Multifunctional Effects of Biguanide Derivative in the Application of Highly Efficient Tin-Lead Perovskite Solar Cells.

Tin-lead (Sn-Pb) mixed perovskites is beneficial to a single-junction or all-perovskite tandem device. However, the poor quality of the perovskite surface resulting from Sn2+ oxidation and uncontrollable crystallization degrades device performance and stability. Herein, based on interface engineering, a novel biguanide derivative of PZBGACl is employed that integrates different types of N-related groups to reconstruct the surface/grain boundaries of Sn-Pb perovskite. Combined with the microcorrosion effect of isopropanol solvent, PZBGACl can induce surface recrystallization of perovskite, and passivate various types of defects via hydrogen bond or Lewis acid-base interaction, leading to an excellent perovskite film with reduced stress, larger grain size, and more n-type surface. As a result, the obtained Sn-Pb solar cell achieves a power conversion efficiency of 22.0%, and exhibits excellent N2 storage/operation stability.

A Newly Crosslinked-double Network PEDOT:PSS@PEGDMA toward Highly-Efficient and Stable Tin-Lead Perovskite Solar Cells.

Until now, poly(3,4-ethylenedioxythiophene):poly(styrensulfonate) (PEDOT:PSS) is widely used in Sn-Pb perovskite solar cells (PSCs) due to its many advantages, including high optical transparency, suitable conductivity, superior wettability, and so on. However, the acidic and hydroscopic properties of the PSS component, as well as the incongruous energy level of the hole transport layer (HTL), may lead to unsatisfying interface properties and decreased device performance. Herein, by adding polyethylene glycol dimethacrylate (PEGDMA) into PEDOT:PSS, a newly crosslinked-double-network obtain of PEDOT:PSS@PEGDMA film, which could not only optimize nucleation and crystallinity of Sn-Pb perovskite films, but also suppress defect density and optimize energy level alignment at the HTL/perovskite interface. As a result, the achieves highly efficient and stable mixed Sn-Pb PSCs with an encouraging power conversion efficiency of 20.9%. Additionally, the device can maintain good stability under N2 atmosphere.

Multifunctional Ionic Liquid as an Interfacial Modifier for High-Performance and Stable NiOx-Based Inverted Perovskite Solar Cells.

Interface instability has evolved into the primary aspect that limits the durability improvement of perovskite solar cells (PSCs). Interface modification with suitable molecules is widely considered an effective path for improving the interface state. Herein, an ionic liquid modified layer, 1-ethyl-3-methylimidazolium aminoacetate (EMIMAE), is brought to modify NiOx/perovskite interface. The EMIMAE layer can interact with the adjacent layer to regulate the perovskite growth, passivate defects in the film, and promote charge transport in PSCs. Eventually, the optimized device's efficiency rises to 18.6%, which is a substantial improvement over the control device. Particularly, after 1000 h of continuous maximum power point tracking, the device can still retain 95% of its initial efficiency. This work proposes a simple idea to ameliorate the device interface and boost the commercialization of NiOx based devices.

In Situ Perovskitoid Engineering at SnO2 Interface toward Highly Efficient and Stable Formamidinium Lead Triiodide Perovskite Solar Cells.

The black-phase formamidinium lead triiodide (α-FAPbI3) perovskite has turned out to be one of the most efficient light harvesting materials. However, the phase stability of FAPbI3 is a long-standing issue. Herein, we introduce a layer of tetrabutylammonium fluoride (TBAF) on SnO2, which would form an in situ layer of TBAPbI3 perovskitoid at the SnO2/FAPbI3 interface by interacting with PbI2. The results show that this strategy could improve the conductivity of SnO2, passivate the defects in perovskite, improve the phase stability of α-FAPbI3, and retard the nonradiative recombination in the device. As a result, we obtain a champion device with a power conversion efficiency of 23.1% under AM 1.5 G illumination of 100 mW/cm2. The unencapsulated devices can maintain excellent stability under illumination, thermal stress, and humidity conditions, respectively.

Stable Layered 2D Perovskite Solar Cells with an Efficiency of over 19% via Multifunctional Interfacial Engineering.

Layered 2D perovskites have been extensively investigated by scientists with photovoltaics (PV) expertise due to their good environmental stability. However, a random phase distribution in the perovskite film could affect both the performance and stability of the devices. To overcome this problem, we propose multifunctional interface engineering of 2D GA2MA4Pb5I16 perovskite by employing guanidinium bromide (GABr) on top of it to optimize the secondary crystallization process. It is found that GABr treatment can facilitate to form a shiny and smooth surface of the 2D GA2MA4Pb5I16 film with excellent optoelectronic properties. Thus, we realize efficient and stable 2D perovskite solar cells (PSCs) with a champion power conversion efficiency (PCE) of 19.3% under AM 1.5G illumination. Additionally, the optimized device without encapsulation could retain 94% of the initial PCE for more than 3000 h after being stored under ambient conditions.

Enhanced Ultraviolet Damage Resistance in Magnesium Doped Lithium Niobate Crystals through Zirconium Co-Doping.

MgO-doped LiNbO3 (LN:Mg) is famous for its high resistance to optical damage, but this phenomenon only occurs in visible and infrared regions, and its photorefraction is not decreased but enhanced in ultraviolet region. Here we investigated a series of ZrO2 co-doped LN:Mg (LN:Mg,Zr) regarding their ultraviolet photorefractive properties. The optical damage resistance experiment indicated that the resistance against ultraviolet damage of LN:Mg was significantly enhanced with increased ZrO2 doping concentration. Moreover, first-principles calculations manifested that the enhancement of ultraviolet damage resistance for LN:Mg,Zr was mainly determined by both the increased band gap and the reduced ultraviolet photorefractive center O2-/-. So, LN:Mg,Zr crystals would become an excellent candidate for ultraviolet nonlinear optical material.

Linear Tuning of Phase-Matching Temperature in LiNbO3:Zr Crystals by MgO Co-Doping.

We grew a series of co-doped LiNbO3 crystals with fixed 1.5 mol % ZrO2 and various MgO concentrations (1.0, 3.0, 4.0, 6.0 mol %), and investigated their optical properties and defect structures. By 3.0 mol % MgO co-doping, the optical damage resistance at 532 nm reached 6.5 × 106 W/cm2, while the phase-matching temperature for doubling 1064 nm was only 29.3 °C-close to room temperature-which was conducive to realizing the 90° phase matching at room temperature by slightly modulating the incident angle of the fundamental beam. Notably, we found that the phase-matching temperature increased linearly with the increase of MgO doping, and this linear dependence helped us to grow the high-quality crystal for room temperature 90° phase matching. Moreover, the defect analysis indicated that the linear tuning of phase-matching temperature might be attributed to Mg Li + + Zr Nb - neutral pairs in crystals.

Near-Infrared Light-Driven Controllable Motions of Gold-Hollow-Microcone Array.

Micro/nanomotors can effectively convert other forms of energy into mechanical energy, which have been widely used in microscopic fields. However, it is still challenging to integrate the micro/nanomotors to perform complex tasks for broad applications. Herein, a new mode for driving the collective motion behaviors of integrated micro/nanomotors in a liquid by plasmonic heating is reported. The integrated micro/nanomotors, constituted by gold hollow microcone array (AuHMA), are fabricated via colloidal lithography. Owing to the excellent plasmonic-heating property of the AuHMA, the integrated micro/nanomotors can generate vapor bubbles in the liquid as exposure to near-infrared (NIR) irradiation, therefore inducing versatile motions via on/off NIR irradiation. The floating-diving motions are reversible for at least 60 cycles without fatigue. In addition, precise manipulation of the coordinated motion behaviors, including bending, convex, and jellyfish-like floating motions, can be realized by adjusting the irradiated positions of incident NIR light together with the sizes and shapes of AuHMA films. Moreover, the AuHMA film can act as a robust motor to drive a foam craft over 57-folds of its own weight as exposure to NIR irradiation. Our investigation into the NIR-driven AuHMA film provides a facile approach for obtaining integrated micro/nanomotors with controllable collective motions, which holds promise in remotely controlled smart devices and soft robotics in liquids.

Room temperature 90° phase-matching in zirconium and magnesium co-doped lithium niobate crystals.

Laser has been widely used in many aspects, by now it is difficult to get each frequency that we want, and frequency conversion is an effective way to obtain different frequency laser through a nonlinear optical crystal. MgO-doped LiNbO3 (Mg:LN) crystal has usually been used for second harmonic generation (SHG) through temperature-matching configuration with a stove, till now a room temperature 90° phase-matching is still lacking. Here we find that the SHG of Nd:YAG laser is achieved at 26.1 °C while the optical damage resistance is higher than 6.5 MW/cm2 in the ZrO2 and MgO co-doped LiNbO3 (Zr,Mg:LN) crystal. Moreover, the monotonic decrease of phase-matching temperature is firstly found with the increase of doping concentration. These unusual properties may be attributed to the formation of [Formula: see text] + [Formula: see text] defect pairs. Our work suggests that Zr,Mg:LN crystal may be an attractive candidate for nonlinear optical applications.

Polystyrene sulfonate threaded in MIL-101Cr(iii) as stable and efficient acid catalysts.

A series of polystyrene sulfonate threaded in MIL-101Cr(iii) composites both with and without cross-linkers were synthesized. These composites demonstrated superior activity and durability for the acid catalyzed reaction, thus highlighting the importance of surface properties, mobility and accessibility of active sites in determining the catalytic performance.