RESUMO
Gas imaging has become one of the research hotspots in the field of gas detection due to its significant advantages, such as high efficiency, large range, and dynamic visualization. It is widely used in industries such as natural gas transportation, chemical, and electric power industries. With the development of infrared detector technology, uncooled thermal imagers are undergoing a developmental stage of technological advancement and widespread application. This article introduces a gas imaging principle and radiation transfer model, focusing on passive imaging technology and active imaging technology. Combined with the actual analysis, the application scenarios using uncooled thermal imaging cameras for gas imaging measurement are analyzed. Finally, the limitations and challenges of the development of gas imaging technology are analyzed.
RESUMO
All-solid-state sodium ion batteries (ASIBs) possess enhanced safety and desired cycling life compared with conventional liquid sodium batteries, showing great potential in large-scale energy storage systems. Polymer electrolytes based on poly(ethylene oxide) (PEO) have been extensively studied for ASIBs due to superior flexibility and processability. However, PEO-based electrolyte without any modification can hardly meet the requirements of ASIBs at room temperature. In the past decade, unremitting efforts have been attached to inhibiting crystallization of PEO, especially via ionic liquid plasticizing. However, the plasticizing mechanism is not clear. Here we incorporated Pyr13FSI into PEO-NaClO4 electrolyte to investigate the plasticizing effect by infrared spectrum characterizations and DFT calculations. The results indicate that FSI- anions tend to adhere to the PEO backbone, generating enhanced coordination ability and more coordination sites. Solid-state sodium ion batteries using PEO-NaClO4-40 wt % Pyr13FSI as polymer electrolyte exhibit good cycling and rate performance. Insights into the plasticizing mechanism contribute to fabricating polymer electrolyte with high performance for ASIBs.
RESUMO
As a typical multielectron cathode material for lithium-ion batteries, iron fluoride (FeF3) and its analogues suffer from poor electronic conductivity and low actual specific capacity. Herein, we introduce Ag nanoparticles by silver mirror reaction into the FeF3·0.33H2O cathode to build the electronic bridge between the solid (active materials) and liquid (electrolyte) interface. The crystal structures of as-prepared samples are characterized by X-ray diffraction and Rietveld refinement. Moreover, the density of states of FeF3·0.33H2O and FeF3·0.33H2O/Ag (Ag-decorated FeF3·0.33H2O) samples are calculated using the first principle density functional theory. The FeF3·0.33H2O/Ag cathodes exhibit significant enhancements on the electrochemical performance in terms of the cycle performance and rate capability, especially for the Ag-decorated amount of 5%. It achieves an initial capacity of 168.2 mA h g-1 and retains a discharge capacity of 128.4 mA h g-1 after 50 cycles in the voltage range of 2.0-4.5 V. It demonstrates that Ag decoration can reduce the band gap, improve electronic conductivity, and elevate intercalation/deintercalation kinetics.