Multifunctional Regulation of SnO2 Nanocrystals by Snail Mucus for Preparation of Rigid or Flexible Perovskite Solar Cells in Air.

Tin oxide (SnO2) is widely used as an inorganic electron transport layer (ETL) for rigid and flexible perovskite solar cells (PSCs). In this work, an extract of snail shell, the sodium salt of polyaspartic acid (S-PASP), a water-soluble polypeptide polymer, has been used to multifunctionally regulate SnO2 nanograins. S-PASP has a strong chelating and dispersing effect; thus, chemically adsorbed SnO2 can inhibit agglomeration. The S-PASP:SnO2 ETL also improved the extraction and transferability of carriers, reducing body defects and interfacial charge. Moreover, the S-PASP:SnO2 ETL promotes the vertical growth of the perovskite crystals due to its bottom-up morphology, wettability, and strain release, which is conducive to improving the photoelectric performance of the device. The optimized rigid device prepared under open-air conditions obtained a PCE of 20.92%. In addition, due to the stress compensation of the S-PASP long chain, which prevented the cracking and displacement of the ETL, the optimal PCE of the flexible device was 17.96%, and the initial efficiency was maintained at 82.8% after 100 bends. This work introduces a molecular doping mechanism for organic-inorganic hybrid electronics.

Air-processed MAPbI3 perovskite solar cells achieve 20.87% efficiency and excellent bending resistance enabled via a polymer dual-passivation strategy.

In recent years, air-processed MAPbI3 perovskite solar cells (PSCs) have attracted widespread interest from researchers worldwide because of their simple and low-cost fabrication process. Nonetheless, the ambient conditions usually bring about many adverse effects, such as imperfect crystallization and numerous defects in perovskite films, which seriously impact both the photoelectric performance and stability of the device. Therefore, in this work, a polymer dual-passivation strategy was employed by introducing ammonium polyphosphate (APP) as an additive to the green anti-solvent to accurately modify the perovskite layer. APP, which has abundant phosphate and ammonium groups, could simultaneously fill the I/Pb vacancies by Lewis acid-base reactions to restrain defect formation and improve the power conversion efficiency (PCE) of the ultimate device. On the other hand, the long molecular chains of the polymer with a certain flexural ability were easily congregated at the grain boundaries of the perovskite grains, thus enhancing the bending resistance. Consequently, high-quality perovskite films with a dense morphology and large grain size were obtained. Because of the reduced defect density and suppressed non-radiative recombination, the optimal PSC attained a champion PCE of 20.87% with negligible hysteresis. Furthermore, the non-encapsulated APP-modified flexible device also exhibited excellent bending resistance. Only 20% of its normalized PCE was lost after 150 bending cycles at room temperature. This simple, green, low-cost, and reliable strategy for preparing high-efficiency PSCs with good stability can facilitate its commercialization.

Reduction-Active Antisolvent: A Universal and Innovative Strategy of Further Ameliorating Additive Optimization for High Efficiency Perovskite Solar Cells.

To further ameliorate current additive engineering of perovskites for viable applications, the inherent limitations should be overcome; these include weakened coordination of the dopants to the [PbI6]4- octahedra during crystallization and ubiquity of ineffective bonding sites. Herein, we introduce a facile strategy for synthesizing a reduction-active antisolvent. Washing with reduction-active PEDOT:PSS-blended antisolvent substantially enhances the intrinsic polarity of the Lewis acid (Pb2+) in [PbI6]4- octahedra, which causes significant strengthening of the coordinate bonding between additives and perovskite. Thus, coordination of the additive to the perovskite becomes much stable. Additionally, the enhanced coordination ability of Pb2+ can enhance the effective bonding sites and further enhance the efficacy of additive optimization to the perovskite. Here, we demonstrate five different additives as dopant bases and repeatedly verify the universality of this approach. The photovoltaic performance and stability of doped-MAPbI3 devices are further improved, revealing the advanced potential of additive engineering.

Silicon/nickel oxide core/shell nanospheres as a hole transport layer for high efficiency and light-stable perovskite solar cells.

Metal halide perovskite solar cells (PSCs) possess huge potential due to their high power conversion efficiency. However, instability is still a key factor limiting their applications. Therefore, we have found a feasible strategy to improve the light stability of PSCs. Specifically, a core-shell material with a silicon nanosphere core and a nickel oxide nanosheet shell serves as the hole transport layer in our PSCs. Due to the selective absorption of ultraviolet light by the silicon nanoparticles, the ultraviolet light content of the natural light that reaches the perovskite layer is reduced. Compared with a control device (without Si), the PSCs with the silicon/nickel oxide hole transport layer possessed a higher current density of 22.09 mA cm-2 and a higher power conversion efficiency of 18.54%, with both values increased by 2.7% and 6.1%, respectively. More importantly, the PSCs based on a silicon/nickel oxide hole transport layer maintains 85% of its initial power conversion efficiency value after 700 hours of natural light exposure. These results indicate that the silicon/nickel oxide hole transport layer is an important functional component of the PSCs, which improves the photovoltaic performance and reduces ultraviolet light-induced photodegradation, thereby improving the device stability.

Aggregation-induced Emission Materials for High-efficiency Perovskite Solar Cells.

The perovskite solar cells (PSCs) with high efficiency and stability are in great demand for commercial applications. Although the remarkable photovoltaic feature of perovskite layer plays a great role in improving the PCE of PSCs, the inevitable defects and poor stability of perovskite, etc. are the bottleneck and restrict the commercialization of PSCs. Herein, a review provides a strategy of applying aggregation-induced emission (AIE) molecules, containing passivation functional groups and distinct AIE character, which serves as the alternative materials for fabricating high-efficiency and high-stability PSCs. The methods of introducing AIE molecules to PSCs are also summarized, including additive engineering, interfacial engineering, hole transport materials and so on. In addition, the functions of AIE molecule are discussed, such as defects passivation, morphology modulation, well-matched energy level, enhanced stability, hole transport ability, carrier recombination suppression. Finally, the detailed functions of AIE molecules are offered and further research trend for high performance PSCs based on AIE materials is proposed.

Hydrazone dye passivator for high-performance and stable perovskite solar cells.

There has been rapid development of organic-inorganic perovskite solar cells (PSCs) in recent years, but efficiency and stability challenges remain due to the massive defects in perovskite films. Here, the organic dye Th-azi-Pyr (ethyl 2-(2-(3-methyl-5-oxo-1-phenyl-1,5-dihydro-4H-pyrazol-4-ylidene) hydrazineyl)-4,5,6,7-tetrahydrobenzo[b]thiophene-3-carboxylate) with carbonyl, pyrazolone structure, and benzene ring was synthesized and used to prepare high-quality perovskite film as an additive. Th-azi-Pyr formed relatively stable intermediate ligands with uncoordinated Pb and I, slowing the crystal growth and reducing the grain boundary defects of perovskite. In addition, the benzene ring in the dye protected against moisture and increased the stability of the perovskite film. Therefore, the Th-azi-Pyr-modified PSC assembled in an air environment exhibited a promising power conversion efficiency (PCE) of 19.27%, which is superior to the 15.33% of the control PSC. Additionally, 88% of the original performance was maintained after 300 h at 25 ± 5 °C and 50 ± 10% relative humidity, implying that the modified PSCs exhibited greater stability than the untreated PSCs. This work indicates that simple and low-cost organic dyes are excellent defect passivators for high-performance PSCs.

When Aggregation-Induced Emission Meets Perovskites: Efficient Defect-Passivation and Charge-Transfer for Ambient Fabrication of Perovskite Solar Cells.

The intrinsic defects in perovskite film can serve as non-radiative recombination center to limit the performance and stability of metal halide perovskite solar cells (PSCs). The additive engineering in perovskite film is always applied to produce high-efficiency PSCs in recent years. Here, a typical donor-acceptor (D-A) structured aggregation-induced emission (AIE) molecule tetraphenylethene-2-dicyano-methylene-3-cyano-4,5,5-trimethyl-2,5-dihydrofuran (TPE-TCF) was introduced into perovskite film. The D-A structure of TPE-TCF molecule provided additional charge transfer channels, contributing to transporting electron of TPE-TCF-based device. The cyano (C≡N) of TPE-TCF can interact with the uncoordinated Pb to from a relatively stable intermediate, PbI2 ⋅TPE-TCF, resulting in the slower crystal growth, reduced the defects at the grain boundaries and suppressed carrier recombination. As a consequence, the power conversion efficiency (PCE) of TPE-TCF-modified PSCs achieved a remarkably enhanced from 15.63 to 19.66 % with negligible hysteresis, which was prominent in methylammonium lead iodide-based devices fabricated under ambient condition. Furthermore, the PSCs modified by AIE molecule possessed an outstanding stability and maintain about 86 % of the initial PCE after 300 h storage in air at 25-35 °C with a high relative humidity (RH) of ≈85 %. This work suggests that incorporating AIE molecule into perovskite is a promising strategy for facilitating high-performance PSCs commercialization in ambient environment without glovebox.

The disappearing additive: introducing volatile ethyl acetate into a perovskite precursor for fabricating high efficiency stable devices in open air.

In recent years, organic-inorganic halide perovskite solar cells (PSCs) have attracted massive attention because of their high power conversion efficiency (PCE). However, it is difficult to prepare perovskite films with good performance in open air due to the poor stability of perovskite materials in high humidity, which is seriously hindering the practical application and development of PSCs. Herein, ethyl acetate (EA) is introduced into the perovskite precursor to enhance the crystallinity of perovskite for fabricating high efficiency stable devices in the atmospheric environment. Interestingly, volatile EA, which is often used as an anti-solvent, could quickly evaporate and accelerate the nuclei formation during perovskite crystallization. More impressively, the Lewis base nature of EA can form strong chemical bonding interactions with perovskite to passivate the defects during crystallization. As a result, the EA-modified perovskite film demonstrates dense and defect-less morphology with large grain size (the maximum achieves 0.9 µm). The EA-treated device has a dramatic efficiency of 19.53% and negligible hysteresis of the photocurrent. Furthermore, both the temperature and humidity resistances of EA-modified PSC are significantly improved. The normalized PCE of the EA-modified device without encapsulation can still retain over 80% of its initial value after being stored in 60% relative humidity (RH) in the dark for 500 hours. This contribution provides a promising channel for facilitating the commercialization of PSCs.

NiCo2O4 arrays with a tailored morphology as hole transport layers of perovskite solar cells.

Inorganic p-type semiconductors have broadly served as hole transport materials (HTLs) in perovskite solar cells (PSCs) in recent years. Among them, NiCo2O4 with its excellent conductivity and hole mobility is the emerging candidate for HTLs and is attracting increasing attention. Here, we employ a simple hydrothermal method to fabricate high-quality mesoporous NiCo2O4 films as HTLs of PSCs. The study finds that the morphology of NiCo2O4 can be regulated from nanosheets (NSs) to nanowires (NWs) as the hydrothermal reaction time increases, and the morphology of NiCo2O4 significantly affects the device performance. Specially, the device with NWs achieves a best efficiency of 11.58%, ascribed to the fact that such a one dimension material could provide a straight path for hole extraction/transport. And benefiting from the mesoporous structures of NiCo2O4 films, all the devices exhibited a very repeatable and desirable long-term stability. Overall, this work develops alternative NiCo2O4 nanostructure-based HTLs and opens up new opportunities in fabricating PSCs.

Electrospun cellulose polymer nanofiber membrane with flame resistance properties for lithium-ion batteries.

Current developments of lithium-ion batteries (LIBs) are mainly focused on improving security and cycle performance. Herein, a novel polyvinylidene fluoride (PVDF)/triphenyl phosphate (TPP)/cellulose acetate (CA) nanofiber membrane was fabricated by one-step electrospinning and used as separator in lithium-ion batteries. Compared to traditional polyethylene membrane, the obtained composite showed higher porosity, elevated thermal stability, superior electrolyte wettability, and improved flame resistance. In addition, batteries assembled with PVDF/TPP/CA membrane exhibited excellent electrochemical properties and cycle stability. The enhanced performances were attributed to the porous structure and presence of CA and TPP. Overall, the proposed hybrid organic cellulose-based composite polymer membranes look promising as separators for advanced LIBs.

3 D NiO Nanowall Hole-Transporting Layer for the Passivation of Interfacial Contact in Inverted Perovskite Solar Cells.

Nickel oxide (NiO) materials with excellent stability and favorable energy bands are desirable candidates for hole-selective contact (HSC) of inverted perovskite solar cell (PSC). However, studies that focus on addressing interfacial issues, which are induced by the poor NiO/perovskite contact or other defects, are scarce. In this study, a facile one-step hydrothermal strategy is demonstrated for the development of a 3 D NiO nanowall (NW) film as a promising HSC. The new NiO NWs HSC exhibits a robust and homogenous mesoporous network structure, which improved the NiO/perovskite interface contact, passivated the interfacial defect and improved the quality of the perovskite film. The optimized interface features enabled a power conversion efficiency (PCE) approaching 18 %. A diethanolamine (DEA) interlayer was introduced to further passivate the intrinsic defect of the NiO surface, resulting in better charge transfer with suppressed recombination loss. As a result, the champion PCE of the NiO NWs/DEA-based device was increased to 19.16 % with a high open-circuit voltage (≈1.11 V) and fill factor (>80 %), which is prominent in methylammonium lead iodide-based inverted PSCs. Furthermore, the device exhibited better stability and lower hysteresis behavior than a conventional solution-based NiO nanocrystal device.

Novel NiO Nanoforest Architecture for Efficient Inverted Mesoporous Perovskite Solar Cells.

Inverted perovskite solar cells (PSCs) demonstrate attractive features in developing an air-stable photovoltaic device, by employing inorganic hole transport layers (HTLs). However, their power conversion efficiencies are still inferior to that of mesoporous n-i-p devices, mainly attributed to the undesirable hole extraction and interfacial recombination loss. Here, we design a novel one-dimensional NiO nanotube (NT) nanoforest as efficient mesoporous HTLs. Such a NiO NT mesoporous structure provides a highly conductive pathway for rapid hole extraction and depresses interfacial recombination loss. Furthermore, excellent light capturing could be achieved by optimizing the length and branch growth of the NiO NT nanoforest, which mimics the evolution of the natural forest. Therefore, this inverted mesoporous PSCs yield an optimal efficiency of 18.77%, which is still prominent in state-of-the-art NiO-based devices. Alternatively, the mesoporous device exhibits greatly improved long-term stability. This work provides a new design perspective for developing high-performance inverted PSCs.

Microwave Hydrothermal Synthesis of Basalt Fibers/Titanium Dioxide and Their Photocatalytic Activity for the Degradation of Rhodamine B.

Basalt fibers loaded with titanium dioxide (BFs/TiO2) were successfully fabricated via a simple and cost effective microwave hydrothermal method. The morphology and structure of the BFs/TiO2 were characterized by transmission electron microscopy, scanning electron microscopy, and X-ray diffraction. The photocatalytic activity of the BFs/TiO2 was validated by the photodegradation test of Rhodamine B (RhB) under ultraviolet light irradiation. The photocatalytic reaction result revealed the excellent photocatalytic activity of the BFs/TiO2, with 94% of RhB decomposed at 5 h after irradiation. Furthermore, the recycling test indicated that the BFs/TiO2 exhibited excellent recyclability with photocatalytic degradation rate still maintained at 86% in the fifth cycling test.

Preparation and the luminescent properties of Tb3+-doped Gd2O3 fluorescent nanofibers via electrospinning.

Tb(3+)-doped Gd(2)O(3) (Gd(2)O(3):Tb(3+)) nanofibers were prepared via a simple electrospinning technique using poly(ethylene oxide) (PEO) and rare-earth acetate tetrahydrates (Ln(CH(3)COO)(3)·4H(2)O (Ln = Gd, Tb)) as precursors. The obtained nanofibers have an average diameter of about 80 nm and are composed of pure cubic Gd(2)O(3) phase. A possible formation mechanism for the nanofibers is proposed on the basis of the experimental results, which reveals that PEO acts as the structure directing template during the whole electrospinning and subsequent calcination process. The luminescent properties of the nanofibers were investigated in detail. The nanofibers exhibit a favorable fluorescent property symbolized by the characteristic green emission (545 nm) resulting from the 5D4-->7F5 transition of Tb(3+). Concentration quenching occurs when the Tb(3+) concentration is 3 at.%, indicating that the Gd(2)O(3):Tb(3+) nanofibers have an optimum luminescent intensity under such a doping concentration.