RESUMEN
In this study, 7075 aluminum alloy welding wire with TiB2 nanoparticle reinforcement as an additive together with the variable polarity TIG welding arc as a heat source were applied to produce thin-walled deposited layer samples. Results indicated that the performance of the deposited structure of 7075 aluminum alloy with a TiB2 reinforcement phase was significantly improved compared to the deposited structure of ordinary 7075 aluminum alloy welding wire. Meanwhile, the precipitation of the TiB2 reinforcement phase was insufficient within the structure, and the enhancing effect could not be fully exerted. Moreover, the 7-series aluminum alloy contained a large amount of Zn and Mg elements inside. If the soluble crystalline phase was not fully dissolved, severe stress corrosion could be caused, which inevitably led to a decrease in the mechanical properties. To further improve the performance of the deposited layer, a T6 heat treatment process was performed at 470 °C for 2 h, followed by rapid cooling with distilled water and artificial aging at 120 °C for 24 h. After heat treatment, many second phases appeared in the microstructure of the deposited layer, and the tensile strength increased from (361.8 ± 4.8) MPa to (510.2 ± 5.4) MPa together with the elongation which increased from (9.5 ± 0.5) % to (10.2 ± 0.4) %. The fracture mode of the fracture was a ductile fracture along grain boundaries. The microhardness increased from (145 ± 5) HV to (190 ± 4) HV and exhibited good corrosion resistance in a 3.5% NaCl solution corrosion test.
RESUMEN
As an important part of perovskite solar cells (PSCs), hole transporting layer (HTL) has a critical impact on the performance and stability of the devices. In an attempt to alleviate the moisture and thermal stability issues from the commonly used HTL Spiro-OMeTAD with dopant, it is urgent to develop novel HTLs with high stability. In this study, a new class of polymers D18 and D18-Cl are applied as undoped HTL for CsPbI2Br-based PSCs. In addition to the excellent hole transporting properties, we unveil that D18 and D18-Cl with larger thermal expansion coefficient than that of CsPbI2Br could impose a compressive stress onto the CsPbI2Br film upon thermal treatment, which could release the residual tensile stress in the film. As a result, the efficiency of CsPbI2Br-based PSCs with D18-Cl as HTL reaches 16.73%, and the fill factor (FF) exceeds 85%, which is one of the highest FF records for the conventional-structured device to date. The devices also show impressive thermal stability with over 80% of the initial PCE retained after 85 °C heating for 1500 h.
RESUMEN
In this investigation, 1060Al/AZ31B welded joints were obtained by magnetic pulse welding technique. In order to test the microstructure and mechanical properties of the joints, the welded joints were annealed at different temperatures and then examined by optical microscopy (OM), scanning electron microscopy (SEM), energy spectrum analysis (EDS) and mechanical properties testing. The testing results of the welded joints annealed at different temperatures showed that the Al-Mg MPW welded joints were well bonded. The changing of the microstructure and mechanical properties of Al/Mg welded joints was not apparent under the temperature of 200 °C. However, Al12Mg17 intermetallic compound layer formed at 200 °C. Al12Mg17 and Al3Mg2 intermetallic compound layers formed at the temperature of 300 °C. The diffusion rate of Mg and Al elements is proportional to the annealing temperature and the intermetallic compounds layer is gradually formed. The microhardness near the interface decreased first and then increased on account of the brittleness of intermetallic compounds. In the tensile shear tests, the fracture mechanism of Al/Mg MPW welded joints were analyzed. When the temperature was lower than 200 °C the joints did not crack. At 200 °C and 250 °C, the joints fracture along the Al12Mg17-Al interface. The joint cracks along the interface of Al12Mg17-Al3Mg2 at the temperature of 300 °C.
RESUMEN
The Mg/Al composite plate was developed in aerospace and other fields. At present, through the corrugated rolling method, the bonding strength of Mg/Al composite plate could be increased and the warpage could be reduced. However, this still requires the straightening process to reach the parameters' range. In this work, the original interface morphology of Mg/Al corrugated composite plate was obtained by experimental characterization. Based on the principle of elastoplastic mechanics, the equations of straightener parameters and straightening process parameters were obtained and the influencing factors were deduced. So, the straightening model was established in an Abaqus. The effects of straightener parameters and straightening process parameters on the interface morphology were analyzed and the interface morphology was expressed by amplitude and period length of the equation. The results showed that bending moment, shear strength and the reduction of second roll played roles on the interface morphology. After the first straightening unit, the amplitude increased by 1.1% and the period length increased by 3%. Finally, a complete straightening parameter was designed, which included straightener parameters, straightening process parameters and straightening temperature. The aim of this work was to provide a theoretical basis for establishing a high precision Mg/Al corrugated composite plate straightening model, which could improve the bonding strength while ensuring the straightening effect.
RESUMEN
Increasing working voltage is a promising way to increase the energy density of lithium-ion batteries. Cycling and rate performance deteriorated due to excessive electrolyte decomposition and uncontrolled formation of a cathode-electrolyte interface (CEI) layer at a high voltage. A new concept is proposed to construct a high-voltage-stable electrode-electrolyte interface. An elastomeric poly(dimethyl siloxane) (PDMS) binder is incorporated into the electrode to modify the LiNi0.5Co0.2Mn0.3O2 (NCM 523) particle surface via an in situ cross-linking reaction between hydroxy-terminated PDMS and methyl trimethoxy silane promoted by moisture at ambient conditions (MPDMS). Improved electrochemical performance is achieved with the MPDMS binder in terms of reversible capacity (201 vs 185 mAh·g-1 at 0.2C), capacity retention (80 vs 68%, after 300 cycles at 1C), and rate performance (55.6% increase at 5C), as demonstrated by the NCM 523||Li half-cell. The NCM 523||graphite full-cell also shows improved performance at 4.6 V (147 vs 128 mAh·g-1, 82 vs 76%, after 200 cycles at 1C). The mechanism studies indicate that MPDMS exerts multiple effects, including cathode surface passivation, solvation structure tuning, electrolyte uptake enhancement, and mechanical stress relief. This work provides an inspiring route to realize high-voltage application of lithium-ion battery technology.
RESUMEN
Polyurethane elastomer electrolyte (PUEE) represents a promising class of polymer solid electrolytes for the preparation and packaging of flexible devices by anodic bonding. In this work, PUEEs were designed and prepared via a pre-polymerization method and cured at room temperature using polypropylene glycol (PPG), toluene-2,4-diisocyanate (TDI) and 1,4-butanediol (BDO) in the presence of varying amounts of lithium bis(trifluoromethanesulphonyl)imide (LiTFSI). All PUEEs exhibited high thermal stability and conductivity, with the highest ionic conductivity of 9.6 × 10-5 S cm-1 for PUEE6 (n [NHCOO]/Li+ = 1) at 55 °C. The results showed that LiTFSI was dissolved completely in the polyurethane matrix, and the complexing reactions occurred between the lithium ions and the polar groups of polyurethane. After that, the prepared PUEE and the Al sheet were successfully joined by the anodic bonding process. The microstructures of the bonded interface between PUEE and the Al sheet with a clear intermediate bonding layer could be observed in the cross-section scanning electron microscopy (SEM) images, and the elements in each layer were also detected by energy dispersive spectroscopy (EDS), which indicated that the PUEE and the Al sheet were bonded together. The maximum tensile strength for bonded PUEE6/Al was up to 0.45 MPa. All these results demonstrated that the prepared PUEE material would be a promising candidate for the preparation and packaging of flexible devices by anodic bonding.
