interface ͉ photovoltaic ͉ solar energy

We report the fabrication of organic bulk-heterojunction solar cells based, for the first time, on squaraine/PCBM blends. The most efficient device, solution-processed in air, exhibits J(sc) = 5.70 mA/cm(2), V(oc) = 0.62 V, fill-factor = 0.35, and power conversion efficiency = 1.24%, one of the highest to date for a small molecule solution-processed bulk-heterojunction cell.

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The effects of anode/active layer interface modification in bulk‐heterojunction organic photovoltaic (OPV) cells is investigated using poly(3,4‐ethylenedioxythiophene):poly(styrene sulfonate) (PEDOT:PSS) and/or a hole‐transporting/electron‐blocking blend of 4,4′‐bis[(p‐trichlorosilylpropylphenyl)‐phenylamino]biphenyl (TPDSi2) and poly[9,9‐dioctylfluorene‐co‐N‐[4‐(3‐methylpropyl)]‐diphenylamine] (TFB) as interfacial layers (IFLs). Current–voltage data in the dark and AM1.5G light show that the TPDSi2:TFB IFL yields MDMO‐PPV:PCBM OPVs with substantially increased open‐circuit voltage (Voc), power conversion efficiency, and thermal stability versus devices having no IFL or PEDOT:PSS. Using PEDOT:PSS and TPDSi2:TFB together in the same cell greatly reduces dark current and produces the highest Voc (0.91 V) by combining the electron‐blocking effects of both layers. ITO anode pre‐treatment was investigated by X‐ray photoelectron spectroscopy to understand why oxygen plasma, UV ozone, and solvent cleaning markedly affect cell response in combination with each IFL. O2 plasma and UV ozone treatment most effectively clean the ITO surface and are found most effective in preparing the surface for PEDOT:PSS deposition; UV ozone produces optimum solar cells with the TPDSi2:TFB IFL. Solvent cleaning leaves significant residual carbon contamination on the ITO and is best followed by O2 plasma or UV ozone treatment.

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This contribution describes the design, synthesis, characterization, and organic photovoltaic (OPV) device implementation of a novel interfacial layer (IFL) for insertion between the anode and active layer of poly(3-hexylthiophene) (P3HT):[6,6]-phenyl-C 61butyric acid methyl ester (PCBM) bulk-heterojunction solar cells. The IFL precursor, 5,5′-bis[(p-trichlorosilylpropylphenyl)phenylamino]-2,2′-bithiophene (PABTSi 2 ), covalently anchors to the Sn-doped In 2 O 3 (ITO) surface via the -SiCl 3 groups and incorporates a bithiophene unit to align the highest occupied molecular orbital (HOMO) energy with that of P3HT (5.0 eV). The synthesis and subsequent electrochemical analysis of PABTSi 2 indicates a HOMO energy of 4.9 eV, while the lowest uoccupied molecular orbital level remains sufficiently high, at 2.2 eV, to effectively block electron leakage to the OPV ITO anode. For the P3HT:PCBM OPV fabrication, PABTSi 2 is used as a spin-coated cross-linked (via -SiCl 3 hydrolysis and condensation) 1:2 blend with poly [9,9-dioctylfluorene-co-N-[4-(3methylpropyl)]-diphenylamine] (TFB). Such devices exhibit an average power conversion efficiency of 3.14%, a fill factor of 62.7%, an open-circuit voltage of 0.54 V, and a short-circuit current of 9.31 mA/cm 2 , parameters rivaling those of optimized PEDOT:PSSbased devices.

The aims of this paper are twofold: first, to gain a fuller understanding of factors that foster community cohesion and contribute to the residents' social and economic well‐being; and, second, to move beyond previous research that used larger spatial units such as states, counties, or aggregates of counties and to focus instead on American small towns (population 2,500–20,000). The data on small towns are drawn from public‐use files and from confidential microdata from various economic censuses. From these sources we construct measures of locally oriented firms, self‐employment, business establishments that serve as gathering places, and associations. The local capitalism and civic engagement variables generally perform as hypothesized; in some cases they are related quite strongly to civic welfare outcomes such as income levels, poverty rates, and nonmigration rates. We discuss the advantages and disadvantages of working with place‐level data and suggest some strategies for subsequent work on small towns and other incorporated places.

The functionality of NiO interfacial layers in enhancing bulk heterojunction (BHJ) organic photovoltaic (OPV) cell performance is investigated by integrated characterization of the electrical properties, microstructure, electronic structure, and optical properties of thin NiO films grown on glass/ITO electrodes. These NiO layers are found to be advantageous in BHJ OPV applications due to favorable energy band levels, interface passivation, p-type character, crystallinity, smooth surfaces, and optical transparency. The NiO overlayers are fabricated via pulsed-laser deposition and found to have a work function of ∼5.3 eV. They are investigated by both topographic and conductive atomic force microscopy and shown to passivate interfacial charge traps. The films also have an average optical transparency of >80% in the visible range, crucial for efficient OPV function, and have a near-stoichiometric Ni:O surface composition. By grazing-incidence X-ray diffraction, the NiO thin films are shown to grow preferentially in the (111) direction and to have the fcc NaCl crystal structure. Diodes of pÀn structure and first-principles electronic structure calculations indicate that the NiO interlayer is preferentially conductive to holes, with a lower hole charge carrier effective mass versus that of electrons. Finally, the implications of these attributes in advancing efficiencies for state-of-the-art OPV systems-in particular, improving the open circuit voltage (V OC )-are discussed.