ABSTRACT
Light exposure has been proven to have a significant impact on human health. As a result, researchers are increasingly exploring its potential benefits and drawbacks. With advancements in understanding light and the manufacturing of light sources, modern health lighting has become widely utilized in daily life and plays a critical role in the prevention and treatment of various illnesses. The use of light in healthcare is a global trend, with many countries actively promoting the development and application of relevant scientific research and medical technology. This field has gained worldwide attention and support from scientists and doctors alike. In this review, we examine the application of lighting in human health and recent breakthroughs in light exposure related to pathology, therapeutic strategies, molecular changes, and more. Finally, we also discuss potential future developments and areas of application.
Subject(s)
Light , Humans , Health , Phototherapy , LightingABSTRACT
Confocal Raman microscopy (CRM) has found applications in many fields as a consequence of being able to measure molecular fingerprints and characterize samples without the need to employ labelling methods. However, limited spatial resolution has limited its application when identification of sub-micron features in materials is important. Here, we propose a differential correlation-confocal Raman microscopy (DCCRM) method to address this. This new method is based on the correlation product method of Raman scattering intensities acquired when the confocal Raman pinhole is placed at different (defocused) positions either side of the focal plane of the Raman collection lens. By using this correlation product, a significant enhancement in the spatial resolution of Raman mapping can be obtained. Compared with conventional CRM, these are 23.1% and 33.1% in the lateral and axial directions, respectively. We illustrate these improvements using in situ topographic imaging and Raman mapping of graphene, carbon nanotube, and silicon carbide samples. This work can potentially contribute to a better understanding of complex nanostructures in non-real time spectroscopic imaging fields.
ABSTRACT
Lithium (Li), as the lightest metal and the most important powerful material in battery fabrication, is widely used in many fields. The fast detection of Li is necessary for industrial application. The slow-speed detection methods, including atomic absorption spectroscopy and inductively coupled plasma mass spectroscopy with high accuracy and low limit of detection, are hard to utilize in in situ industrial control due to complex prepreparation of samples. Here, through the analysis of the typical spectrum line at Li I 670.79 nm, Li ions in water were detected quantitatively in 1 min, including sample preparation by laser-induced breakdown spectroscopy (LIBS) with filter paper as the adsorption substrate. The calibration curve by polynomial function fitting is used to predict the Li+ concentration. The limit of detection (LOD) as low as 18.4 ppb is obtained, which is much lower than the results ever reported by using filter paper. The related factor R2 reaches 99%, and the prediction error is lower than 2%, proving the fast and online monitor for Li+ by LIBS is feasible. Furthermore, by comparison with the results with filter paper enrichment, the Li+ detection from water directly shows higher LOD to 10.5 ppm. Moreover, the plasma images, by gate-controlled intensified charge-coupled device, illustrate a different morphology and evolution between that on water surface and filter paper surface through visual observation. This study provides experimental and theoretical experience in a fast way for the quantitative detection of the lightest metal ion (Li+) in liquid.
