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In this contribution, we report on bulk-heterojunction solar cells using a solution-processable neutral green conjugated copolymer based on 3,4-dioxythiophene and 2,1,3-benzothiadiazole as the donor and [6,6]phenyl-C61 butyric acid methyl ester (PCBM) as the acceptor. We have found that the short-circuit current is very sensitive to the composition of the donor-acceptor blend and it increases with increasing acceptor concentration. The device with a donor-acceptor ratio of 1:8 gives the best performance with a short-circuit current of 5.56 mA/cm(2), an open-circuit voltage of 0.77 V, and a power conversion efficiency of 1.9% under AM 1.5 solar illumination. The incident photon-to-current efficiency (IPCE) of the green solar cells shows two bands, one with a maximum of 57% in the UV region corresponding to absorption of PCBM and a second one with a maximum of 42% at longer wavelengths corresponding to the absorption of the green polymer.
ACS Appl Mater Interfaces 2009 Jun
PMID:Efficient green solar cells via a chemically polymerizable donor-acceptor heterocyclic pentamer. 2035 5

We report herein a detailed study of the thermal and hole-transport properties of poly[2,7-(9,9-dihexylfluorene)-alt-bithiophene] (F6T2) and its photovoltaic performance in a bulk-heterojunction (BHJ) solar cell. This crystalline polymer has a high weight-average molecular weight (M(w) = 52 400) with a polydispersity index of 1.99. With a band gap of 2.36 eV, F6T2 exhibits strong absorption in the 300-500 nm region. BHJ solar cells blending F6T2 with [6,6]-phenyl-C(61)-butyric acid methyl ester (PCBM) (1:3 weight ratio) as the active layer present a high open-circuit voltage (V(oc) approximately 0.9 V) and a promising power conversion efficiency of 2.4% under simulated solar light AM1.5G (100 mW/cm(2)). Furthermore, F6T2 shows sufficient hole mobility [ca. 8.4 x 10(-5) cm(2)/(V s) at 310 K and 2.5 x 10(5) V/cm applied electric field] by a time-of-flight transient photocurrent technique, allowing efficient charge extraction and a good fill factor for solar cell application. Nanoscale phase separation was observed in F6T2/PCBM films with a surface roughness lower than 60 nm.
ACS Appl Mater Interfaces 2009 Jul
PMID:Hole transport in Poly[2,7-(9,9-dihexylfluorene)-alt-bithiophene] and high-efficiency polymer solar cells from its blends with PCBM. 2035 50

We have used ultraviolet photoelectron spectroscopy to investigate the energy-level and band alignment near the anode for poly(3-hexylthiophene)/[6,6]-phenyl-C(61)-butyric acid methyl ester (P3HT/PCBM)-based organic solar cells. Analysis of various batches of indium-tin oxide (ITO) revealed that the photoresist residues had a strong effect, reducing the work functions of ITO (Phi(ITO)) by as much as 0.61 eV. The energy-level alignment of poly(3,4-ethylenedioxythiophene)/ITO (Phi(PEDOT/ITO)) interfaces obey the Mott-Schottky rule at values of Phi(ITO) of less than 3.92 eV. In contrast, we observed Fermi-level pinning for the blend/PEDOT interfaces at values of Phi(PEDOT/ITO) greater than 4.26 eV; this finding is consistent with a previous report that the positive polaronic energy of P3HT is equal to 4.0 eV. Consequently, we suspect that the similar efficiency levels and open-circuit voltages of devices prepared from various ITO samples were due mainly to the constant interfacial energy barrier at the blend/PEDOT interface with Fermi-level pinning.
ACS Appl Mater Interfaces 2009 Apr
PMID:Energy level alignment at the anode of poly(3-hexylthiophene)/fullerene-based solar cells. 2035 97

Significant conductivity enhancement was observed on transparent and conductive poly(3,4-ethylene dioxythiophene):poly(styrene sulfonate) (PEDOT:PSS) films after a treatment with organic and inorganic acids, including acetic acid, propionic acid, butyric acid, oxalic acid, sulfurous acid, and hydrochloric acid. The conductivity could be enhanced from 0.2 to over 200 S cm(-1), that is, by a factor of more than 1000. The conductivity enhancement was dependent on the structure of the acids and the experimental conditions during the treatment, such as the acid concentration and the temperature. The optimal temperature was in the range of 120 to 160 degrees C. The resistance dropped rapidly when a PEDOT:PSS film was treated with acid solution of high concentration, whereas it gradually increased and then decreased when it was treated with an acid solution of low concentration. The mechanism for this conductivity enhancement was studied by various chemical and physical characterizations. The temperature dependence of conductivity indicates that the energy barrier for charge hopping among the PEDOT chains become lower in the highly conductive PEDOT:PSS film after the acid treatment. The ultraviolet-visible-near-infrared (UV-vis-NIR) absorption spectroscopy, the X-ray photoelectron spectroscopy (XPS) and scanning electron microscopy (SEM) indicate the loss of polystyrene sulfonic acid (PSSH) chains from the PEDOT:PSS film after the acid treatment, and the atomic force microscopy (AFM) suggest conformational change of the polymer chains. Therefore, the conductivity enhancement is attributed to the loss of PSSH chains from the PEDOT:PSS film and the conformational change of the PEDOT chains, which are induced by the acids.
ACS Appl Mater Interfaces 2010 Feb
PMID:Significant conductivity enhancement of conductive poly(3,4-ethylenedioxythiophene): poly(styrenesulfonate) films through a treatment with organic carboxylic acids and inorganic acids. 2035 94

We present herein efficient bulk heterojunction (BHJ) solar cells via mixing poly[2,7-(9,9-dihexylfluorene)-alt-bithiophene] (F6T2) and 6,6-phenyl C61 butyric acid methyl ester (PCBM) with variable weight ratios. The photo-physics and morphology of F6T2:PCBM blend films and the electrical characteristics of their corresponding single cells were studied in details by changing PCBM concentration. The complete photoluminescence quenching of F6T2 emission occurs with only a small fraction of PCBM blended, demonstrating effective photoinduced charge transfer between F6T2 and PCBM. Morphology images from atomic force microscopy and scanning electron microscopy (SEM) reveal that the phase separation in F6T2:PCBM blend films becomes pronounced with the increase of PCBM concentration, resulting in the increased fill factor from 25.2% (1:1) to 56.9% (1:6). A SEM image also shows the phase separation is within the range of 10 - 20 nm. With the optimized F6T2:PCBM weight ratio (1:2), the single cell exhibits a highest power conversion efficiency of 2.46% due to the balance of light absorption and charge transport. Finally, the polymer-small molecule tandem cells are constructed using F6T2:PCBM BHJ as the bottom cell and copper phthalocyanine (CuPc):fullerene (C(60)) as the top cell. The open-circuit voltage (V(oc)) of tandem cell (1.27 V) is equal to the summation of the V(oc) values of the bottom cell (0.86 V) and the top cell (0.43 V).
ACS Appl Mater Interfaces 2010 Mar
PMID:Efficient bulk heterojunction solar cells with poly[2,7-(9,9-dihexylfluorene)-alt-bithiophene] and 6,6-phenyl C61 butyric acid methyl ester blends and their application in tandem cells. 2035 88

The donor, 2,4-bis[4-(N,N-diisobutylamino)-2,6-dihydroxyphenyl] squaraine (SQ) is used with the acceptor, [6,6]-phenyl C70 butyric acid methyl ester (PC70BM) to result in efficient, solution-processed, small-molecule bulk heterojunction photovoltaic cells. The distribution of the donor nanoparticles in the acceptor matrix as a function of relative concentrations results in a trade-off between exciton dissociation and hole mobility (and hence, cell series resistance). A bulk heterojunction solar cell consisting of an active region with a component ratio of SQ to PC70BM of 1:6 has a power conversion efficiency of 2.7 +/- 0.1% with a 8.85 +/- 0.22 mA/cm(2) short-circuit current density and an open-circuit voltage of 0.89 +/- 0.01 V obtained under simulated 1 sun (100 mW/cm(2)) air mass 1.5 global (AM1.5 G) solar illumination. This is a decrease from 3.3 +/- 0.3% at 0.2 sun intensity, and is less than that of a control planar heterojunction SQ/C60 cell with 4.1 +/- 0.2% at 1 sun, suggesting that the nanoparticle morphology introduces internal resistance into the solution-based thin film. The nanomorphology and hole mobility in the films is strongly dependent on the SQ-to-PC70BM ratio, increasing by greater than 2 orders of magnitude as the ratio increases from 28% to 100% SQ.
ACS Nano 2010 Apr 27
PMID:Solution-processed squaraine bulk heterojunction photovoltaic cells. 2035 89

The charge mobility in a new hole transporting polymer, poly(2,6-bis(thiophene-2-yl)-3,5-dipentadecyldithieno[3,2-b;2',3'-d]thiophene) (PBTDTT-15), and its blend with (6,6)-phenyl-C(70)-butyric acid methyl ester (PC(70)BM) in a weight ratio of 1:3 at ambient atmosphere condition was investigated using time-of-flight (TOF) photoconductivity and photoinduced charge extraction by linearly increasing voltage (PhotoCELIV) techniques. The bulk heterojunction based photovoltaic (PV) blend (PBTDTT-15:PC(70)BM (1:3)) exhibited a promising power conversion efficiency (PCE) of 3.23% under air mass 1.5 global (AM 1.5G) illumination of 100mW/cm(2). The charge mobility and recombination properties of the best performing cells were investigated. The hole mobility in the pure PBTDTT-15 was in the range of 4 x 10(-4) cm(2)/(V s), which was reduced almost 5 times in the PBTDTT-15:PC(70)BM (1:3) blend. The PhotoCELIV transient observed for the photovoltaic (PV) blend was dominated by electrons, with the charge mobility of the order of 10(-3) cm(2)/(V s), and a weak shoulder at a long time scale due to holes. The effective bimolecular recombination coefficient (beta) obtained for the PV blend deviated significantly from the Langevin recombination coefficient (beta(L)) indicating a phase-separated morphology. The obtained results indicate that the PBTDTT-15:PC(70)BM blend can be potential for organic solar cell applications.
ACS Appl Mater Interfaces 2010 May
PMID:Charge mobility and recombination in a new hole transporting polymer and its photovoltaic blend. 2041 40

We have developed polymer solar cells featuring a buffer layer of polythiophene (PT) sandwiched between the active layer and the poly(3,4-ethylenedioxythiophene):poly(styrenesulfonate) (PEDOT:PSS) layer. We attribute the improvement in power conversion efficiency of these polymer solar cells, relative to that of those based on poly(3-hexylthiophene):[6,6]-phenyl-C(61)-butyric acid methyl ester (P3HT:PCBM), to a reduction in the degree of carrier recombination at the junction interface. Because the conductivity and the energy level of PT can be tuned simply by applying a bias to it in an electrolytic solution, we also investigated the effect of the energy level on the devices' performances. The power conversion efficiency of a solar cell containing a PT buffer layer reached 4.18% under AM 1.5 G irradiation (100 mW/cm(2)).
ACS Appl Mater Interfaces 2010 May
PMID:A strategic buffer layer of polythiophene enhances the efficiency of bulk heterojunction solar cells. 2045 Jan 93

The utilization of graphene oxide (GO) thin films as the hole transport and electron blocking layer in organic photovoltaics (OPVs) is demonstrated. The incorporation of GO deposited from neutral solutions between the photoactive poly(3-hexylthiophene) (P3HT):phenyl-C61-butyric acid methyl ester (PCBM) layer and the transparent and conducting indium tin oxide (ITO) leads to a decrease in recombination of electrons and holes and leakage currents. This results in a dramatic increase in the OPV efficiencies to values that are comparable to devices fabricated with PEDOT:PSS as the hole transport layer. Our results indicate that GO could be a simple solution-processable alternative to PEDOT:PSS as the effective hole transport and electron blocking layer in OPV and light-emitting diode devices.
ACS Nano 2010 Jun 22
PMID:Solution-processable graphene oxide as an efficient hole transport layer in polymer solar cells. 2048 12

In an aim to harvest UV-near-visible (360-440 nm) photons as well as to increase the morphology in the bulk heterojunction solar cells, we report herein the strategic design, synthesis, and characterization of a novel excited-state intramolecular proton-transfer dye, 3-hydroxy-2-(5-(5-(5-(3-hydroxy-4-oxo-4H-chromen-2-yl)thiophen-2-yl)thiophen-2-yl)thiophen-2-yl)-4H-chromen-4-one (FT), which bears two key functional groups, namely 3-hydroxychromone chromophore and trithiophene backbone and is then exploited into the blends of regioregular poly(3-hexylthiophene) (RR-P3HT) and phenyl-C(61)-butyric acid methyl ester (PCBM). FT acts as an excellent UV-near visible absorber, which then undergoes excited-state intramolecular proton transfer, giving rise to an orange-red proton-transfer emission that was reabsorbed by P3HT via a Forster type of energy transfer. Introduction of FT to P3HT/PCBM blend films also improves the morphology of phase separated structure, in particular, enhances the interaction of P3HT chains and the hole mobility. In this work, under the optimized condition of P3HT: PCBM:FT of 15:9:2 in weight ratio, the best performance of the device B-FT2 revealed consistent enhancements in the efficiency (eta) 4.28% and short-circuit current (J(sc)) 12.53 mAcm(-2), which are higher than that (3.68% and 10.28 mAcm(-2)) of the best performance of the control device B (P3HT:PCBM 15:9 in weight ratio) by 16 and 22%, respectively.
ACS Appl Mater Interfaces 2010 Jun
PMID:Design and synthesis of trithiophene-bound excited-state intramolecular proton transfer dye: enhancement on the performance of bulk heterojunction solar cells. 2049 80


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