole pairs governing optical and transport properties in organic semiconductors, have long resisted direct experimental access to their full quantum-mechanical wave functions. Here, we use femtosecond time-resolved photoemission orbital tomography (trPOT) combining high-harmonic probe pulses with time- and momentum-resolved photoelectron spectroscopy to directly image the momentum-space distribution and ultrafast dynamics of excitons in 𝛼-sexithiophene thin films. We introduce a model that enables reconstruction of the exciton wave function in real space, including both its spatial extent and its internal phase structure. The reconstructed wave function reveals coherent delocalization across approximately three molecular units and exhibits a characteristic phase modulation, consistent with ab initio calculations within the framework of many-body perturbation theory. Time-resolved measurements further indicate an approximately 25% contraction of the exciton radius within 400 fs, suggesting self-trapping driven by exciton-phonon coupling. These results establish trPOT as a general and experimentally accessible approach for resolving exciton wave functions—with spatial, phase, and temporal sensitivity—in a broad class of molecular and low-dimensional materials.

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Contributing Institute(s):
  1. Quantum Nanoscience (PGI-3)
Research Program(s):
  1. 5213 - Quantum Nanoscience (POF4-521) (POF4-521)
  2. Orbital Cinema - Photoemission Orbital Cinematography: An ultrafast wave function lab (101071259) (101071259)

Appears in the scientific report 2026
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 Datensatz erzeugt am 2026-08-31, letzte Änderung am 2026-08-31


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