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Gion Calzaferri

Publications and source records attributed to Gion Calzaferri.

At least 19 recordsLinked to original sources
PubMed2006

Transfer of electronic excitation energy between randomly mixed dye molecules in the channels of zeolite L.

Host-guest materials containing strongly fluorescent donor and acceptor molecules have been prepared. Fine-tuning of the donor to acceptor distance in this material allows beautiful visible and quantitative observation of electronic excitation energy transfer phenomena. Oxonine and pyronine have been used as guest molecules and zeolite L as host. The dyes have been inserted by ion exchange. Stationary state and time-resolved experiments have been carried out with zeolite crystals of 300 and 700 nm size in the dye concentration range of 10(-4) mol/L up to 0.042 mol/L. The fluorescence decay of the donor and the pumping of the acceptor via energy transfer, which can be well observed, became faster with increasing loading. The behavior of the system follows requirements expected for Förster energy transfer material.

Journal Article↗
PubMed2005

Synthesis and luminescence properties of Ag2S and PbS clusters in zeolite A.

Zeolite A provides a suitable environment to host Ag2S and PbS clusters, so that spectroscopic investigations on very small particles are possible. The Ag2S monomer is colorless and shows photoluminescence at 490 nm with a lifetime of 300 micros, while the absorption and luminescence of Ag4S2 and larger clusters are red-shifted. The properties of these Ag2S/zeolite A materials depend on the co-cations. Results for Li+, Na+, K+, Rb+, Cs+, Mg2+, Ca2+, and Sr2+ are reported. Excitation energy transfer between Ag2S and Ag4S2 has been studied in materials containing Ca2+ co-cations. PbS particles can be prepared by the same method as Ag2S in the cavities of zeolite A. The PbS monomers obtained are yellow and show photoluminescence at 570 nm, with a lifetime of 700 ns.

Journal Article↗
PubMed2005

Particle distribution in a microporous material: theoretical concept.

Particle distribution and exchange equilibria in a microporous host material, built up of equivalent particle sites, which are grouped in larger subsets, are described. Simplified descriptions evolve from the exact formulae in the thermodynamic limit. We find that, for example, a single zeolite A nanocrystal consisting of about 1000 pseudo-unit-cells fixes a lower limit for the use of the approximate formula describing particle distribution. A rational selectivity coefficient, which is approximately constant over the whole exchange range, only results if a single zeolite crystal consists of one million pseudo-unit-cells or more, or if a sufficiently large number of smaller crystals is considered. On the basis of the statistical particle distribution model, a closed, simple formula for the ion-exchange isotherm is then derived, which is valid for systems involving a variable number of coupled-exchange reactions. Its similarity to the Langmuir isotherm is discussed. The theory on ion-exchange equilibria is used to derive formulae for the change of free-energy, enthalpy, and entropy occurring in coupled ion-exchange reactions. The findings, though applicable to virtually any particle exchanging system with the structural properties described above, are applied to zeolite A, since this material can be treated as a nearly ideal model. The results derived can straightforwardly be used to evaluate experimental data quantitatively, since the common inequivalence of the host sites can be taken into account.

Models, Chemical↗
PubMed2005

Particle distribution in a microporous material: experiments with zeolite A.

The theory on particle distribution and exchange equilibria in a microporous material is applied to experimental ion-exchange data involving zeolite Na-A and zeolite K-A, with silver ions as the exchanging species. The presented method enables direct evaluation of the measured data and consideration of nonequivalent particle sites. The isotherms of the K+ versus Ag+ exchange in zeolite K-A rise much more steeply, at low exchange degrees, than those of the Na+ versus Ag+ exchange in zeolite Na-A. This result implies a different course of the ion-exchange reactions. Spectroscopic measurements on dehydrated, partly silver-exchanged zeolites Na-A and K-A do indeed show that in zeolite Na-A, the Na+ ions occupying four-ring positions are exchanged faster for Ag+ than the Na+ ions occupying eight- and six-ring positions, while in zeolite K-A the exchange does not start with the four-ring ion but with six-ring ions, followed by the four-ring ion. These findings are consistent with the results obtained from evaluation of the ion-exchange data. The resulting thermodynamic quantities significantly differ from published reference values, which we suggest should be revised.

Journal Article↗
PubMed2004

Injecting electronic excitation energy into an artificial antenna system through an Ru2+ complex.

The Ru2+ complex [Ru(bpy)2(bpy-ph4-Si(CH3)3)]2+ can be electrostatically bound to the negatively charged channel entrances of dye-loaded zeolite L crystals where it acts as a functional stopcock molecule. Impressive electronic triplet-singlet excitation energy transfer from the Ru2+ complex to the acceptor dye oxazine 1 (Ox1) located inside the channels can be observed when the donor molecule is selectively excited. Time-resolved luminescence experiments have been performed on the separate components and on the assembled donor-acceptor material. The luminescence lifetime of the Ru2+ complex attached to the zeolite is reduced by a factor of 30 when Ox1 acceptor molecules are present. The fluorescence decay of Ox1 incorporated in zeolite L is single exponential with a lifetime of 3 ns. The much longer lifetime in zeolite L than in solution is due to the fact, that the diethyl groups are sterically restricted when the dye is inside the host.

Cations, Divalent↗
PubMed2004

Water splitting with silver chloride photoanodes and amorphous silicon solar cells.

A thin silver chloride layer deposited on a conducting support photocatalyzes the oxidation of water to O(2) in the presence of a small excess of silver ions in solution. The light sensitivity in the visible part of the spectrum is due to self-sensitization caused by reduced silver species. Anodic polarization reoxidizes the reduced silver species. To test its water splitting capability, AgCl photoanodes as well as gold colloid modified AgCl photoanodes were combined with an amorphous silicon solar cell. The AgCl layer was employed in the anodic part of a setup for photoelectrochemical water splitting consisting of two separate compartments connected through a salt bridge. A platinum electrode and an amorphous silicon solar cell were used in the cathodic part. Illumination of the AgCl photoanode and the amorphous Si solar cell led to photoelectrochemical water splitting to O(2) and H(2). For AgCl photoanodes modified with gold colloids an increased photocurrent, and consequently a higher O(2) and H(2) production, were observed.

Journal Article↗
PubMed2004

Electronic and vibrational properties of fluorenone in the channels of zeolite L.

Fluorenone (C13H8O) was inserted into the channels of zeolite L by using gas-phase adsorption. The size, structure, and stability of fluorenone are well suited for studying host-guest interactions. The Fourier transform IR, Raman, luminescence, and excitation spectra, in addition to thermal analysis data, of fluorenone in solution and fluorenone/zeolite L are reported. Normal coordinate analysis of fluorenone was performed, based on which IR and Raman bands were assigned, and an experimental force field was determined. The vibrational spectra can be used for nondestructive quantitative analysis by comparing a characteristic dye band with a zeolite band that has been chosen as the internal standard. Molecular orbital calculations were performed to gain a better understanding of the electronic structure of the system and to support the interpretation of the electronic absorption and luminescence spectra. Fluorenone shows unusual luminescence behavior in that it emits from two states. The relative intensity of these two bands depends strongly on the environment and changes unexpectedly in response to temperature. In fluorenone/zeolite L, the intensity of the 300 nm band (lifetime 9 micros) increases with decreasing temperature, while the opposite is true for the 400 nm band (lifetime 115 micros). A model of the host-guest interaction is derived from the experimental results and calculations: the dye molecule sits close to the channel walls with the carbonyl group pointing to an Al3+ site of the zeolite framework. A secondary interaction was observed between the fluorenone's aromatic ring and the zeolite's charge-compensating cations.

Journal Article↗
PubMed2003

Host-guest antenna materials.

The focus of this review is on host-guest composites with photonic antenna properties. The material generally consists of cylindrical zeolite L crystals the channels of which are filled with dye molecules. The synthesis is based on the fact that molecules can diffuse into individual channels. This means that, under the appropriate conditions, they can also leave the zeolite by the same way. In some cases, however, it is desirable to block their way out by adding a closure molecule. Functionalization of the closure molecules allows tuning of, for example, wettability, refractive index, and chemical reactivity. The supramolecular organization of the dyes inside the channels is a first stage of organization. It allows light harvesting within a certain volume of a dye-loaded nanocrystalline zeolite and radiationless transport to both ends of the cylinder or from the ends to the center. The second stage of organization is the coupling to an external acceptor or donor stopcock fluorophore at the ends of the channels, which can trap or inject electronic excitation energy. The third stage of organization is the coupling to an external device through a stopcock molecule. The wide-ranging tunability of these highly organized materials offers fascinating new possibilities for exploring excitation-energy-transfer phenomena, and challenges for developing new photonic devices.

Journal Article↗
PubMed2003

Electronic excitation energy migration in a photonic dye--zeolite antenna.

Electronic excitation energy migration in a photonic antenna host-guest material has been investigated by time-resolved fluorescence experiments and by Monte Carlo calculations. The host consists of a linear channel system (zeolite L). The channels are filled with energy transporting dyes (donors) in their middle section and by one or several monolayers of a strongly luminescent trapping dye (acceptors) at each end of the channels. Excitation energy is transported among the donors in a series of steps until it reaches an acceptor at one end of the channels, or it is somehow trapped on its way, or it escapes by spontaneous emission. We describe the organization of dyes in the channels by means of Monte Carlo simulation and we report time-resolved data on a variety of pyronine-, oxonine-, and oxonine, pyronine-zeolite L materials. In the latter, the pyronine acts as donor and oxonine as acceptor. We find that the luminescence decay of crystals containing only one kind of dye is single exponential for moderate loading if measured under oxygen-free conditions, but biexponential otherwise. The main characteristic of the time evolution of oxonine, pyronine-zeolite L crystals is that the acceptor intensity is first built up before it starts to decay. This intensity increase becomes faster with increasing donor loading, a fact that beautifully supports the interpretation that the crystals behave as photonic antenna in which excitation energy is transported preferentially along the channels by a Förster-type mechanism until it reaches the acceptor, where it is emitted as red luminescence.

Journal Article↗
PubMed2003

The electronic structure of Cu+, Ag+, and Au+ zeolites.

A variety of procedures have been used to prepare d10-zeolite materials. The electronic structure of these materials can be regarded to a first approximation as a superposition of the framework, of the charge compensating ions, of solvent molecules and of guest species. Zeolite oxygen to d10-ion charge transfer transitions dominate the electronic spectra if the ions coordinate to the zeolite oxygens. Specific coordination sites can influence the energy and the intensity of these transitions remarkably. Intra guest transitions dominate in quantum dot materials, as discussed in detail for luminescent Ag2S zeolite A. The zeolite is not needed for the photocatalytic water oxidation on Ag+/AgCl photo anodes with visible light. It can, however, be used to increase the active surface area substantially.

Journal Article↗