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The practical application of lithium metal anodes is significantly impeded by poor interfacial stability and uncontrolled dendrite growth. Herein, we introduce methyl trifluoroacetate (MTFA), a low-melting-point small molecule, as an electrolyte additive in an ether-based electrolyte. This additive facilitates the formation of an in situ composite solid electrolyte interphase (SEI) layer that is rich in LiF and features an ester-based flexible matrix. The resulting composite layer exhibits high ionic conductivity and mechanical stability, effectively regulating the lithium deposition behavior over a broad temperature range and inhibiting dendrite formation. Based on MTFA, the Li||Li symmetrical cell achieves a lifespan exceeding 5000 h at room temperature and 800 h at -20 °C, both with ultralow overpotential and exceptional cycling stability. In Li||LiFePO 4 full cells with a high-area loading (10.52 mg cm -2 ) and an N/P ratio of 1.68, an average capacity decay of merely 0.096% per cycle is observed over 200 cycles. Even at -20 °C, the Li||LiFePO 4 cell shows a CE of over 99% and maintains stable cycling performance. This work provides an innovative approach for optimizing lithium metal anode interfaces and enhancing low-temperature operation capabilities through the use of electrolyte additives.

Innovative titania nanostructures were synthesized via efficient and prolific liquid phase deposition route and efficiently utilized for catalytic degradation of Eosin Y. The as-synthesized TiO 2 @ITO nanostructures were subjected to various characterization tactics that confirmed the efficacious fabrication of nanostructures. The minute size of particles around 5-6 nm having anatase crystalline phase and concrete like morphology was greatly revealed by atomic force microscopy, XRD, and SEM, respectively. The resulting nanoconcretes were employed for photocatalytic degradation of Eosin Y dye in aqueous medium. The effects of various experimental parameters such as the reducing agent concentration, sunlight, time, catalytic dose, and microwave power were investigated for the potential photocatalytic degradation. The proposed TiO 2 @ITO nanostructures showed potential photocatalytic efficiency then previously reported nanomaterial for degradation of toxic Eosin Y dye; it shows approximately 99.8% dye degraded within 50-60 s using only 100 μg of nanocatalyst under optimized conditions. Owing to minute size, topography and electron-hole pair abilities TiO 2 @ITO nanostructures suggest an exceptional icon at the commercial level for successful degradation of toxic pollutants.Graphical abstract.

In this study, nano-sized ITO supported Pt-Pd bimetallic catalyst was synthesized for the degradation of methyl parathion pesticide, a common extremely toxic contaminant in aqueous solution. On the characterization with different techniques, a beautiful scenario of honeycomb architecture composed of ultra-small nanoneedles or fine hairs was found. Average size of nanocatalyst also confirmed which was in the range of 3-5 nm. High percent degradation (94%) was obtained in 30 s using 1.5 × 10 - 1  mg of synthesized nanocatalyst, 0.5 mM NaBH 4 , and 110 W microwave radiations power. Recyclability of nanocatalyst was efficient till 4th cycle observed during study of reusability. The supported Pt-Pd bimetallic nanocatalyst on ITO displayed many advantages over conventional methods for degradation of methyl parathion pesticide, such as high percent degradation, short reaction time, small amount of nanocatalyst, and multitime reusability. Graphical abstract Schematic illustration of reaction for degradation of methyl parathion.