Abstract

Electronic wave functions of planar molecules can be reconstructed via inverse Fourier transform of angle-resolved photoelectron spectroscopy (ARPES) data, provided the phase of the electron wave in the detector plane is known. Since the recorded intensity is proportional to the absolute square of the Fourier transform of the initial state wave function, information about the phase distribution is lost in the measurement. It was shown that the phase can be retrieved in some cases by iterative algorithms using a priori information about the object such as its size and symmetry. We suggest a more generalized and robust approach for the reconstruction of molecular orbitals based on state-of-the-art phase-retrieval algorithms currently used in coherent diffraction imaging (CDI). We draw an analogy between the phase problem in molecular orbital imaging by ARPES and of that in optical CDI by performing an optical analogue experiment on micrometer-sized structures. We successfully reconstruct amplitude and phase of both the micrometer-sized objects and a molecular orbital from the optical and photoelectron far-field intensity distributions, respectively, without any prior information about the shape of the objects.

Highlights

  • Organic semiconductors play a key role in modern devices such as organic light-emitting diodes and photovoltaic cells [1, 2]

  • Detailed information about the electronic structure of molecular systems can be inferred from angle-resolved photoelectron spectroscopy (ARPES) of well-ordered molecular layers on single-crystalline substrates [7,8,9,10,11,12]

  • We suggest that the phase problem in ARPES-based molecular orbital imaging can be solved in a more robust manner by utilizing the analogy to the phase problem in coherent diffraction imaging (CDI) [15]

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Summary

Introduction

Organic semiconductors play a key role in modern devices such as organic light-emitting diodes and photovoltaic cells [1, 2]. Tailoring the physical properties of molecular optoelectronic devices [4,5,6] crucially depends on a deep understanding of the charge transfer mechanisms at metal-organic interfaces. The time-resolved spatial visualization of such processes would be highly desirable. The frontier orbitals, i.e. the highest occupied and lowest unoccupied molecular orbitals (HOMO and LUMO), largely determine the chemical reactivity and electronic properties of molecular systems. Detailed information about the electronic structure of molecular systems can be inferred from angle-resolved photoelectron spectroscopy (ARPES) of well-ordered molecular layers on single-crystalline substrates [7,8,9,10,11,12]

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