ABSTRACT
Valeriana jatamansi Jones is a commonly used traditional Chinese medicine, boasting rich effective compositions with versatile chemical structures and wide polarity, including iridoids, chlorogenic acid, and flavonoids. Previous reports indicate that conventional high-performance liquid chromatography (HPLC) analytical methods have proven inefficient performance in comprehensively characterizing components in Valeriana jatamansi. In the present study, a hybrid online analytical platform combining supercritical fluid extraction with both conventional HPLC separation (reverse phase) and supercritical fluid chromatography (normal phase) has been established and validated. This system can provide online extraction with two different chromatographic separation modes to increase separation ability and has been connected to a mass spectrometer to acquire high-resolution mass spectrometry data. Then, the online platform was applied to screening components in Valeriana jatamansi. A total of 117 compounds were identified, including five lignans, 18 organic acids, six flavonoids, and 88 iridoids. Thirty-three compounds were reported from Valeriana jatamansi for the first time. These results enrich our understanding of the components of Valeriana jatamansi and prove that the developed online platform in this study is a robust approach for accelerating working efficiency in comprehensively analyzing complicated samples.
Subject(s)
Chromatography, Supercritical Fluid , Valerian , Valerian/chemistry , Chromatography, High Pressure Liquid , Mass Spectrometry , Iridoids/analysis , Flavonoids/analysisABSTRACT
Reaction kinetics can be improved by the enhanced electrical contact between different components growing symbiotically. But so far, due to the necessity for material synthesis conditions match, the component structures of cooperative growth are similar, and the materials are of the same type. The collaborative growth of high-reaction kinetics composite homogeneous core-shell heterostructure between various materials is innovatively proposed with different structures in one step. The NiCo-LDH and PPy successfully symbiotically grow on activated carbon fiber fabric in one step. The open channel structure of the NiCo-LDH nanosheets is preserved while PPy effectively wrapped around the NiCo-LDH. The well-defined nanostructure with abundant active sites and convenient ion diffusion paths is favorable for electrolyte entry into the entire nanoarrays. In addition, owing to the enhanced electronic interaction between different components through XPS analysis, the NiCo-LDH@PPy electrode shows outstanding reaction kinetics and structural stability. The as-synthesized NiCo-LDH@PPy exhibited excellent super-capacitive storage capabilities, robust capacitive activity, and good rate survival. Furthermore, an asymmetric supercapacitor (ASC) device made of NiCo-LDH@PPy and activated carbon (AC) is able to maintain a long cycle life while achieving high power and energy densities.
ABSTRACT
Cobalt tetraoxide (Co3O4) is regarded as a promising anode material for Li-ion batteries owing to its high theoretical capacity (890 mAh g-1), simple preparation, and controllable morphology. Nanoengineering has been proven to be an effective method for producing high-performance electrode materials. However, systematic research on the influence of material dimensionality on battery performance is lacking. Herein, we prepared Co3O4 with various dimensionalities (one-dimensional (1D) Co3O4 nanorod (NR), two-dimensional (2D) Co3O4 nanosheet (NS), three-dimensional (3D) Co3O4 nanocluster (NC), and 3D Co3O4 nanoflower (NF)) using a simple solvothermal heat treatment method, and their morphologies were controlled by varying the precipitator type and solvent composition. The 1D Co3O4 NR and 3D samples (3D Co3O4 NC and 3D Co3O4 NF) exhibited poor cyclic and rate performances, respectively, while the 2D Co3O4 NS exhibited the best electrochemical performance. The mechanism analysis revealed that the cyclic stability and rate performance of the Co3O4 nanostructures are closely related to their intrinsic stability and interfacial contact performance, respectively, and the 2D thin-sheet structure can achieve an optimal balance between the two, resulting in the best performance. This work presents a comprehensive study on the effect of dimensionality on the electrochemical performance of Co3O4 anodes, providing a new concept for the nanostructure design of conversion-type materials.
ABSTRACT
Nano-sized two-dimensional carbonaceous materials have been widely used as the matrix for alloying-type and conversion-type anode materials for Li-ion batteries (LIBs) to improve structural stability and rate performance. However, relevant synthesis usually requires rigorous conditions and chronic reaction processes. Herein, we have designed a simple solvothermal reaction and heat treatment to prepare a novel CoO/Co/C two-dimensional nanosheet (CoO/Co/C 2DNS) by adopting cellulose nanofibers (CNFs) as the precursor. The unique characteristics of CNFs facilitate the uniform distribution of active materials on the surface and the construction of two-dimensional nanostructure via self-assembly. It is worth noting that CoO/Co/C 2DNS exhibits a striking synergistic effect since the porous 2D carbon framework offers additional pseudo-capacitance and enhances the electronic conductivity, while the ultrafine active materials encapsulated inside shorten the Li-ions diffusion pathways and relieve the volume change. Benefit from the unique structure, the composite anode delivered outstanding rate performance (â¼500 mAh g-1 at 10 A g-1) and superior long-range cycling performance up to 800 cycles even at 2 A g-1. This work provides a new strategy for the synthesis of nano-sized 2D composite, offering a promising route to construct high performance conversion-type anodes for next-generation LIBs.
Subject(s)
Lithium , Nanofibers , Cellulose , Electric Power Supplies , ElectrodesABSTRACT
Time of flight and photometric stereo are two three-dimensional (3D) imaging techniques with complementary properties, where the former can achieve depth accuracy in discontinuous scenes, and the latter can reconstruct surfaces of objects with fine depth details and high spatial resolution. In this work, we demonstrate the surface reconstruction of complex 3D fields with discontinuity between objects by combining the two imaging methods. Using commercial LEDs, a single-photon avalanche diode camera, and a mobile phone device, high resolution of surface reconstruction is achieved with a RMS error of 6% for an object auto-selected from a scene imaged at a distance of 50 cm.
ABSTRACT
Multispectral and 3-D imaging are useful for a wide variety of applications, adding valuable spectral and depth information for image analysis. Single-photon avalanche diode (SPAD) based imaging systems provide photon time-of-arrival information, and can be used for imaging with time-correlated single photon counting techniques. Here we demonstrate an LED based synchronised illumination system, where temporally structured light can be used to relate time-of-arrival to specific wavelengths, thus recovering reflectance information. Cross-correlation of the received multi-peak histogram with a reference measurement yields a time delay, allowing depth information to be determined with cm-scale resolution despite the long sequence of relatively wide (â¼10 ns) pulses. Using commercial LEDs and a SPAD imaging array, multispectral 3-D imaging is demonstrated across 9 visible wavelength bands.