Optimizing graphene content in scaffolds for evenly distributed crumpled MoS2paper wads as anodes for high-performance Li-ion batteries.

Lithium-ion batteries (LIBs) have revolutionized portable electronics, yet their conventional graphite anodes face capacity limitations. Integrating graphene and 3D molybdenum disulfide (MoS2) offers a promising solution. Ensuring a uniform distribution of 3D MoS2nanostructures within a graphene matrix is crucial for optimizing battery performance and preventing issues like agglomeration and capacity degradation. This study focuses on synthesizing a uniformly distributed paper wad structure by optimizing a composite of reduced graphene oxide RGO@MoS2through structural and morphological analyses. Three composites with varying graphene content were synthesized, revealing that the optimized sample containing 30 mg RGO demonstrates beneficial synergy between MoS2and RGO. The interconnected RGO network enhances reactivity and conductivity, addressing MoS2aggregation. Experimental results exhibit an initially superior capacity of 911 mAh g-1, retained at 851 mAh g-1even after 100 cycles at 0.1 A g-1current density, showcasing improved rate efficiency and long-term stability. This research underscores the pivotal role of graphene content in customizing RGO@MoS2composites for enhanced LIB performance.

Reversible synthesis of GO: Role of differential bond structure transformation in fine-tuning photodetector response.

The controlled modification of graphene's electronic band structure poses serious challenges. In the present work, we study the effect of sp 2 cluster size variation on the electronic band gap and photoconductive properties of reduced graphene oxide (RGO). This is achieved by performing reversible functionalization of RGO with oxygen species. The reversible functionalization of RGO results in its partial transformation to graphene oxide (GO) so that the size of the sp 2 clusters within the sp 3 matrix varies, thereby affecting the π-π* band structure and photoconductive properties. The study reveals: (1) incremental creation/elimination of oxygenated surface bonds' related energy states within the π-π* band; (2) customized tuning of the sp 2/sp 3 ratio; (3) the presence/absence of oxygenated states impacts the optical transition processes both from band-to-band and oxygenated states; and (4) the incremental addition/depletion of surface states in a tunable manner directly influences the carrier transport in the photoconductive device. Experiments show a two-stage transformation of RGO electronic properties with changing oxygen functionalities: oxidation (Stage I) and decomposition or erosion (Stage II). Sp 2 cluster size variation induced bandgap change was analyzed by Raman and photoluminescence studies, indicating the possibility for photodetection in a specific band encompassing NIR to UV, depending on the sp 2/sp 3 ratio. Energy-dispersive x-ray spectroscopy and Fourier transform infrared studies confirm the surface oxygenation/de-oxygenation during plasma treatment, and XRD confirms partial transformation of RGO to GO and its amorphization at higher plasma exposure times. In addition, the photodetector performance is optimized in terms of carrier generation-recombination and carrier-lattice scattering. Thus, manipulating better photoconductive response is possible through suitable handling of the parameters involved in the plasma treatment process. This is the first study on the influence of the sp 2/sp 3 ratio-induced lattice structure evolution on photodetection.

New lithium metal polymer solid state battery for an ultrahigh energy: nano C-LiFePO4 versus nano Li1.2V3O8.

Novel lithium metal polymer solid state batteries with nano C-LiFePO4 and nano Li1.2V3O8 counter-electrodes (average particle size 200 nm) were studied for the first time by in situ SEM and impedance during cycling. The kinetics of Li-motion during cycling is analyzed self-consistently together with the electrochemical properties. We show that the cycling life of the nano Li1.2V3O8 is limited by the dissolution of the vanadium in the electrolyte, which explains the choice of nano C-LiFePO4 (1300 cycles at 100% DOD): with this olivine, no dissolution is observed. In combination with lithium metal, at high loading and with a stable SEI an ultrahigh energy density battery was thus newly developed in our laboratory.

WS2 Quantum Dots on e-Textile as a Wearable UV Photodetector: How Well Reduced Graphene Oxide Can Serve as a Carrier Transport Medium?

We document the fabrication and investigations of a novel photodetector based on a WS2 quantum dots and reduced graphene oxide (RGO) (WS2-QDs/RGO) heterostructure. The proposed photodetector is simple, scalable, cost-effective, and flexible and works in an ambient environment. An enhanced photodetection efficiency is observed due to the superior electronic properties of WS2-QDs and excellent electrical as well as thermal properties of the carrier transportation medium, RGO. For device fabrication, GO and WS2-QDs were separately synthesized via different chemistry followed by decorating WS2-QDs on RGO coated cotton textile. Characterization studies confirm the transformation of exfoliated WS2-2D flakes into WS2-0D quantum dots and graphene oxide (GO) to RGO. The optimized photodetection performance of WS2-QDs/RGO demonstrates its photoresponsivity of 5.22 mA W-1 at 1.4 mW mm-2 power density of a 405 nm illumination source. Other sensor parameters such as photosensitivity (∼20.2%), resolution (∼0.031 mW mm-2 µA-1), response time (1.57 s), recovery time (1.83 s), and specific detectivity (∼1.6 × 106 jones) are found for WS2-QDs/RGO sensor, and a few of these parameters are comparable and even superior to some of the devices as reported. Photosensing mechanism is explained in terms of charge transfer caused by appropriate band alignment across the interface between WS2-QDs and RGO, where dimensionality and quantum confinement of nanostructures synergistically enhance the overall performance of the heterostructure. The device flexibility is examined through bending, stretching, and twisting experiments and successfully demonstrated its potentiality. Sensor performance even after being soaked in water and subsequent drying shows the possibility of reuse. The attributes of flexibility, high sensitivity and responsivity, superior resolution, and cost-effectiveness of our novel flexible photodetector indicate its promising potential for flexible and wearable optical detectors operating in UV band. Although negative photoconductance of the WS2-QDs/RGO sensor is a major cause for not allowing the sensor to show its best performance, a trade-off is made with improved device design to qualify the expectations of being a competitive device, and this has been demonstrated with experimental facts.

Li2TiO3/Ni foam composite as high-performance electrode for energy storage and conversion.

Li2TiO3/Ni foam composites were prepared by a solid-state reaction process. They crystallized in the monoclinic Li2TiO3 structure with C2/c space group. SEM images show that the Li2TiO3 particles are monodispersed crystallites of average size 49 nm, infused into porous scaffold Ni foam. As an anode in lithium battery, the composite delivered a discharge capacity of 153 mAh g-1 in an aqueous electrolyte and retained 95% of its initial capacity after 30 cycles. Moreover, the Li2TiO3/Ni foam composite as a negative electrode of pseudo-supercapacitor delivered a specific capacitance of 593 F g-1 and retained 95% of its initial capacitance after 1000 cycles. The enhanced capacity of Li2TiO3/Ni composite is due to porous scaffold Ni foam, which provides high conductivity to the Li2TiO3 particles and high effective surface area for redox reactions. The performance of the Li2TiO3/Ni foam as an electrode material for both lithium-ion batteries (LIBs) and supercapacitors (SCs) shows that this composite is promising for energy storage devices.

Oxidation and metal-insertion in molybdenite surfaces: evaluation of charge-transfer mechanisms and dynamics.

Molybdenum disulfide (MoS2), a layered transition-metal dichalcogenide, has been of special importance to the research community of geochemistry, materials and environmental chemistry, and geotechnical engineering. Understanding the oxidation behavior and charge-transfer mechanisms in MoS2 is important to gain better insight into the degradation of this mineral in the environment. In addition, understanding the insertion of metals into molybdenite and evaluation of charge-transfer mechanism and dynamics is important to utilize these minerals in technological applications. Furthermore, a detailed investigation of thermal oxidation behavior and metal-insertion will provide a basis to further explore and model the mechanism of adsorption of metal ions onto geomedia.The present work was performed to understand thermal oxidation and metal-insertion processes of molybdenite surfaces. The analysis was performed using atomic force microscopy (AFM), scanning electron microscopy (SEM), transmission electron microscopy (TEM), Rutherford backscattering spectrometry (RBS), and nuclear reaction analysis (NRA).Structural studies using SEM and TEM indicate the local-disordering of the structure as a result of charge-transfer process between the inserted lithium and the molybdenite layer. Selected area electron diffraction measurements indicate the large variations in the diffusivity of lithium confirming that the charge-transfer is different along and perpendicular to the layers in molybdenite. Thermal heating of molybenite surface in air at 400 degrees C induces surface oxidation, which is slow during the first hour of heating and then increases significantly. The SEM results indicate that the crystals formed on the molybdenite surface as a result of thermal oxidation exhibit regular thin-elongated shape. The average size and density of the crystals on the surface is dependent on the time of annealing; smaller size and high density during the first one-hour and significant increase in size associated with a decrease in density with further annealing.

Structural stability and phase transitions in WO3 thin films.

Tungsten oxide (WO3) thin films have been produced by KrF excimer laser (lambda = 248 nm) ablation of bulk ceramic WO3 targets. The crystal structure, surface morphology, chemical composition, and structural stability of the WO3 thin films have been studied in detail. Characterization of freshly grown WO3 thin films has been performed using X-ray diffraction (XRD), atomic force microscopy (AFM), energy-dispersive X-ray spectroscopy (EDX), Raman spectroscopy (RS), transmission electron microscopy (TEM), and selected area electron diffraction (SAED) measurements. The results indicate that the freshly grown WO3 thin films are nearly stoichiometric and well crystallized as monoclinic WO3. The surface morphology of the resulting WO3 thin film has grains of approximately 60 nm in size with a root-mean-square (rms) surface roughness of 10 nm. The phase transformations in the WO3 thin films were investigated by annealing in the TEM column at 30-500 degrees C. The phase transitions in the WO3 thin films occur in sequence as the temperature is increased: monoclinic --> orthorhombic --> hexagonal. Distortion and tilting of the WO6 octahedra occurs with the phase transitions and significantly affects the electronic properties and, hence, the electrochemical device applications of WO3.

FTIR features of lithium-iron phosphates as electrode materials for rechargeable lithium batteries.

The essential structural features of lithium-metal phosphates (LMP) have been studied using FTIR spectroscopy which is a sensitive tool to probe the local environment in the solid materials. Various LMP materials where M is iron have been investigated including phospho-olivine LiFePO(4), diphosphate LiFeP(2)O(7), Nasicon-type phosphate Li(3)Fe(2)(PO(4))(3) and dihydrate FePO(4).2H(2)O. Vitreous and amorphous materials are also considered. Analysis of internal and external modes of vibration allows to distinguish between the different phases and the type of cationic environment in the framework. Results corroborate the contribution of the main factors which are responsible for the complexity of the spectra, i.e. departure from ideal symmetry, interactions between polyhedra, bridging atoms and lattice distortion.

Lattice vibrations of manganese oxides. Part I. Periodic structures.

Raman scattering (RS) and Fourier transform-infrared (FT-IR) spectroscopy have been applied to the structural characterisation of manganese dioxides (MDOs). A variety of synthetic battery-grade MDOs are investigated for comparison to the natural phases. The RS and FT-IR spectra are analysed on the basis of the local environment in the MDO structures considering the vibrations of the MnO6 octahedral building the lattices. The vibrational modes of the MnO6 units expand over 400-650 cm(-l) with additional bands in the low-wavelength region. Structural trends are deduced from the comparison of the vibrational spectra of the MDO phases investigated: birnessite, bixbyite, coronadite, groutite, hausmannite, hollandite, manganosite, pyrolusite, ramsdellite, romanechite, spinel, and todorokite.