Amir Dindar

A Universal Method to Produce Low–Work Function Electrodes for Organic Electronics

A Sturdy Electrode Coating To operate efficiently, organic devices—such as light-emitting diodes—require electrodes that emit or take up electrons at low applied voltages (that is, have low work functions). Often these electrodes are metals, such as calcium, that are not stable in air or water vapor and have to be protected from environmental damage. Zhou et al. (p. 327; see the Perspective by Helander) report that a coating polymer containing aliphatic amine groups can lower the work functions of various types of electrodes by up to 1.7 electron volts and can be used in a variety of devices. Air-stable, physisorbed polymers containing aliphatic amine groups can improve the efficiency of organic electronic devices. Organic and printed electronics technologies require conductors with a work function that is sufficiently low to facilitate the transport of electrons in and out of various optoelectronic devices. We show that surface modifiers based on polymers containing simple aliphatic amine groups substantially reduce the work function of conductors including metals, transparent conductive metal oxides, conducting polymers, and graphene. The reduction arises from physisorption of the neutral polymer, which turns the modified conductors into efficient electron-selective electrodes in organic optoelectronic devices. These polymer surface modifiers are processed in air from solution, providing an appealing alternative to chemically reactive low–work function metals. Their use can pave the way to simplified manufacturing of low-cost and large-area organic electronic technologies.

Recyclable organic solar cells on cellulose nanocrystal substrates

Solar energy is potentially the largest source of renewable energy at our disposal, but significant advances are required to make photovoltaic technologies economically viable and, from a life-cycle perspective, environmentally friendly, and consequently scalable. Cellulose nanomaterials are emerging high-value nanoparticles extracted from plants that are abundant, renewable, and sustainable. Here, we report on the first demonstration of efficient polymer solar cells fabricated on optically transparent cellulose nanocrystal (CNC) substrates. The solar cells fabricated on the CNC substrates display good rectification in the dark and reach a power conversion efficiency of 2.7%. In addition, we demonstrate that these solar cells can be easily separated and recycled into their major components using low-energy processes at room temperature, opening the door for a truly recyclable solar cell technology. Efficient and easily recyclable organic solar cells on CNC substrates are expected to be an attractive technology for sustainable, scalable, and environmentally-friendly energy production.

Stable Solution‐Processed Molecular n‐Channel Organic Field‐Effect Transistors

A new solution-processable small-molecule containing electron-poor naphthalene diimide and tetrazine moieties has been synthesized. The optimized spin-coated n-channel OFETs on glass substrate shows electron mobility value up to 0.15 cm(2) V(-1) s(-1) . Inkjet-printed OFETs are fabricated in ambient atmosphere on flexible plastic substrates, which exhibits an electron mobility value up to 0.17 cm(2) V(-1) s(-1) and also shows excellent environmental and operational stability.

All-plastic solar cells with a high photovoltaic dynamic range

We report on semitransparent air-processed all-plastic solar cells, fabricated from vacuum-free processes, comprising two polymer electrodes, a polymeric work-function modification layer and a polymer:fullerene photoactive layer. The active layer and the top PEDOT:PSS electrode were prepared by sequential film-transfer lamination on polyethylenimine-modified PEDOT:PSS bottom electrodes. The transferring of films offers ease of layer patterning and the misalignment of defects in the different layers resulting from the additive film transfer lamination process yields high shunt resistance values of 108 ohm cm2. Consequently, all-plastic solar cells fabricated with this process exhibit very low reverse bias dark current and can operate in the photovoltaic quadrant with light irradiance varying over five orders of magnitude. The analysis of the values of the open-circuit voltage as a function of light irradiance over that wide dynamic range points toward an ideality factor of n = 1.82 and a reverse saturation current density of 6.2 × 10−11 A cm−2 for solar cells with an active layer comprised of a blend of poly(3-hexylthiophene) and an indene fullerene bis-adduct.

Organic Photovoltaic Cells with Stable Top Metal Electrodes Modified with Polyethylenimine

Efficient organic photovoltaic cells (OPV) often contain highly reactive low-work-function calcium electron-collecting electrodes. In this work, efficient OPV are demonstrated in which calcium electrodes were avoided by depositing a thin layer of the amine-containing nonconjugated polymer, polyethylenimine (PEIE), between the photoactive organic semiconductor layer and stable metal electrodes such as aluminum, silver, or gold. Devices with structure ITO/poly(3,4-ethylenedioxythiophene):poly(styrenesulfonate) (PEDOT:PSS)/poly(3-hexylthiophene):indene-C60-bis-adduct (P3HT:ICBA)/PEIE/Al demonstrated overall photovoltaic device performance comparable to devices containing calcium electron-collecting electrodes, ITO/PEDOT:PSS/P3HT:ICBA/Ca/Al, with open-circuit voltage of 775±6 mV, short-circuit current density of 9.1±0.5 mA cm(-2), fill factor of 0.65±0.01, and power conversion efficiency of 4.6±0.3%, averaged over 5 devices at 1 sun.

Systematic Reliability Study of Top-Gate p- and n-Channel Organic Field-Effect Transistors

We report on a systematic investigation on the performance and stability of p-channel and n-channel top-gate OFETs, with a CYTOP/Al2O3 bilayer gate dielectric, exposed to controlled dry oxygen and humid atmospheres. Despite the severe conditions of environmental exposure, p-channel and n-channel top-gate OFETs show only minor changes of their performance parameters without undergoing irreversible damage. When correlated with the conditions of environmental exposure, these changes provide new insight into the possible physical mechanisms in the presence of oxygen and water. Photoexcited charge collection spectroscopy experiments provided further evidence of oxygen and water effects on OFETs. Top-gate OFETs also display outstanding durability, even when exposed to oxygen plasma and subsequent immersion in water or operated under aqueous media. These remarkable properties arise as a consequence of the use of relatively air stable organic semiconductors and proper engineering of the OFET structure.

Stable low-voltage operation top-gate organic field-effect transistors on cellulose nanocrystal substrates.

We report on the performance and the characterization of top-gate organic field-effect transistors (OFETs), comprising a bilayer gate dielectric of CYTOP/Al2O3 and a solution-processed semiconductor layer made of a blend of TIPS-pentacene:PTAA, fabricated on recyclable cellulose nanocrystal-glycerol (CNC/glycerol) substrates. These OFETs exhibit low operating voltage, low threshold voltage, an average field-effect mobility of 0.11 cm(2)/(V s), and good shelf and operational stability in ambient conditions. To improve the operational stability in ambient a passivation layer of Al2O3 is grown by atomic layer deposition (ALD) directly onto the CNC/glycerol substrates. This layer protects the organic semiconductor layer from moisture and other chemicals that can either permeate through or diffuse out of the substrate.

Polyvinylpyrrolidone-modified indium tin oxide as an electron-collecting electrode for inverted polymer solar cells

We report on the photovoltaic properties of inverted polymer solar cells that use a polyvinylpyrrolidone (PVP) modified indium tin oxide (ITO) layer as the electron-collecting electrode. An ultrathin PVP layer, prepared by spin-coating, on top of ITO, was used to induce a reduction of its work function, allowing it to act as an electron-collecting electrode. Devices made on pristine ITO showed s-shape current-voltage characteristics, which were removed after exposure to ultraviolet radiation due to a reduction of the work function of ITO. Inverted solar cells with ITO/PVP electrodes yield efficiencies comparable to devices with ITO/ZnO electron-selective electrodes.

Metal-oxide complementary inverters with a vertical geometry fabricated on flexible substrates

We report on the fabrication of p-channel thin film transistors (TFTs) and vertically stacked complementary inverters comprised of a p-channel copper oxide TFT on top of an n-channel indium gallium zinc oxide TFT fabricated on a flexible polyethersulfone substrate. The p- and n-channel TFTs showed saturation mobility values of 0.0022 and 1.58 cm2/Vs, respectively, yielding inverters with a gain of 120 V/V. This level of performance was achieved by reducing the copper oxide channel thickness, allowing oxygen diffusion into the copper oxide layer at medium processing temperature (150 °C).

Self-(Un)rolling Biopolymer Microstructures: Rings, Tubules, and Helical Tubules from the Same Material†

We have demonstrated the facile formation of reversible and fast self-rolling biopolymer microstructures from sandwiched active-passive, silk-on-silk materials. Both experimental and modeling results confirmed that the shape of individual sheets effectively controls biaxial stresses within these sheets, which can self-roll into distinct 3D structures including microscopic rings, tubules, and helical tubules. This is a unique example of tailoring self-rolled 3D geometries through shape design without changing the inner morphology of active bimorph biomaterials. In contrast to traditional organic-soluble synthetic materials, we utilized a biocompatible and biodegradable biopolymer that underwent a facile aqueous layer-by-layer (LbL) assembly process for the fabrication of 2D films. The resulting films can undergo reversible pH-triggered rolling/unrolling, with a variety of 3D structures forming from biopolymer structures that have identical morphology and composition.