Retaining soluble polysulfides in the sulfur cathodes and allowing for deep redox are essential to develop high-performance lithium-sulfur batteries. The versatile textures and physicochemical characteristics of abundant biomass offer a great opportunity to prepare biochar materials that can enhance the performance of Li-S batteries in sustainable mode. Here, we exploit micro-/mesoporous coconut shell carbon (CSC) with high specific surface areas as a sulfur host for Li-S batteries. The sulfur-infiltrated CSC materials show superior discharge-charge capacity, cycling stability, and high rate capability. High discharge capacities of 1599 and 1500 mA h g were achieved at current rates of 0.5 and 2.0 C, respectively. A high reversible capacity of 517 mA h g was retained at 2.0 C even after 400 cycles. The results demonstrate a high retention and a deep lithiation of the CSC-confined sulfur. The success of this strategy provides insights into seeking high-performance biochar materials for Li-S batteries from abundant bioresources.
In this work, a multilayer-modified paper-based colorimetric sensing platform with improved color uniformity and intensity was developed for the sensitive and selective determination of uric acid and glucose with smartphone as signal readout. In detail, chitosan, different kinds of chromogenic reagents, and horseradish peroxidase (HRP) combined with a specific oxidase, e.g., uricase or glucose oxidase (GOD), were immoblized onto the paper substrate to form a multilayer-modified test paper. Hydrogen peroxide produced by the oxidases (uricase or GOD) reacts with the substrates (uric acid or glucose), and could oxidize the co-immoblized chromogenic reagents to form colored products with HRP as catalyst. A simple strategy by placing the test paper on top of a light-emitting diode lamp was adopted to efficiently prevent influence from the external light. The color images were recorded by the smartphone camera, and then the gray values of the color images were calculated for quantitative analysis. The developed method provided a wide linear response from 0.01 to 1.0 mM for uric acid detection and from 0.02 to 4.0 mM for glucose detection, with a limit of detection (LOD) as low as 0.003 and 0.014 mM, respectively, which was much lower than for previously reported paper-based colorimetric assays. The proposed assays were successfully applied to uric acid and glucose detection in real serum samples. Furthermore, the enhanced analytical performance of the proposed method allowed the non-invasive detection of glucose levels in tear samples, which holds great potential for point-of-care analysis. Graphical abstract ᅟ.
Taking advantage of technology of spatio-temporal reconstruction and dispersive Fourier transform (DFT), we experimentally observed the buildup dynamics of dissipative soliton in an ultrafast fiber laser in the net-normal dispersion regime. The soliton buildup dynamics were analyzed in both the spectral and temporal domains. We firstly revealed that the appearing of the spectral sharp peaks with oscillation structures during the mode-locking transition is caused by the formation of structural dissipative soliton. The experimental results were explained by the numerical simulations. These findings would give some new insights into the dissipative soliton buildup dynamics in ultrafast fiber lasers.
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