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Davydov splitting and singlet fission in excitonically coupled pentacene dimers

2019, Basel, Bettina Sabine, Hetzer, Constantin, Zirzlmeier, Johannes, Thiel, Dominik, Guldi, Rebecca, Hampel, Frank, Kahnt, Axel, Clark, Timothy, Guldi, Dirk Michael, Tykwinski, Rik R.

Singlet fission (SF) allows two charges to be generated from the absorption of a single photon and is, therefore, potentially transformative toward improving solar energy conversion. Key to the present study of SF is the design of pentacene dimers featuring a xanthene linker that strictly places two pentacene chromophores in a rigid arrangement and, in turn, enforces efficient, intramolecular π-overlap that mimics interactions typically found in condensed state (e.g., solids, films, etc.). Inter-chromophore communication ensures Davydov splitting, which plays an unprecedented role toward achieving SF in pentacene dimers. Transient absorption measurements document that intramolecular SF evolves upon excitation into the lower Davydov bands to form a correlated triplet pair at cryogenic temperature. At room temperature, the two spin-correlated triplets, one per pentacene moiety within the dimers, are electronically coupled to an excimer state. The presented results are transferable to a broad range of acene morphologies including aggregates, crystals, and films. © 2019 The Royal Society of Chemistry.

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Judging the feasibility of TiO2 as photocatalyst for chemical energy conversion by quantitative reactivity determinants

2019, Dilla, Martin, Moustakas, Nikolaos G., Becerikli, Ahmet E., Peppel, Tim, Springer, Armin, Schlögl, Robert, Strunk, Jennifer, Ristig, Simon

In this study we assess the general applicability of the widely used P25-TiO2 in gas-phase photocatalytic CO2 reduction based on experimentally determined reactivity descriptors from classical heterogeneous catalysis (productivity) and photochemistry (apparent quantum yield/AQY). A comparison of the results with reports on the use of P25 for thermodynamically more feasible reactions and our own previous studies on P25-TiO2 as photocatalyst imply that the catalytic functionality of this material, rather than its properties as photoabsorber, limits its applicability in the heterogeneous photocatalytic CO2 reduction in the gas phase. The AQY of IrOx/TiO2 in overall water splitting in a similar high-purity gas-solid process was four times as high, but still far from commercial viability.