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Register a new userExcited State Photophysics of Squaraine Dyes for Photovoltaic Applications: an Alternative Deactivation Scenario
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Added by
Francesco Scotognella
Publication date
2017
fields
Physics
and research's language is
English
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Squaraine dyes (SQs) represent a versatile class of functional molecules with strong absorption and emission features, widely used as near-infrared sensitizers in organic and hybrid photovoltaic devices. In this context, the photodynamics of such molecules has been seen to influence dramatically the efficiency of the photogeneration process. The most accepted interpretation of excited state deactivation in SQs is represented by a trans-cis photoisomerization around a CC double bond of the polymethinic-like bridge, although such scenario does not explain satisfyingly the decay route of SQs dyes in conformational constrained systems or in highly viscous environments. Here we combine steady-state and time-resolved spectroscopic techniques with high level ab initio calculations to shed light into the photophysics of cis-locked indolenine-based SQs. Our results point towards alternative deactivation routes, possibly involving a dark state in molecules lacking central substitution and the rotation of the central substituent in the core-functionalized ones. These novel results can suggest a synthetic rationale to design dyes that permit quantitative and effective charge generation/diffusion and collection in photovoltaic diodes and, thus, enhance their efficiency.
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Pumping water using multiple energy sources is the ideal solution for supplying of potable water in isolated or arid areas. In this paper, an effective control and energy management strategy for a stand-alone photovoltaic-batteries water pumping system for agriculture applications is presented. The system is composed of photovoltaic solar panels as primary energy sources, and Lead-Acid batteries as seconder energy sources to supply the brushless DC motor and the centrifugal pump. The energy management strategy uses an intelligent algorithm to satisfy the energy demanded by the motor, also to maintain the state-of-charge of the battery between safe margins in order to eliminate the full discharge and the destruction of the batteries. Drift is a major problem in photovoltaic systems; this phenomenon occurs when the solar irradiation changes rapidly. Classical MPPT algorithms do not solve this problem, for this reason a modified P&O has been implemented, the obtained results shown the efficiency of the algorithm compared to the conventional P&O. Computer simulation results confirm the effectiveness of the proposed energy management algorithm under random meteorological conditions.
Nd doped phosphate glasses have been studied before and after gamma irradiation in order to understand the effect of glass composition and radiation induced defects on the optical properties of glasses. UV, Vis absorption and photoluminescence spectra of these glasses are found strongly dependent on the composition of glass matrix, particularly on the ratio of oxygen (O) and neodymium (Nd) concentration obtained from energy dispersive X-ray spectroscopic (EDX) measurement. Gamma irradiation of glass modifies the transmission below 700 nm due to generation of some new absorption bands corresponding to different types of defects. Observations indicate toward possibility of change in the valence state of Nd3+ to Nd2+ and generation of oxygen vacancies in glass matrix. EDX and X-ray photoelectron spectroscopic (XPS) measurements indicate change in the composition of glasses particularly decrease in the relative concentration of oxygen in glass samples after gamma irradiation.
In the context of gravitational collapse and black hole formation, we reconsider the problem to describe analytically the critical collapse of a massless and minimally coupled scalar field in $2+1$ gravity.
Here were report a study of picene nano-cristalline thin films doped with pentacene molecules. The thin films were grown by supersonic molecular beam deposition with a doping concentration that ranges between less than one molecules of pentacene every 104 picene molecules up to about one molecule of pentacene every 102 of picene. Morphology and opto-electronic properties of the films were studied as a function of the concentration of dopants. The optical response of the picene films, characterized by absorption, steady-state and time-resolved photoluminescence measurements, changes dramatically after the doping with pentacene. An efficient energy transfer from the picene host matrix to the pentacene guest molecules was observed giving rise to an intense photoluminescence coming out from pentacene. This efficient mechanism opens the possibility to exploit applications where the excitonic states of the guest component, pentacene, are of major interest such as MASER. The observed mechanism could also serve as prototypical system for the study of the photophysics of host guest systems based on different phenacenes and acenes.
Angle-resolved photoelectron spectroscopy is an extremely powerful probe of materials to access the occupied electronic structure with energy and momentum resolution. However, it remains blind to those dynamic states above the Fermi level that determine technologically relevant transport properties. In this work, we extend band structure mapping into the unoccupied states and across the entire Brillouin zone by using a state-of-the-art high repetition rate, extreme ultraviolet fem- tosecond light source to probe optically excited samples. The wide-ranging applicability and power of this approach are demonstrated by measurements on the 2D semiconductor WSe2, where the energy-momentum dispersion of valence and conduction bands are observed in a single experiment. This provides a direct momentum-resolved view not only on the complete out-of-equilibrium band gap but also on its renormalization induced by electron-hole interaction and screening. Our work establishes a new benchmark for measuring the band structure of materials, with direct access to the energy-momentum dispersion of the excited-state spectral function.
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