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Journal articleMoia D, Cappel UB, Leijtens T, et al., 2015,
The Role of Hole Transport between Dyes in Solid-State Dye-Sensitized Solar Cells
, Journal of Physical Chemistry C, Vol: 119, Pages: 18975-18985, ISSN: 1932-7447 -
Journal articleYao J, Kirchartz T, Vezie MS, et al., 2015,
Quantifying losses in open-circuit voltage in solution-processable solar cells
, Physical Review Applied, Vol: 4, ISSN: 2331-7019The maximum open-circuit voltage of a solar cell can be evaluated in terms of its ability to emit light. We herein verify the reciprocity relation between the electroluminescence spectrum and subband-gap quantum efficiency spectrum for several photovoltaic technologies at different stages of commercial development, including inorganic, organic, and a type of methyl-ammonium lead- halide CH3NH3PbI3−xClx perovskite solar cells. Based on the detailed balance theory and reciprocity relations between light emission and light absorption, voltage losses at open circuit are quantified and assigned to specific mechanisms, namely, absorption edge broadening and nonradiative recombination. The voltage loss due to nonradiative recombination is low for inorganic solar cells (0.04–0.21 V), while for organic solar cell devices it is larger but surprisingly uniform, with values of 0.34–0.44 V for a range of material combinations. We show that, in CH3NH3PbI3−xClx perovskite solar cells that exhibit hysteresis, the loss to nonradiative recombination varies substantially with voltage scan conditions. We then show that for different solar cell technologies there is a roughly linear relation between the power conversion efficiency and the voltage loss due to nonradiative recombination.
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Journal articleLeguy AMA, Frost JM, McMahon AP, et al., 2015,
Corrigendum: The dynamics of methylammonium ions in hybrid organic–inorganic perovskite solar cells
, Nature Communications, Vol: 6, ISSN: 2041-1723 -
Journal articleLeguy AMA, Frost JM, McMahon AP, et al., 2015,
The dynamics of methylammonium ions in hybrid organic-inorganic perovskite solar cells
, Nature Communications, Vol: 6, ISSN: 2041-1723Methylammonium lead iodide perovskite can make high-efficiency solar cells, which also show an unexplained photocurrent hysteresis dependent on the device-poling history. Here we report quasielastic neutron scattering measurements showing that dipolar CH3NH3+ ions reorientate between the faces, corners or edges of the pseudo-cubic lattice cages in CH3NH3PbI3 crystals with a room temperature residence time of ~14 ps. Free rotation, π-flips and ionic diffusion are ruled out within a 1–200-ps time window. Monte Carlo simulations of interacting CH3NH3+ dipoles realigning within a 3D lattice suggest that the scattering measurements may be explained by the stabilization of CH3NH3+ in either antiferroelectric or ferroelectric domains. Collective realignment of CH3NH3+ to screen a device’s built-in potential could reduce photovoltaic performance. However, we estimate the timescale for a domain wall to traverse a typical device to be ~0.1–1 ms, faster than most observed hysteresis.
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Journal articleLeguy AMA, Hu Y, Campoy-Quiles M, et al., 2015,
Reversible hydration of CH(3)NH(3)Pbl(3) in films, single crystals, and solar cells
, Chemistry of Materials, Vol: 27, Pages: 3397-3407, ISSN: 0897-4756Solar cells composed of methylammonium lead iodide perovskite (MAPI) are notorious for their sensitivity to moisture. We show that (i) hydrated crystal phases are formed when MAPI is exposed to water vapor at room temperature and (ii) these phase changes are fully reversed when the material is subsequently dried. The reversible formation of CH3NH3PbI3·H2O followed by (CH3NH3)4PbI6·2H2O (upon long exposure times) was observed using time-resolved XRD and ellipsometry of thin films prepared using “solvent engineering”, single crystals, and state-of-the-art solar cells. In contrast to water vapor, the presence of liquid water results in the irreversible decomposition of MAPI to form PbI2. MAPI changes from dark brown to transparent on hydration; the precise optical constants of CH3NH3PbI3·H2O formed on single crystals were determined, with a bandgap at 3.1 eV. Using the single-crystal optical constants and thin-film ellipsometry measurements, the time-dependent changes to MAPI films exposed to moisture were modeled. The results suggest that the monohydrate phase forms independent of the depth in the film, suggesting rapid transport of water molecules along grain boundaries. Vapor-phase hydration of an unencapsulated solar cell (initially Jsc ≈ 19 mA cm–2 and Voc ≈ 1.05 V at 1 sun) resulted in more than a 90% drop in short-circuit photocurrent and ∼200 mV loss in open-circuit potential; however, these losses were fully reversed after the device was exposed to dry nitrogen for 6 h. Hysteresis in the current–voltage characteristics was significantly increased after this dehydration, which may be related to changes in the defect density and morphology of MAPI following recrystallization from the hydrate. Based on our observations, we suggest that irreversible decomposition of MAPI in the presence of water vapor only occurs significantly once a grain has been fully converted to the monohydrate phase.
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Journal articleDeledalle F, Kirchartz T, Vezie MS, et al., 2015,
Understanding the Effect of Unintentional Doping on Transport Optimization and Analysis in Efficient Organic Bulk-Heterojunction Solar Cells
, PHYSICAL REVIEW X, Vol: 5, ISSN: 2160-3308- Author Web Link
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- Citations: 46
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Journal articleDimitrov SD, Wheeler S, Niedzialek D, et al., 2015,
Polaron pair mediated triplet generation in polymer/fullerene blends
, Nature Communications, Vol: 6, ISSN: 2041-1723Electron spin is a key consideration for the function of organic semiconductors in light-emitting diodes and solar cells, as well as spintronic applications relying on organic magnetoresistance. A mechanism for triplet excited state generation in such systems is by recombination of electron-hole pairs. However, the exact charge recombination mechanism, whether geminate or nongeminate and whether it involves spin-state mixing is not well understood. In this work, the dynamics of free charge separation competing with recombination to polymer triplet states is studied in two closely related polymer-fullerene blends with differing polymer fluorination and photovoltaic performance. Using time-resolved laser spectroscopic techniques and quantum chemical calculations, we show that lower charge separation in the fluorinated system is associated with the formation of bound electron-hole pairs, which undergo spin-state mixing on the nanosecond timescale and subsequent geminate recombination to triplet excitons. We find that these bound electron-hole pairs can be dissociated by electric fields.
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Journal articleEmmott CJM, Roehr JA, Campoy-Quiles M, et al., 2015,
Organic photovoltaic greenhouses: a unique application for semi-transparent PV?
, Energy & Environmental Science, Vol: 8, Pages: 1317-1328, ISSN: 1754-5706Organic photovoltaics are an emerging solar power technology which embody properties such astransparency, flexibility, and rapid, roll to roll manufacture, opening the potential for unique nicheapplications. We report a detailed techno-economic analysis of one such application, namely thephotovoltaic greenhouse, and discuss whether the unique properties of the technology can provideadvantages over conventional photovoltaics. The potential for spectral selectivity through the choice ofOPV materials is evaluated for the case of a photovoltaic greenhouse. The action spectrum of typicalgreenhouse crops is used to determine the impact on crop growth of blocking different spectral rangesfrom the crops. Transfer matrix optical modelling is used to assess the efficiency and spectrally resolvedtransparency of a variety of commercially available semi-conducting polymer materials, in addition to anon-commercial low-band-gap material with absorption outside that required for crop growth. Economicanalysis suggests there could be a huge potential for OPV greenhouses if aggressive cost targets can bemet. Technical analysis shows that semi-transparent OPV devices may struggle to perform better thanopaque crystalline silicon with partial coverage, however, OPV devices using the low-band-gap materialPMDPP3T, as well as a high efficiency mid-band-gap polymer PCDTBT, can demonstrate improvedperformance in comparison to opaque, flexible thin-film modules such as CIGS. These results stress theimportance of developing new, highly transparent electrode and interlayer materials, along with highefficiency active layers, if the full potential of this application is going to be realised.
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Journal articleFew S, Frost JM, Nelson J, 2015,
Models of charge pair generation in organic solar cells
, PHYSICAL CHEMISTRY CHEMICAL PHYSICS, Vol: 17, Pages: 2311-2325, ISSN: 1463-9076- Author Web Link
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- Citations: 139
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Journal articleDattani R, Gibson KF, Few S, et al., 2015,
Fullerene oxidation and clustering in solution induced by light
, Journal of Colloid and Interface Science, Vol: 446, Pages: 24-30, ISSN: 1095-7103We investigate the environmental stability of fullerene solutions by static and dynamic light scattering, FTIR, NMR and mass spectroscopies, and quantum chemical calculations. We find that visible light exposure of fullerene solutions in toluene, a good solvent, under ambient laboratory conditions results in C60 oxidation to form fullerene epoxides, and subsequently causes fullerene clustering in solution. The clusters grow with time, even in absence of further illumination, and can reach dimensions from ≈100 nm to the μm scale over ≈1 day. Static light scattering suggests that resulting aggregates are fractal, with a characteristic power law (df) that increases from approximately 1.3 to 2.0 during light exposure. The clusters are bound by weak Coulombic interactions and are found to be reversible, disintegrating by mechanical agitation and thermal stress, and reforming over time. Our findings are relevant to the solution processing of composites and organic photovoltaics, whose reproducibility and performance requires control of fullerene solution stability under storage conditions.
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Journal articleMacLachlan AJ, Rath T, Cappel UB, et al., 2015,
Polymer/Nanocrystal Hybrid Solar Cells: Influence of Molecular Precursor Design on Film Nanomorphology, Charge Generation and Device Performance
, ADVANCED FUNCTIONAL MATERIALS, Vol: 25, Pages: 409-420, ISSN: 1616-301X- Author Web Link
- Open Access Link
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- Citations: 42
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Journal articleHolliday S, Ashraf RS, Nielsen CB, et al., 2015,
A rhodanine flanked nonfullerene acceptor for solution-processed organic photovoltaics
, Journal of the American Chemical Society, Vol: 137, Pages: 898-904, ISSN: 0002-7863A novel small molecule, FBR, bearing 3-ethylrhodanine flanking groups was synthesized as a nonfullerene electron acceptor for solution-processed bulk heterojunction organic photovoltaics (OPV). A straightforward synthesis route was employed, offering the potential for large scale preparation of this material. Inverted OPV devices employing poly(3-hexylthiophene) (P3HT) as the donor polymer and FBR as the acceptor gave power conversion efficiencies (PCE) up to 4.1%. Transient and steady state optical spectroscopies indicated efficient, ultrafast charge generation and efficient photocurrent generation from both donor and acceptor. Ultrafast transient absorption spectroscopy was used to investigate polaron generation efficiency as well as recombination dynamics. It was determined that the P3HT:FBR blend is highly intermixed, leading to increased charge generation relative to comparative devices with P3HT:PC60BM, but also faster recombination due to a nonideal morphology in which, in contrast to P3HT:PC60BM devices, the acceptor does not aggregate enough to create appropriate percolation pathways that prevent fast nongeminate recombination. Despite this nonoptimal morphology the P3HT:FBR devices exhibit better performance than P3HT:PC60BM devices, used as control, demonstrating that this acceptor shows great promise for further optimization.
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Journal articleSteiner F, Foster S, Losquin A, et al., 2015,
Distinguishing the influence of structural and energetic disorder on electron transport in fullerene multi-adducts
, MATERIALS HORIZONS, Vol: 2, Pages: 113-119, ISSN: 2051-6347- Author Web Link
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- Citations: 43
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Journal articleManke F, Frost JM, Vaissier V, et al., 2015,
Influence of a nearby substrate on the reorganization energy of hole exchange between dye molecules
, PHYSICAL CHEMISTRY CHEMICAL PHYSICS, Vol: 17, Pages: 7345-7354, ISSN: 1463-9076- Author Web Link
- Open Access Link
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- Citations: 12
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Journal articleHermerschmidt F, Kalogirou AS, Min J, et al., 2015,
4<i>H</i>-1,2,6-Thiadiazin-4-one-containing small molecule donors and additive effects on their performance in solution-processed organic solar cells
, JOURNAL OF MATERIALS CHEMISTRY C, Vol: 3, Pages: 2358-2365, ISSN: 2050-7526- Author Web Link
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- Citations: 26
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Journal articleWade J, Steiner F, Niedzialek D, et al., 2014,
Charge mobility anisotropy of functionalized pentacenes in organic field effect transistors fabricated by solution processing
, JOURNAL OF MATERIALS CHEMISTRY C, Vol: 2, Pages: 10110-10115, ISSN: 2050-7526 -
Journal articleGuilbert AAY, Schmidt M, Bruno A, et al., 2014,
Spectroscopic Evaluation of Mixing and Crystallinity of Fullerenes in Bulk Heterojunctions
, ADVANCED FUNCTIONAL MATERIALS, Vol: 24, Pages: 6972-6980, ISSN: 1616-301X- Author Web Link
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- Citations: 26
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Journal articleMadsen MV, Gevorgyan SA, Pacios R, et al., 2014,
Worldwide outdoor round robin study of organic photovoltaic devices and modules
, SOLAR ENERGY MATERIALS AND SOLAR CELLS, Vol: 130, Pages: 281-290, ISSN: 0927-0248- Author Web Link
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- Citations: 21
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Journal articleCredgington D, Liu S-W, Nelson J, et al., 2014,
In Situ Measurement of Energy Level Shifts and Recombination Rates in Subphthalocyanine/C<sub>60</sub> Bilayer Solar Cells
, JOURNAL OF PHYSICAL CHEMISTRY C, Vol: 118, Pages: 22858-22864, ISSN: 1932-7447- Author Web Link
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- Citations: 17
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Journal articleFoster S, Deledalle F, Mitani A, et al., 2014,
Electron Collection as a Limit to Polymer:PCBM Solar Cell Efficiency: Effect of Blend Microstructure on Carrier Mobility and Device Performance in PTB7:PCBM
, ADVANCED ENERGY MATERIALS, Vol: 4, ISSN: 1614-6832- Author Web Link
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- Citations: 148
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Journal articleKirchartz T, Nelson J, 2014,
Device Modelling of Organic Bulk Heterojunction Solar Cells
, MULTISCALE MODELLING OF ORGANIC AND HYBRID PHOTOVOLTAICS, Vol: 352, Pages: 279-324, ISSN: 0340-1022 -
Journal articleVaissier V, Mosconi E, Moia D, et al., 2014,
Effect of Molecular Fluctuations on Hole Diffusion within Dye Monolayers
, CHEMISTRY OF MATERIALS, Vol: 26, Pages: 4731-4740, ISSN: 0897-4756- Author Web Link
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- Citations: 21
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Book chapterEkins-Daukes NJ, Nelson J, 2014,
Quantum Well Solar Cells
, Clean Electricity from Photovoltaics, Editors: Green, Archer, Publisher: Imperial College Press, ISBN: 9781848167674The second edition of Clean Electricity from Photovoltaics, first published in 2001, provides an updated account of the underlying science, technology and market prospects for photovoltaics.
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Journal articleDattani R, Bannock JH, Fei Z, et al., 2014,
A general mechanism for controlling thin film structures in all-conjugated block copolymer: fullerene blends
, JOURNAL OF MATERIALS CHEMISTRY A, Vol: 2, Pages: 14711-14719, ISSN: 2050-7488 -
Journal articleMartinez L, Higuchi S, MacLachlan AJ, et al., 2014,
Improved electronic coupling in hybrid organic-inorganic nanocomposites employing thiol-functionalized P3HT and bismuth sulfide nanocrystals
, Nanoscale, Vol: 6, Pages: 10018-10026, ISSN: 2040-3372In this study, we employ a thiol-functionalized polymer (P3HT-SH) as a leverage to tailor the nanomorphology and electronic coupling in polymer–nanocrystal composites for hybrid solar cells. The presence of the thiol functional group allows for a highly crystalline semiconducting polymer film at low thiol content and allows for improved nanomorphologies in hybrid organic–inorganic systems when employing non-toxic bismuth sulfide nanocrystals. The exciton dissociation efficiency and carrier dynamics at this hybrid heterojunction are investigated through photoluminescence quenching and transient absorption spectroscopy measurements, revealing a larger degree of polaron formation when P3HT-SH is employed, suggesting an increased electronic interaction between the metal chalcogenide nanocrystals and the thiol-functionalized P3HT. The fabricated photovoltaic devices show 15% higher power conversion efficiencies as a result of the improved nanomorphology and better charge transfer mechanism together with the higher open circuit voltages arising from the deeper energy levels of P3HT-SH.
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Journal articleXu W, Zhang X, Hu Q, et al., 2014,
Fluorene-based cathode interlayer polymers for high performance solution processed organic optoelectronic devices
, ORGANIC ELECTRONICS, Vol: 15, Pages: 1244-1253, ISSN: 1566-1199- Author Web Link
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- Citations: 35
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Journal articleEmmott CJM, Ekins-Daukes NJ, Nelson J, 2014,
Dynamic carbon mitigation analysis: the role of thin-film photovoltaics
, ENERGY & ENVIRONMENTAL SCIENCE, Vol: 7, Pages: 1810-1818, ISSN: 1754-5692- Author Web Link
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- Citations: 15
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Journal articleMacKenzie RCI, Goeritz A, Greedy S, et al., 2014,
Theory of Stark spectroscopy transients from thin film organic semiconducting devices
, PHYSICAL REVIEW B, Vol: 89, ISSN: 2469-9950- Author Web Link
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- Citations: 12
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Journal articleFew S, Frost JM, Kirkpatrick J, et al., 2014,
Influence of Chemical Structure on the Charge Transfer State Spectrum of a Polymer:Fullerene Complex
, JOURNAL OF PHYSICAL CHEMISTRY C, Vol: 118, Pages: 8253-8261, ISSN: 1932-7447- Author Web Link
- Cite
- Citations: 60
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Journal articleMacLachlan AJ, O'Mahony FTF, Sudlow AL, et al., 2014,
Solution- Processed Mesoscopic Bi2S3: Polymer Photoactive Layers
, CHEMPHYSCHEM, Vol: 15, Pages: 1019-1023, ISSN: 1439-4235- Author Web Link
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- Citations: 30
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Contact
Jenny Nelson
Professor of Physics
1007, Huxley Building
South Kensington, London, SW7 2AZ