Green Organic Solar Cells from a Water Soluble Polymer and Nancrystalline TiO2

The cost of the present generation of inorganic silicon solar cells is very high and further breakthroughs in cost and efficiency using traditional materials are becoming less and less likely after over 50 years of development. Next generation organic solar cells offer a solution to the limitations of silicon through the vision of low-cost, liquid-based, large area fabrication technology based on polymer and nanomaterials at room temperature. However, most polymers used in solar cells are dissolved in organic solvents such as xylene, toluene, chloroform, and chlorobenzene. Such solvents are harmful to people and environments, leading to higher costs due to complicated waste disposal processing. This is in conflict with the low cost, green, and renewable energy for which we are aiming. To realize a green organic solar cell, a novel solar cell has been created using an environmentally friendly water-soluble thiophene polymer [(Sodium poly[2-(3-thienyl)-ethoxy-4-butylsulfonate])] (PTEBS) and nanocrystalline TiO2. This novel system has shown great potential in photovoltaics the work has garnered the attention of the international community.In our innovative solar cells, the water-soluble polythiophene (PTEBS) is used as electron donor. Nanoparticle TiO2 acts as electron acceptor. PTEBS/TiO2 solar cells with various structures including bilayer heterojunctions, bulk heterojunctions and a hybrid of bilayer and bulk heterojunctions have been developed and explored. These results are comparable to the best polymer/metal-oxide solar cells reported by other groups using organic solvents.In summary, this is the first time that green solar cells have been fabricated from environmentally friendly water-soluble polymers. By using water as the solvent and utilizing liquid-based processing, the cost of the energy generated by this type of solar cell will be further lowered. In addition, the flexible polymer offers the ease of fabrication and integration into different devices

Hybrid solar cells from water-soluble polymers

We report on the use of a water-soluble, light-absorbing polythiophene polymer to fabricate novel photovoltaic devices. The polymer is a water-soluble thiophene known as sodium poly[2-(3-thienyl)-ethoxy-4-butylsulfonate] or PTEBS. The intention is to take advantage of the properties of conjugated polymers (flexible, tunable, and easy to process) and incorporate the additional benefits of water solubility (easily controlled evaporation rates and environmentally friendly). The PTEBS polythiophene has shown significant photovoltaic response and has been found to be effective for making solar cells. To date, solar cells in three different configurations have been produced: titanium dioxide (TiO2) bilayer cells, TiO2 bulk heterojunction solar cells, and carbon nanotubes (CNTs) in bulk heterojunctions. The best performance thus far has been achieved with TiO2 bilayer devices. These devices have an open circuit voltage (Voc) of 0.84V, a short circuit current (Jsc) of 0.15 mA/cm2, a fill factor (ff) of 0.91, and an efficiency (η) of 0.15 %

Water-soluble polythiophene∕nanocrystalline TiO2 solar cells

We report the characteristics of polymer∕nanocrystalline solar cells fabricated using an environmentally friendly water-soluble polythiophene and TiO2 in a bilayer configuration. The cells were made by dropping the polymer onto a TiO2nanocrystallinefilm and then repeatedly sweeping a clean glass rod across the polymer as it dried. The devices showed an open circuit voltage of 0.81 V, a short circuit current density of 0.35mA/cm2, a fill factor of 0.4, and an energy conversion efficiency of 0.13%. The water-soluble polythiophene showed significant photovoltaic behavior and the potential for use in solar cells

Functionalized Carboxylate Deposition of Triphenylamine-based Organic Dyes for Efficient Dye-sensitized Solar Cells

he standard dip-coating dye-loading technique for dye-sensitized solar cells (DSSCs) remains essentially unchanged since modern DSSCs were introduced in 1991. This technique constitutes up to 80% of the DSSC fabrication time. Dip-coating of DSSC dyes not only costs time, but also generates a large amount of dye waste, necessitates use of organic solvents, requires sensitization under dark conditions, and often results in inefficient sensitization. Functionalized Carboxylate Deposition (FCD) was introduced as an alternative dye deposition technique, requiring only 2% of the fabrication time, eliminating the need for solvents, and significantly reducing dye waste. In this study, FCD was used to deposit two relatively large triphenylamine-based organic dyes (L1 and L2). These dyes were sublimated and deposited in \u3c20 minutes via a customized FCD instrument using a vacuum of ∼0.1 mTorr and temperatures ≤280 °C. FCD-based DSSCs showed better efficiency (i.e., 5.03% and 5.46% for L1 and L2 dyes, respectively) compared to dip-coating (i.e., 4.36% and 5.35% for L1 and L2, respectively) in a fraction of the deposition time. With multiple advantages over dip-coating, FCD was shown to be a viable alternative for future ultra-low cost DSSC production

Characteristics of water-soluble polythiophene: TiO2 composite and its application in photovoltaics

We have studied the characteristics of composites of an environmentally friendly water-soluble polythiophene sodium poly[2-(3-thienyl)-ethoxy-4-butylsulfonate] (PTEBS) and TiO2. We observed that the ultraviolet-visible absorption spectrum of low molecular weight PTEBS is redshifted possibly due to the formation of aggregates. Cyclic voltammetry reveals the values of highest occupied molecular orbitals and lowest unoccupied molecular orbitals for PTEBS. A factor of 7 in photoluminescence quenching indicates that the exciton dissociation and charge separation occur successfully at the PTEBS: TiO2 (1:1 by weight) interface. This enhances the possibility that the separated charges will reach the electrodes before recombining. Scanning electron micrograph images show how the PTEBS and TiO2 are interconnected and form paths to the electrodes to improve charge transport. Photovoltaic devices with TiO2:PTEBS composite achieved an energy conversion efficiency of η=0.015%, a short circuit current of JSC=0.22mA/cm2, an open circuit voltage of VOC=0.72V, and a fill factor of FF=0.29 under ∼300mW/cm2 white light illumination

Hybrid Solar Cells from Water-Soluble Polymers

We report on the use of a water-soluble, light-absorbing polythiophene polymer to fabricate novel photovoltaic devices. The polymer is a water-soluble thiophene known as sodium poly[2-(3-thienyl)-ethoxy-4-butylsulfonate] or PTEBS. The intention is to take advantage of the properties of conjugated polymers (flexible, tunable, and easy to process) and incorporate the additional benefits of water solubility (easily controlled evaporation rates and environmentally friendly). The PTEBS polythiophene has shown significant photovoltaic response and has been found to be effective for making solar cells. To date, solar cells in three different configurations have been produced: titanium dioxide (TiO 2 ) bilayer cells, TiO 2 bulk heterojunction solar cells, and carbon nanotubes (CNTs) in bulk heterojunctions. The best performance thus far has been achieved with TiO 2 bilayer devices. These devices have an open circuit voltage (V oc ) of 0.84 V, a short circuit current (J sc ) of 0.15 mA/cm 2 , a fill factor (ff ) of 0.91, and an efficiency (η) of 0.15%

Employing PCBTDPP as an efficient donor polymer for high performance ternary polymer solar cells

A compatible low-bandgap donor polymer (poly[N-90-heptadecanyl-2,7carbazole-alt-3,6-bis(thiophen-5-yl)-2,5-dioctyl-2,5-dihydropyrrolo[3,4]pyrrole-1,4-dione], PCBTDPP) was judicially introduced into the archetypal poly(3-hexylthiophene):[6,6]-phenyl-C61-butyric acid methyl ester (P3HT:PC61BM) photoactive system to fabricate highly efficient ternary based bulk heterojunction polymer solar cells (PSCs). The PCBTDPP ternary-based PSC with optimal loading (0.2 wt.%) displayed outstanding performance with a champion power conversion efficiency (PCE) of 5.28% as compared to the PCE (4.67%) for P3HT:PC61BM-based PSC (reference). The improved PCE for PCBTDPP ternary-based PSC can be mainly attributed to the incorporation of PCBTDPP into P3HT:PC61BM that beneficially improved the optical, morphological, electronic, and photovoltaic (PV) performance. This work instills a rational strategy for identifying components (donor/acceptor (D/A) molecules) with complementary beneficial properties toward fabricating efficient ternary PSCs

Long-Term Efficacy of Ultrasound-Guided Percutaneous Transluminal Angioplasty for Arteriovenous Fistula Outflow Stenosis Caused by Venous Valve

Introduction: Venous valve-related stenosis (VVRS) is an uncommon type of failure of arteriovenous fistula among patients with end-stage renal disease (ESRD). There is a paucity of data on the long-term efficacy of ultrasound-guided percutaneous transluminal angioplasty (PTA) for VVRS. Methods: ESRD patients who underwent PTA because of VVRS between January 2017 and December 2021 at the First Affiliated Hospital of Chongqing Medical University were enrolled. Patients were classified into three cohorts (cohort1, VVRS located within 3 cm of the vein adjacent to the anastomosis; cohort2, VVRS located over 3 cm away from the anastomosis; cohort3, multiple stenoses). The patency rates were assessed by the Kaplan-Meier method and compared using the log-rank test. Univariate and multivariate Cox analyses were performed to identify the risk factors. Results: A total of 292 patients were enrolled, including 125 (42.8%), 111 (38.0%), and 56 (19.2%) patients in cohort1, cohort2, and cohort3, respectively. The median follow-up was 34.8 months. The 6-month, 1-year, 2-year, and 3-year primary patency rates were 86.0%, 69.4%, 47.5%, and 35.3%, respectively. The secondary patency rates were 94.5%, 89.4%, 75.5%, and 65.3%, respectively. Cohort1 showed a relatively better primary patency compared to cohort2 and cohort3. The secondary patency rates were comparable in the three cohorts. Duration of dialysis and VVRS type were potential factors associated with primary patency. Conclusions: This study showed acceptable long-term primary and secondary patency rates after PTA for VVRS in ESRD patients, especially for those with VVRS located within 3 cm of the vein adjacent to the anastomosis