Analysed current trends in development of garnet-type structured Li7La3Zr2O12-based oxides as solid electrolytes for next-generation all-solid-state lithium batteries.
Highly fluorescent crystalline carbon nanoparticles (CNPs) have been synthesized by one step microwave irradiation of sucrose with phosphoric acid at 100 W for 3 min 40 s. This method is very simple, rapid and economical and hence can be used for large scale applications. The average particle sizes are 3 to 10 nm and they emit bright green fluorescence under the irradiation of UV-light. Therefore, the particles can be used as a unique material for bioimaging as well as drug delivery. To further increase the fluorescence property of the synthetic carbon nanoparticles we simply functionalized them by using different organic dyes, such as fluorescein, rhodamine B and α-naphthylamine; the maximum fluorescence intensity was observed for the particles functionalized with fluorescein. It is very interesting to note that all of those compounds show maximum fluorescence intensity at 225 nm excitation wavelength and for any excitation wavelength the peak positions are exactly same the position as that of CNPs itself, which is completely different from the individual precursors (dyes). All of the above compounds, including CNPs, have also been successfully introduced into the erythrocyte enriched fraction of healthy human blood cells with minimum cytotoxicity.
Development of efficient electrocatalyst based on non-precious metal that favors the four-electron pathway for the reduction of oxygen in alkaline fuel cell is a challenging task. Herein, we demonstrate a new facile route for the synthesis of hybrid functional electrocatalyst based on nitrogen-doped reduced graphene oxide (N-rGO) and Mn3O4 with pronounced electrocatalytic activity towards oxygen reduction reaction (ORR) in alkaline solution. The synthesis involves one-step in situ reduction of both graphene oxide (GO) and Mn(VII), growth of Mn3O4 nanocrystals and nitrogen doping onto the carbon framework using a single reducing agent, hydrazine. The X-ray photoelectron (XPS), Raman and FTIR spectral, and X-ray diffraction measurements confirm the reduction of GO and growth of nanosized Mn3O4. The XPS profile reveals that N-rGO has pyridinic (40%), pyrrolic (53%), and pyridine N oxide (7%) types of nitrogen. The Mn3O4 nanoparticles are single crystalline and randomly distributed over the wrinkled N-rGO sheets. The hybrid material has excellent ORR activity and it favors the 4-electron pathway for the reduction of oxygen. The electrocatalytic performance of the hybrid catalyst is superior to the N-rGO, free Mn3O4 and their physical mixture. The hybrid material shows an onset potential of -0.075 V, which is 60-225 mV less negative than that of the other catalyst tested. It has excellent methanol tolerance and high durability. The catalytic current density achieved with the hybrid material at 0.1 mg cm(-2) is almost equivalent to that of the commercial Pt/C (10%). The synergistic effect of N-rGO and Mn3O4 enhances the overall performance of the hybrid catalyst. The nitrogen in N-rGO is considered to be at the interface to bridge the rGO framework and Mn3O4 nanoparticles and facilitates the electron transfer.
Following
the prevalence of the Li-ion battery for electrical energy
storage systems (EESs), the world is looking toward alternative, cost-effective,
electrical EESs for portable electronics, electric vehicles, and grid
storage from renewable sources. Na-based batteries are the most promising
candidates and show similar chemistry as Li-based batteries. All-solid-state
sodium batteries (AS3Bs) have attracted great attention
due to safe operation, high energy density, and wide operational temperature.
Herein, current development of solid-state crystalline borate- and
chalcogenide-based Na-ion conductors is discussed together with historically
important Na-β-alumina and Na superionic conductors (NASICONs).
Furthermore, we report on engineering a ceramic Na-ion electrolyte
and electrode interface, which is considered a bottleneck for practical
applications of solid-state electrolytes in AS3Bs. A soft
Na-ion conducting interlayer is critical to suppress the interfacial
Na-ion charge transfer resistance between the solid electrolyte and
electrode. Several Na-ion conducting ionic liquids, polymers, gels,
crystalline plastics interlayers, and other interfacial modification
strategies have been effectively employed in advanced AS3Bs.
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