Samuel D. Collins

High‐Efficiency Polymer Solar Cells Enhanced by Solvent Treatment

A significant enhancement of efficiency in thieno[3,4-b]-thiophene/benzodithiophene:[6,6]-phenyl C71-butyric acid methyl ester (PTB7:PC70 BM) solar cells can be achieved by methanol treatment. The effects of methanol treatment are shown in an improvement of built-in voltage, a decrease in series resistance, an enhanced charge-transport property, an accelerated and enlarged charge extraction, and a reduced charge recombination, which induce a simultaneous enhancement in open-circuit voltage (Voc), short-circuit current (Jsc), and fill factor (FF) in the devices.

Polymer Homo‐Tandem Solar Cells with Best Efficiency of 11.3%

Rational materials design and interface engineering are both essential to realize a high performance for tandem cells. Two identical bulk heterojunctions are connected in series using novel interconnection layers combining pH-neutral conjugated polyelectrolytes and a thin film of ZnO nanoparticles by a solution process. The best performing tandem cells achieve a power conversion efficiency of 11.3%, with 25% enhancement in efficiency compared with single cells, which arises primarily from the increased light absorption.

Conductive Conjugated Polyelectrolyte as Hole-Transporting Layer for Organic Bulk Heterojunction Solar Cells

Poly(3,4-ethylenedioxythiophene):poly(styrenesulfonate) (PEDOT:PSS) has been extensively used as the hole-transporting layer (HTL) in bulk heterojunction (BHJ) solar cells, however, its anisotropic electrical conduction and intrinsic acidic nature generally limit the device performance. Here we demonstrate the application of a water/alcohol soluble CPE (CPE-K) as HTLs in BHJ solar cells, achieving a PCE up to 8.2%. The more superior and uniform vertical electrical conductivity found in CPE-K reduces the series resistance and provides efficient hole extraction.

Enhanced Efficiency of Single and Tandem Organic Solar Cells Incorporating a Diketopyrrolopyrrole‐Based Low‐Bandgap Polymer by Utilizing Combined ZnO/Polyelectrolyte Electron‐Transport Layers

Power conversion efficiency up to 8.6% is achieved for a solution-processed tandem solar cell based on a diketopyrrolopyrrole-containing polymer as the low-bandgap material after using a thin polyelectrolyte layer to modify the electron-transport ZnO layers, indicating that interfacial engineering is a useful approach to further enhancing the efficiency of tandem organic solar cells.

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).

DNA Interlayers Enhance Charge Injection in Organic Field‐Effect Transistors

By inserting DNA interlayers beneath the Au contact, the contact resistance of PC(70) BM field-effect transistorss is reduced by approximately 30 times at a gate bias of 20 V. The electron and hole mobilities of ambipolar diketopyrrolopyrrole transistors are increased by one order of magnitude with a reduction of the threshold voltage from 12 to 6.5 V.

Interplay of solvent additive concentration and active layer thickness on the performance of small molecule solar cells.

A relationship between solvent additive concentration and active layer thickness in small-molecule solar cells is investigated. Specifically, the additive concentration must scale with the amount of semiconductor material and not as absolute concentration in solution. Devices with a wide range of active layers with thickness up to 200 nm can readily achieve efficiencies close to 6% when the right concentration of additive is used.

All-conjugated triblock polyelectrolytes.

All-conjugated triblock polyfluorenes with well-defined molecular weights and low polydispersities are synthesized via chain-growth Suzuki-Miyaura polymerization. Ionization of pendant alkylbromide chains by pyridine affords amphiphilic triblock polyelectrolytes with neutral/charged/neutral or charged/neutral/charged segments. The immiscible blocks lead to aggregation in polar and nonpolar solvents, and to complex surface morphologies depending on the polarity of the substrate. These triblock polyelectrolytes can also be used as interfacial layers in polymer light-emitting diodes to facilitate electron injection from aluminum.

Enhancement of the Photoresponse in Organic Field-Effect Transistors by Incorporating Thin DNA Layers**

A mechanistic study of the DNA interfacial layer that enhances the photoresponse in n-type field-effect transistors (FET) and lateral photoconductors using a solution-processed fullerene derivative embedded with disperse-red dye, namely PCBDR, is reported. Incorporation of the thin DNA layer simultaneously leads to increasing the electron injection from non-Ohmic contacts into the PCBDR active layer in dark and to increasing the photocurrent under irradiation. Such features lead to the observation of the enhancement of the photoresponsivity in PCBDR FETs up to 10(3) . Kelvin probe microscopy displays that in the presence of the DNA layer, the surface potential of PCBDR has a greater change in response to irradiation, which is rationalized by a larger number of photoinduced surface carriers. Transient absorption spectroscopy confirms that the increase in photoinduced carriers in PCBDR under irradiation is primarily ascribed to the increase in exciton dissociation rates through the PCBDR/DNA interface and this process can be assisted by the interfacial dipole interaction.

Rectifying Electrical Noise with an Ionic‐Organic Ratchet

Electronic ratchets can rectify AC signals that are extracted from unpredictable energy fluctuations. A device is presented with ratchet-like current-voltage characteristics, which delivers record high electrical currents of 2.6 and 1.7 μA when driven with an AC signal of square wave and random amplitude, respectively. The device is based on a poly(3-hexylthiophene-2,5-diyl):salt blend, which acquires rectification properties after a voltage stress in a transistor configuration.