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.

Slow dynamic processes in lead halide perovskite solar cells. Characteristic times and hysteresis

Abstract: Characteristic times of perovskite solar cells (PSCs) have been measured by different techniques: transient photovoltage decay, transient photoluminescence, and impedance spectroscopy. A slow dynamic process is detected that shows characteristic times in the seconds to milliseconds scale, with good quantitative agreement between transient photovoltage decay and impedance spectroscopy. Here, we show that this characteristic time is related with a novel slow dynamic process caused by the peculiar structural properties of lead halide perovskites and depending on perovskite crystal size and organic cation nature. This new process may lie at the basis of the current–voltage hysteresis reported for PSCs and could have important implications in PSC performance because it may give rise to distinct dynamical behavior with respect to other classes of photovoltaic devices. Furthermore, we show that low-frequency characteristic time, commonly associated with electronic carrier lifetime in other photovoltaic devices, ...

Silver Iodide Formation in Methyl Ammonium Lead Iodide Perovskite Solar Cells with Silver Top Electrodes

Abstract: Silver is a low-cost candidate electrode material for perovskite solar cells. However, in such cells the silver electrodes turn yellow within days of device fabrication. The color change is also accompanied by a dramatic decrease in the power conversion efficiency when compared to otherwise identical devices using gold electrodes. Here, it is shown that the color change results from silver oxidation to silver iodide, due to a reaction with iodine in methyl ammonium lead perovskite. The change in X-ray diffraction and X-ray photo­electron spectroscopy is discussed. Exposure to air accelerates corrosion of the Ag electrodes when compared to dry nitrogen gas exposure. However, iodine not reacted with silver is observed by X-ray photoelectron spectroscopy even for the perovskite solar cell kept in dry nitrogen gas. It is proposed that silver iodide is formed when methyl ammonium iodide migration is facilitated by the small pinholes in the hole transport layer spiro-MeOTAD.

11% Efficient Perovskite Solar Cell Based on ZnO Nanorods: An Effective Charge Collection System

Abstract: A perovskite solar cell based on ZnO nanorods was prepared, and its photovoltaic performance was investigated. ZnO nanorods were grown on the ZnO seed layer from solution, and their diameters and lengths were controlled by precursor concentration and growth time. CH3NH3PbI3 perovskite infiltrated ZnO nanorods showed a power conversion efficiency of 11.13% with short-circuit current density Jsc of 20.08 mA/cm2, open-circuit voltage Voc of 991 mV and fill factor of 0.56. Square spectral feature of external quantum efficiency (EQE) was observed, where EQE exceeded 80% in almost the entire wavelength range from 400 to 750 nm, and the integrated current density of 20.03 mA/cm2 calculated from EQE data was in good agreement with the observed Jsc. Compared to the perfect spectral response of ZnO nanorods, a perovskite solar cell based on TiO2 nanorods exhibited an integrated current density (16 mA/cm2) much lower than the measured Jsc (20.9 mA/cm2). In addition, time-limited photocurrent response under 530 and 7...

Scalable fabrication of efficient organolead trihalide perovskite solar cells with doctor-bladed active layers

Abstract: Organolead trihalide perovskites (OTPs) are nature abundant materials with prospects as future low-cost renewable energy sources boosted by the solution process capability of these materials. Here we report the fabrication of efficient OTP devices by a simple, high throughput and low-cost doctor-blade coating process which can be compatible with the roll-to-roll fabrication process for the large scale production of perovskite solar cell panels. The formulation of appropriate precursor inks by removing impurities is shown to be critical in the formation of continuous, pin-hole free and phase-pure perovskite films on large area substrates, which is assisted by a high deposition temperature to guide the nucleation and grain growth process. The domain size reached 80–250 μm in 1.5–2 μm thick bladed films. By controlling the stoichiometry and thickness of the OTP films, highest device efficiencies of 12.8% and 15.1% are achieved in the devices fabricated on poly(3,4-ethylenedioxythiophene) polystyrene sulfonate and cross-linked N4,N4′-bis(4-(6-((3-ethyloxetan-3-yl)methoxy)hexyl)phenyl)–N4,N4′-diphenylbiphenyl-4,4′-diamine covered ITO substrates. Interestingly, the carrier diffusion length in doctor-bladed OTP films is beyond 3.5 μm which is significantly larger than in the spin-coated films, due to the formation of crystalline grains with a very large size by the doctor-blade coating method.

Low-bandgap mixed tin-lead iodide perovskite absorbers with long carrier lifetimes for all-perovskite tandem solar cells

Abstract: Tandem solar cells using only metal-halide perovskite sub-cells are an attractive choice for next-generation solar cells. However, the progress in developing efficient all-perovskite tandem solar cells has been hindered by the lack of high-performance low-bandgap perovskite solar cells. Here, we report efficient mixed tin–lead iodide low-bandgap (∼1.25 eV) perovskite solar cells with open-circuit voltages up to 0.85 V and over 70% external quantum efficiencies in the infrared wavelength range of 700–900 nm, delivering a short-circuit current density of over 29 mA cm−2 and demonstrating suitability for bottom-cell applications in all-perovskite tandem solar cells. Our low-bandgap perovskite solar cells achieve a maximum power conversion efficiency of 17.6% and a certified efficiency of 17.01% with a negligible current–voltage hysteresis. When mechanically stacked with a ∼1.58 eV bandgap perovskite top cell, our best all-perovskite 4-terminal tandem solar cell shows a steady-state efficiency of 21.0%. All-perovskite tandem solar cells hold the promise of high efficiencies whilst safeguarding the ease of fabrication intrinsic to perovskites. Here, Zhao et al. present a certified 17% efficient tin and lead perovskite solar cell, which is integrated as the low-bandgap component of a tandem device with 21% efficiency.