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The water catalysis at oxygen cathodes of lithium–oxygen cells

机译:锂氧电池氧阴极上的水催化

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摘要

Lithium–oxygen cells have attracted extensive interests due to their high theoretical energy densities. The main challenges are the low round-trip efficiency and cycling instability over long time. However, even in the state-of-the-art lithium–oxygen cells the charge potentials are as high as 3.5 V that are higher by 0.70 V than the discharge potentials. Here we report a reaction mechanism at an oxygen cathode, ruthenium and manganese dioxide nanoparticles supported on carbon black Super P by applying a trace amount of water in electrolytes to catalyse the cathode reactions of lithium–oxygen cells during discharge and charge. This can significantly reduce the charge overpotential to 0.21 V, and results in a small discharge/charge potential gap of 0.32 V and superior cycling stability of 200 cycles. The overall reaction scheme will alleviate side reactions involving carbon and electrolytes, and shed light on the construction of practical, rechargeable lithium–oxygen cells.
机译:锂氧电池由于其较高的理论能量密度而引起了广泛的兴趣。主要挑战是长期往返效率低和自行车不稳定。但是,即使在最先进的锂氧电池中,充电电位也高达3.5 V,比放电电位高0.70 0.7V。在这里,我们报告了在炭黑Super P上负载的氧阴极,钌和二氧化锰纳米颗粒上的反应机理,方法是在电解质中施加微量水以催化锂氧电池在放电和充电过程中的阴极反应。这样可以将电荷超电势大大降低至0.21 V,并导致0.32 V的小放电/充电电势差和200个循环的出色循环稳定性。总体反应方案将减轻涉及碳和电解质的副反应,并为实用的可充电锂氧电池的构造提供启示。

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