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Calcium (Ca) and lanthanum (La) doping into mesoporous TiO2 prevents nucleation and growth of particles during synthesis and calcination at high temperature, resulting in smaller particle sizes and a decrease in the band gap of TiO2. These collectively have a positive affect on the efficiency of dye-sensitized solar cells (DSSCs) when employed as the anode. When designing an effective DSSC anode, the efficiency of dye adsorption must also be considered. This work investigates the adsorption properties of N719 dye onto La and Ca doped mesoporous TiO2 anodes for DSSCs. Near edge X-ray absorption fine structure spectroscopy (NEXAFS) identified the presence of La and Ca dopants in the TiO2 nanoparticles. Performance of DSSCs with Ca and La doped mesoporous TiO2 anodes demonstrated that doping of TiO2 enhances the overall efficiency of the devices. Both doped TiO2 nanoparticles showed higher dye adsorption concentration than that of pure TiO2, as shown in Brunauer-Emmett-Teller (BET) characterization. By employing Langmuir and Freundlich isotherms, dye adsorption behaviour was modelled. Pure and Ca doped TiO2 demonstrated good correlation to both isotherms, whereas La doped TiO2 only showed good correlation with Langmuir isotherm. Irrespective of its single layer adsorption kinetics, 0.1 mol.% La doped TiO2 has shown the highest dye adsorption and efficiency due to increase in surface area and oxygen vacancies induced by La doping.

The interfacial compatibility between the graphite/carbon black composite counter electrode (Gr/CB CE) and the perovskite layer is a crucial determinant of the performance of the hole-transport-layer-free carbon-based perovskite solar cells, and judicious selection of the Gr/CB CE application method is essential for achieving an optimum contact. In this work, three different types of Gr/CB CEs application methods are investigated: (1) deposition of Gr/CB on the fluorine-doped tin oxide (FTO) substrate, followed by clamping to the perovskite layer, (2) direct deposition of Gr/CB onto the perovskite layer, and (3) deposition of Gr/CB onto the PbI

In this work, we investigated the morphology, electrical conductivity, catalytic properties, and binding energies of electronic states of a system consisting of acetylene carbon black (AB) and graphite as efficient and low-cost counter electrodes (CEs) for dye-sensitized solar cells (DSSCs), where ratios of AB to graphite of 0:1, 1:3, 1:1, 3:1, and 1:0 were investigated. These carbon-based CEs were characterized using four-point probe conductivity measurement, field emission scanning electron microscope (FE-SEM), X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), near-edge X-ray absorption fine structure (NAXAFS), electrochemical impedance spectrum (EIS), and current-voltage (I-V) performance. Introduction of small AB particles into graphite paste enhanced the electronic conductivity of AB-graphite composite due to the bridging of the graphite flakes for electrocatalytic activity of triiodide reduction. AB particles also offer large surface area to provide high electrochemical performance in DSSCs. The overall highest power conversion efficiency of 5.06% was achieved for the DSSC fabricated with a CE consisting of AB-graphite ratio of 3:1, which is comparable to the DSSC performance with conventional platinum (Pt) CE. These findings suggest that AB and graphite composite could be a promising CE for low-cost DSSCs.

In this work, we have investigated the performance of acetylene carbon black/graphite (AB/G) composite counter electrodes (CEs) by incorporating TiO2 as a binder in dye-sensitized solar cells (DSSCs). We obtained five types of composite CE films at different weight ratios of 0:1, 1:3, 1:1, 3:1 and 1:0 by adding a constant amount of TiO2 to a mixture of AB/G. The performance of the composite electrodes was assessed by using X-ray diffraction, X-ray photoelectron spectroscopy, scanning electron microscopy, electrochemical impedance spectroscopies and photocurrent density–voltage characteristics. The results have shown enhanced DSSC efficiency due to improved charge transfer properties of the CE when adding TiO2. TiO2 enhances the binding of the electrode to the substrate. AB/G/TiO2 composites show superior overall results compared to AB/TiO2 and G/TiO2. Since AB has high catalytic activity and surface area, as the AB content of the composite is increased, the electrochemical properties of the CEs are improved. The DSSC with AB:G (3:1) exhibited the maximum power conversion efficiency (PCE) of 5.9% with the highest fill factor (FF) of 0.55, which are comparable to those DSSCs employing platinum CEs with PCE of 6.2% and FF of 0.67.