Progress In Perovskite Solar Cells Research Articles

Imidazole-Based Ionic Liquid Engineering for Perovskite Solar Cells with High Efficiency and Excellent Stability.

Despite the remarkable progress of perovskite solar cells (PSCs), the substantial inherent defects within perovskites restrict the achievement of higher efficiency and better long-term stability. Herein, we introduced a novel multifunctional imidazole analogue, namely, 1-benzyl-3-methylimidazolium bromide (BzMIMBr), into perovskite precursors to reduce bulk defects and inhibit ion migration in inverted PSCs. The electron-rich environment of -N- in the BzMIMBr structure, which is attributed to the electron-rich adjacent benzene ring-conjugated structure, effectively passivates the uncoordinated Pb2+ cations. Moreover, the interaction between the BzMIMBr additive and perovskite can effectively hinder the deprotonation of formamidinium iodide/methylammonium iodide (FAI/MAI), extending the crystallization time and improving the quality of the perovskite precursors and films. This interaction also effectively inhibits ion migration to subsequent deposited films, leading to a noteworthy decrease in trap states. Various characterization studies show that the BzMIMBr-doped films exhibit superior film morphology and surface uniformity and reduced nonradiative carrier recombination, consequently enhancing crystallinity by reducing bulk/surface defects. The PSCs fabricated on the BzMIMBr-doped perovskite thin film exhibit a power conversion efficiency of 23.37%, surpassing that of the pristine perovskite device (20.71%). Additionally, the added BzMIMBr substantially increased the hydrophobicity of perovskite, as unencapsulated devices still retained 93% of the initial efficiency after 1800 h of exposure to air (45% relative humidity).

Perovskite solar cells with ferroelectricity

AbstractHalide perovskites show excellent optoelectronic properties for solar cell application. Notably, perovskite crystalline structures have been widely reported to deliver superior ferroelectric properties. As a result, the integration of the ferroelectric process with the photon‐to‐electron energy conversion process becomes feasible to generate interesting photo‐physical properties and further boost the device performance of perovskite solar cells (PSCs), which have started to attract more and more attention in recent years. Here, we have reviewed the recent progress in PSCs with ferroelectricity (FE‐PSCs), by classifying them into three regimes according to the degree of phase segregation, for example, the layer‐structured ferroelectric/halide perovskite composite, micro phase‐separated ferroelectric/halide perovskite composite, and the intrinsic ferroelectric halide perovskite composite. The different composite structures enable a large range of interesting optoelectronic properties and the specific structure significantly enhances the device performance of PSCs. The most prominent contribution of ferroelectricity is that it can provide an extra electrical field to drive charge generation, transport, and collection. Further, key challenges and opportunities of the integration of ferroelectricity with photovoltaics are discussed. We hope our work can draw intensive attention in this field to accelerate the establishment of the basic theories in ferroelectricity and the commercialization of PSCs.

Fluorinated Polyimide Tunneling Layer for Efficient and Stable Perovskite Photovoltaics

AbstractDespite the remarkable progress of perovskite solar cells (PSCs), challenges remain in terms of finding effective and viable strategies to enhance their long‐term stability while maintaining high efficiency. In this study, a new insulating and hydrophobic fluorinated polyimide (FPI: 6FDA‐6FAPB) was used as the interface layer between the perovskite layer and the hole transport layer (HTL) in PSCs. The functional groups of FPI play a pivotal role in passivating interface defects within the device. Due to its high work function, FPI demonstrates field‐effect passivation (FEP) capabilities as an interface layer, effectively mitigating non‐radiative recombination at the interface. Notably, the FPI insulating interface layer does not impede carrier transmission at the interface, which is attributed to the presence of hole tunneling effects. The optimized PSCs achieve an outstanding power conversion efficiency (PCE) of 24.61 % and demonstrate excellent stability, showcasing the efficacy of FPI in enhancing device performance and reliability.

Fluorinated Polyimide Tunneling Layer for Efficient and Stable Perovskite Photovoltaics.

Despite the remarkable progress of perovskite solar cells (PSCs), challenges remain in terms of finding effective and viable strategies to enhance their long-term stability while maintaining high efficiency. In this study, a new insulating and hydrophobic fluorinated polyimide (FPI: 6FDA-6FAPB) was used as the interface layer between the perovskite layer and the hole transport layer (HTL) in PSCs. The functional groups of FPI play a pivotal role in passivating interface defects within the device. Due to its high work function, FPI demonstrates field-effect passivation (FEP) capabilities as an interface layer, effectively mitigating non-radiative recombination at the interface. Notably, the FPI insulating interface layer does not impede carrier transmission at the interface, which is attributed to the presence of hole tunneling effects. The optimized PSCs achieve an outstanding power conversion efficiency (PCE) of 24.61 % and demonstrate excellent stability, showcasing the efficacy of FPI in enhancing device performance and reliability.

Boosting optoelectronic performance of (FA)X(MA)1-XPbI3 perovskite solar cells: Via FAI post-treatment engineering

Complex composition engineering of mixed-cations perovskite (FAxMA1-xPbI3) has recently supported rapid progress in perovskite solar cells (PSCs). Nevertheless, it is insufficient to embed and accommodate formamidinium (FA) cation into the MAPbI3 lattice structure via existing methods, leaving behind masses of FA or lead halide content and deteriorating photovoltaic performance. Herein, we present facile surface engineering via post-treated methodology, the surface of CH3NH3PbI3 (MAPbI3) films post-treated with formamidinium iodide (FAI) solution and that results get mixed-cation FAxMA1-xPbI3 perovskite films. The mixed-cation-based FAXMA1-XPbI3 perovskite with significant and large grain size, uniform and compact morphology, highly crystallization, and consequently reducing defect density of the perovskite films can be produced via the present method. It is observed that the film, post-treated with FAI-2, shows results in a very stable and highly crystalline lattice structure with attributes such as extended carrier lifetime, better electron transport, and decreased defect density. The optimized device demonstrates a promising power conversion efficiency (PCE) of 21.89%, and higher than that of the non-treated (19.08%) devices. Furthermore, the devices based on the novel FAI-post-treatment engineering exhibit significantly enhanced stability compared to non-treated devices. Therefore, this approach provides a novel methodology that offers a simple method for producing superior mixed perovskite films, potentially paving the way for the future exploitation of the boosted performance of perovskite solar cells.

Low-cost dopant-free fluoranthene-based branched hole transporting materials for efficient and stable n-i-p perovskite solar cells

It has been widely recognized that hole transporting materials (HTMs) play a key role in the rapid progress of perovskite solar cells (PVSCs). However, common organic HTMs such as spiro-OMeTAD not only suffer from high synthetic costs, but also usually require the additional chemical doping process to improve their hole transport ability, which unfortunately induces the terrible stability issue. Therefore, it is urgent to develop low-cost dopant-free HTMs for efficient and stable PVSCs. In this work, we have successfully developed a new class of efficient dopant-free fluoranthene-based HTMs (TPF1–5) with quite low lab synthetic costs by combining donor-acceptor and branched structure designs. The detailed structure-property study revealed that tuning the twisted arms at different substitution sites would regulate the intermolecular interactions and film-forming ability, thereby significantly affecting the performance of the HTMs. By applying these HTMs in conventional PVSCs, the dopant-free TPF1-based devices not only achieved the best efficiency of 21.76%, which is comparable to that of the doped spiro-OMeTAD control devices, but also showed much better operational stability, which maintained over 87% of the initial efficiency under maximum power point tracking after 1038 h.

High-Quality Hybrid Perovskite Thin Films by Post-Treatment Technologies in Photovoltaic Applications.

Incredible progress in photovoltaic devices based on hybrid perovskite materials has been made in the past few decades, and a record-certified power conversion efficiency (PCE) of over 26% has been achieved in single-junction perovskite solar cells (PSCs). In the fabrication of high-efficiency PSCs, the postprocessing procedures toward perovskites are essential for designing high-quality perovskite thin films; developing efficient and reliable post-treatment techniques is very important to promote the progress of PSCs. Here, recent post-treatment technological reforms toward perovskite thin films are summarized, and the principal functions of the post-treatment strategies on the design of high-quality perovskite films have been thoroughly analyzed by dividing into two categories in this review: thermal annealing (TA)-related technique and TA-free technique. The latest research progress of the above two types of post-treatment techniques is summarized and discussed, focusing on the optimization of postprocessing conditions, the regulation of perovskite qualities, and the enhancement of device performance. Finally, an outlook of the prospect trends and future challenges for the fabrication of the perovskite layer and the production of highly efficient PSCs is given.

Synergistic Full‐Scale Defect Passivation Enables High‐Efficiency and Stable Perovskite Solar Cells

AbstractDespite remarkable progress in perovskite solar cells (PSCs), the unsatisfying stability strongly interrelated with the defect density remains the main obstacle for commercialization. Herein, a synergetic defect passivation method is judiciously designed that consists of a precursor engineering strategy based on an ionic liquid 1‐butylsulfonate‐3‐methylimidazolium dihydrogen phosphate (BMDP), and two‐stage annealing (TSA) treatment to sufficiently passivate defects and enhance performance further. It is found that the multifunctional groups from BMDP have strong chemical interactions and form chelated complexes with perovskite components thus effectively passivating the intrinsic defects. Synergized by the sequential TSA treatment, the formed hydrophobic complexes can be precisely controlled with filling along grain boundaries (GBs) and on surfaces, leading to a wrapping of perovskite grains and significant passivation of GBs. Consequently, both deep‐ and shallow‐level defects in the bulk, at GBs and surface are sufficiently passivated, resulting in a champion efficiency of 24.20%. Impressively, the resultant unencapsulated films and corresponding devices exhibit admirable stability with maintaining 83.9% of initial composition for 4000 h of aging in moist air, 81.7% original structure after continuous heating for 1600 h, and 97% initial power conversion efficiency for 1000 h under continuous illumination. This work provides an efficient strategy toward improved efficiency and stability PSCs.

Recent Progress of Low-Toxicity Poor-Lead All-Inorganic Perovskite Solar Cells.

Organic-inorganic hybrid perovskite solar cells (PSCs) have achieved an impressive certified efficiency of 25.7%, which is comparatively higher than that of commercial silicon solar cells (23.3%), showing great potential toward commercialization. However, the low stability and high toxicity due to the presence of volatile organic components and toxic metal lead in the perovskites pose significant challenges. To obtain robust and low-toxicity PSCs, substituting organic cations with pure inorganic cations, and partially or fully replacing the toxic Pb with environmentally benign metals, is one of the promising methods. To date, continuous efforts have been made toward the construction of highly performed low-toxicity inorganic PSCs with astonishing breakthroughs. This review article provides an overview of recent progress in inorganic PSCs in terms of lead-reduced and lead-free compositions. The physical properties of poor-lead all-inorganic perovskites are discussed to unveil the major challenges in this field. Then, it reports notable achievements for the experimental studies to date to figure out feasible methods for efficient and stable poor-lead all-inorganic PSCs. Finally, a discussion of the challenges and prospects for poor-lead all-inorganic PSCs in the future is presented.

Progress and Challenges of Chloride–Iodide Perovskite Solar Cells: A Critical Review

Chloride–iodide perovskites have received substantial interest due to their better photovoltaic performance compared to pure iodide ones. The superior properties of chloride–iodide perovskites boost photovoltaic performance. However, quantifying the Cl composition in perovskite films remains challenging. Hence, it is not easy to correlate the Cl quantity with the improved photovoltaic performance. Considering this critical issue, it is still necessary to determine the correlation between the Cl quantity and the improved photovoltaic performance to solve this puzzle. Here, a critical review is presented showcasing the significant impacts of the Cl quantity on chloride–iodide perovskites and related solar cell devices. This review provides an up-to-date picture of different strategic methods to overcome the challenges of Cl incorporation in I-based perovskites, aiming to improve photovoltaic performance. Finally, some valuable remedies are prescribed for potential future research strategies to study the photovoltaic performance of chloride–iodide perovskite solar cells. Hopefully, this review will be a noteworthy scientific contribution to the advancement of the continuous progress of perovskite solar cells.

Carbon Dots in Perovskite Solar Cells: Properties, Applications, and Perspectives

Perovskite solar cells (PSCs) have attracted substantial research interest owing to their flexible fabrication, high efficiency, and low cost. Currently, the power conversion efficiency (PCE) of PSCs has reached 25.7%, meeting the requirements for commercialization. In recent years, as a novel type of carbon nanomaterial, carbon dots (CDs) with abundant and tunable surface functional groups have shown great potential in regulating the efficiency and stability of PSCs because of their tunable photovoltaic properties, high photochemical stability, and energy down-shift properties. These CDs not only modify the interface of PSCs to control their energy level structure but also induce the growth of perovskite crystals to improve crystal quality, ultimately improving the efficiency and stability of PSCs. This review systematically summarizes the photoelectric properties of CDs and their application progress in PSCs as an active layer dopant, electron transport layer, hole transport layer, interface modification layer, and energy down-shift material after briefly introducing the structures and types of PSCs. Finally, the existing problems and challenges of CDs applied in PSCs are pointed out; specific solutions are proposed; and the future development prospects are presented.

Scalable Two‐Step Production of High‐Efficiency Perovskite Solar Cells and Modules

Perovskite solar cells (PSCs) fabricated in laboratories have already achieved a power conversion efficiency (PCE) comparable to market‐dominant crystalline silicon solar cells. However, this promising photovoltaic technology suffers from severe loss of PCE during scaling up, limiting its progress toward commercialization. One critical question is to develop scalable, low‐cost, high throughput, and well‐controlled production methods to deposit high‐quality perovskite films. Among various approaches, two‐step sequential deposition methods have their unique advantages but have been long overlooked. This review provides an overview of two‐step methods for fabricating efficient and stable perovskite solar modules (PSMs). The mechanisms of two‐step perovskite conversion and advanced engineering approaches to modulate the perovskite formation process are discussed first. The progress of efficient PSCs prepared by different two‐step methods is surveyed and the advantages and disadvantages of each method for the scalable production of PSMs are compared. Particularly, it is highlighted that the vapor‐based two‐step methods are promising for high‐throughput in‐line production of PSMs. Finally, insights into the challenges and outlook of the industrialization of two‐step processes for producing PSMs are provided.

Stabilization of Perovskite Solar Cells: Recent Developments and Future Perspectives.

Exceptional power conversion efficiency (PCE) of 25.7% in perovskite solar cells (PSCs) has been achieved, which is comparable with their traditional rivals (Si-based solar cells). However, commercialization-worthy efficiency and long-term stability remain a challenge. In this regard, there are increasing studies focusing on the interface engineering in PSC devices to overcome their poor technical readiness. Herein, the roles of electrode materials and interfaces in PSCs are discussed in terms of their PCEs and perovskite stability. All the current knowledge on the factors responsible for the rapid intrinsic and external degradation of PSCs is presented. Then, the roles of carbonaceous materials as substitutes for noble metals are focused on, along with the recent research progress in carbon-based PSCs. Furthermore, a sub-category of PSCs, that is, flexible PSCs, is considered as a type of exceptional power source due to their high power-to-weight ratios and figures of merit for next-generation wearable electronics. Last, the future perspectives and directions for research in PSCs are discussed, with an emphasis on their commercialization.

Recent progress in perovskite solar cells: from device to commercialization

Recent progress in perovskite solar cells: from device to commercialization

The effect of B-site alloying on the electronic and opto-electronic properties of RbPbI3: A DFT study

Divalent cations mixed lead halide perovskites with enhanced performances, high stabilities, and reduced toxicity are requisite to make persistent progress in perovskite solar cells. However, the mixing strategy is not reported extensively in search of a lead reduced structure. Herein, we report the structural, electronic and optical properties of RbPb1-xMxI3 (where, M = {Sn,Ge} and x = {0.25, 0.50, 0.75}) by alloying the B-site with Sn and Ge, using the density functional theory. The formation enthalpy is estimated for all RbPb1-xMxI3 (with x = 0.25, 0.50, 0.75), which confirms stability for all the structures. The energy bandgap and density of states (DOS) have been thoroughly investigated. The energy bandgap decreases with the increasing Sn/Ge contents, the lowest bandgap of 1.850eV is observed at x=0.50 in the case of RbPb1-xGexI3 systems. Further, the effective masses and the binding energy of excitons and spectroscopic limited maximum efficiency (SLME) are also estimated for all the mixed systems. The exciton type is observed to change from Mott–Wannier to Frenkel type with increasing the contents of both Sn and Ge at the B-site. The maximum efficiency of 23% is achieved using an active layer containing an equal admixture of Sn/Ge and Pb. The estimated parameters of both the mixed systems are consistent with the available literature of similar types.

Manipulate energy transport via fluorinated spacers towards record-efficiency 2D Dion-Jacobson CsPbI3 solar cells

Two-dimensional (2D) Dion-Jacobson (D-J)-type cesium lead iodide CsPbI3 perform remarkably in terms of stability. However, the complex interactions between spacer and inorganic layers limit its excellent progress in perovskite solar cells (PSCs). Herein, starting from the considerable structural diversity of organic spacers, we engineer 2D CsPbI3 with fine-tuning functionalities. Specifically, for the first time we embedded fluorinated aromatic cations in 2D D-J CsPbI3, and successfully applied it into construction of high-performance PSCs. Compared with constitutive 1,4-diaminobenzene (PDA), the fluorinated 2-fluorobenzene-1,4-diamine (F-PDA) component greatly expands the dipole moment from 0.59D to 3.47D, which reduces the exciton binding energy of the system. A theoretical study shows that the spacer layer and inorganic plane are more enriched with charge accumulation in (F-PDA)Csn–1PbnI3n+1. The results show that (F-PDA)Csn–1PbnI3n+1 demonstrates more significant charge transfer between organic and inorganic layers than (PDA)Csn–1PbnI3n+1, and it is confirmed in the femtosecond transient absorption experiment. Moreover, the interactions of the fluorinated spacer with the [PbI6]4– plane effectively manipulate the crystallization quality, and thus the ion migration and defect formation of target 2D CsPbI3 are inhibited. As a result, we obtained a record power conversion efficiency (PCE) beyond 15% for 2D D-J (F-PDA)Cs3Pb4I13 (n = 4) PSCs with significantly improved environmental stability compared with the three-dimensional (3D) counterparts.

Azo‐Initiator‐Induced Cascade Defect Passivation for Efficient and Stable Planar Perovskite Solar Cells

Remarkable progress in perovskite solar cells (PSCs) has been made by virtue of surface and bulk modification for defect control of perovskite layers, however, the interior defects in the perovskite layer can be hardly passivated by means of conventional passivation strategies, which makes perovskites prone to decomposition with inferior device performance. Here, the authors propose a cascade defect passivation strategy to doubly reduce perovskite defects by introducing a series of azo radical initiators. The primary passivation process of the azo compounds is realized on the perovskite surfaces through strong coordination interactions between Pb2+ and carbonyl/cyano groups. The secondary passivation occurs after thermal treatment, and the decomposed products diffuse into the interior defects of the initial passivated perovskite films through grain boundaries to accomplish the cascade defect passivation. Excitingly, this passivation strategy inhibits unwanted defect‐assisted recombination effectively, and thus CH3NH3PbI3 (MAPbI3)‐based inverted PSCs exhibit a significant increase in power conversion efficiency (PCE) from 16.92% to 19.69%. Moreover, the dual‐passivated PSCs show only 10% PCE loss after 3000 h in an inert atmosphere. Overall, the first proposed cascade defect passivation strategy is highly efficient in promoting defect healing of perovskites, demonstrating a new way to prepare high‐quality perovskite films for high‐performance PSCs.

Construction of Charge Transport Channels at the NiOx/Perovskite Interface through Moderate Dipoles toward Highly Efficient Inverted Solar Cells.

NiOx-based perovskite solar cells (PSCs) have attracted much attention because of their low fabrication temperature, suppressed hysteresis, and superior stability. However, the poor interfacial contacts between NiOx and perovskite layers always limit the progress of PSCs. Here, we applied 2-thiophenemethylamine (TPMA) as charge transport channels at the interface between NiOx and perovskite layers. The introduction of TPMA provides moderate dipole moment pointing to the perovskite side and effectively promotes the charge transportation. Meanwhile, TPMA anchorage also passivates the defect states at the surfaces of both NiOx and MAPbI3, which compensates the voltage loss due to the change in NiOx work function induced by the dipole. Thus, the device performance has been significantly enhanced in both electrochemical properties and power conversion efficiency. Our work has demonstrated a new way of improving current and voltage in the NiOx-based PSCs simultaneously through a moderate interfacial dipole moment toward highly efficient PSCs.

Decomposition of Organic Perovskite Precursors on MoO3: Role of Halogen and Surface Defects.

Despite the rapid progress in perovskite solar cells, their commercialization is still hindered by issues regarding long-term stability, which can be strongly affected by metal oxide-based charge extraction layers next to the perovskite material. With MoO3 being one of the most successful hole transport layers in organic photovoltaics, the disastrous results of its combination with perovskite films came as a surprise but was soon attributed to severe chemical instability at the MoO3/perovskite interface. To discover the atomistic origin of this instability, we combine density functional theory (DFT) calculations and X-ray photoelectron spectroscopy (XPS) measurements to investigate the interaction of MoO3 with the perovskite precursors MAI, MABr, FAI, and FABr. From DFT calculations we suggest a scenario that is based upon oxygen vacancies playing a key role in interface degradation reactions. Not only do these vacancies promote decomposition reactions of perovskite precursors, but they also constitute the reaction centers for redox reactions leading to oxidation of the halides and reduction of Mo. Specifically iodides are proposed to be reactive, while bromides do not significantly affect the oxide. XPS measurements reveal a severe reduction of Mo and a loss of the halide species when the oxide is interfaced with I-containing precursors, which is consistent with the proposed scenario. In line with the latter, experimentally observed effects are much less pronounced in case of Br-containing precursors. We further find that the reactivity of the MoO3 substrate can be moderated by reducing the number of oxygen vacancies through a UV/ozone treatment, though it cannot be fully eliminated.

A short review on progress in perovskite solar cells

The performance of hybrid metal halide perovskite-based solar cells has been improved at an exceptional rate compared to other solar cells. Just in a decade, the efficiency of perovskite solar cells (PSC) could be increased from 3.8% to 25.5%. The halide-based perovskite materials have gained increased attention for optoelectronics applications because of their simple synthesis method and the ability to achieve high-efficiency solar cells. In this article, we have reviewed the significant developments in PSC that have contributed to the high-efficiency achievements. These include the evolution of device structure, the development of absorber layer materials as well as charge selective layers, and the advancement in the device fabrication techniques targeting to improve the control over perovskite film morphology, crystallinity, composition, and the interface properties of the devices leading to enhancement in the overall performances. We have also discussed the challenges and prospects for PSC research and development towards commercialization.