Fusing Science with Industry: Perovskite Photovoltaics Moving Rapidly into Industrialization.

The organic-inorganic lead halide perovskite materials have emerged as highly promising contenders in the field of photovoltaic technology, offering exceptional efficiency and cost-effectiveness. The commercialization of perovskite photovoltaics hinges on successfully transitioning from lab-scale perovskite solar cells to large-scale perovskite solar modules (PSMs). However, the efficiency of PSMs significantly diminishes with increasing device area, impeding commercial viability. Central to achieving high-efficiency PSMs is fabricating uniform functional films and optimizing interfaces to minimize energy loss. In this review, we shed light on the path towards large-scale PSMs, emphasizing the pivotal role of integrating cutting-edge scientific research with industrial technology. By exploring scalable deposition techniques and optimization strategies, we reveal the advancements and challenges in fabricating large-area perovskite films. Subsequently, we delve into the architecture and contact materials of PSMs while addressing pertinent interface issues. Crucially, we analyze efficiency loss during scale-up and stability risks encountered by PSMs. Furthermore, we highlight the advancements in industrial efforts towards perovskite commercialization, emphasizing the perspective of PSMs in revolutionizing renewable energy. By highlighting the scientific and technical challenges in developing PSMs, we stress the importance of combining science and industry to drive their industrialization and pave the way for future advancements. This article is protected by copyright. All rights reserved.

A-D-A Molecule-Bridge Interface for Efficient Perovskite Solar Cells and Modules.

As the photovoltaic field endeavors to transition perovskite solar cells (PSCs) to industrial applications, inverted PSCs, which incorporate fullerene as electron transport layers, have emerged as a compelling choice due to their augmented stability and cost-effectiveness. However, these attributes suffer from performance issues stemming from suboptimal electrical characteristics at the perovskite/fullerene interface. To surmount these hurdles, an interface bridging strategy (IBS) is proposed to attenuate the interface energy loss and enhance the interfacial stability by designing a series of A-D-A type perylene monoimide (PMI) derivatives with multifaceted advantages. In addition to passivating defects, the IBS plays a crucial role in facilitating the binding between perovskite and fullerene, thereby enhancing interface coupling and importantly, improving the formation of fullerene films. The PMI derivatives, functioning as bridges, serve as a protective barrier to enhance the device stability. Consequently, the IBS enables a remarkable efficiency of 24.62% for lab-scale PSCs and an efficiency of 18.73% for perovskite solar modules craft on 156 × 156 mm2 substrates. The obtained efficiencies represent some of the highest recorded for fullerene-based devices, showcasing significant progress in designing interfacial molecules at the perovskite/fullerene interface and offering a promising path to enhance the commercial viability of PSCs.

Hydrophobic Hydrogen-Bonded Polymer Network for Efficient and Stable Perovskite/Si Tandem Solar Cells.

The pursuit of highly efficient and stable wide-band gap (WBG) perovskite solar cells (PSCs), especially for monolithic perovskite/silicon tandem devices, is a key focus in achieving the commercialization of perovskite photovoltaics. In this study, we initially designed poly(ionic liquid)s (PILs) with varying alkyl chain lengths based on density functional theory calculations. Results pinpoint that PILs with longer alkyl chain lengths tend to exhibit more robust binding energy with the perovskite structure. Then we synthesized the PILs to craft a hydrophobic hydrogen-bonded polymer network (HHPN) that passivates the WBG perovskite/electron transport layer interface, inhibits ion migration and serves as a barrier layer against water and oxygen ingression. Accordingly, the HHPN effectively curbs nonradiative recombination losses while facilitating efficient carrier transport, resulting in substantially enhanced open-circuit voltage (Voc ) and fill factor. As a result, the optimized single-junction WBG PSC achieves an impressive efficiency of 23.18 %, with Voc as high as 1.25 V, which is the highest reported for WBG (over 1.67 eV) PSCs. These devices also demonstrate outstanding thermostability and humidity resistance. Notably, this versatile strategy can be extended to textured perovskite/silicon tandem cells, reaching a remarkable efficiency of 28.24 % while maintaining exceptional operational stability.

Wide-Bandgap Organic-Inorganic Lead Halide Perovskite Solar Cells.

Under the groundswell of calls for the industrialization of perovskite solar cells (PSCs), wide-bandgap (>1.7 eV) mixed halide perovskites are equally or more appealing in comparison with typical bandgap perovskites when the former's various potential applications are taken into account. In this review, the progress of wide-bandgap organic-inorganic hybrid PSCs-concentrating on the compositional space, optimization strategies, and device performance-are summarized and the issues of phase segregation and voltage loss are assessed. Then, the diverse applications of wide-bandgap PSCs in semitransparent devices, indoor photovoltaics, and various multijunction tandem devices are discussed and their challenges and perspectives are evaluated. Finally, the authors conclude with an outlook for the future development of wide-bandgap PSCs.

Perovskite Quantum Dots in Solar Cells.

Perovskite quantum dots (PQDs) have captured a host of researchers' attention due to their unique properties, which have been introduced to lots of optoelectronics areas, such as light-emitting diodes, lasers, photodetectors, and solar cells. Herein, the authors aim at reviewing the achievements of PQDs applied to solar cells in recent years. The engineering concerning surface ligands, additives, and hybrid composition for PQDSCs is outlined first, followed by analyzing the reasons of undesired performance of PQDSCs. Subsequently, a novel overview that PQDs are utilized to improve the photovoltaic performance of various kinds of solar cells, is provided. Finally, this review is summarized and some challenges and perspectives concerning PQDs are also discussed.

Hole-Storage Enhanced a-Si Photocathodes for Efficient Hydrogen Production.

Ferrihydrite (Fh) has been demonstrated as an effective interfacial layer for photoanodes to achieve outstanding photoelectrochemical (PEC) performance for water oxidation reaction owing to its unique hole-storage function. However, it is unknown whether such a hole-storage layer can be used to construct highly efficient photocathodes for hydrogen evolution reaction (HER). In this work, we report Fh interfacial engineering of amorphous silicon photocathode (with nickel as HER cocatalyst) achieving a photocurrent density of 15.6 mA cm-2 at 0 V vs. the reversible hydrogen electrode and a half-cell energy conversion efficiency of 4.08 % in alkaline solution, outperforming most of reported a-Si based photocathodes including multi-junction configurations integrated with noble metal cocatalysts in acid solution. Besides, the photocurrent density is maintained above 14 mA cm-2 for 175 min with 100 % Faradaic efficiency for HER in alkaline solution. Our results demonstrate a feasible approach to construct efficient photocathodes via the application of a hole-storage layer.

High-Efficiency Perovskite Solar Cells with Imidazolium-Based Ionic Liquid for Surface Passivation and Charge Transport.

Surface defects have been a key constraint for perovskite photovoltaics. Herein, 1,3-dimethyl-3-imidazolium hexafluorophosphate (DMIMPF6 ) ionic liquid (IL) is adopted to passivate the surface of a formamidinium-cesium lead iodide perovskite (Cs0.08 FA0.92 PbI3 ) and also reduce the energy barrier between the perovskite and hole transport layer. Theoretical simulations and experimental results demonstrate that Pb-cluster and Pb-I antisite defects can be effectively passivated by [DMIM]+ bonding with the Pb2+ ion on the perovskite surface, leading to significantly suppressed non-radiative recombination. As a result, the solar cell efficiency was increased to 23.25 % from 21.09 %. Meanwhile, the DMIMPF6 -treated perovskite device demonstrated long-term stability because the hydrophobic DMIMPF6 layer blocked moisture permeation.

High-Pressure Nitrogen-Extraction and Effective Passivation to Attain Highest Large-Area Perovskite Solar Module Efficiency.

Slot-die coating holds advantages over other large-scale technologies thanks to its potential for well-controlled, high-throughput, continuous roll-to-roll fabrication. Unfortunately, it is challenging to control thin.film uniformity over a large area while maintaining crystallization quality. Herein, by using a high-pressure nitrogen-extraction (HPNE) strategy to assist crystallization, a wide processing window in the well-controlled printing process for preparing high-quality perovskites is achieved. The yellow-phase perovskite generated by the HPNE acts as a crucial intermediate phase to produce large-area high-quality perovskite film. Furthermore, an ionic liquid is developed to passivate the perovskite surface to reduce surface defect density and to suppress carrier recombination, resulting in significantly increased efficiency to 22.7%, the highest for large-area fabrication. The strategies are successfully extended to large-area device fabrication, making it possible to produce a 40 × 40 mm2 module with stabilized PCE as high as 19.4%, the highest-efficiency for a large-area module to date.