The influence of siloxane side-chains on the photovoltaic performance of a conjugated polymer

The effect of gradually replacing the branched alkyl side chains of a diketopyrrolopyrrole (DPP) conjugated polymer by linear side chains containing branched siloxane end groups on the photovoltaic performance of blends of these polymers with a common fullerene acceptor is investigated. With an increasing proportion of siloxane side chains, the molecular weight and solubility of the polymers decreases. While the siloxane containing polymers exhibit a higher hole mobility in field-effect transistors, their performance in solar cells is less than the polymer with only alkyl sides chains. Using grazing-incidence wide-angle X-ray scattering, transmission electron microscopy, and fluorescence spectroscopy we identify two main reasons for the reduced performance of siloxane containing polymers in solar cells. The first one is a somewhat coarser phase-separated morphology with slightly wider polymer fibers. This is unexpected as often the fiber width is inversely correlated with polymer solubility. The second one is stronger non-radiative decay of the pristine polymers containing siloxane side chains

Effect of Different Bromine Sources on the Dual Cation Mixed Halide Perovskite Solar Cells

Recent research has shown that perovskite solar cells with a mixed dual A-cation have much better structural stability without loss of efficiency than single cation devices. Mixed cation perovskites create a lot of questions about the salts being used for the formation of the best-quality layer. Here, we have investigated three sources of bromide in the perovskite absorption layer, using lead bromide (PbBr2), formamidinium bromide (FABr), and cesium bromide (CsBr). The experimental results have shown better performance for FABr and CsBr sources of bromide in comparison to the regularly used PbBr2. This effect has been explained with the complex species present in the not-annealed perovskite films which changes the defect states during the crystallization of the absorber layer. It has been found with numerical simulations that the observed phenomenon directly impacts the rates of the trap-assisted recombination. The results of this study are one more step forward in understanding the physics behind the crystallization process which is crucial in further improvement of the perovskite solar cells

Analysis of the Performance of Narrow-Bandgap Organic Solar Cells Based on a Diketopyrrolopyrrole Polymer and a Nonfullerene Acceptor

The combination of narrow-bandgap diketopyrrolopyrrole (DPP) polymers and nonfullerene acceptors (NFAs) seems well-matched for solar cells that exclusively absorb in the near infrared but they rarely provide high efficiency. One reason is that processing of the active layer is complicated by the fact that DPP-based polymers are generally only sufficiently soluble in chloroform (CF), while NFAs are preferably processed from halogenated aromatic solvents. By using a ternary solvent system consisting of CF, 1,8-diiodooctane (DIO), and chlorobenzene (CB), the short-circuit current density is increased by 50% in solar cells based on a DPP polymer (PDPP5T) and a NFA (IEICO-4F) compared to the use of CF with DIO only. However, the open-circuit voltage and fill factor are reduced. As a result, the efficiency improves from 3.4 to 4.8% only. The use of CB results in stronger aggregation of IEICO-4F as inferred from two-dimensional grazing-incidence wide-angle X-ray diffraction. Photo- A nd electroluminescence and mobility measurements indicate that the changes in performance can be ascribed to a more aggregated blend film in which charge generation is increased but nonradiative recombination is enhanced because of reduced hole mobility. Hence, while CB is essential to obtain well-ordered domains of IEICO-4F in blends with PDPP5T, the morphology and resulting hole mobility of PDPP5T domains remain suboptimal. The results identify the challenges in processing organic solar cells based on DPP polymers and NFAs as near-infrared absorbing photoactive layers

Phase separation of VO2 and SiO2 on SiO2-Coated float glass yields robust thermochromic coating with unrivalled optical properties

Vanadium dioxide displays thermochromic properties based on its structural phase transition from monoclinic VO2 (M) to rutile VO2 (R) and vice versa, and the accompanying reversible metal-insulator transition. We developed a single layer coating comprising VO2 (M) and SiO2. We applied the coating from an alcoholic solution comprising vanadium(IV) oxalate complex and pre-oligomerized tetra ethoxy silane to SiO2-coated float glass using dip coating, and thermally annealed the dried xerocoat in a two-step process. The addition of SiO2 as coating matrix resulted in non-scattering coatings with low surface roughness and random distribution of VO2 nanodomains (≤200 nm). Furthermore, the formation of the coating, comprising a phase separation yielding SiO2 and VO2 nanodomains during the thermal anneal, was studied in detail. The coating displays unrivalled optical properties, combining high visible light transmission Tvis > 60% and large solar modulation ΔTsol ≥ 10%. When applied in insulating glass units, the coating has a positive impact on energy savings for heating and cooling of buildings in intermediate climates, which we demonstrated through building energy simulations. For a typical house in the Netherlands, energy savings up to 24% were obtained. In addition, we demonstrate a coating stability comparable to current energy-efficient window coatings during processing into and in insulating glass units through (accelerated) life time tests

Precise Control of Phase Separation Enables 12% Efficiency in All Small Molecule Solar Cells

Compared to conjugated polymers, small-molecule organic semiconductors present negligible batch-to-batch variations, but presently provide comparatively low power conversion efficiencies (PCEs) in small-molecular organic solar cells (SM-OSCs), mainly due to suboptimal nanomorphology. Achieving precise control of the nanomorphology remains challenging. Here, two new small-molecular donors H13 and H14, created by fluorine and chlorine substitution of the original donor molecule H11, are presented that exhibit a similar or higher degree of crystallinity/aggregation and improved open-circuit voltage with IDIC-4F as acceptor. Due to kinetic and thermodynamic reasons, H13-based blend films possess relatively unfavorable molecular packing and morphology. In contrast, annealed H14-based blends exhibit favorable characteristics, i.e., the highest degree of aggregation with the smallest paracrystalline π–π distortions and a nanomorphology with relatively pure domains, all of which enable generating and collecting charges more efficiently. As a result, blends with H13 give a similar PCE (10.3%) as those made with H11 (10.4%), while annealed H14-based SM-OSCs have a significantly higher PCE (12.1%). Presently this represents the highest efficiency for SM-OSCs using IDIC-4F as acceptor. The results demonstrate that precise control of phase separation can be achieved by fine-tuning the molecular structure and film formation conditions, improving PCE and providing guidance for morphology design

Precise Control of Phase Separation Enables 12% Efficiency in All Small Molecule Solar Cells

Compared to conjugated polymers, small-molecule organic semiconductors present negligible batch-to-batch variations, but presently provide comparatively low power conversion efficiencies (PCEs) in small-molecular organic solar cells (SM-OSCs), mainly due to suboptimal nanomorphology. Achieving precise control of the nanomorphology remains challenging. Here, two new small-molecular donors H13 and H14, created by fluorine and chlorine substitution of the original donor molecule H11, are presented that exhibit a similar or higher degree of crystallinity/aggregation and improved open-circuit voltage with IDIC-4F as acceptor. Due to kinetic and thermodynamic reasons, H13-based blend films possess relatively unfavorable molecular packing and morphology. In contrast, annealed H14-based blends exhibit favorable characteristics, i.e., the highest degree of aggregation with the smallest paracrystalline π–π distortions and a nanomorphology with relatively pure domains, all of which enable generating and collecting charges more efficiently. As a result, blends with H13 give a similar PCE (10.3%) as those made with H11 (10.4%), while annealed H14-based SM-OSCs have a significantly higher PCE (12.1%). Presently this represents the highest efficiency for SM-OSCs using IDIC-4F as acceptor. The results demonstrate that precise control of phase separation can be achieved by fine-tuning the molecular structure and film formation conditions, improving PCE and providing guidance for morphology design

Efficient thick-film polymer solar cells with enhanced fill factors via increased fullerene loading

Developing effective methods to make efficient bulk-heterojunction polymer solar cells at roll-to-roll relevant active layer thickness is of significant importance. We investigate the effect of fullerene content in polymer:fullerene blends on the fill factor (FF) and on the performance of thick-film solar cells for four different donor polymers PTB7-Th, PDPP-TPT, BDT-FBT-2T, and poly[5,5′-bis(2-butyloctyl)-(2,2′-bithiophene)-4,4′-dicarboxylate-alt-5,5′-2,2′-bithiophene] (PDCBT). At a few hundreds of nanometers thickness, increased FFs are observed in all cases and improved overall device performances are obtained except for PDCBT upon increasing fullerene content in blend films. This fullerene content effect was studied in more detail by electrical and morphological characterization. The results suggest enhanced electron mobility and suppressed bimolecular recombination upon increasing fullerene content in thick polymer:fullerene blend films, which are the result of larger fullerene aggregates and improved interconnectivity of the fullerene phases that provide continuous percolating pathways for electron transport in thick films. These findings are important because an effective and straightforward method that enables fabricating efficient thick-film polymer solar cells is desirable for large-scale manufacturing via roll-to-roll processing and for multijunction devices