Perovskite solar cell

About: Perovskite solar cell is a research topic. Over the lifetime, 4701 publications have been published within this topic receiving 216807 citations. The topic is also known as: PSC.

Flexible organo-metal halide perovskite solar cells on a Ti metal substrate

Abstract: Organo-metal halide perovskite solar cells have received much attention in the field of photovoltaics in recent years. Herein, we report a flexible perovskite solar cell based on a metal substrate. It showed a power conversion efficiency of over 6% for the first time using a silver thin film as a semi-transparent top electrode on a Ti substrate.

Zn2SnO4-Based Photoelectrodes for Organolead Halide Perovskite Solar Cells

Abstract: We report a new ternary Zn2SnO4 (ZSO) electron-transporting electrode of a CH3NH3PbI3 perovskite solar cell as an alternative to the conventional TiO2 electrode. The ZSO-based perovskite solar cells have been prepared following a conventional procedure known as a sequential (or two-step) process with ZSO compact/mesoscopic layers instead of the conventional TiO2 counterparts, and their solar cell properties have been investigated as a function of the thickness of either the ZSO compact layer or the ZSO mesoscopic layer. The presence of the ZSO compact layer has a negligible influence on the transmittance of the incident light regardless of its thickness, whereas the thickest compact layer blocks the back-electron transfer most efficiently. The open-circuit voltage and fill factor increase with the increasing thickness of the mesoscopic ZSO layer, whereas the short-circuit current density decreases with the increasing thickness except for the thinnest one (∼100 nm). As a result, the device with a 300 nm-th...

Electronic structure, optical property and improved stability of mixed halide perovskite CH$_3$NH$_3$Pb(I$_{1-x}$Br$_x$)$_3$ by virtual crystal approximation within DFT

Abstract: We investigate the structural, electronic and optical properties of mixed bromide-iodide lead perovskite solar cell CH$_3$NH$_3$Pb(I$_{1-x}$Br$_x$)$_3$ by means of the virtual crystal approximation (VCA) within density functional theory (DFT). Optimizing the atomic positions and lattice parameters increasing the bromide content $x$ from 0.0 to 1.0, we fit the calculated lattice parameter and energy band gap to the linear and quadratic function of Br content, respectively, which are in good agreement with the experiment, respecting the Vegard's law. With the calculated exciton binding energy and light absorption coefficient, we make sure that VCA gives consistent results with the experiment, and the mixed halide perovskites are suitable for generating the charge carriers by light absorption and conducting the carriers easily due to their strong photon absorption coefficient, low exciton bindign energy, and high carrier mobility at low Br contents. Furthermore analyzing the bonding lengths between Pb and X (I$_{1-x}$Br$_x$: virtual atom) as well as C and N, we stress that the stability of perovskite solar cell is definitely improved at $x$=0.2.

Plasmonic Metal Nanoparticles with Core–Bishell Structure for High-Performance Organic and Perovskite Solar Cells

Abstract: To maximize light coupling into the active layer, plasmonic nanostructures have been incorporated into both active layers of organic solar cells (OSCs) and perovskite solar cells (PSCs) with the aim of increasing light absorption, but reports have shown controversial results in electrical characteristics. In this work, we introduce a core-bishell concept to build plasmonic nanoparticles (NPs) with metal-inorganic semiconductor-organic semiconductor nanostructure. Specifically, Ag NPs were decorated with a titania/benzoic-acid-fullerene bishell (Ag@TiO2@Pa), which enables the NPs to be compatible with fullerene acceptors or a perovskite absorber. Moreover, coating the Ag@TiO2 NP with a fullerene shell can activate efficient plasmon-exciton coupling and eliminate the charge accumulation, thus facilitating exciton dissociation and reducing the monomolecular recombination. The improved light absorption and enhanced carrier extraction of devices with Ag@TiO2@Pa nanoparticles are responsible for the improved short-circuit current and fill factor, respectively. On the basis of the synergistic effects (optical and electrical), a series of plasmonic OSCs exhibited enhancement of 12.3-20.7% with a maximum power conversion efficiency of 13.0%, while the performance of plasmonic PSCs also showed an enhancement by 10.2% from 18.4% to 20.2%. This core-bishell design concept of plasmonic nanostructures demonstrates a general approach to improving the photovoltaic performance with both optical and electrical contributions.

Thermodynamic regulation of CH3NH3PbI3 crystal growth and its effect on photovoltaic performance of perovskite solar cells

Abstract: We report a theoretical analysis on the crystallization of CH3NH3PbI3 and the control of grain sizes by varying the two-step reaction temperature from −10 °C to 50 °C based on the present analysis. The thermodynamic equation for CH3NH3PbI3 crystallization is derived by considering the change in Gibbs free energy and the equilibrium concentration of the reaction between the PbI2 film and CH3NH3I solution. The photovoltaic performance of a perovskite solar cell is found to depend on the reaction temperature, which is critical in determining the crystal size of perovskite. The reaction temperature was varied between −10 °C and 50 °C, and the optimal temperature was found to be around 20 °C in our two-step process. The performance enhancement controlled by the grain size with the increase of reaction temperature could be compensated by the generation of defects for a large crystal perovskite layer device.