Publications by authors named "John Tritsch"

The efficiency of a conventional solar cell may be enhanced if one incorporates a molecular material capable of singlet fission, that is, the production of two triplet excitons from the absorption of a single photon. To implement this, we need to successfully harvest the two triplets from the singlet fission material. Here we show in the tetracene (Tc)/copper phthalocyanine (CuPc) model system that triplets produced from singlet fission in the former can transfer to the later on the timescale of 45±5 ps.

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The absorption of one photon by a semiconductor material usually creates one electron-hole pair. However, this general rule breaks down in a few organic semiconductors, such as pentacene and tetracene, where one photon absorption may result in two electron-hole pairs. This process, where a singlet exciton transforms to two triplet excitons, can have quantum yields as high as 200%.

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Article Synopsis
  • Photocurrent in organic photovoltaics (OPVs) is generated when excitons dissociate into free electrons and holes, but strong Coulomb interactions in organic materials complicate this process.
  • Recent findings suggest that hot charge-transfer (CT) excitons play a crucial role in overcoming these interactions.
  • Using advanced optical techniques and simulations, researchers observed that hot CT excitons form almost instantaneously and then cool down, which impacts the efficiency of charge separation and photocurrent generation.
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Singlet fission, the creation of two triplet excitons from one singlet exciton, is being explored to increase the efficiency of solar cells and photo detectors based on organic semiconductors, such as pentacene and tetracene. A key question is how to extract multiple electron-hole pairs from multiple excitons. Recent experiments in our laboratory on the pentacene/C(60) system (Chan, W.

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Article Synopsis
  • The study investigates how the interface dipole influences electronic energy alignment in donor/acceptor interfaces crucial for organic photovoltaics.
  • Combining density functional theory (DFT) with ultraviolet photoemission spectroscopy (UPS) and time-of-flight secondary ion mass spectrometry (TOF-SIMS), researchers found a significant interface dipole in the face-on orientation that aligns with UPS measurements, while ruling out charge transfer as the cause.
  • The research also reveals that the interfacial structure of the CuPc/C60 bilayer exhibits molecular intermixing, highlighting how the interfacial morphology can impact the characteristics of the interface dipole.
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Surface states play essential roles in condensed matter physics, e.g., as model two-dimensional (2D) electron gases and as the basis for topological insulators.

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Methanobactin (mb) is a novel chromopeptide that appears to function as the extracellular component of a copper acquisition system in methanotrophic bacteria. To examine this potential physiological role, and to distinguish it from iron binding siderophores, the spectral (UV-visible absorption, circular dichroism, fluorescence, and X-ray photoelectron) and thermodynamic properties of metal binding by mb were examined. In the absence of Cu(II) or Cu(I), mb will bind Ag(I), Au(III), Co(II), Cd(II), Fe(III), Hg(II), Mn(II), Ni(II), Pb(II), U(VI), or Zn(II), but not Ba(II), Ca(II), La(II), Mg(II), and Sr(II).

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