4-terminal tandem photovoltaic cell using two layers of PTB7:PC71BM for optimal light absorption

This document is the Accepted Manuscript version of a Published Work that appeared in final form in ACS applied materials and interfaces, copyright © American Chemical Society, after peer review and technical editing by the publisher and may be found at http://dx.doi.org/10.1021/acsami.5b04537A 4-terminal architecture is proposed in which two thin active layers (<100 nm) of PTB7:PC71BM are deposited on a two-sided ITO covered glass substrate. By modeling the electric field distribution inside the multilayer structure and applying an inverse solving problem procedure, we designed an optimal device architecture tailored to extract the highest photocurrent possible. By adopting such a 4-terminal configuration, we numerically demonstrated that even when the two subcells use identical absorber materials, the performance of the 4-terminal device may overcome the performance of the best equivalent single-junction device. In an experimental implementation of such a 4-terminal device, we demonstrate the viability of the approach and find a very good match with the trend of the numerical predictions.Peer ReviewedPostprint (author's final draft

1D and 3D supramolecular structures exhibiting weak ferromagnetism in three Cu(II) complexes based on malonato and di-alkyl-2,2’-bipyridines

Abstract Manganese coordination polymers {Mn(- fum)(5dmb)(H2O)2}n (1) and {[Mn2(fum)2(4dmb)2] H2O}n (2) (fum= fumarato; 5dmb = 5,50-dimethyl-2,20-bipyridine; 4dmb = 4,40-dimethyl-2,20-bipyridine) were obtained from one-pot, solution reactions under ambient conditions. The fum ligand acquires different coordination modes in the presence of the different dmb ancillary ligands, promoting distinctive crystal structures, including divergent dimensionalities. Thus, X-ray single-crystal data reveal that complex 1 crystallizes in a monoclinic system with C2/c space group and forms an infinite one-dimensional polymer. The Mn(II) center is six-coordinated and displays a distorted octahedral configuration. In addition, the solid-state selfassembly of the polymeric structure of 1 gives rise to a twodimensional (2D) supramolecular framework, mainly through hydrogen bonding. In contrast, complex 2 crystallizes in a monoclinic system with a Cc space group and forms an infinite 2D coordination polymer having dinuclear units. The Mn(II) center has a distorted octahedral configuration. The thermal stabilities of both coordination polymers were investigated. Variable-temperature magnetic measurements show that complex 1 is paramagnetic, while complex 2 exhibits weak antiferromagnetic coupling between adjacent Mn(II) centers.supported by CONACyT project 129293, DGAPA-UNAM project IN106014, and ICYTDF, project PICCO

Ultrathin oxidized Ti to increase stability and smoothness of Al doped ZnO transparent conductors for high efficiency indium-free polymer solar cells

We propose a transparent electrode consisting of an aluminum doped zinc oxide (AZO) layer capped with an ultrathin oxidized Ti film for indium-free bulk-heterojunction polymer solar cells (PSCs). The oxidized Ti increases the chemical, environmental, stability and the surface smoothness of AZO while still maintaining its electrical and optical properties. The application potential of the proposed transparent electrode is demonstrated in an inverted PSC, which shows an efficiency of 6.3%, very close to the value (7%) obtained in a similar structure using indium tin oxide. This efficiency is the highest reported to date for PSCs incorporating AZO electrodes.Peer ReviewedPostprint (published version

Semi-transparent polymer solar cells

Copyright 2015 Society of Photo Optical Instrumentation Engineers (SPIE). One print or electronic copy may be made for personal use only. Systematic reproduction and distribution, duplication of any material in this publication for a fee or for commercial purposes, or modification of the contents of the publication are prohibited.Over the last three decades, progress in the organic photovoltaic field has resulted in some device features which make organic cells applicable in electricity generation configurations where the standard silicon-based technology is not suitable, for instance, when a semi-transparent photovoltaic panel is needed. When the thin film solar cell performance is evaluated in terms of the device's visible transparency and power conversion efficiency, organic solar cells offer the most promising solution. During the last three years, research in the field has consolidated several approaches for the fabrication of high performance semi-transparent organic solar cells. We have grouped these approaches under three categories: devices where the absorber layer includes near-infrared absorption polymers, devices incorporating one-dimensional photonic crystals, and devices with a metal cavity light trapping configuration. We herein review these approaches.Peer ReviewedPostprint (author's final draft

Enhanced stability in semi-transparent PTB7/PC71BM photovoltaic cells

© 2015. This version is made available under the CC-BY-NC-ND 4.0 license http://creativecommons.org/licenses/by-nc-nd/4.0/We studied the performance over time of opaque and semi-transparent PTB7:PC71BM bulk heterojunction solar cells. For unsealed inverted configuration cells we observe that when the isolation from the environment is improved, the degradation observed is dominated by one single exponential decay. We demonstrate that a dielectric multilayer stack of approximately 550 nm provides an isolation that increases the lifetime of the cell close to ten times. In that event the fill factor appears to be the PV parameter dominating cell degradation resulting from a decrease in the shunt resistance. An Impedance analysis we performed indicates that a Warburg element, attributed to the presence of slowly moving charges such as heavy ions, must be included in the description of the experimental data. The contribution from such element increases as the cell degrades in good agreement with a degradation dominated by the corrosive effects from external agents reaching the active layer of the device.Peer ReviewedPostprint (author's final draft

All-optical aggregation and distribution of traffic in large metropolitan area networks using multi-Tb/s S-BVTs

Current metropolitan area network architectures are based on a number of hierarchical levels that aggregate traffic toward the core at the IP layer. In this setting, routers are interconnected by means of fixed transceivers operating on a point-to-point basis where the rates of transceivers need to match. This implies a great deal of intermediate transceivers to collect traffic and groom and send it to the core. This paper proposes an alternative scheme based on sliceable bandwidth/bitrate variable transceivers (S-BVTs) where the slice-ability property is exploited to perform the aggregation of traffic from multiple edges �� -to-1 rather than 1-to-1. This approach can feature relevant cost reductions through IP offloading at intermediate transit nodes but requires viable optical signal-to-noise ratio (OSNR) margins for all-optical transmission through the network. In this work, we prove through simulation the viability and applicability of this technique in large metro networks with a vertical-cavity-surface-emitting laser-based S-BVT design to target net capacities per channel of 25, 40, and 50 Gb/s. The study reveals that this technology can support most of the paths required for IP offloading after simulation in a semi-synthetic topology modeling a 20-million-inhabitant metropolitan area. Moreover, OSNR margins enable the use of protection paths (secondary disjoint paths) between the target node and the core much longer than primary paths in terms of both the number of intermediate hops and kilometers.European Union H2020 project PASSION, grant no. 780326 (http://www.passion-project.eu/)

Antimicrobial photodynamic polymeric films bearing biscarbazol triphenylamine end-capped dendrimeric Zn(II) porphyrin

A novel biscarbazol triphenylamine end-capped dendrimeric zinc(II) porphyrin (DP 5) was synthesized by click chemistry. This compound is a cruciform dendrimer that bears a nucleus of zinc(II) tetrapyrrolic macrocycle substituted at the meso positions by four identical substituents. These are formed by a tetrafluorophenyl group that possesses a triazole unit in the para position. This nitrogenous heterocyclic is connected to a 4,4′-di(N-carbazolyl)triphenylamine group by means of a phenylenevinylene bridge, which allows the conjugation between the nucleus and this external electropolymerizable carbazoyl group. In this structure, dendrimeric arms act as light-harvesting antennas, increasing the absorption of blue light, and as electroactive moieties. The electrochemical oxidation of the carbazole groups contained in the terminal arms of the DP 5 was used to obtain novel, stable, and reproducible fully π-conjugated photoactive polymeric films (FDP 5). First, the spectroscopic characteristics and photodynamic properties of DP 5 were compared with its constitutional components derived of porphyrin P 6 and carbazole D 7 moieties in solution. The fluorescence emissions of the dendrimeric units in DP 5 were more strongly quenched by the tetrapyrrolic macrocycle, indicating photoinduced energy transfer. In addition, FDP 5 film showed the Soret and Q absorption bands and red fluorescence emission of the corresponding zinc(II) porphyrin. Also, FDP 5 film was highly stable to photobleaching, and it was able to produce singlet molecular oxygen in both N,N-dimethylformamide (DMF) and water. Therefore, the porphyrin units embedded in the polymeric matrix of FDP 5 film mainly retain the photochemical properties. Photodynamic inactivation mediated by FDP 5 film was investigated in Staphylococcus aureus and Escherichia coli. When a cell suspension was deposited on the surface, complete eradication of S. aureus and a 99% reduction in E. coli survival were found after 15 and 30 min of irradiation, respectively. Also, FDP 5 film was highly effective to eliminate individual bacteria attached to the surface. In addition, photodynamic inactivation (PDI) sensitized by FDP 5 film produced >99.99% bacterial killing in biofilms formed on the surface after 60 min irradiation. The results indicate that FDP 5 film represents an interesting and versatile photodynamic active material to eradicate bacteria as planktonic cells, individual attached microbes, or biofilms.Fil: Heredia, Daniel Alejandro. Universidad Nacional de Río Cuarto. Instituto para el Desarrollo Agroindustrial y de la Salud. - Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Córdoba. Instituto para el Desarrollo Agroindustrial y de la Salud; ArgentinaFil: Martinez, Sol Romina. Universidad Nacional de Río Cuarto. Instituto para el Desarrollo Agroindustrial y de la Salud. - Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Córdoba. Instituto para el Desarrollo Agroindustrial y de la Salud; ArgentinaFil: Durantini, Andres Matías. Universidad Nacional de Río Cuarto. Instituto para el Desarrollo Agroindustrial y de la Salud. - Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Córdoba. Instituto para el Desarrollo Agroindustrial y de la Salud; ArgentinaFil: Pérez, María Eugenia. Universidad Nacional de Río Cuarto. Instituto para el Desarrollo Agroindustrial y de la Salud. - Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Córdoba. Instituto para el Desarrollo Agroindustrial y de la Salud; ArgentinaFil: Mangione, Maria Ines. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Rosario. Instituto de Química Rosario. Universidad Nacional de Rosario. Facultad de Ciencias Bioquímicas y Farmacéuticas. Instituto de Química Rosario; ArgentinaFil: Durantini, Javier Esteban. Universidad Nacional de Río Cuarto. Facultad de Ciencias Exactas Fisicoquímicas y Naturales. Instituto de Investigaciones en Tecnologías Energéticas y Materiales Avanzados. - Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Córdoba. Instituto de Investigaciones en Tecnologías Energéticas y Materiales Avanzados; ArgentinaFil: Gervaldo, Miguel Andres. Universidad Nacional de Río Cuarto. Facultad de Ciencias Exactas Fisicoquímicas y Naturales. Instituto de Investigaciones en Tecnologías Energéticas y Materiales Avanzados. - Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Córdoba. Instituto de Investigaciones en Tecnologías Energéticas y Materiales Avanzados; ArgentinaFil: Otero, Luis Alberto. Universidad Nacional de Río Cuarto. Facultad de Ciencias Exactas Fisicoquímicas y Naturales. Instituto de Investigaciones en Tecnologías Energéticas y Materiales Avanzados. - Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Córdoba. Instituto de Investigaciones en Tecnologías Energéticas y Materiales Avanzados; ArgentinaFil: Durantini, Edgardo Néstor. Universidad Nacional de Río Cuarto. Instituto para el Desarrollo Agroindustrial y de la Salud. - Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Córdoba. Instituto para el Desarrollo Agroindustrial y de la Salud; Argentin

Neutral water splitting catalysis with a high FF triple junction polymer cell

This document is the Accepted Manuscript version of a Published Work that appeared in final form in CS catalysis, copyright © American Chemical Society, after peer review and technical editing by the publisher and may be found at http://dx.doi.org/10.1021/acscatal.6b01036We report a photovoltaics-electrochemical (PV-EC) assembly based on a compact and easily processable triple homojunction polymer cell with high fill factor (76%), optimized conversion efficiencies up to 8.7%, and enough potential for the energetically demanding water splitting reaction (V-oc = 2.1 V). A platinum-free cathode made of abundant materials is coupled to a ruthenium oxide on glassy carbon anode (GC-RuO2) to perform the reaction at optimum potential (Delta E = 1.70-1.78 V, overpotential = 470-550 mV). The GC-RuO2 anode contains a single monolayer of catalyst corresponding to a superficial concentration (Gamma) of 0.15 nmol cm(-2) and is highly active at pH 7. The PV-EC cell achieves solar to hydrogen conversion efficiencies (STH) ranging from 5.6 to 6.0%. As a result of the solar cell's high fill factor, the optimal photovoltaic response is found at 1.70 V, the minimum potential at which the electrodes used perform the water splitting reaction. This allows generating hydrogen at efficiencies that would be very similar (96%) to those obtained as if the system were to be operating at 1.23 V, the thermodynamic potential threshold for the water splitting reaction.Peer ReviewedPostprint (author's final draft

Transition path to a dense efficient-packed post-delafossite phase. Crystal structure and evolution of the chemical bonding

[EN] A(I)B(III)O(2) delafossite-type oxides are important technological compounds characterized by the linear coordination of the monovalent A metal by oxygen atoms. Based on results of in situ synchrotron X-ray diffraction measurements and ab initio calculations, we herein report on the high-pressure behavior of AgGaO2, to the best of our knowledge the first compound showing step-wise transitions of Ag coordination from linear (2) to octahedral (6), through a leaning delafossite structure. These transformations take place at similar to 10.5 and similar to 16.5 GPa, respectively. Our structural analysis evidences that the initial rhombohedral delafossite structure first becomes dynamically unstable, and distorts continuously via a gliding motion of the [GaO2] octahedral layers within the ab plane, and subsequently transform into another rhombohedral phase 8% denser. This structural sequence is associated with a simultaneous decrease in the bond order of the Ag-O bonds and an increase in the ionicity of the crystal. These results may help to unveil the high-pressure phases of several delafossite compounds which were reported to undergo phase transitions under compression that could not be identified.We are thankful for the financial support received from the Spanish Ministerio de Ciencia e Innovacion and the Agencia Estatal de Investigacion under national projects PGC2018-094417-B-I00 (co-financed by EU FEDER funds), MAT2016-75586-C4-1-P/2-P, FIS2017-83295-P, PID2019-106383GB-C41/C42 and RED2018-102612-T (MALTA Consolider), and from Generalitat Valenciana under project PROMETEO/2018/123. D.S-P, A.O.R, and J.A.S acknowledge financial support of the Spanish MINECO for the RyC-2014-15643, RyC-2016-20301, and RyC-2015-17482 Ramon y Cajal Grants, respectively. Authors thank ALBA-CELLS synchrotron for providing beamtime (ALBA experiments 2012010170).Chuliá-Jordán, R.; Santamaria-Perez, D.; Pellicer-Porres, J.; Otero-De-La-Roza, A.; Martinez-Garcia, D.; García-Domene, B.; Gomis, O.... (2021). Transition path to a dense efficient-packed post-delafossite phase. Crystal structure and evolution of the chemical bonding. Journal of Alloys and Compounds. 867. https://doi.org/10.1016/j.jallcom.2021.15901215901286

Joint Observation of the Galactic Center with MAGIC and CTA-LST-1

MAGIC is a system of two Imaging Atmospheric Cherenkov Telescopes (IACTs), designed to detect very-high-energy gamma rays, and is operating in stereoscopic mode since 2009 at the Observatorio del Roque de Los Muchachos in La Palma, Spain. In 2018, the prototype IACT of the Large-Sized Telescope (LST-1) for the Cherenkov Telescope Array, a next-generation ground-based gamma-ray observatory, was inaugurated at the same site, at a distance of approximately 100 meters from the MAGIC telescopes. Using joint observations between MAGIC and LST-1, we developed a dedicated analysis pipeline and established the threefold telescope system via software, achieving the highest sensitivity in the northern hemisphere. Based on this enhanced performance, MAGIC and LST-1 have been jointly and regularly observing the Galactic Center, a region of paramount importance and complexity for IACTs. In particular, the gamma-ray emission from the dynamical center of the Milky Way is under debate. Although previous measurements suggested that a supermassive black hole Sagittarius A* plays a primary role, its radiation mechanism remains unclear, mainly due to limited angular resolution and sensitivity. The enhanced sensitivity in our novel approach is thus expected to provide new insights into the question. We here present the current status of the data analysis for the Galactic Center joint MAGIC and LST-1 observations