Ultra-High Proportion of Grain Boundaries in Zinc Metal Anode Spontaneously Inhibiting Dendrites Growth.

Aqueous Zn-ion batteries are an attractive electrochemical energy storage solution for their budget and safe properties. However, dendrites and uncontrolled side reactions in anodes detract the cycle life and energy density of the batteries. Grain boundaries in metals are generally considered as the source of the above problems but we present a diverse result. This study introduces an ultra-high proportion of grain boundaries on zinc electrodes through femtosecond laser bombardment to enhance stability of zinc metal/electrolyte interface. The ultra-high proportion of grain boundaries promotes the homogenization of zinc growth potential, to achieve uniform nucleation and growth, thereby suppressing dendrite formation. Additionally, the abundant active sites mitigate the side reactions during the electrochemical process. Consequently, the 15 µm Fs-Zn||MnO2 pouch cell achieves an energy density of 249.4 Wh kg-1 and operates for over 60 cycles at a depth-of-discharge of 23 %. The recognition of the favorable influence exerted by UP-GBs paves a new way for other metal batteries.

Femtosecond laser induced in-situ crystallization of Tb-based luminescent metal organic framework.

Luminescent metal-organic frameworks (LMOFs) are a class of interesting and well-investigated MOF materials, which have shown remarkable prospects in the past and have been widely applied in different fields. However, due to their organic hybrid aspect, micro-/nano-patterning LMOFs in devices via a conventional semiconductor process is very challenging. In this work, we have introduced an elegant technique via nonlinear photon-chemical effect to induce the synthesis and growth of LMOFs. A facile technique for local synthesis and micro-pattering Tb-based luminescent metal organic frameworks (Tb(BTC)·G) from a solution of precursors is achieved. A single step approach micro-patterning for device integration with simultaneous chemical synthesis was proposed. Micro-devices with excellent fluorescence performance based on Tb(BTC)·G have been demonstrated. This work first suggested a high resolution bottom-up micro-patterning technique for MOF device fabrication using femtosecond laser direct writing, showing great potential on MOF based micro/nano-devices integration, especially promising for patterning high resolution luminescent MOF devices.

Ultrafast Photoexcitation Induced Passivation for Quasi-2D Perovskite Photodetectors.

Quasi-2D perovskites exhibit great potential in photodetectors due to their exceptional optoelectronic responsivity and stability, compared to their 3D counterparts. However, the defects are detrimental to the responsivity, response speed, and stability of perovskite photodetectors. Herein, an ultrafast photoexcitation-induced passivation technique is proposed to synergistically reduce the dimensionality at the surface and induce oxygen doping in the bulk, via tuning the photoexcitation intensity. At the optimal photoexcitation level, the excited electrons and holes generate stretching force on the Pb─I bonds at the interlayered [PbI6]-, resulting in low dimensional perovskite formation, and the absorptive oxygen is combined with I vacancies at the same time. These two induced processes synergistically boost the carrier transport and interface contact performance. The most outstanding device exhibits a fast response speed with rise/decay time of 201/627 ns, with a peak responsivity/detectivity of 163 mA W-1/4.52 × 1010 Jones at 325 nm and the enhanced cycling stability. This work suggests the possibility of a new passivation technique for high performance 2D perovskite optoelectronics.

Photoexcitation-induced passivation of SnO2 thin film for efficient perovskite solar cells.

A high-quality tin oxide electron transport layer (ETL) is a key common factor to achieve high-performance perovskite solar cells (PSCs). However, the conventional annealing technique to prepare high-quality ETLs by continuous heating under near-equilibrium conditions requires high temperatures and a long fabrication time. Alternatively, we present a non-equilibrium, photoexcitation-induced passivation technique that uses multiple ultrashort laser pulses. The ultrafast photoexcitation and following electron-electron and electron-phonon scattering processes induce ultrafast annealing to efficiently passivate surface and bulk defects, and improve the crystallinity of SnO2, resulting in suppressing the carrier recombination and facilitating the charge transport between the ETL and perovskite interface. By rapidly scanning the laser beam, the annealing time is reduced to several minutes, which is much more efficient compared with conventional thermal annealing. To demonstrate the university and scalability of this technique, typical antisolvent and antisolvent-free processed hybrid organic-inorganic metal halide PSCs have been fabricated and achieved the power conversion efficiency (PCE) of 24.14% and 22.75% respectively, and a 12-square-centimeter module antisolvent-free processed perovskite solar module achieves a PCE of 20.26%, with significantly enhanced performance both in PCE and stability. This study establishes a new approach towards the commercialization of efficient low-temperature manufacturing of PSCs.

Periodic Acid Modification of Chemical-Bath Deposited SnO2 Electron Transport Layers for Perovskite Solar Cells and Mini Modules.

Chemical bath deposition (CBD) has been demonstrated as a remarkable technology to fabricate high-quality SnO2 electron transport layer (ETL) for large-area perovskite solar cells (PSCs). However, surface defects always exist on the SnO2 film coated by the CBD process, impairing the devices' performance. Here, a facile periodic acid post-treatment (PAPT) method is developed to modify the SnO2 layer. Periodic acid can react with hydroxyl groups on the surface of SnO2 films and oxidize Tin(II) oxide to Tin(IV) oxide. With the help of periodic acid, a better energy level alignment between the SnO2 and perovskite layers is achieved. In addition, the PAPT method inhibits interfacial nonradiative recombination and facilitates charge transportation. Such a multifunctional strategy enables to fabricate PSC with a champion power conversion efficiency (PCE) of 22.25%, which remains 93.32% of its initial efficiency after 3000 h without any encapsulation. Furthermore, 3 × 3 cm2 perovskite mini-modules are presented, achieving a champion efficiency of 18.10%. All these results suggest that the PAPT method is promising for promoting the commercial application of large-area PSCs.

Passive Deicing CFRP Surfaces Enabled by Super-Hydrophobic Multi-Scale Micro-Nano Structures Fabricated via Femtosecond Laser Direct Writing.

Carbon fiber reinforced plastic (CFRP) is the main material of aircraft skin. Preparing superhydrophobic anti-icing/deicing surface on the CFRP is of great importance for aircraft flight safety. In this work, a variety of multi-scale micro-nano structures were imprinted on CFRP by femtosecond laser processing, and a transition from hydrophilic to superhydrophobic CFRP was realized. After being optimized by different geometries and laser conditions, the water contact angle, which is tested at 24.3 °C and 34% humidity, increased from 88 ± 2° (pristine) to 149 ± 3° (100 µm groove) and 153 ± 3° (80 µm grid). A further anti-icing test at -10 °C (measured on the cooling platform) and 28% humidity showed that the freezing time was increased from 78 ± 10 s (pristine) to 282 ± 25 s (80 µm grid). Most importantly, the tensile tests showed that the femtosecond laser processing method did not deteriorate the mechanical properties of CFRP. This work provides great significance for aircraft passive deicing technology.

Fiber Optical Hydrogen Sensor Based on WO3-Pd2Pt-Pt Nanocomposite Films.

In this paper, WO3-Pd2Pt-Pt nanocomposite films were deposited on a single mode fiber as the hydrogen sensing material, which changes its reflectivity under different hydrogen concentration. The reflectivity variation was probed and converted to an electric signal by a pair of balanced InGaAs photoelectric detectors. In addition, the performance of the WO3-Pd2Pt-Pt composite film was investigated under different optical powers, and the irrigating power was optimized at 5 mW. With the irrigation of this optical power, the hydrogen sensitive film exhibits quick response toward 100 ppm hydrogen in air atmosphere at a room temperature of 25 °C. The experimental results demonstrate a high resolution at 5 parts per million (ppm) within a wide range from 100 to 5000 ppm in air. This simple and compact sensing system can detect hydrogen concentrations far below the explosion limit and provide early alert for hydrogen leakage, showing great potential in hydrogen-related applications.

Lead halide-templated crystallization of methylamine-free perovskite for efficient photovoltaic modules.

Upscaling efficient and stable perovskite layers is one of the most challenging issues in the commercialization of perovskite solar cells. Here, a lead halide-templated crystallization strategy is developed for printing formamidinium (FA)-cesium (Cs) lead triiodide perovskite films. High-quality large-area films are achieved through controlled nucleation and growth of a lead halide•N-methyl-2-pyrrolidone adduct that can react in situ with embedded FAI/CsI to directly form α-phase perovskite, sidestepping the phase transformation from δ-phase. A nonencapsulated device with 23% efficiency and excellent long-term thermal stability (at 85°C) in ambient air (~80% efficiency retention after 500 hours) is achieved with further addition of potassium hexafluorophosphate. The slot die-printed minimodules achieve champion efficiencies of 20.42% (certified efficiency 19.3%) and 19.54% with an active area of 17.1 and 65.0 square centimeters, respectively.

Enhancing the thermal stability of the carbon-based perovskite solar cells by using a Cs x FA1-x PbBr x I3-x light absorber.

Despite the impressive photovoltaic performance with a power conversion efficiency beyond 23%, perovskite solar cells (PSCs) suffer from poor long-term stability, failing by far the market requirements. Although many efforts have been made towards improving the stability of PSCs, the thermal stability of PSCs with CH3NH3PbI3 as a perovskite and organic hole-transport material (HTM) remains a challenge. In this study, we employed the thermally stable (NH2)2CHPbI3 (FAPbI3) as the light absorber for the carbon-based and HTM-free PSCs, which can be fabricated by screen printing. By introducing a certain amount of CsBr (10%) into PbI2, we obtained a phase-stable Cs x FA1-x PbBr x I3-x perovskite by a "two-step" method and improved the device power conversion efficiency from 10.81% to 14.14%. Moreover, the as-prepared PSCs with mixed-cation perovskite showed an excellent long-term stability under constant heat (85 °C) and thermal cycling (-30 °C to 85 °C) conditions. These thermally stable and fully-printable PSCs would be of great significance for the development of low-cost photovoltaics.

Alleviate the J-V hysteresis of carbon-based perovskite solar cells via introducing additional methylammonium chloride into MAPbI3 precursor.

The hysteretic phenomenon commonly exists in the J-V curves of perovskite solar cells with different structures, especially for carbon-based mesoscopic perovskite solar cells without hole-conductor (carbon-based PSCs). By adding moderate amounts of methylammonium chloride (MACl) into MAPbI3 perovskite precursor, we found the J-V hysteresis of carbon-based PSCs could be significantly alleviated and the crystallinity of MAPbI3 perovskite could also be influenced. With the increasing amount of MACl, MAPbI3 perovskite showed better and better crystallinity until the MACl came to 0.45 M. The champion device with 0.45 M of additional MACl exhibited a preferable PCE of 14.27% for reverse-scan (RS) and 14.50% for forward-scan (FS), significantly higher than that of the pristine device (8.74% for RS and 4.80% for FS). What's more, the J-V hysteretic index of the device gradually decreased along with the increasing amount of MACl, and kept at low value even when the crystallinity of MAPbI3 perovskite became poor. Through XRD and PL analysis, we demonstrated that the recombination rate of the accumulated charges at the perovskite/TiO2 interface is the main reason for photocurrent hysteresis in carbon-based PSCs. High quality of perovskite crystals is an important contributing factor for high-performance PSCs with low hysteresis, but there is no necessary correlation between low hysteresis and good crystallinity. This research presents an effective way to fabricate carbon-based PSCs with low-hysteresis, and at the same time, provides evidence for investigating the origin of J-V hysteresis of PSCs.