Publications by authors named "Tristan Dilbeck"

Correction for 'Extracting accurate information from triplet-triplet annihilation upconversion data with a mass-conserving kinetic model' by Abhishek Kalpattu , , 2022, , 28174-28190, https://doi.org/10.1039/D2CP03986A.

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Triplet-triplet annihilation upconversion (TTA-UC) is a process that shows promise for applications such as energy-harvesting and light-generation technologies. The irradiance dependent performance of TTA-UC systems is typically gauged using a graphical analysis, rather than a detailed model. Additionally, kinetic models for TTA-UC rarely incorporate mass conservation, which is a phenomenon that can have important consequences under experimentally relevant conditions.

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Natural photosynthesis uses an array of molecular structures in a multiphoton Z-scheme for the conversion of light energy into chemical bonds (i.e., solar fuels).

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The pressure behavior of crystalline CsUOCl has been explored using a diamond anvil cell. The uranyl fluorescence intensity decreases dramatically with increasing pressure. Using the O-U-O symmetric stretching frequency, an apparent linear decrease in bond length with increasing pressure was observed.

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M(TpyNO)(NO)(HO)·THF (M = La, Nd, Sm, Eu, Tb, Am; TpyNO = 4'-nitrophenyl terpyridyl) have been prepared from the reaction of M(NO)· nHO with TpyNO in THF. Structural analysis shows that the metal centers are 10-coordinate, providing the first example of Am with this coordination number. Further spectroscopic and theoretical evaluation of these complexes reveals utilization of the 5f orbitals in bonding in the Am complex.

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Molecular photon upconversion via triplet-triplet annihilation (TTA-UC) is an intriguing strategy to increase solar cell efficiencies and surpass the Shockley-Quiesser (SQ) limit. In this Perspective, we recount our group's efforts to harness TTA-UC by directly incorporating metal ion linked multilayers of acceptor and sensitizer molecules into an organic-inorganic hybrid solar cell architecture. These self-assembled multilayers facilitate both upconverted emission and photocurrent generation from the upconverted state with a record contribution of 0.

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Organic-inorganic hybrid metal halide perovskites have emerged as a highly promising class of light emitters, which can be used as phosphors for optically pumped white light-emitting diodes (WLEDs). By controlling the structural dimensionality, metal halide perovskites can exhibit tunable narrow and broadband emissions from the free-exciton and self-trapped excited states, respectively. Here, we report a highly efficient broadband yellow light emitter based on zero-dimensional tin mixed-halide perovskite (CNHBr)SnBrI (x = 3).

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High surface area metal oxides offer a unique substrate for the assembly of multiple molecular components at an interface. The choice of molecules, metal oxide, and the nature of the assembly method can have a profound influence on the mechanism, rate, and efficiency of photoinduced energy and electron transfer events at the interface. Owing to their diversity and high level of control, these interfacial assemblies are of interest for numerous applications including solar energy conversion, photoelectrosynthesis, photo-writable memory, and more.

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We report precise manipulation of the potential-energy surfaces (PESs) of a series of butterfly-like pyrazolate-bridged platinum binuclear complexes, by synthetic control of the electronic structure of the cyclometallating ligand and the steric bulkiness of the pyrazolate bridging ligand. Color tuning of dual emission from blue/red, to green/red and red/deep red were achieved for these phosphorescent molecular butterflies, which have two well-controlled energy minima on the PESs. The environmentally dependent photoluminescence of these molecular butterflies enabled their application as self-referenced luminescent viscosity sensor.

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Printed organometal halide perovskite light-emitting diodes (LEDs) are reported that have indium tin oxide (ITO) or carbon nanotubes (CNTs) as the transparent anode, a printed composite film consisting of methylammonium lead tribromide (Br-Pero) and poly(ethylene oxide) (PEO) as the emissive layer, and printed silver nanowires as the cathode. The fabrication can be carried out in ambient air without humidity control. The devices on ITO/glass have a low turn-on voltage of 2.

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Molecular photon upconversion via triplet-triplet annihilation (TTA-UC), combining two or more low energy photons to generate a higher energy excited state, is an intriguing strategy to surpass the maximum efficiency for a single junction solar cell (<34%). Here, we introduce self-assembled bilayers on metal oxide surfaces as a strategy to facilitate TTA-UC emission and demonstrate direct charge separation of the upconverted state. A 3-fold enhancement in transient photocurrent is achieved at light intensities as low as two equivalent suns.

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