Tb- and Eu-doped yttrium oxyselenides as novel absorber layers for superstrate thin-film photovoltaics: improved spectral optical absorption and green-red phosphor activation.

To generate and deliver alternative sustainable energy in the face of the current energy crisis, new materials that can capture solar energy and transform it into other useful energies are required. Rare-earth (RE) oxychalcogenides are now being used more frequently as up/down-conversion materials in established photovoltaic (PV) devices to boost their PV performance. Here, through an efficient microwave assisted synthesis procedure, novel nanoplate/sheet shaped nanomaterials of yttrium oxyselenide (YOSe) and its analogues doped with Tb and Eu (YOSe:Tb and YOSe:Eu) were successfully synthesized. Analyses of the structure, stability, morphology, light absorption, and electrochemistry were performed. This work showed that the parent YOSe exhibited green (543 nm) and red (615 nm) emission luminescence when doped with Tb and Eu with a luminescence quantum yield (LQY) of 0.56 and 0.53 for YOSe:Tb and YOSe:Eu nanomaterials, respectively. The surface and material conductivity of YOSe improved with the addition of the dopant elements, with the best outcome shown in YOSe:Eu, according to electrokinetic research evidenced by the enhanced current peaks, reduced charge-transfer resistance (Rct) and low impedance magnitude (Zmag) through electrochemical experiments. These improvements were induced by the distinctive properties of the dopant elements. PCEs of 0.25%, 0.67%, and 1.20% were obtained for YOSe, YOSe:Tb, and YOSe:Eu-based PV devices, respectively, using the nanomaterials as novel absorber layers in a superstrate device design. Our results can initiate further exploitation of the doped host structure for effective down-conversion NIR luminescence for applications in PV devices and to boost the PV performance of existing solar cells.

Microscopic, Spectroscopic, and Electrochemical Characterization of Novel Semicrystalline Poly(3-hexylthiophene)-Based Dendritic Star Copolymer.

In this study, electron-donating semicrystalline generation 1 poly(propylene thiophenoimine)-co-poly(3-hexylthiophene) star copolymer, G1PPT-co-P3HT was chemically prepared for the first time. Copolymerization was achieved with high molecular weight via facile green oxidative reaction. 1H NMR analyses of the star copolymer demonstrated the presence of 84% regioregular (rr) head-to-tail (HT) P3HT, which accounts for the molecular ordering in some grain regions in the macromolecule's morphology, as revealed by the high-resolution scanning electron microscopy (HRSEM) and Selected Area Electron Diffraction (SAED) images, and X-ray diffraction spectroscopy (XRD) measurements. The star copolymer also exhibited good absorption properties in the ultraviolet-visible (UV-Vis) and the near infrared (NIR) spectral regions, which give rise to an optical energy bandgap value as low as 1.43 eV. A HOMO energy level at -5.53 eV, which is below the air-oxidation threshold, was obtained by cyclic voltammetry (CV). Electrochemical impedance spectroscopy (EIS) ascertained the semiconducting properties of the macromolecule, which is characterized by a charge transfer resistance, Rct, value of 3.57 kΩ and a Bode plot-phase angle value of 75°. The combination of the EIS properties of G1PPT-co-P3HT and its highly electron-donating capability in bulk heterojunction (BHJ) active layer containing a perylene derivative, as demonstrated by photoluminescence quenching coupled to the observed Förster Resonance charge transfer, suggests its suitability as an electron-donor material for optoelectronic and photovoltaic devices.

Pseudocapacitive Effects of Multi-Walled Carbon Nanotubes-Functionalised Spinel Copper Manganese Oxide.

Spinel copper manganese oxide nanoparticles combined with acid-treated multi-walled carbon nanotubes (CuMn2O4/MWCNTs) were used in the development of electrodes for pseudocapacitor applications. The CuMn2O4/MWCNTs preparation involved initial synthesis of Mn3O4 and CuMn2O4 precursors followed by an energy efficient reflux growth method for the CuMn2O4/MWCNTs. The CuMn2O4/MWCNTs in a three-electrode cell assembly and in 3 M LiOH aqueous electrolyte exhibited a specific capacitance of 1652.91 F g-1 at 0.5 A g-1 current load. Similar investigation in 3 M KOH aqueous electrolyte delivered a specific capacitance of 653.41 F g-1 at 0.5 A g-1 current load. Stability studies showed that after 6000 cycles, the CuMn2O4/MWCNTs electrode exhibited a higher capacitance retention (88%) in LiOH than in KOH (64%). The higher capacitance retention and cycling stability with a Coulombic efficiency of 99.6% observed in the LiOH is an indication of a better charge storage behaviour in this electrolyte than in the KOH electrolyte with a Coulombic efficiency of 97.3%. This superior performance in the LiOH electrolyte than in the KOH electrolyte is attributed to an intercalation/de-intercalation mechanism which occurs more easily in the LiOH electrolyte than in the KOH electrolyte.