Bifunctional Organic Spacers for Formamidinium-Based Hybrid Dion-Jacobson Two-Dimensional Perovskite Solar Cells.

Three-dimensional (3D) perovskite materials display remarkable potential in photovoltaics owing to their superior solar-to-electric power conversion efficiency, with current efforts focused on improving stability. Two-dimensional (2D) perovskite analogues feature greater stability toward environmental factors, such as moisture, owing to a hydrophobic organic cation that acts as a spacer between the inorganic layers, which offers a significant advantage over their comparatively less stable 3D analogues. Here, we demonstrate the first example of a formamidinium (FA) containing Dion-Jacobson 2D perovskite material characterized by the BFA Pb I formulation through employing a novel bifunctional organic spacer (B), namely 1,4-phenylenedimethanammonium (PDMA).

Strong Photocurrent Amplification in Perovskite Solar Cells with a Porous TiO2 Blocking Layer under Reverse Bias.

We investigate two different types of TiO2 blocking layer (BL) deposition techniques commonly used in solid-state methylammonium lead triiodide perovskite (MaPbI3)-based solar cells. Although these BLs lead to similar photovoltaic device performance, their structure and blocking capability is actually very different. In one case, the "blocking" layer is porous, allowing an intimate contact of the perovskite with the fluorine-doped tin-dioxide (FTO)-covered glass substrate serving as transparent electron collector.

Nanowire perovskite solar cell.

Organolead iodide perovskite, CH3NH3PbI3, was prepared in the form of nanowire by means of a small quantity of aprotic solvent in two-step spin-coating procedure. One-dimensional nanowire perovskite with the mean diameter of 100 nm showed faster carrier separation in the presence of hole transporting layer and higher lateral conductivity than the three-dimensional nanocuboid crystal. Reduction in dimensionality resulted in the hypsochromic shift of both absorption and fluorescence spectra, indicative of more localized exciton states in nanowires.

Water photolysis at 12.3% efficiency via perovskite photovoltaics and Earth-abundant catalysts.

Although sunlight-driven water splitting is a promising route to sustainable hydrogen fuel production, widespread implementation is hampered by the expense of the necessary photovoltaic and photoelectrochemical apparatus. Here, we describe a highly efficient and low-cost water-splitting cell combining a state-of-the-art solution-processed perovskite tandem solar cell and a bifunctional Earth-abundant catalyst. The catalyst electrode, a NiFe layered double hydroxide, exhibits high activity toward both the oxygen and hydrogen evolution reactions in alkaline electrolyte.

Growth of CH3NH3PbI3 cuboids with controlled size for high-efficiency perovskite solar cells.

Perovskite solar cells with submicrometre-thick CH(3)NH(3)PbI(3) or CH(3)NH(3)PbI(3-x)Cl(x) active layers show a power conversion efficiency as high as 15%. However, compared to the best-performing device, the average efficiency was as low as 12%, with a large standard deviation (s.d.

3-D TiO2 nanoparticle/ITO nanowire nanocomposite antenna for efficient charge collection in solid state dye-sensitized solar cells.

TiO2 nanoparticle (NP)/ITO nanowire (NW) nanocomposites for use as photoelectrode materials were fabricated to improve the charge collection efficiency in solid state dye sensitized solar cells (ss-DSSCs). The average current density for ss-DSSCs containing TiO2 NP/ITO NW arrays was 7.2 mA cm(-2) that was 98% higher than that for the conventional TiO2 NP ss-DSSCs.

Lead iodide perovskite sensitized all-solid-state submicron thin film mesoscopic solar cell with efficiency exceeding 9%.

We report on solid-state mesoscopic heterojunction solar cells employing nanoparticles (NPs) of methyl ammonium lead iodide (CH(3)NH(3))PbI(3) as light harvesters. The perovskite NPs were produced by reaction of methylammonium iodide with PbI(2) and deposited onto a submicron-thick mesoscopic TiO(2) film, whose pores were infiltrated with the hole-conductor spiro-MeOTAD. Illumination with standard AM-1.

Size-tunable, fast, and facile synthesis of titanium oxide nanotube powders for dye-sensitized solar cells.

Size-tunable titanium oxide (TiO(2)) nanotube powders offering both a light-scattering effect and a light-harvesting function were synthesized by a fast and facile anodizing method. When used to prepare the TiO(2) layer for a photoanode, their photovoltaic performances were much worse than that of a nanocrystal TiO(2) layer. However, when the TiO(2) nanotube powders were used as a light-scattering layer on a nanocrystal TiO(2) layer, the highest conversion efficiency was obtained because of more noticeable light absorption of the longer wavelength, which was not attainable from a pure nanocrystal TiO(2) layer or the combination of nanocrystal TiO(2)/commercialized light-scattering particles.

Synthesis, structure, and photovoltaic property of a nanocrystalline 2H perovskite-type novel sensitizer (CH3CH2NH3)PbI3.

A new nanocrystalline sensitizer with the chemical formula (CH3CH2NH3)PbI3 is synthesized by reacting ethylammonium iodide with lead iodide, and its crystal structure and photovoltaic property are investigated. X-ray diffraction analysis confirms orthorhombic crystal phase with a = 8.7419(2) Å, b = 8.

6.5% efficient perovskite quantum-dot-sensitized solar cell.

Highly efficient quantum-dot-sensitized solar cell is fabricated using ca. 2-3 nm sized perovskite (CH(3)NH(3))PbI(3) nanocrystal. Spin-coating of the equimolar mixture of CH(3)NH(3)I and PbI(2) in γ-butyrolactone solution (perovskite precursor solution) leads to (CH(3)NH(3))PbI(3) quantum dots (QDs) on nanocrystalline TiO(2) surface.

Pseudo first-order adsorption kinetics of N719 dye on TiO2 surface.

We have investigated the adsorption kinetics of Ru-based N719 dye on TiO(2) surface in dye-sensitized solar cell using 0.5 mM and 5 mM dye solutions. The amount of adsorbed dye on TiO(2) surface of ca.