Novel room temperature ionic liquids of hexaalkyl substituted guanidinium salts for dye-sensitized solar cells

A novel family of room temperature ionic liquids, N,N-diethyl-N′,N′-dipropyl-N′′-hexyl-N′′-methylguanidinium iodide (SGI) and N,N,N′,N′-tetramethyl-N′′,N′′-dipentylguanidinium tricyanomethanide (SGTM) were designed and synthesized. Due to the strong charge delocalization on the tricyanomethanide anion and, thus, weaker ion-pairing, SGTM has a lower viscosity than SGI salt that has iodide as an anion. SGI was successfully used as an iodide resource for dye-sensitized nanocrystalline solar cells. The device with a solvent-free, SGI-based electrolyte achieved a 5.9% power conversion efficiency under an air mass 1.5 incident light of 9.47mW/cm

Enhanced light harvesting in mesoporous TiO2/P3HT hybrid solar cells using a porphyrin dye

We report panchromatic light harvesting in hybrid TiO2/P3HT photovoltaic devices using a porphyrin dye that complements the light absorption of P3HT. The high short circuit photocurrent (12.1 mA cm(-2)) obtained is found to be due, in part, to Forster resonance energy transfer from the P3HT to the dye

Optimization of distyryl-Bodipy chromophores for efficient panchromatic sensitization in dye sensitized solar cells

Versatility of Bodipy (4,4-difluoro-4-bora-3a,4a-diaza-s-indacene) dyes was further expanded in recent dye-sensitized solar cell applications. Here we report a series of derivatives designed to address earlier problems in Bodipy sensitized solar cells. In the best case example, an overall efficiency of a modest 2.46% was achieved, but panchromatic nature of the dyes is quite impressive. This is the best reported efficiency in liquid electrolyte solar cells with Bodipy dyes as photosensitizers. © The Royal Society of Chemistry 2011

Consensus statement for stability assessment and reporting for perovskite photovoltaics based on ISOS procedures

Funder: 2017 SGR 329 Severo Ochoa program from Spanish MINECO (Grant No. SEV-2017-0706)Funder: This article is based upon work from COST Action StableNextSol MP1307 supported by COST (European Cooperation in Science and Technology). M. V. K., E. A. K., V. B., and A. Osherov thank the financial support of the United States – Israel Binational Science Foundation (grant no. 2015757). E. A. K., A. A., and I. V.-F. acknowledge a partial support from the SNaPSHoTs project in the framework of the German-Israeli bilateral R&D cooperation in the field of applied nanotechnology. M. S. L. thanks the financial support of NSF (ECCS, award #1610833). S. C., M. Manceau and M. Matheron thank the financial support of European Union’s Horizon 2020 research and innovation programme under grant agreement No 763989 (APOLO project). F. De R. and T. M. W. would like to acknowledge the support from the Engineering and Physical Sciences Research Council (EPSRC) through the SPECIFIC Innovation and Knowledge Centre (EP/N020863/1) and express their gratitude to the Welsh Government for their support of the Ser Solar programme. P. A. T. acknowledges financial support from Russian Science Foundation (project No. 19-73-30020). J.K. acknowledges the support by the Solar Photovoltaic Academic Research Consortium II (SPARC II) project, gratefully funded by WEFO. M.K.N. acknowledges financial support from Innosuisse project 25590.1 PFNM-NM, Solaronix, Aubonne, Switzerland. C.-Q. M. would like to acknowledge The Bureau of International Cooperation of Chinese Academy of Sciences for the support of ISOS11 and the Ministry of Science and Technology of China for the financial support (No 2016YFA0200700). N.G.P. acknowledges financial support from the National Research Foundation of Korea (NRF) grants funded by the Ministry of Science, ICT Future Planning (MSIP) of Korea under contracts NRF-2012M3A6A7054861 and NRF-2014M3A6A7060583 (Global Frontier R&D Program on Center for Multiscale Energy System). CSIRO’s contribution to this work was conducted with funding support from the Australian Renewable Energy Agency (ARENA) through its Advancing Renewables Program. A. F. N gratefully acknowledges support from FAPESP (Grant 2017/11986-5) and Shell and the strategic importance of the support given by ANP (Brazil’s National Oil, Natural Gas and Biofuels Agency) through the R&D levy regulation. Y.-L.L. and Q.B. acknowledge support from the National Science Foundation Division of Civil, Mechanical and Manufacturing Innovation under award #1824674. S.D.S. acknowledges the European Research Council (ERC) under the European Union’s Horizon 2020 research and innovation programme (HYPERION, grant agreement No. 756962), and the Royal Society and Tata Group (UF150033). The work at the National Renewable Energy Laboratory was supported by the U.S. Department of Energy (DOE) under contract DE-AC36-08GO28308 with Alliance for Sustainable Energy LLC, the manager and operator of the National Renewable Energy Laboratory. The authors (J.J.B, J.M.L., M.O.R, K.Z.) acknowledge support from the De-risking halide perovskite solar cells program of the National Center for Photovoltaics, funded by the U.S. Department of Energy, Office of Energy Efficiency and Renewable Energy, Solar Energy Technology Office. The views expressed in the article do not necessarily represent the views of the DOE or the U.S. Government. The U.S. Government retains and the publisher, by accepting the article for publication, acknowledges that the U.S. Government retains a nonexclusive, paid-up, irrevocable, worldwide license to publish or reproduce the published form of this work, or allow others to do so, for U.S. Government purposes. H.J.S. acknowledges the support of EPSRC UK, Engineering and Physical Sciences Research Council. V.T. and M. Madsen acknowledges ‘Villum Foundation’ for funding of the project CompliantPV, under project number 13365. M. Madsen acknowledges Danmarks Frie Forskningsfond, DFF FTP for funding of the project React-PV, No. 8022-00389B. M.G. and S.M.Z. thank the King Abdulaziz City for Science and technology (KACST) for financial support. S.V. acknowledges TKI-UE/Ministry of Economic Affairs for financial support of the TKI-UE toeslag project POP-ART (No. 1621103). M.L.C. and H.X. acknowledges the support from Spanish MINECO for the grant GraPErOs (ENE2016-79282-C5-2-R), the OrgEnergy Excellence Network CTQ2016-81911- REDT, the Agència de Gestiód'Ajuts Universitaris i de Recerca (AGAUR) for the support to the consolidated Catalonia research group 2017 SGR 329 and the Xarxa de Referència en Materials Avançats per a l'Energia (Xarmae). ICN2 is supported by the Severo Ochoa program from Spanish MINECO (Grant No. SEV-2017-0706) and is funded by the CERCA Programme / Generalitat de Catalunya.Abstract: Improving the long-term stability of perovskite solar cells is critical to the deployment of this technology. Despite the great emphasis laid on stability-related investigations, publications lack consistency in experimental procedures and parameters reported. It is therefore challenging to reproduce and compare results and thereby develop a deep understanding of degradation mechanisms. Here, we report a consensus between researchers in the field on procedures for testing perovskite solar cell stability, which are based on the International Summit on Organic Photovoltaic Stability (ISOS) protocols. We propose additional procedures to account for properties specific to PSCs such as ion redistribution under electric fields, reversible degradation and to distinguish ambient-induced degradation from other stress factors. These protocols are not intended as a replacement of the existing qualification standards, but rather they aim to unify the stability assessment and to understand failure modes. Finally, we identify key procedural information which we suggest reporting in publications to improve reproducibility and enable large data set analysis

Solvent-Free Ionic Liquid Electrolytes for Mesoscopic Dye-Sensitized Solar Cells

Ionic liquids have been identified as a new class of solvent that offers opportunities to move away from the traditional solvents. The physical-chemical properties of ionic liquids can be tuned and controlled by tailoring their structures. The typical properties of ionic liquids, such as non-volatility, electrochemical stability and high conductivity, render them attractive as electrolytes for dye-sensitized solar cells. However, the high viscosity of ionic liquids leads to mass transport limitations on the photocurrents in the solar cells at full sunlight intensity, but the contribution of a Grotthous-type exchange mechanism in these viscous electrolytes helps to alleviate these diffusion problems. This article discusses recent developments in the field of high-performance dye-sensitized solar cells with ionic liquid-based electrolytes and their characterization by electrochemical impedance analysis

Molecular Wiring of Olivine LiFeP04 by Ruthenium(II)-Bipyridine Complexes and by Their Assemblies with Single-Walled Carbon Nanotubes

The undoped and carbon-free olivine, LiFePO4 was bonded with 5% PVDF, and deposited on F-doped SnO2 support (FTO). The electrodes were modified by a monolayer of three different complexes: NaRu(4,4′-dicarboxylic acid-2,2′-bipyridine)(4,4′-dinonyl-2,2′-bipyridine)(NCS)2, coded as Z-907Na, Ru-bis(4,4′-diethoxycarbonyl-2,2′-bipyridine)(4,4′-dicarboxylic acid-2,2′-bipyridine), coded Z-974, and Ru-bis(4,4′-dicarboxylic acid-2,2′-bipyridine)(4,4′-dinonyl-2,2′-bipyridine), coded Z-975. These complexes have redox potentials from 3.5 to 4.45 V versus Li/Li+ and are active for molecular wiring of LiFePO4. The Ru-complexes contacting FTO are reversibly oxidized, which allows the holes to be transported via the adsorbed monolayer across the olivine surface, where a subsequent chemical delithiation occurs toward FePO4. The supramolecular assembly of Z-907Na with single-walled carbon nanotubes (SWNT) is more active for molecular wiring than pure Z-907Na. In this case, the LiFePO4/FePO4 system can be charged/discharged by currents larger by 1 order of magnitude, and the performance of the assembly depends on the type of SWNT. This study improved our understanding of molecular wiring in general, and the enhancement of wiring activity by SWNT in particular

Interface Modification of Dye-sensitized Solar Cells with Pivalic Acid to Enhance the Open-circuit Voltage

Pivalic acid (PVA) was used as a new coadsorbent to dyesensitized solar cells (DSCs) to modify the interface between the TiO2 films and electrolyte. The addition of PVA improved the light-to-electricity conversion efficiency of devices by 8% by enhancing the open-circuit voltage

Heterogeneous electron transfer from dye-sensitized nanocrystalline TiO2 to [Co(bpy)3]3+: Insights gained from impedance spectroscopy

10.1021/ja311743mJournal of the American Chemical Society135103939-3952JACS

The influence of dye structure on charge recombination in dye-sensitized solar cells

10.1039/c0cp02605kPhysical Chemistry Chemical Physics13146637-6648PPCP