Spin and Phonon Design in Modular Arrays of Molecular Qubits
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Photon upconversion, particularly via triplet-triplet annihilation (TTA), could prove beneficial in expanding the efficiencies and overall impacts of optoelectronic devices across a multitude of technologies. The recent development of bulk metal halide perovskites as triplet sensitizers is one potential step toward the industrialization of upconversion-enabled devices. In this work, we investigate the impact of varying additions of bromide into a lead iodide perovskite thin film on the TTA upconversion process in the annihilator molecule rubrene. We find an interplay between the bromide content and the overall device efficiency. In particular, a higher bromide content results in higher internal upconversion efficiencies, enabled by more efficient charge extraction at the interface, likely due to a more favorable band alignment. However, the external upconversion efficiency decreases, as the absorption cross section in the near infrared is reduced. The highest upconversion performance is found in our study for a bromide content of 5%. This result can be traced back to a high absorption cross section in the near infrared and higher photoluminescence quantum yield in comparison to the iodide-only perovskite, as well as an increased driving force for charge transfer.
A van der Waals coupled Weyl semimetal NbIrTe 4 is investigated by combining scanning tunneling microscopy/spectroscopy and first-principles calculations. Here we observe a sharp peak in the tunneling conductance near the Fermi energy (E F ). Comparison with calculations indicates that the peak originates from a van Hove singularity (vHs) associated with a Lifshitz transition of the surface Fermi-arc state. Interestingly, our tunneling spectroscopy also shows signatures of strong electron-boson coupling. This is potentially due to an anomalously enhanced charge susceptibility coming from the near-E F vHs formation.
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Single Crystal ARCS data of TiO2 at several temperatures
Logarithmic decrements of quartz crystal driven in torsional vibration mode at resonant frequency determined as function of temperature in liquid helium
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Abstract Erstmalig wurde Synchrotron‐basierte nukleare inelastische Streuung (NIS) unter Nutzung des Mößbauer‐Isotops 161 Dy für die Untersuchung der vibronischen Eigenschaften eines Dy III ‐basierten Einzelmolekülmagneten, [Dy(Cy 3 PO) 2 (H 2 O) 5 ]Br 3 ⋅2 (Cy 3 PO)⋅2 H 2 O⋅2 EtOH, eingesetzt. Die experimentelle partielle Phononen‐Zustandsdichte, die alle Schwingungen mit einer Auslenkung des Dy III ‐Ions enthält, wurde mit Hilfe von auf Dichtefunktionaltheorie (DFT) basierenden Simulationen reproduziert, was die Zuordnung aller intramolekularen Schwingungsmoden des Moleküls ermöglicht. Diese Studie zeigt, dass 161 Dy‐NIS als eine experimentelle Methode ein hohes Potential besitzt, um zur Klärung der Rolle von Phononen in Einzelmolekülmagneten beizutragen.