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      Morphology control of nickel oxalate by soft chemistry and conversion to nickel oxide for application in photocatalysis

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          Chemistry and properties of nanocrystals of different shapes.

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            Nano-sized transition-metal oxides as negative-electrode materials for lithium-ion batteries.

            Rechargeable solid-state batteries have long been considered an attractive power source for a wide variety of applications, and in particular, lithium-ion batteries are emerging as the technology of choice for portable electronics. One of the main challenges in the design of these batteries is to ensure that the electrodes maintain their integrity over many discharge-recharge cycles. Although promising electrode systems have recently been proposed, their lifespans are limited by Li-alloying agglomeration or the growth of passivation layers, which prevent the fully reversible insertion of Li ions into the negative electrodes. Here we report that electrodes made of nanoparticles of transition-metal oxides (MO, where M is Co, Ni, Cu or Fe) demonstrate electrochemical capacities of 700 mA h g(-1), with 100% capacity retention for up to 100 cycles and high recharging rates. The mechanism of Li reactivity differs from the classical Li insertion/deinsertion or Li-alloying processes, and involves the formation and decomposition of Li2O, accompanying the reduction and oxidation of metal nanoparticles (in the range 1-5 nanometres) respectively. We expect that the use of transition-metal nanoparticles to enhance surface electrochemical reactivity will lead to further improvements in the performance of lithium-ion batteries.
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              Environmental effects on vibronic band intensities in pyrene monomer fluorescence and their application in studies of micellar systems

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                Author and article information

                Journal
                RSCACL
                RSC Advances
                RSC Adv.
                Royal Society of Chemistry (RSC)
                2046-2069
                2013
                2013
                : 3
                : 17
                : 6106
                Article
                10.1039/c3ra21978j
                1ee053dd-3bc8-45ea-85dd-ccbbdfa5bf1d
                © 2013
                History

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