Perovskite Precursor Solution Research Articles

Mechanism of defect passivation achieved by chemical interaction in inverted perovskite solar cells

A variety of defects exist in the solution-processed polycrystalline perovskites, resulting in photovoltaic output losses and degradation. Chemical interaction is a promising way to realize the passivation of defects. Herein, cetyl pyridinium bromide (CPB) containing both pyridine units and long-chain alkyl groups was introduced in the perovskite precursor solution as a passivation agent. Experimental results show that pyridine unit in CPB formed coordination with uncoordinated Pb2+, which also interact with N–H in MAPbI3. Meanwhile, long-chain alkyl groups in CPB had interaction with MAI and PbI2 in MAPbI3. Thus, trace amount of CPB in the precursor solution improved the optoelectronic properties of perovskite films and suppressed non-radiative carrier recombination in perovskite solar cell (PSC). CPB-modified perovskite films exhibit a lower trap-state density and stronger carrier migration capability. It enables the significant enhancement of PCE values of the p-i-n structured PSC from 18.27 % to 20.53 %, accompanied by the improved stability. Our work exhibits more possibility between passivating additive and PSC performance.

Effective of l-tyrosine hydrochloride on the photovoltaic performance of tin-based perovskite solar cells by suppressing tin (II) oxidation

Additive engineering has been widely concerned to improve the photovoltaic performance of tin-based perovskite solar cells (PSCs). Here, the tin-based perovskite precursor solution is modified with L-Tyrosine hydrochloride (LTHCl). The results demonstrate that the defect state density of tin-based perovskite films is reduced by improving their morphology and crystallinity. The electrical properties of tin-based perovskite film are enhanced by suppressing the Sn2+ oxidation. As a result, the open-circuit voltage of tin-based PSCs is increased from 0.53 V to 0.59 V. The best power conversion efficiency of the tin-based PSC with LTHCl is up to 8.63 %, which is higher than that of the pristine device (7.65 %). Meanwhile, the tin-based PSC with LTHCl retains 84 % of its initial efficiency after over 1140 h in a nitrogen glove box.

Surface modification of paper substrates by a printed UV curing varnish layer and a transferred transparent PEDOT:PSS electrode for paper-based perovskite light-emitting devices in ambient air

Paper, a low-cost and eco-friendly substrate, can be used to prepare flexible electronic devices by resorting to surface modification technology. In this study, we investigated the surface modification of paper substrates, including those that were uncoated or coated with traditional mineral coatings, to analyze the enhancements to surface flatness and water resistance using a UV curing varnish layer. Furthermore, we explored the formation of perovskite films on the surface-modified paper substrates utilizing a PEO-doped perovskite precursor solution in ambient air, and the surface morphology, crystallinity, photoluminescence properties, and absorption properties of the prepared perovskite films were discussed accordingly. Considering the nontransparent feature of paper-based substrates, the inverted perovskite light-emitting device was finally assembled by transfer printing a transparent PEDOT:PSS layer as a top electrode. The conductive and optical properties of the electrode layer were thus analyzed as well. It is found that the surface modification of paper substrates via printing the UV curing varnish can illustrate significant improvements, such as pore-filling on the surface, a more than 10-fold reduction in roughness, and downward penetration. Moreover, prepared perovskite films on the surface-modified coated paper exhibit superior enhancements, including photoluminescence, higher crystallinity, and surface roughness and porosity. Devices fabricated on the surface-modified substrates are less susceptible to short-circuiting. The electroluminescence on the surface-modified coated paper substrate is 2.16 times higher than the prepared device on the surface-modified base paper substrate and even 3.23 times higher than on the PET substrate. Therefore, it is quite feasible to fabricate a perovskite light-emitting device on the modified surface of a paper substrate by using a printed UV curing varnish layer, which is expected to be a promising coating to polish the paper surface in the preparation of electroluminescent devices.

Symmetrical dicyano-based imidazole molecule-assisted crystallization and defects passivation for high-performance perovskite solar cells

Benefiting from the simple and low-cost fabrication of the one-step anti-solvent spin-coating process, the perovskite solar cells (PSCs) have a boost development. However, a great number of defects are generated during solution-fabrication process, retarding the development of PSCs seriously. In this study, the utilization of 4,5-dicyanoimidazole (DCI) as an additive for perovskite precursor solution was investigated. The presence of the double –CN groups in DCI facilitated the formation of Lewis acid-base coordination with unsaturated Pb2+ ions, as well as interaction with I- anions by the –NH- moiety, resulting in the enhanced perovskite film crystallinity, the reduced grain boundaries, and a significant reduction in the defects density of the perovskite film. The decreased trap-assisted recombination and voltage open circuit (VOC) losses in the PSC resulted in the improved photovoltaic performance of device treated by DCI molecule, the PCE increased from 19.59 % to 21.87 % significantly. Moreover, the unencapsulated device with DCI additive exhibited a remarkable 87.8 % retention of its initial PCE after exposure under 10–20 % relative humidity for 60 days, demonstrating an excellent stability than control device.

Disperse PbI2 clusters with 4-Difluoromethyl-Benzylamine Hydrochloride to improve the efficiency and stability of perovskite solar cells

Generally, an excess of PbI2 is used in the perovskite precursor solution to increase the crystallinity of the perovskite. However, excessive PbI2 will form PbI2 clusters during the annealing process of the perovskite film, which will cause the decomposition of perovskite solar cells (PSCs) and affect the stability of the device. Here we use 4-Difluoromethyl-Benzylamine Hydrochloride (4F2M-BACl) to do interfacial doping of the perovskite film to passivate the defects on the surface of the perovskite film and disperse the PbI2 clusters through the interaction with PbI2. Under the passivation effect of 4F2M-BACl, the power conversion efficiency (PCE) of PSCs was increased from 18.51% to 21.51%, and the hysteresis indicator (HI) was lower. In addition, the hydrophobic functional group F and benzene ring of 4F2M-BACl and the dispersing effect of 4F2M-BACl on PbI2 have significantly improved the stability of the device. Unencapsulated devices with 4F2M-BACl modification were able to maintain over 85% of the initial PCE after 170 h at 80% relative humidity (RH).

Break through the Steric Hindrance of Ionic Liquids with Carbon Quantum Dots to Achieve Efficient and Stable Perovskite Solar Cells.

Overcoming the negative impact of residual ionic liquids (ILs) on perovskite films based on an in-depth understanding of chemical interactions between ionic liquids and preparing perovskite precursor solutions is a great challenge when aiming to simultaneously achieve long-term stability and high efficiency within IL-based perovskite solar cells (PSCs). Herein, 1-butyl-3-methylimidazolium tetrafluoroborate (BMIMBF4), a type of IL, was introduced into the perovskite precursor solution, and carbon quantum dots (CQDs) were further introduced into the antisolvent to enhance the photovoltaic properties of PSCs. Both ILs and CQDs synergistically manipulate the crystallization process and passivate defects to obtain high-quality perovskite films. Besides serving as passivation sites to strengthen the collaboration between additives and perovskite materials, the cointroduction of CQDs further promotes the carrier transport process since it not only provides carrier channels at grain boundaries but also forms better energy alignment, which effectively overcomes the charge transfer loss caused by the steric hindrance of ILs. Based on such a synergistic effect of ILs and CQDs, the n-i-p MAPbI3-based PSCs achieve the highest efficiency of 20.84% with improved stability. This simple and low-cost synergistic integration method will subsequently provide direction for optimizing ILs to improve the photovoltaic performance of PSCs.

Crystallization Retardation and Synergistic Trap Passivation in Perovskite Solar Cells Incorporated with Magnesium-Decorated Graphene Quantum Dots.

One of the encouraging strategies for enhancing the efficiency of perovskite solar cells (PSCs) is to reduce defects, trap states of pinholes, and charge recombination rate in the light absorber layer of perovskite, which can be addressed by increasing the perovskite grain size. The utilization of Mg-decorated graphene quantum dots (MGQD) or graphene quantum dots (GQDs) into a perovskite precursor solution for further crystal modification is introduced in this study. Studies on the crystalline structure and morphology of MGQD generated from GQDs demonstrate that MGQD has a greater crystal size than GQD. Therefore, higher light absorption in the whole UV-vis spectrum and a larger grain size for the perovskite/MGQD layer compared to the perovskite/GQD sample are achieved. Moreover, more photoluminescence peak quenching of perovskite/MGQD and extended carrier recombination lifetime (from 3 to 40 ns) verify the surface and grain boundary trap passivation compared to pristine perovskite. Consequently, PSCs in an n-i-p configuration containing perovskite/MGQD show a higher performance of 10.2% in comparison to the pristine perovskite at 7.2%, attributed to the enhanced JSC from 13.2 to 19.1 mA cm-2. Thus, incorporating MGQDs into the perovskite layer is a hopeful approach for obtaining a superior perovskite film with impressive charge extraction and decreased nonradiative charge recombination.

Inhibition of Sn2+ Oxidation in FASnI3 Perovskite Precursor Solution and Enhanced Stability of Perovskite Solar Cells by Reductive Additive.

Tin-based halide perovskite solar cells (Sn-PSCs) have attracted a progressive amount of attention as a potential alternative to lead-based PSCs (Pb-PSCs). Sn-perovskite films are fabricated by a solution process spin-coating technique. However, the efficiency of these devices varies significantly with the different batches of precursor solution due to the poor chemical stability of SnI2-DMSO and the oxidation of Sn2+ to Sn4+. This study investigated the origin of Sn2+ oxidation before film formation, and it was identified that the ionization of SnI2 in dimethyl sulfoxide (DMSO) causes the oxidation of free Sn2+ and I- ions. To address these issues, this study introduces the reductive additive 4-fluorophenylhydrazine hydrochloride (4F-PHCl) in the FASnI3 perovskite precursor solution. The hydrazine functional (-NH-NH2) group converted detrimental Sn4+ and I2 defects back to Sn2+ and I- in precursor solution while retaining the properties of the perovskite solution. Furthermore, the addition of 4F-PHCl in the precursor solution effectively slows the crystallization process, enhancing the crystallinity of FASnI3 perovskite films and guaranteeing the Sn2+/I- stoichiometric ratio, ultimately leading to a power conversion efficiency (PCE) of 10.86%. The hydrophobic fluorinated benzene ring in 4F-PHCl ensures moisture stability in perovskite films, allowing unencapsulated PSCs to retain over 92% of their initial PCE in an N2-filled glovebox for 130 days. Moreover, the 4F-PHCl-modified encapsulated PSCs showed superior operational stability for 420 h and maintained 95% of their initial PCE for 300 h under maximum power point tracking at 1 sun continuous illumination. This study's findings provide a promising pathway to create a controlled Sn-based perovskite precursor solution for highly reproducible and stable Pb-free Sn-PSCs.

Benzophenone: A Small Molecule Additive for Enhanced Performance and Stability of Inverted Perovskite Solar Cells.

In this study, we investigated the impact of benzophenone (BP), a small molecule additive, on the performance and stability of inverted perovskite solar cells (PSCs). Specifically, we introduced BP into the perovskite precursor solution of FAPbI3 to fabricate PSCs with an ITO/PEDOT:PSS/BP:FAPbI3/PCBM/C60/PCB/Ag architecture. The incorporation of BP with an optimum concentration of 2 mg mL-1 significantly enhanced the power conversion efficiency (PCE) of the inverted PSC from 13.12 to 18.84% with negligible hysteresis. Notably, the BP-based PSCs retained ∼90% of their initial PCE after being stored in ambient air with 30% relative humidity at 25 °C for 700 h. In contrast, control devices showed rapid degradation, retaining only 30% of their initial value within 300 h under the same conditions. We attributed the superior performance and stability of the BP-based PSCs to the grain boundary passivation of the perovskite film. The improvement was mainly attributed to the intermolecular interaction between the O-donor Lewis base BP material and both Pb2+ and FA+ in FAPbI3. This effectively suppresses trap-assisted recombination and promotes the conversion of the δ-phase to photoactive and stable α-phase FAPbI3. Overall, our findings suggest that BP is a promising additive for improving the performance and stability of inverted PSCs.

Ionic Liquid Additives for Efficient and Durable Two-Step Perovskite Photovoltaic Devices

Ionic liquids (ILs) have found widespread use in controlling the crystallization process of perovskites, optimizing the morphology and enhancing the device performance, especially in the one-step method. However, research regarding the effects of ionic liquids on perovskite devices prepared using the two-step method remains relatively scarce. Here, an IL 1-Hexyl-3-methylimidazolium Tetrafluoroborate (HMIMBF4) is selected as an additive in the perovskite precursor solution for the fabrication of PSCs using the two-step method. Our study involves a systematic exploration of the precise effects of ILs on the morphology of perovskite thin films, defect density, and photovoltaic performance. IL HMIMBF4 is convincingly shown to possess a robust chemical affinity with perovskite components, thereby establishing a basis for the inhibition of ion migration. Concurrently, ILs play a pivotal role in governing the morphology of perovskite while also facilitating the conversion of lead iodide into the perovskite structure. Benefiting from the regulation of the perovskite morphology and defect states by IL HMIMBF4, the devices with an efficiency exceeding 23% is ultimately achieved. Our research provides a comprehensive comprehension and contributes to advancing the utilization of ILs in two-step photovoltaic devices.

Dimension-Controlled Synthesis of Hybrid-Mixed Halide Perovskites for Solar Cell Application.

Despite the rapid improvement of photovoltaic (PV) efficiency in hybrid organic-inorganic metal halide perovskites (HOIPs), the fabrication procedure of a compact thin film in a large-area application is still a tedious work. Apart from the quality of the thin film, the stability of the perovskite materials and the expensive organic hole transport layer (HTL) within the HOIP-based PV device are the major issues that need to be addressed prior to their commercialization. Herein, a unique glass rod-based facile fabrication technique for producing a compact and stable thin film utilizing a mixed-halide-based perovskite precursor solution is demonstrated. The fabricated devices deliver high photoconversion efficiency (PCE) without the use of any HTL and show an excellent stability under ambient conditions. By varying the organic CH3NH3I (MAI) and inorganic PbBr2 content, perovskite materials with different dimensions, i.e., 3D, 2D, and 1D, are synthesized to produce an active layer for PV devices. Although a 2D single-halide perovskite is reported earlier, herein two different mixed-halide 2D perovskites, i.e., MA2PbI2Br2 and MAPb2IBr4, are synthesized successfully, and their performance is compared in detail along with that of 1D and 3D mixed-halide perovskites. The facile synthesized mixed-halide 2D-based MA2PbI2Br2 perovskite shows a PCE of 10.14% with a high stability of 92% after 100 days without encapsulation, which is much superior as compared to that of the mixed-halide 3D MAPbIBr2. The semiconducting behavior as well as the nature of the bandgap of the synthesized compounds is examined by pursuing density functional theory calculations. Specifically, the role of iodine doping to modify the electronic band structure is investigated, and introduction of iodine is found to reduce the effective masses of both electrons and holes in the perovskite material.

Efficient and stable Sn based perovskite solar cells by the modulation of crystallization with bulky organic cation for large nucleation cluster

Organic-inorganic hybrid halide perovskite have been attracting much attention as promising photovoltaic materials owing to their exceptional photovoltaic characteristics. However, even though the rise of progress for the perovskite solar cell was increased, it was still remained the concern for the toxicity of lead in hybrid organolead based perovskite solar cell, which is the harmful materials to the environmental system.Herein, we incorpoarted the homopiperazium (HP2+) into the FASnI3 perovskite to prepare a high-quality perovskite film with a lower defect density. Since the HP is the largest organic cation, that can not enter 3D perovskite but it played a significant role in modulating the crystallinity, morphology and optoelectronic properties of FASnI3 perovskite. When the HPI2 introduced the perovskite precursor solution, it affects the nucleation of perovskite solution by the formation of large pre-nulceation cluster through the linked colloids. It decrease the energy barrier, resulting in a high-quality perovskite film with a lower defect density. Highly oriented perovskite film exhibits the PCE up to a high at 6.88%, with high long-term stability as well which is much higher than that of the pristine FASnI3 perovskite film (4.71%).

A facile strategy for highly efficient perovskite crystals fabricated in a high moisture environment via solvent engineering process

BackgroundHybrid organic perovskite solar cells (PSCs) have recently gained recognition for their excellent photovoltaic properties. However, most PSCs were fabricated in a nitrogen-filled glovebox to prevent damage from moisture. Overcoming humidity damage is crucial for PSC fabrication in an ambient atmosphere. Fabricating perovskite solar cells (PSCs) under ambient atmosphere conditions needs the aid of substrate heating or air-knife flow to rapidly evaporate solvents. MethodsHerein, we propose a facile solvent engineering method without extra equipment or processes for fabricating highly efficient PSCs in a high moisture condition by a one-step spin-coating process. Acetone incorporation into the perovskite precursor solution not only prevents the ingress of moisture, but also accelerates the volatilization of solvents during the crystallization process. Significant findingsThe as-prepared PSCs feature low trap-state density, high charge recombination resistance, low hysteresis, and long charge lifetime. Little MABr and PbBr2 are separated out to passivate interface/grain-boundary defects. At a 10% acetone incorporation, the highest power conversion efficiency can reach 17.75% for the PSC fabricated in 70% relative humidity. The work provides a facile, promising method to prepare highly efficient PSCs in an ambient atmosphere.

Effect of HBr additive on the performance of all-inorganic Cs3Bi2Br9 halide perovskite resistive switching memory

Non-toxic, stable Cs3Bi2Br9 halide perovskite films prepared using a one-step solution method have become the active layer of resistive switching memory. Here, we control the nucleation and growth of Cs3Bi2Br9 perovskite by introducing an appropriate amount of HBr to adjust the supersaturation of the perovskite precursor solution, thus improving the film formation quality and optimizing the device performance. The memory prepared for this film has a significant bipolar resistive behavior with a high switching ratio of 105, a cycle time of 300 and a retention time of 104 s. In addition, the current transient response of the device under pulsed voltage is investigated. By different the pulse voltage parameters (pulse amplitude, duration and time interval) to study the variation of the device current value, the term "TJUT" is finally encoded and decoded using different the number of pulses and repetitions.

Triiodide Attacks the Organic Cation in Hybrid Lead Halide Perovskites: Mechanism and Suppression.

Molecular I2 can be produced from iodide-based lead perovskites under thermal stress; triiodide, I3 - , is formed from this I2 and I- . Triiodide attacks protic cation MA+ - or FA+ -based lead halide perovskites (MA+ , methylammonium; FA+ , formamidinium) as explicated through solution-based nuclear magnetic resonance (NMR) studies: triiodide has strong hydrogen-bonding affinity for MA+ or FA+ , which leads to their deprotonation and perovskite decomposition. Triiodide is a catalyst for this decomposition that can be obviated through perovskite surface treatment with thiol reducing agents. In contrast to methods using thiol incorporation into perovskite precursor solutions, no penetration of the thiol into the bulk perovskite is observed, yet its surface application stabilizes the perovskite against triiodide-mediated thermal stress. Thiol applied to the interface between FAPbI3 and Spiro-OMeTAD ("Spiro") prevents oxidized iodine species penetration into Spiro and thus preserves its hole-transport efficacy. Surface-applied thiol affects the perovskite work function; it ameliorates hole injection into the Spiro overlayer, thus improving device performance. It helps to increase interfacial adhesion ("wetting"): fewer voids are observed at the Spiro/perovskite interface if thiols are applied. Perovskite solar cells (PSCs) incorporating interfacial thiol treatment maintain over 80% of their initial power conversion efficiency (PCE) after 300h of 85°C thermal stress.

Phase Behavior and Role of Organic Additives for Self-Doped CsPbI3 Perovskite Semiconductor Thin Films.

The phase change of all-inorganic cesium lead halide (CsPbI3) thin film from yellow δ-phase to black γ-/α-phase has been a topic of interest in the perovskite optoelectronics field. Here, the main focus is how to secure a black perovskite phase by avoiding a yellow one. In this work, we fabricated a self-doped CsPbI3 thin film by incorporating an excess cesium iodide (CsI) into the perovskite precursor solution. Then, we studied the effect of organic additive such as 1,8-diiodooctane (DIO), 1-chloronaphthalene (CN), and 1,8-octanedithiol (ODT) on the optical, structural, and morphological properties. Specifically, for elucidating the binary additive-solvent solution thermodynamics, we employed the Flory-Huggins theory based on the oligomer level of additives' molar mass. Resultantly, we found that the miscibility of additive-solvent displaying an upper critical solution temperature (UCST) behavior is in the sequence CN:DMF > ODT:DMF > DIO:DMF, the trends of which could be similarly applied to DMSO. Finally, the self-doping strategy with additive engineering should help fabricate a black γ-phase perovskite although the mixed phases of δ-CsPbI3, γ-CsPbI3, and Cs4PbI6 were observed under ambient conditions. However, the results may provide insight for the stability of metastable γ-phase CsPbI3 at room temperature.

Tuning the Surface Energy of Hole Transport Layers Based on Carbazole Self‐Assembled Monolayers for Highly Efficient Sn/Pb Perovskite Solar Cells

AbstractRecently, carbazole‐based self‐assembled monolayers (SAMs) have been utilized as hole transport layers (HTLs) in perovskite solar cells. However, their application in Sn or mixed Sn/Pb perovskite solar cells has been hindered by the poor wettability of the perovskite precursor solution on the carbazole surface. Here a self‐assembled bilayer (SAB) comprising a covalent monolayer (Br‐2PACz) and a noncovalent wetting layer (4CzNH3I) as the HTL in a Cs0.25FA0.75Sn0.5Pb0.5I3 perovskite solar cell is proposed. It is demonstrated that the wetting layer completely solves the problem due to the higher polarity of the surface and, furthermore, the ammonium groups help in the passivation of trap states at the buried SAB/perovskite interface. The introduction of the SAB enhances the device reproducibility with an average efficiency of 18.98 ± 0.28% (19.45% for the best device), compared to 11.54 ± 9.36% (19.34% for the best device) for the SAM‐only devices. Furthermore, the improved perovskite processability on the SAB helps to increase the reproducibility of larger size device, where, a 12.5% efficiency for a 0.8 cm2 active area device compared to 0.68% for the best SAM‐based solar cell is demonstrated. Finally, the device's operational stability is also improved to 358 hours (T80%), compared to 220 hours for the SAM‐based solar cell.

Facile growth of perovskite nanoparticles confined on dimension-controlled Si nanorod arrays for various promising photophysical applications

In this study, a facile growth of hybrid perovskite nanoparticles (NPs) has been demonstrated on mesoporous, high-aspect ratio, morphology-controlled Si nanorod (NR) arrays. A generic method of directly confining perovskite nanocrystallites (average size <7 nm) on a mesoporous substrate without the use of colloidal stabilization was introduced. The perovskite NPs coated on dimension-and position-controlled Si NR arrays were systematically investigated by their various photophysical properties such as optical reflectance, cathodoluminescence (CL), and photoluminescence (PL) behaviors at both room temperature and low temperature. The dimension and position of the Si NR arrays were controlled by e-beam lithography followed by selective metal-assisted chemical etching (MACE). Organic-inorganic perovskite NPs were synthesized on the surface of Si NR array by spin coating of perovskite precursor solution and followed by annealing. The porous and rough sites on the surface of the NR arrays acted as nucleation centers for the formation of perovskite NPs. Due to the excitonic recombination of CH3NH3PbBr3, the NPs confined on the various NR templates exhibited strong PL emission in the 505–510 nm region. Furthermore, due to greater radiative recombination and lesser carrier trapping in the NPs, the PL and CL emission intensities of the perovskite NPs localized on the surface of the NR array were dramatically increased (PL enhancement factor ∼ 7.7, when NR aspect ratio ∼ 17.2) as compared to the bulk perovskite microcrystals. The low-temperature PL study revealed higher exciton binding energy of the NPs as compared to the bulk microcrystalline film. A systematic investigation revealed that the optical absorption, as well as the emission color of the perovskite NPs, can be tuned by the aspect ratio of the Si NR arrays. The results of our studies indicate the application of bandgap engineering of perovskite nanocrystals through confinement in a mesoporous, well-organized, regularly-ordered template as a powerful tool for tuning the emission wavelength in next-generation photonic sources. Furthermore, the important findings on the periodic array of photoactive nanoscale materials introduced in this manuscript may open up huge opportunities in numerous cutting-edge applications such as light emitting diode arrays, photodetector arrays, individually addressable devices, display devices with controlled pixel size and pixel density, etc.

Postdeposition Halide Exchange for Achieving Deep-Blue Perovskite Light-Emitting Diodes: The Role of the Organic Cations in the Chloride Source.

Postdeposition halide exchange has been a popular strategy for tuning the emission wavelength of metal halide perovskites and is particularly attractive in achieving deep-blue perovskite light-emitting diodes (PeLEDs), where the quality of the emissive layer is largely limited by the low solubility of chlorides in perovskite precursor solution. In this work, the halide exchange strategy isexamined for deep-blue PeLEDs, with a focus on understanding the role of the organic cations of the halide salt (i.e., the chloride source for ion exchange) in modifying the properties of the perovskite films and consequently the PeLED performances. By comparatively investigating the treatment effects of two model systems, namely phenethylammonium chloride and 2,2-diphenylethylammonium chloride (DPEACl), it isfound that although the two chlorides produce highly similar photoluminescence properties of the perovskite films, they create different landscapes for current flow in the PeLEDs. In particular, the bulky branch-structured DPEA cations exhibit minimal disturbance to the perovskite grains while providing highly effective inter-grain void filling and thus leakage current blocking, leading to 3D perovskite-based PeLEDs with a record high peak external quantum efficiency of 6.4% at 462nm. The study highlights the importance of organic cation selection in the halide exchange processes for PeLEDs.

Long-Chain Gemini Surfactant-Assisted Blade Coating Enables Large-Area Carbon-Based Perovskite Solar Modules with Record Performance

HighlightsTrace amounts of long-chain gemini surfactants are essential for blade-coating of high-quality perovskite films, enabling a 17.05% efficient full printed carbon-based module (50 cm2 active area).Only when the surfactant chain is over a critical length will the gemini surfactant be effective for blade-coating of perovskite films.The surfactants increase the capillary number of perovskite precursor solution, reduce the local disturbance and combat inhomogeneous solidification during blade coating, thus allowing high-quality perovskite films to be formed.