Imaging the photophysics of organic semiconductors using polarisation-resolved and near-field optical spectroscopies

James Kerfoot; Tyler James; Takashi Taniguchi; Kenji Watanabe; Peter H. Beton; Graham A. Rance; Michael W. George

doi:10.1016/j.optcom.2025.131945

論文 Imaging the photophysics of organic semiconductors using polarisation-resolved and near-field optical spectroscopies

James Kerfoot ; Tyler James ; Takashi Taniguchi (National Institute for Materials Science) ; Kenji Watanabe (National Institute for Materials Science) ; Peter H. Beton ; Graham A. Rance ; Michael W. George

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James Kerfoot, Tyler James, Takashi Taniguchi, Kenji Watanabe, Peter H. Beton, Graham A. Rance, Michael W. George. Imaging the photophysics of organic semiconductors using polarisation-resolved and near-field optical spectroscopies. Optics Communications. 2025, 588 (), 131945. https://doi.org/10.1016/j.optcom.2025.131945

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(abstract)

Imaging techniques that enable the structure of organic semiconductors to be determined across length scales are essential for optimisation of their luminescence properties. In this study, we prepare well-ordered monolayer films of perylene-3,4,9,10-tetracarboxylic-3,4,9,10-diimide (PTCDI) both on the surface of hexagonal boron nitride (hBN) and confined within few-layer thick hBN vertical heterostructures, and apply polarisation-resolved and tip-enhanced optical spectroscopies to image the effects of molecular orientation and dielectric environment on the photoluminescence (PL) exhibited by this prototype organic semiconductor translated at the micro and nano length scales, respectively. Using this combined approach, we show that PTCDI self-assembles into two discrete types of few-micron-sized grains at sub-monolayer coverage, each exhibiting characteristic shifts in PL emission energy related to their registry on hBN surfaces. Through examination of the near-field PL spectra extracted from images of individual grains, we further reveal the existence of nanoscale inhomogeneities within the molecular layer which influence both the energy of PL emission and ratio of vibronic sidebands and provide compelling evidence that variations in the degree of resonant coupling are present on length scales comparable to the resolution of the near-field measurement. Together these imaging tools enable a more comprehensive understanding of the molecular-level photophysics of organic semiconductor aggregates to be established, all under ambient conditions, critical for their development and integration into next-generation technologies, including light-emitting diodes, solar cells and sensors.

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