Assessing the Influence of Illumination on Ion Conductivity in Perovskite Solar Cells.

Whether illumination influences the ion conductivity in lead-halide perovskite solar cells containing iodide halides has been an ongoing debate. Experiments to elucidate the presence of a photoconductive effect require special devices or measurement techniques and neglect possible influences of the enhanced electronic charge concentrations. Here, we assess the electronic-ionic charge transport using drift-diffusion simulations and show that the well-known increase in capacitance at low frequencies under illumination is caused by electronic currents that are amplified due to the screening of the alternating electric field by the ions.

A Newly Crosslinked-double Network PEDOT:PSS@PEGDMA toward Highly-Efficient and Stable Tin-Lead Perovskite Solar Cells.

Until now, poly(3,4-ethylenedioxythiophene):poly(styrensulfonate) (PEDOT:PSS) is widely used in Sn-Pb perovskite solar cells (PSCs) due to its many advantages, including high optical transparency, suitable conductivity, superior wettability, and so on. However, the acidic and hydroscopic properties of the PSS component, as well as the incongruous energy level of the hole transport layer (HTL), may lead to unsatisfying interface properties and decreased device performance. Herein, by adding polyethylene glycol dimethacrylate (PEGDMA) into PEDOT:PSS, a newly crosslinked-double-network obtain of PEDOT:PSS@PEGDMA film, which could not only optimize nucleation and crystallinity of Sn-Pb perovskite films, but also suppress defect density and optimize energy level alignment at the HTL/perovskite interface.

Interface Modification for Efficient and Stable Inverted Inorganic Perovskite Solar Cells.

Due to their excellent thermal stability and ideal bandgap, metal halide inorganic perovskite based solar cells (PSCs) with inverted structure are considered as an excellent choice for perovskite/silicon tandem solar cells. However, the power conversion efficiency (PCE) of inverted inorganic perovskite solar cells (PSCs) still lags far behind that of conventional n-i-p PSCs due to interfacial energy level mismatch and high nonradiative charge recombination. Herein, the performance of inverted PSCs is significantly improved by interfacial engineering of CsPbI Br films with 2-mercapto-1-methylimidazole (MMI).

Combined Vacuum Evaporation and Solution Process for High-Efficiency Large-Area Perovskite Solar Cells with Exceptional Reproducibility.

Organic-inorganic hybrid perovskites exhibit outstanding performances in perovskite solar cells (PSCs). However, the complex solution chemistry of perovskites precursors renders it difficult to prepare large-area devices in a reproducible way, which is a prerequisite for the technology to make an impact beyond lab scale. Vacuum processing, instead, is an established technology for large-scale coating of thin films.

Simultaneous Lattice Engineering and Defect Control via Cadmium Incorporation for High-Performance Inorganic Perovskite Solar Cells.

Doping of all-inorganic lead halide perovskites to enhance their photovoltaic performance and stability has been reported to be effective. Up to now most studies have focused on the doping of elements in to the perovskite lattice. However, most of them cannot be doped into the perovskite lattice and the roles of these dopants are still controversial.

Multifunctional succinate additive for flexible perovskite solar cells with more than 23% power-conversion efficiency.

Flexible perovskite solar cells (FPSCs) have emerged as power sources in versatile applications owing to their high-efficiency characteristics, excellent flexibility, and relatively low cost. Nevertheless, undesired strain in perovskite films greatly impacts the power-conversion efficiency (PCE) and stability of PSCs, particularly in FPSCs. Herein, a novel multifunctional organic salt, methylammonium succinate, which can alleviate strain and reinforce grain boundaries, was incorporated into the perovskite film, leading to relaxed microstrain and a lower defect concentration.

A Transparent Electrode Based on Solution-Processed ZnO for Organic Optoelectronic Devices.

Achieving high-efficiency indium tin oxide (ITO)-free organic optoelectronic devices requires the development of high-conductivity and high-transparency materials for being used as the front electrode. Herein, sol-gel-grown zinc oxide (ZnO) films with high conductivity (460 S cm) and low optical absorption losses in both visible and near-infrared (NIR) spectral regions are realized utilizing the persistent photoinduced doping effect. The origin of the increased conductivity after photo-doping is ascribed to selective trapping of photogenerated holes by oxygen vacancies at the surface of the ZnO film.

Sequential vacuum-evaporated perovskite solar cells with more than 24% efficiency.

Vacuum evaporation is promising for the high-throughput fabrication of perovskite solar cells (PSCs) because of its solvent-free characteristic, precise control of film thickness, and compatibility with large-scale production. Nevertheless, the power conversion efficiency (PCE) of PSCs fabricated by vacuum evaporation lags behind that of solution-processed PSCs. Here, we report a Cl-containing alloy-mediated sequential vacuum evaporation approach to fabricate perovskite films.

Conformal quantum dot-SnO layers as electron transporters for efficient perovskite solar cells.

Improvements to perovskite solar cells (PSCs) have focused on increasing their power conversion efficiency (PCE) and operational stability and maintaining high performance upon scale-up to module sizes. We report that replacing the commonly used mesoporous-titanium dioxide electron transport layer (ETL) with a thin layer of polyacrylic acid-stabilized tin(IV) oxide quantum dots (paa-QD-SnO) on the compact-titanium dioxide enhanced light capture and largely suppressed nonradiative recombination at the ETL-perovskite interface. The use of paa-QD-SnO as electron-selective contact enabled PSCs (0.

Interfaces and Interfacial Layers in Inorganic Perovskite Solar Cells.

Owing to their superior thermal stability, metal halide inorganic perovskite materials continue to attract interest for photovoltaics applications. The highest reported power conversion efficiency (PCE) for solar cells based on inorganic perovskites is over 20 %. As this PCE corresponds to 73 % of the theoretical limit, there remains more room for further improving the device PCEs than for improving organic-inorganic hybrid perovskite solar cells (PSCs).

Mobile ions determine the luminescence yield of perovskite light-emitting diodes under pulsed operation.

The external quantum efficiency of perovskite light-emitting diodes (PeLEDs) has advanced quickly during the past few years. However, under pulsed operation, an operation mode which is important for display and visible light communication, the performance of PeLEDs changes a lot and requires in-depth understanding to facilitate these applications. Here, we report the response of PeLEDs under pulsed operation in the range of 10 Hz to 20 kHz.

Crystal-Size-Induced Band Gap Tuning in Perovskite Films.

A comprehensive picture explaining the effect of the crystal size in metal halide perovskite films on their opto-electronic characteristics is currently lacking. We report that perovskite nanocrystallites exhibit a wider band gap due to concurrent quantum confinement and size dependent structural effects, with the latter being remarkably distinct and attributed to the perturbation from the surface of the nanocrystallites affecting the structure of their core. This phenomenon might assist in the photo-induced charge separation within the perovskite in devices employing mesoporous layers as they restrict the size of nanocrystallites present in them.

Vapor-assisted deposition of highly efficient, stable black-phase FAPbI perovskite solar cells.

Mixtures of cations or halides with FAPbI (where FA is formamidinium) lead to high efficiency in perovskite solar cells (PSCs) but also to blue-shifted absorption and long-term stability issues caused by loss of volatile methylammonium (MA) and phase segregation. We report a deposition method using MA thiocyanate (MASCN) or FASCN vapor treatment to convert yellow δ-FAPbI perovskite films to the desired pure α-phase. NMR quantifies MA incorporation into the framework.

Ba-induced phase segregation and band gap reduction in mixed-halide inorganic perovskite solar cells.

All-inorganic metal halide perovskites are showing promising development towards efficient long-term stable materials and solar cells. Element doping, especially on the lead site, has been proved to be a useful strategy to obtain the desired film quality and material phase for high efficient and stable inorganic perovskite solar cells. Here we demonstrate a function by adding barium in CsPbIBr.

Perovskite Solar Cells Yielding Reproducible Photovoltage of 1.20 V.

High photovoltages and power conversion efficiencies of perovskite solar cells (PSCs) can be realized by controlling the undesired nonradiative charge carrier recombination. Here, we introduce a judicious amount of guanidinium iodide into mixed-cation and mixed-halide perovskite films to suppress the parasitic charge carrier recombination, which enabled the fabrication of >20% efficient and operationally stable PSCs yielding reproducible photovoltage as high as 1.20 V.

Review on Recent Progress of All-Inorganic Metal Halide Perovskites and Solar Cells.

All-inorganic perovskites are considered to be one of the most appealing research hotspots in the field of perovskite photovoltaics in the past 3 years due to their superior thermal stability compared to their organic-inorganic hybrid counterparts. The power-conversion efficiency has reached 17.06% and the number of important publications is ever increasing.

Origin of apparent light-enhanced and negative capacitance in perovskite solar cells.

So-called negative capacitance seems to remain an obscure feature in the analysis of the frequency-dependent impedance of perovskite solar cells. It belongs to one of the puzzling peculiarities arising from the mixed ionic-electronic conductivity of this class of semiconductor. Here we show that apparently high capacitances in general (positive and negative) are not related to any capacitive feature in the sense of a corresponding charge accumulation.

Electroluminescence Dynamics in Perovskite Solar Cells Reveals Giant Overshoot Effect.

High performance of both photovoltaic and electroluminescent devices requires low nonradiative recombination losses. In perovskites, such loses strongly depend on the carrier traps related to the mobile ions and vacancies, causing I- V hysteresis of solar cells and influencing the performance of other optoelectronic devices, such as photodetectors and LEDs. To address the dynamics of the mobile ions, here we investigate electroluminescence time evolution in perovskite solar cells under constant and pulsed voltage conditions.

Design rules for minimizing voltage losses in high-efficiency organic solar cells.

The open-circuit voltage of organic solar cells is usually lower than the values achieved in inorganic or perovskite photovoltaic devices with comparable bandgaps. Energy losses during charge separation at the donor-acceptor interface and non-radiative recombination are among the main causes of such voltage losses. Here we combine spectroscopic and quantum-chemistry approaches to identify key rules for minimizing voltage losses: (1) a low energy offset between donor and acceptor molecular states and (2) high photoluminescence yield of the low-gap material in the blend.

Reducing Surface Recombination by a Poly(4-vinylpyridine) Interlayer in Perovskite Solar Cells with High Open-Circuit Voltage and Efficiency.

Identifying and reducing the dominant recombination processes in perovskite solar cells is one of the major challenges for further device optimization. Here, we show that introducing a thin interlayer of poly(4-vinylpyridine) (PVP) between the perovskite film and the hole transport layer reduces nonradiative recombination. Employing such a PVP interlayer, we reach an open-circuit voltage of 1.

Planar Perovskite Solar Cells with High Open-Circuit Voltage Containing a Supramolecular Iron Complex as Hole Transport Material Dopant.

In perovskite solar cells (PSCs), the most commonly used hole transport material (HTM) is spiro-OMeTAD, which is typically doped by metalorganic complexes, for example, based on Co, to improve charge transport properties and thereby enhance the photovoltaic performance of the device. In this study, we report a new hemicage-structured iron complex, 1,3,5-tris(5'-methyl-2,2'-bipyridin-5-yl)ethylbenzene Fe(III)-tris(bis(trifluoromethylsulfonyl)imide), as a p-type dopant for spiro-OMeTAD. The formal redox potential of this compound was measured as 1.

Poly(ethylene glycol)-[60]Fullerene-Based Materials for Perovskite Solar Cells with Improved Moisture Resistance and Reduced Hysteresis.

A series of [60]fullerenes covalently functionalized with the polymer poly(ethylene glycol) is presented. These new [60]fullerene-based materials have been incorporated as additives in CH NH PbI (MAPbI ), the most common organic-inorganic perovskite used in perovskite solar cells. The extensive photovoltaic study performed by using these materials shows several beneficial effects on the performance of these cells, including a reduction in hysteresis and an increased stability against moisture, whereby the solar cells retain up to 97 % of their initial power conversion efficiency in an ambient atmosphere.