Christopher J. Takacs

Solution-processed small-molecule solar cells with 6.7% efficiency

Organic photovoltaic devices that can be fabricated by simple processing techniques are under intense investigation in academic and industrial laboratories because of their potential to enable mass production of flexible and cost-effective devices. Most of the attention has been focused on solution-processed polymer bulk-heterojunction (BHJ) solar cells. A combination of polymer design, morphology control, structural insight and device engineering has led to power conversion efficiencies (PCEs) reaching the 6-8% range for conjugated polymer/fullerene blends. Solution-processed small-molecule BHJ (SM BHJ) solar cells have received less attention, and their efficiencies have remained below those of their polymeric counterparts. Here, we report efficient solution-processed SM BHJ solar cells based on a new molecular donor, DTS(PTTh(2))(2). A record PCE of 6.7% under AM 1.5 G irradiation (100 mW cm(-2)) is achieved for small-molecule BHJ devices from DTS(PTTh(2))(2):PC(70)BM (donor to acceptor ratio of 7:3). This high efficiency was obtained by using remarkably small percentages of solvent additive (0.25% v/v of 1,8-diiodooctane, DIO) during the film-forming process, which leads to reduced domain sizes in the BHJ layer. These results provide important progress for solution-processed organic photovoltaics and demonstrate that solar cells fabricated from small donor molecules can compete with their polymeric counterparts.

Inverted Polymer Solar Cells Integrated with a Low‐Temperature‐Annealed Sol‐Gel‐Derived ZnO Film as an Electron Transport Layer

BHJ solar cells are typically fabricated with a transparent conductive anode (e.g. indium tin oxide, ITO), a low-work-function metal cathode (e.g., Al, Ca), and an active layer (a mixture of conjugated polymer and fullerene derivative) sandwiched between the anode and cathode. The BHJ layer and cathode dramatically affect the stability. In particular, the cathode is susceptible to degradation by oxygen and water vapor. Poly(3,4ethylenedioxythiophene):poly(styrene sulfonate) (PEDOT:PSS) is often used as an anode buffer layer. Long-term stability is a problem because PEDOT:PSS is hygroscopic and acidic. [ 17–21 ]

Efficient, Air-Stable Bulk Heterojunction Polymer Solar Cells Using MoOx as the Anode Interfacial Layer

The use of molybdenum oxide as the anode interfacial layer in conventional bulk heterojunction polymer solar cells leads to an improved power conversion efficiency and also dramatically increases the device stability. This indicates that the engineering of improved anode interface materials is an important method by which to fabricate efficient and stable polymer solar cells.

Effect of processing additive on the nanomorphology of a bulk heterojunction material.

The bulk heterojunction (BHJ) material Si-PDTBT:PC(70)BM is sensitive to the use of a small amount of 1-chloronaphthalene (CN) as a processing additive; CN as a cosolvent (e.g., 4% in chlorobenzene) causes in a factor of 2 increase in the power conversion efficiency of BHJ solar cells. The morphology of the BHJ material, prepared with and without the CN additive is studied with top-down transmission electron microscopy, cross-sectional transmission electron microscopy, and atomic force microscopy. The improved performance is the result of changes in the nanoscale morphology. Field-effect transistor measurements are consistent with the observed changes in morphology.

Solubility-limited extrinsic n-type doping of a high electron mobility polymer for thermoelectric applications.

The thermoelectric properties of a highperformance electron-conducting polymer, (P(NDIOD-T2), extrinsically doped with dihydro-1H-benzoimidazol-2-yl (NDBI) derivatives, are reported. The highest thermoelectric power factor that has been reported for a solution-processed n-type polymer is achieved; and it is concluded that engineering polymerdopant miscibility is essential for the development of organic thermoelectrics.

Spontaneous Formation of Bulk Heterojunction Nanostructures: Multiple Routes to Equivalent Morphologies

Bulk heterojunction (BHJ) layers based on poly(3-hexylthiophene-2,5-diyl) (P3HT) and [6,6]-phenyl C61 butyric acid methyl ester (PCBM) were fabricated by two methods: codeposition of P3HT/PCBM from a common solvent (conventional BHJ) and by sequential, layer-by-layer deposition of P3HT/PCBM from separate solvents (layer-evolved BHJ). Thermally annealed layer-evolved BHJ solar cells show power conversion efficiencies and electron/hole mobilities comparable to conventional BHJ solar cells. The nanomorphology of both active layers is compared in situ by transmission electron microscopy (TEM) using a multilayer cross-sectional sample architecture. No significant difference is observed between the nanomorphology of the conventional BHJ and layer-evolved BHJ material implying that the bulk heterojunction forms spontaneously and that it is the lowest energy state of the two component system.

Harvesting the Full Potential of Photons with Organic Solar Cells

A low-bandgap polymer:fullerene blend that has significantly reduced energetic losses from photon absorption to VOC is described. The charge-transfer state and polymer singlet are of nearly equal energy, yet the short-circuit current still reaches 14 mA cm(-2).

Role of trace impurities in the photovoltaic performance of solution processed small-molecule bulk heterojunction solar cells

The final step in the preparation of ppp-DTS(PTTh222)222 involves end capping of the PT-DTS-PT core with 2-hexylbithiophene units via a microwave assisted Stille cross coupling reaction. Methyl transfer (instead of 2-hexylbithiophene transfer) can occur leading to the formation of (MePT)DTS(PTTh22). Although (MePT)DTS(PTTh22) is difficult to separate from the ppp-DTS(PTTh222)222 product via column chromatography, it is readily extracted using hexanes solvent to give absolute ppp-DTS(PTTh222)222. Trace impurities of (MePT)DTS(PTTh22) in BHJ solar cells fabricated from synthesis batches of ppp-DTS(PTTh222)222 significantly influence the photovoltaic properties, causing a ∼50% reduction in efficiency and affecting all of the relevant device parameters (Jsc, Voc and FF). From a broader perspective, despite molecular design, the suitability of a material for efficient devices is often only determined by trial and error in the device processing laboratory. As shown by the data presented in this publication, promising materials found to be unsuitable for device applications may suffer from highly dilute impurities that act to increase carrier recombination.

Enhancing Fullerene-Based Solar Cell Lifetimes by Addition of a Fullerene Dumbbell†

Cost-effective, solution-processable organic photovoltaics (OPV) present an interesting alternative to inorganic silicon-based solar cells. However, one of the major remaining challenges of OPV devices is their lack of long-term operational stability, especially at elevated temperatures. The synthesis of a fullerene dumbbell and its use as an additive in the active layer of a PCDTBT:PCBM-based OPV device is reported. The addition of only 20 % of this novel fullerene not only leads to improved device efficiencies, but more importantly also to a dramatic increase in morphological stability under simulated operating conditions. Dynamic secondary ion mass spectrometry (DSIMS) and TEM are used, amongst other techniques, to elucidate the origins of the improved morphological stability.

Fractal fronts of diffusion in microgravity

Spatial scale invariance represents a remarkable feature of natural phenomena. A ubiquitous example is represented by miscible liquid phases undergoing diffusion. Theory and simulations predict that in the absence of gravity diffusion is characterized by long-ranged algebraic correlations. Experimental evidence of scale invariance generated by diffusion has been limited, because on Earth the development of long-range correlations is suppressed by gravity. Here we report experimental results obtained in microgravity during the flight of the FOTON M3 satellite. We find that during a diffusion process a dilute polymer solution exhibits scale-invariant concentration fluctuations with sizes ranging up to millimetres, and relaxation times as large as 1,000 s. The scale invariance is limited only by the finite size of the sample, in agreement with recent theoretical predictions. The presence of such fluctuations could possibly impact the growth of materials in microgravity.