Effect of [6,6]‐phenyl‐C61‐butyric acid methyl ester on the morphology of poly(3‐hexylthiophene) film

The change of morphology of poly(3‐hexylthiophene) (P3HT) film as a result of blending with [6,6]‐phenyl‐C₆₁‐butyric acid methyl ester (PCBM) was studied using a freeze‐dry method. A porous structure was observed as the P3HT/PCBM solution was freeze‐dried. The pore size decreased as the proportion of PCBM increased in the P3HT/PCBM blended film. Additionally, the freeze‐dried P3HT/PCBM film was more resistant to the formation of PCBM crystals than that prepared by a spin‐coating method during the thermal annealing process. Homogeneous distribution of PCBM in the freeze‐dried P3HT/PCBM film was the main reason for the reduction of large PCBM crystal formation. Copyright © 2011 Society of Chemical Industry     

Investigation of P3HT/n-Si heterojunction using surface photovoltage spectroscopy

Surface photovoltage spectroscopy (SPS) was used to investigate the interactions of the interface between regioregular poly(3-hexylthiophene) (P3HT) and n-type single crystalline silicon. The SPS responses of silicon and the P3HT/n-Si heterojunction caused by band to band transition of silicon are 30 mV and 160 mV respectively. The band-bending in the silicon side of the P3HT/n-Si structure is larger than that of bare n-Si. The density of the interface states of the P3HT/n-Si heterojunction increased significantly after the deposition of P3HT. Based on the contact potential difference (CPD) transient results, charge transport and separation processes are fast in the silicon substrate and slow in the P3HT layer respectively.     

Enhancement in crystallinity of poly(3-hexylthiophene) thin films prepared by low-temperature drop casting

Low-temperature casting of high molecular weight (HMW > 40 kDa) regioregular poly(3-hexylthiophene) (P3HT) is demonstrated to yield highly crystalline P3HT thin films with well defined and preferentially edge-on oriented [(100) contact plane] nanocrystallites on the pure and silanized Si/SiO₂ substrates. Transmission electron microscopy and X-ray diffraction provide evidence for the increase in preferential edge-on orientation of P3HT-conjugated backbone while decreasing the film preparation temperature below room temperature. The optimum growth temperature is about −12°C for the given concentration (2 mg/mL in CHCl₃). The reduced evaporation rate of the solvent results in a better selection of the thermodynamically stable orientation of nanocrystallites onto the substrate. The degree of preferential orientation and size of the crystallites can be further increased on n-octadecyltrichlorosilane-treated SiO₂ substrates as well as by annealing the films at 200°C for 1 h. © 2012 Wiley Periodicals, Inc. J Appl Polym Sci, 2012     

Ternary Solvent System to Control the Morphology of Active Blend in Inverted Organic Solar Cells

Bulk heterojunction blend of poly(3-hexylthiophene)–[6,6]-phenyl-C₆₁-butyric acid methyl ester prepared using the ternary solvent mixture was used as the active layer of an inverted organic solar cell. The ternary solvent mixture consisted of a good solvent such as ortho-dichlorobenzene and two marginal solvents such as cyclohexanone and toluene offering limited solubility to the poly(3-hexylthiophene) component. Power conversion efficiency of inverted device was found to decrease from 2.74?±?0.05% in the unmodified device to 2.64?±?0.07% in the modified device. UV–visible measurement revealed less efficient photoabsorption in the mixed cosolvent-casted active layer due to insufficient and disordered crystallization of poly(3-hexylthiophene) domains.     

Risk factors associated to musculoskeletal disorder perception in college students,Bogota, 2016

Musculoskeletal disorders (MSD) have a high impact on the health of dual role workers (student and work). The aim of this study was to analyse risk factor (active pauses and job position) associated with MSD in postgraduate students, Bogotá 2016. This Cross-sectional study was conducted in a random sample of 304 college graduate students and statistical analysis in SPSS version 24. We found that significant differences between non-performing active pauses and neck symptoms (P = 0.007), not stretching vs neck symptoms [OR = 2.4048 (1.0133–5.707)]; laptop use vs eyes [OR = 2.7132 (1.457–5.0526)], shoulders [OR = 10.6364 (4.9905–22.6697)], elbows (P = 0.04); non-mouse usage vs elbows (P = 0.028), hand-wrist (P = 0.043); non-forearm support vs lower back (P = 0.009). Results suggest association between non-performing active pauses, stretching and neck; use of laptop and eyes, shoulders and left elbow, non-mouse usage and on elbow and hand/right wrist, no forearm support on table and lower back. Symptom changes in the upper and lower limbs were identified.     

Fabrication of a planar water gated organic field effect transistor using a hydrophilic polythiophene for improved digital inverter performance

A planar water gated OFET (WG-OFET) structure is fabricated by patterning gate, source and drain electrodes on the same plane at the same time. Transistor output characteristics of this novel structure employing commercial regioregular poly(3-hexylthiophene) (rr-P3HT) as polymer semiconductor and deionized (DI) water as gate dielectric show successful field effect transistor operation with an on–off current ratio of 43 A/A and transconductance of 2.5 μA/V. These output characteristics are improved using P3HT functionalized with poly(ethylene glycol) (PEG) (P3HT-co-P3PEGT), which is more hydrophilic, leading to on–off ratio of 130 A/A and transconductance of 3.9 μA/V. Utilization of 100 mM NaCl solution instead of DI water significantly increases the on–off ratio to 141 A/A and transconductance to 7.17 μA/V for commercial P3HT and to 217 A/A and to 11.9 μA/V for P3HT-co-P3PEGT. Finally, transistors with improved transconductances are used to build digital inverters with improved characteristics. Gain of the inverters employing P3HT and P3HT-co-P3PEGT are measured as 2.9 V/V and 10.3 V/V, respectively, with 100 mM NaCl solution.     

Controlling the morphology of poly(3‐hexylthiophene)/methanofullerene film through a dynamic‐cooling and freeze‐drying process

A dynamic‐cooling and freeze‐drying (DCFD) process has been applied to the fabrication of polymer solar cells. The dynamic‐cooling process allows poly(3‐hexylthiophene) molecules to aggregate in solution into a more organized structure during the cooling process; the freeze‐drying process prevents severe agglomeration of [6,6]‐phenyl‐C₆₁‐butyric acid methyl ester (PCBM) during the solvent removing process. Application of these two processes to the preparation of the poly(3‐hexylthiophene)/methanofullerene photoactive layer results in an enhanced poly(3‐hexylthiophene) aggregation and smaller PCBM agglomerates. Devices fabricated using the DCFD process generate 14% more in current density than those prepared by the spin‐coating process under AM1.5G illumination. © 2015 Society of Chemical Industry     

Poly(3-hexylthiophene) and hexafluoro-2-propanol-substituted polysiloxane based OFETs as a sensor for explosive vapor detection

The organic field effect transistors (OFETs) with regioregular poly 3-hexylthiophene (rr-P3HT) and hexafluoro-2-propanol-substituted polysiloxane (SXFA) as an organic layer, have been used for detection of explosive vapors with excellent sensitivity of less than 70 ppt for 1,3,5-trinitro-1,3,5-triazacyclohexane (RDX) and less than 100 ppt for 2,4,6-trinitrotoluene (TNT). The sensor response (% change in saturation current) was found to be 125 ± 10% for TNT and 90 ± 10% for RDX. It was also observed that the incorporation of Cu^II tetraphenylporphyrin (CuTPP) into rr-P3HT/SXFA matrix resulted in an improved selectivity for the vapors of nitro based analytes (TNT, RDX and DNB) as compared to the vapors of non explosive oxidizing agents such as nitrobenzene (NB), benzoquinone (BQ) and benzophenone (BP). This is attributed to the increased binding of the vapors containing nitro compound to the thin films due to the presence of CuTTP. Spin coated thin films were further characterized by Atomic Force Microscopy (AFM) and Electrostatic Force Microscopy (EFM).     

盐酸沙格雷酯的合成

以2-((3-甲氧基)苯乙基)苯酚为起始物料,与环氧氯丙烷进行酚醚化反应得到[[2-[2-(3-甲氧基)苯乙基]苯氧基]甲基]环氧乙烷,与二甲胺进行氨化反应得到1-二甲胺基-3-[2-[2-(3-甲氧基)苯乙基]苯氧基]-2-丙醇,再与丁二酸酐在有机溶剂中进行酯化反应得到沙格雷酯,最后通入氯化氢气体成盐即可制得盐酸沙格雷酯,总收率约67%。