Stability of MAPbI3 perovskite grown on planar and mesoporous electron-selective contact by inverse temperature crystallization.

Single crystalline perovskite solar cells (PSC) are promising for their inherent stability due to the absence of grain boundaries. While the development of single crystals of perovskite with enhanced optoelectronic properties is known, studies on the growth, device performance and understanding of the intrinsic stability of single crystalline perovskite thin film solar cell devices fabricated on electron selective contacts are scarcely explored. In this work, we examine the impact of mesoporous TiO2 (m-TiO2) and planar TiO2 (p-TiO2) on the growth of single crystalline-methyl ammonium lead iodide (SC-MAPbI3) film, PSC device performance and film stability under harsh weather conditions (T ∼ 85 °C and RH ∼ 85%). Self-grown SC-MAPbI3 films are developed on m-TiO2 and p-TiO2 by inverse temperature crystallization under ambient conditions without the need for sophisticated glove-box processing. The best device with m-TiO2 as an electron transport layer showed a promising power conversion efficiency of 3.2% on an active area of 0.3 cm2 in hole transport material free configuration, whereas, only 0.7% was achieved for the films developed on p-TiO2. Complete conversion of precursor to perovskite phase and better surface coverage of the film leading to enhanced absorption and reduced defects of single crystalline perovskite on m-TiO2 compared to its p-TiO2 leads to this large difference in efficiency. Mesoporous device retained more than 70% of its initial performance when stored at 30 °C under dark for more than 5000 h at 50% RH; while the planar device degraded after 1500 h. Thermal and moisture endurance of SC-MAPbI3 films are investigated by subjecting them to temperatures ranging from 35 °C to 85 °C at a constant relative humidity (RH) of 85%. X-ray diffraction studies show that the SC-MAPbI3 films are stable even at 85 °C and 85% RH, with only slight detection (30-35%) of PbI2 at these conditions. This study highlights the superior stability of SC-MAPbI3 films which paves way for further studies on improving the stability and performance of the ambient processed PSCs.

Ordered mesoporous tungsten suboxide counter electrode for highly efficient iodine-free electrolyte-based dye-sensitized solar cells.

A disulfide/thiolate (T(2)/T(-)) redox-couple electrolyte, which is a promising iodine-free electrolyte owing to its transparent and noncorrosive properties, requires alternative counter-electrode materials because conventional Pt shows poor catalytic activity in such an electrolyte. Herein, ordered mesoporous tungsten suboxide (m-WO(3-x)), synthesized by using KIT-6 silica as a hard template followed by a partial reduction, is used as a catalyst for a counter electrode in T(2)/T(-)-electrolyte-based dye-sensitized solar cells (DSCs). The mesoporous tungsten suboxide, which possesses interconnected pores of 4 and 20 nm, provides a large surface area and efficient electrolyte penetration into the m-WO(3-x) pores. In addition to the advantages conferred by the mesoporous structure, partial reduction of tungsten oxide creates oxygen vacancies that can function as active catalytic sites, which causes a high electrical conductivity because of intervalence charge transfer between the W(5+) and W(6+) ions. m-WO(3-x) shows a superior photovoltaic performance (79 % improvement in the power conversion efficiency) over Pt in the T(2)/T(-) electrolyte. The superior catalytic activity of m-WO(3-x) is investigated by using cyclic voltammetry (CV), electrochemical impedance spectroscopy (EIS), and Tafel polarization curve analysis.

Rapid (∼10 min) synthesis of single-crystalline, nanorice TiO2 mesoparticles with a high photovoltaic efficiency of above 8%.

A novel rapid (∼10 min) microwave-hydrothermal synthesis is demonstrated for nanorice TiO(2) mesoparticles as an anode of a dye-sensitized solar cell with an excellent photovoltaic efficiency of above 8%.

Platinum-free tungsten carbides as an efficient counter electrode for dye sensitized solar cells.

Mesoporous tungsten carbides displayed an excellent solar conversion efficiency (7.01%) as a counter electrode for dye sensitized solar cells under 100 mW cm(-2), AM 1.5G illumination, which corresponded to ca. 85% of the efficiency of the conventional platinum electrode.

Large-pore sized mesoporous carbon electrocatalyst for efficient dye-sensitized solar cells.

A counter-electrode comprised of large-pore sized mesoporous carbon exhibits low charge transfer resistance in iodide/triiodide redox electrolyte, thus liquid and quasi-solid dye sensitized solar cells show 8.18% and 3.61% solar to electric energy conversion efficiency, respectively.

Efficient dye-sensitized solar cells with catalytic multiwall carbon nanotube counter electrodes.

We report the successful application of multiwall carbon nanotubes (CNTs) as electrocatalysts for triiodide reduction in a dye-sensitized solar cell (DSSC). Defect-rich edge planes of bamboolike-structure multiwall CNTs facilitate the electron-transfer kinetics at the counter electrode-electrolyte interface, resulting in low charge-transfer resistance and an improved fill factor. In combination with a dye-sensitized TiO2 photoanode and an organic liquid electrolyte, a multiwall CNT counter-electrode DSSC shows 7.7% energy conversion efficiency under 1 sun illumination (100 mW/cm(2), air mass 1.5 G). The short-term stability test at moderate conditions confirms the robustness of CNT counter-electrode DSSCs.