A two-step hybrid evaporation-solution method for fabricating large-area high-efficiency perovskite solar cells

Emerging hybrid organic–inorganic perovskites with superior optoelectronic property demonstrate promising prospect for photovoltaic (PV) applications, in particular for low-lighting indoor applications e.g. within internet of things (IoT) networks or low-energy wireless communication devices. In order to prepare devices with high power output under low-illumination conditions, scalable fabrication techniques are preferred for large-area perovskite solar cells. In additions, one of the key parameters to achieve high-efficiency large-area perovskite solar cells is to minimize the ohmic loss to further boost the solar cell efficiency. Herein, a one-step blade-coating method assisted by hexafluorobenzene (HFB) was developed to deposit dense, large-area smooth and high-quality perovskite films with low ohmic loss. The as-fabricated devices demonstrated power conversion efficiency (PCE) of 20.7% (area of 0.2 cm2) and 16.5% (1 cm2), respectively, under standard (AM 1.5G) illumination conditions. Besides, the large-area (1 cm2) devices demonstrated a remarkable PCE of ∼ 33.8% and ∼ 30.0% under 1000 lx and 100 lx illumination provided by white light-emitting diode (LED) lamp, respectively. We exhibited a series-connected stack of large-area (totally active area ∼ 4 cm2) perovskite photovoltaic device powering up a LED under common indoor environment as an indoor self-power indicator lamp. The analysis using a single diode model suggests that the high performance of the large-area devices under low-lighting indoor conditions is highly associated with the largely reduced ohmic losses, which particularly indicate that the perovskite films by a facile and scalable blade-coating method. The presented scalable approach paves the way to designing high-performance perovskite solar cells for a variety of emerging indoor PV applications.

Efficient MAPbI3-based perovskite solar cells exceeding 21% efficiency via aging treatment

Perovskite solar cells (PSCs) have received a great deal of attention in the science and technology field due to their outstanding power conversion efficiency (PCE), which increased rapidly from 3.9% to 25.5% in less than a decade, comparable to single crystal silicon solar cells. In the past ten years, much progress has been made, e.g. impressive ideas and advanced technologies have been proposed to enlarge PSC efficiency and stability. However, this outstanding progress has always been referred to as small-area (<0.1 cm2) PSCs. Little attention has been paid to the preparation processes and their micro-mechanisms for large-area (>1 cm2) PSCs. Meanwhile, scaling up is an inevitable way for large-scale application of PSCs. Therefore, we firstly summarize the current achievements for high efficiency and stability large-area perovskite solar cells, including precursor composition, deposition, growth control, interface engineering, packaging technology, etc. Then we include a brief discussion and outlook for the future development of large-area PSCs in commercialization.

Electrode Design to Overcome Substrate Transparency Limitations for Highly Efficient 1 cm2 Mesoscopic Perovskite Solar Cells

Photovoltaic technologies based on perovskite absorber materials have led this optoelectronic field into a brand-new horizon. However, the present antisolvents used in the one-step spin-coating method always encounter problems with the very narrow process window. Herein, anisole is introduced into the one-step spin-coating method, and the technology is developed to fabricate perovskite thin films with ultrawide processing window with a dimethylformamide (DMF):dimethyl sulfoxide (DMSO) ratio varying from 6:4 to 9:1 in the precursor solution, anisole dripping time ranging from 5 to 25 s, and an antisolvent volume varying from 0.1 to 0.9 mL. Perovskite thin films as large as 100 cm2 are successfully fabricated using this method. Maximum photoelectric conversion efficiencies of 19.76% for small-area (0.14 cm2 ) and 17.39% for large-area (1.08 cm2 ) perovskite solar cell devices are obtained. It is also found that there are intermolecular hydrogen-bonding forces between anisole and DMF/DMSO that play critical roles in the wide process window. These results provide a deeper understanding of the crystallizing procedure of perovskite during the one-step spin-coating process.

Scalable fabrication of perovskite solar cells (PSCs) with high reliability is one of the most pivotal concerns that must be addressed before they get into the photovoltaic (PV) market. Scaling large-area high-quality perovskite films is of great importance in this process. Here, gaseous therapy has been proposed for the post-treatment of perovskite films with high scalability and low cost. An inspiring evolvement from poor perovskite films to high quality ones is demonstrated under a joint treatment of methylamine gas and hot solvent vapors. The perovskite films are completely reconstructed and repaired regardless of the morphology of the original films. As a consequence, small-area (0.09 cm2) and large-area (4 cm2) PSCs based on the healed MAPbI3 films can afford J-V scanned efficiencies of 19.2 and 16.5% under a reverse sweep, respectively. Furthermore, stabilized power outputs of 18.5 and 15.2% are obtained from the small one and large one under continuous maximum power point tracking.

Enabling high-efficiency ambient-air printable carbon-based large-area perovskite solar cells via effective anionic passivation

Large area, high efficiency and stable perovskite solar cells enabled by fine control of intermediate phase

The performance of large-area perovskite solar cells (PSCs) has been assessed for typical compositions, such as methylammonium lead iodide (MAPbI3 ), using a blade coater, slot-die coater, solution shearing, ink-jet printing, and thermal evaporation. However, the fabrication of large-area all-inorganic perovskite films is not well developed. This study develops, for the first time, an eco-friendly solvent engineered all-inorganic perovskite ink of dimethyl sulfoxide (DMSO) as a main solvent with the addition of acetonitrile (ACN), 2-methoxyethanol (2-ME), or a mixture of ACN and 2-ME to fabricate large-area CsPbI2.77 Br0.23 films with slot-die coater at low temperatures (40-50 °C). The perovskite phase, morphology, defect density, and optoelectrical properties of prepared with different solvent ratios are thoroughly examined and they are correlated with their respective colloidal size distribution and solar cell performance. The optimized slot-die-coated CsPbI2.77 Br0.23 perovskite film, which is prepared from the eco-friendly binary solvents dimethyl sulfoxide:acetonitrile(0.8:0.2 v/v), demonstrates an impressive power conversion efficiency (PCE) of 19.05%. Moreover, the device maintains ≈91% of its original PCE after 1 month at 20% relative humidity in the dark. It is believed that this study will accelerate the reliable manufacturing of perovskite devices.

Two-step ultrasonic spray deposition of CH3NH3PbI3 for efficient and large-area perovskite solar cell

Chemical composition and film quality are two key figures of merit for large-area high-efficiency perovskite solar cells. To date, all studies on mixed perovskites have used solution-processing, which results in imperfect surface coverage and pin-holes generated during solvent evaporation, execrably influencing the stability and efficiency of perovskite solar cells. Herein, we report our development using a vacuum co-evaporation deposition method to fabricate pin-hole-free cesium (Cs)-substituted perovskite films with complete surface coverage. Apart from the simplified procedure, the present method also promises tunable band gap, reduced trap-state density and longer carrier lifetime, leading to solar cell efficiency as high as 20.13%, which is among the highest reported for planar perovskite solar cells. The splendid performance is attributed to superior merits of the Cs-substituted perovskite film including tunable band gap, reduced trap-state density and longer carrier lifetime. Moreover, the Cs-substituted perovskite device without encapsulation exhibits significantly higher stability in ambient air compared with the single-component counterpart. When the Cs-substituted perovskite solar cells are stored in dark for one year, the PCE remains at 19.25%, degrading only 4.37% of the initial efficiency. The excellent stability originates from reduced lattice constant and relaxed strain in perovskite lattice by incorporating Cs cations into the crystal lattice, as demonstrated by the positive peak shifts and reduced peak width in X-ray diffraction analysis.

Development of once-through manufacturing machine for large-area Perovskite solar cell production

An efficient polyelectrolyte hole-transport layer was explored for 2D perovskite solar cells by using a compatible butylamine cation, as reported by Jianyu Yuan and co-workers in their Research Article (e202205111). The tailored polyelectrolyte has an anchoring effect and acts as a passivator for 2D perovskites, which can improve 2D perovskite phase alignment and interfacial charge transfer efficiency, and finally enables high-efficiency and large-area 2D perovskite solar cells.

Multi-flow air knife (MAK): a novel method for large area perovskite film production.

Large-area perovskite solar cells