Molecularly Engineered Multifunctional Bridging Layer Derived from Dithiafulavene Capped Spiroxanthene for Stable and Efficient Perovskite Solar Cells.

This study introduces a novel approach centered around the design and synthesis of an interfacial passivating layer in perovskite solar cells (PSCs). This architectural innovation is realized through the development of a specialized material, termed dithiafulvene end-capped Spiro[fluorene-9,9'-xanthene], denoted by the acronym AF32. In this design architecture, dithiafulvene is thoughtfully attached to the spiroxanthene fluorene core with phenothiazine as the spacer unit, possessing multiple alkyl chains. AF32 passivates interfacial defects by coordinating the sulfur constituents of the phenothiazine and dithiafulvene frameworks to the uncoordinated Pb2+ cations on the surface of the perovskite film, and the alkyl chains construct a hydrophobic environment, preventing moisture from entering the hydrophilic perovskite layer and improving the long-term stability of PSCs. Furthermore, this conductive interlayer facilitates hole transport in PSCs due to its well-aligned molecular orbital levels. Such improvements translated into an enhanced power conversion efficiency (PCE) of 22.6% for the device employing 1.5 mg/mL AF32, and it maintained 85% of its initial PCE after more than 1800 h under ambient conditions [illumination and 45 ± 5% relative humidity (RH)]. This study not only marks progress in photovoltaic technology but also expands our understanding of manipulating interfacial properties for optimized device performance and stability.

Eco-Friendly Boost for Perovskite Photovoltaics: Harnessing Cellulose-Modified SnO2 as a High-Performance Electron Transporting Material.

In this study, a passivated tin oxide (SnO2) film is successfully obtained through the implementation of sodium carboxymethyl cellulose (Na-CMC) modifier agent and used as the electron transporting layer (ETL) within the assembly of perovskite solar cells (PSCs). The strategic incorporation of the Na-CMC modifier agent yields discernible enhancements in the optoelectronic properties of the ETL. Among the fabricated cells, the champion cell based on Na-CMC-complexed SnO2 ETL achieves a conversion efficiency of 22.2% with an open-circuit voltage (VOC) of 1.12 V, short-circuit current density (JSC) of 24.57 mA/cm2, and fill factor (FF) of 80.6%. On the other hand, these values are measured for the pristine SnO2 ETL-based control cell as VOC = 1.11 V, JSC = 23.59 mA/cm2, and FF = 76.7% with an efficiency of 20.1%. This improvement can be ascribed to the high charge extraction ability, higher optical transmittance, better conductivity, and decrease in the trap state density associated with the passivated ETL structure. In addition, the cells employing Na-CMC-complexed SnO2 ETL exhibit prolonged stability under ambient conditions during 2000 h. Based on the preliminary results, this study also presents a set of findings that could have substantial implications for the potential use of the Na-CMC molecule in both large-scale perovskite cells and perovskite/Si tandem configuration.

Facile NaF Treatment Achieves 20% Efficient ETL-Free Perovskite Solar Cells.

Electron transporting layer (ETL)-free perovskite solar cells (PSCs) exhibit promising progress in photovoltaic devices due to the elimination of the complex and energy-/time-consuming preparation route of ETLs. However, the performance of ETL-free devices still lags behind conventional devices because of mismatched energy levels and undesired interfacial charge recombination. In this study, we introduce sodium fluoride (NaF) as an interface layer in ETL-free PSCs to align the energy level between the perovskite and the FTO electrode. KPFM measurements clearly show that the NaF layer covers the surface of rough underlying FTO very well. This interface modification reduces the work function of FTO by forming an interfacial dipole layer, leading to band bending at the FTO/perovskite interface, which facilitates an effective electron carrier collection. Besides, the part of Na+ ions is found to be able to migrate into the absorber layer, facilitating enlarged grains and spontaneous passivation of the perovskite layer. As a result, the efficiency of the NaF-treated cell reaches 20%, comparable to those of state-of-the-art ETL-based cells. Moreover, this strategy effectively enhances the operational stability of devices by preserving 94% of the initial efficiency after storage for 500 h under continuous light soaking at 55 °C. Overall, these improvements in photovoltaic properties are clear indicators of enhanced interface passivation by NaF-based interface engineering.

Efficient and Stable Perovskite Solar Cells Enabled by Dicarboxylic Acid-Supported Perovskite Crystallization.

Defect states at surfaces and grain boundaries as well as poor anchoring of perovskite grains hinder the charge transport ability by acting as nonradiative recombination centers, thus resulting in undesirable phenomena such as low efficiency, poor stability, and hysteresis in perovskite solar cells (PSCs). Herein, a linear dicarboxylic acid-based passivation molecule, namely, glutaric acid (GA), is introduced by a facile antisolvent additive engineering (AAE) strategy to concurrently improve the efficiency and long-term stability of the ensuing PSCs. Thanks to the two-sided carboxyl (-COOH) groups, the strong interactions between GA and under-coordinated Pb2+ sites induce the crystal growth, improve the electronic properties, and minimize the charge recombination. Ultimately, champion-stabilized efficiency approaching 22% is achieved with negligible hysteresis for GA-assisted devices. In addition to the enhanced moisture stability of the devices, considerable operational stability is achieved after 2400 h of aging under continuous illumination at maximum power point (MPP) tracking.

Moisture-Resistant FAPbI3 Perovskite Solar Cell with 22.25 % Power Conversion Efficiency through Pentafluorobenzyl Phosphonic Acid Passivation.

Perovskite solar cells (PSCs) have shown great promise for photovoltaic applications, owing to their low-cost assembly, exceptional performance, and low-temperature solution processing. However, the advancement of PSCs towards commercialization requires improvements in efficiency and long-term stability. The surface and grain boundaries of perovskite layer, as well as interfaces, are critical factors in determining the performance of the assembled cells. Defects, which are mainly located at perovskite surfaces, can trigger hysteresis, carrier recombination, and degradation, which diminish the power conversion efficiencies (PCEs) of the resultant cells. This study concerns the stabilization of the α-FAPbI3 perovskite phase without negatively affecting the spectral features by using 2,3,4,5,6-pentafluorobenzyl phosphonic acid (PFBPA) as a passivation agent. Accordingly, high-quality PSCs are attained with an improved PCE of 22.25 % and respectable cell parameters compared to the pristine cells without the passivation layer. The thin PFBPA passivation layer effectively protects the perovskite layer from moisture, resulting in better long-term stability for unsealed PSCs, which maintain >90 % of the original efficiency under different humidity levels (40-75 %) after 600 h. PFBPA passivation is found to have a considerable impact in obtaining high-quality and stable FAPbI3 films to benefit both the efficiency and the stability of PSCs.

Inorganic CuFeO2 Delafossite Nanoparticles as Effective Hole Transport Materials for Highly Efficient and Long-Term Stable Perovskite Solar Cells.

The regular architecture (n-i-p) of perovskite solar cells (PSCs) has attracted increasing interest in the renewable energy field, owing to high certified efficiencies in the recent years. However, there are still serious obstacles of PSCs associated with spiro-OMeTAD hole transport material (HTM), such as (i) prohibitively expensive material cost (∼150-500 $/g) and (ii) operational instability at elevated temperatures and high humidity levels. Herein, we have reported the highly photo, thermal, and moisture-stable and cost-effective PSCs employing inorganic CuFeO2 delafossite nanoparticles as a HTM layer, for the first time. By exhibiting superior hole mobility and additive-free nature, the best-performing cell achieved a power conversion efficiency (PCE) of 15.6% with a negligible hysteresis. Despite exhibiting a lower PCE as compared to the spiro-OMeTAD-based control cell (19.1%), nonencapsulated CuFeO2-based cells maintained above 85% of their initial efficiency, while the PCE of control cells dropped to ∼10% under continuous illumination at maximum power point tracking after 1000 h. More importantly, the performance of control cells was quickly degraded at above 70 °C, whereas CuFeO2-based cells, retaining ∼80% of their initial efficiency after 200 h, were highly stable even at 85 °C in ambient air under dark conditions. Besides showing significant improvement in stability against light soaking and thermal stress, CuFeO2-based cells exhibited superior shelf stability even at 80 ± 5% relative humidity and retained over 90% of their initial PCE. Overall, we strongly believe that this study highlights the potential of inorganic HTMs for the commercial deployment of long-term stable and low-cost PSCs.